Cannabis, heart disease, and a soy-derived supplement that may help – Medical News Today

Researchers are still learning about the health impacts of cannabis. Derivatives of cannabis may have many health benefits. However, researchers are still learning how to balance these positives with potential health risks.

A recent study published in the journal Cell examined the adverse cardiovascular effects of cannabis and found a particular impact on cardiovascular health.

However, the researchers also found that the compound genistein may help decrease these harmful effects.

Cannabis use is becoming increasingly popular, especially for recreational purposes. But researchers are still seeking to discover the full medicinal benefits of cannabis.

The U.S. Centers for Disease Control and Prevention notes that tetrahydrocannabinol (THC) is the compound in cannabis that produces mind alterations and impaired mental functioning. Specifically, the main compound that causes these effects is delta-9-tetrahydrocannabinol (delta-9-THC). In contrast, the cannabidiol (CBD) compound of cannabis doesnt cause this sort of impairment.

Currently, the U.S. Food and Drug Administration (FDA) has approved the use of Epidiolex, which contains CBD. People can use this drug as a seizure treatment. The FDA has also approved the use of two medications with synthetic THC: Marinol and Syndros. Both of these medications can control nausea and stimulate appetite.

However, in addition to the benefits, cannabis has also been linked to health risks. One particular area of interest is the potential association between cannabis and cardiovascular problems.

When asked to comment, Paul Armentano, deputy director for the National Organization for the Reform of Marijuana Laws (NORML), noted that many studies have yielded inconsistent results regarding the impact of cannabis on cardiovascular health. He explained to Medical News Today:

Population-based studies evaluating the potential link between cannabis exposure and cardiovascular risks have, historically, yielded notoriously inconsistent resultsNonetheless, because of the lack of consistent data, NORML has long urged caution with respect to cannabis exposure among those with a history of heart disease or other cardiovascular issues, among other potentially higher-risk populations.

Therefore, more research is needed in this area.

The study in question sought to explore this link. Researchers first examined the association between cannabis use and heart attacks using the U.K. Biobank, the largest prospective cohort study to date, containing genetic and phenotypic data on 500,000 individuals ages 40-69.

Based on the evaluation of this data, cannabis use was associated with a higher risk for heart attack.

The researchers also recruited participants who smoked cannabis recreationally. They found that these participants had higher levels of inflammatory cytokines after smoking a cannabis cigarette, indicating a greater risk for atherosclerosis.

Next, the study authors examined the impact of delta-9-THC on endothelial cells, which are the cells that make up the cardiovascular system. They found that delta-9-THC caused oxidative stress and inflammation, both of which cause harm to the cardiovascular system.

In mice models, they also discovered that delta-9-THC caused vascular dysfunction. Their research indicates that delta-9-THC could damage the cardiovascular system.

To counteract these effects, the researchers tested the compound genistein derived from soybeans. They found that it helped reduce the impact of inflammation and oxidative stress on the cardiovascular system.

They further discovered that genistein helped lessen the severity of atherosclerosis in mouse models.

Dr. Joseph Wu, professor of cardiovascular medicine and of radiology, and the director of the Stanford Cardiovascular Institute, gave the studys highlights to MNT:

Our study shows that marijuana (cannabis) is linked to cardiovascular disease based on the U.K. biobank, stem cell-derived vascular cells, and mouse models. Using machine learning, we also discover a naturally occurring soybean derivative, genistein, that we can be used to block the bad effects of marijuana on the cardiovascular system. Dr. Joseph Wu

The study had several limitations. Firstly, the researchers could not show a causal relationship between cannabis use and heart attacks. They acknowledge the potential for flaws in the data from the U.K. Biobank cohort.

The study also used mice models, so caution must be exercised when applying any results to people.

Armentano also said that the study may fall short in terms of consistency of research in the area.

This latest paper is simply the latest in a long line of inconsistent results results that likely vary based on how well investigators do or do not control for potential confounding variables and behaviors among subjects.

However, he pointed out that the researchers theory, based on results from their mice studies, was that it could be due to cannabinoids triggering inflammation of the blood vessels and thus atherosclerosis is inconsistent with human observational studies.

Nevertheless, the results indicated that genistein could help mitigate the potentially harmful effects of cannabis while maintaining some of its beneficial effects.

Study authors wrote that [g]enistein, a soybean isoflavone, blocks harmful cardiovascular effects of [delta-9-THC] while reserving clinically useful effects such as sedation and analgesia.

Study author Joseph Wu further elaborated to MNT about the direction of further research in this area:

While we have shown that genistein can block the adverse effects of marijuana on the cardiovascular system using preclinical models, we need to do a randomized clinical trial to test its safety and effectiveness in humans.

Genistein might also be a new lead compound that will lead to the development of new drugs that can treat cardiovascular disease, Wu added.

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Cannabis, heart disease, and a soy-derived supplement that may help - Medical News Today

Global Human Embryonic Stem Cell Market To Be Driven By The Rapid Technological Advancements In The Forecast Period Of 2022-2027 – Digital Journal

The new report by Expert Market Research titled, GlobalHuman Embryonic Stem Cell MarketReport and Forecast 2022-2027, gives an in-depth analysis of the global human embryonic stem cell market, assessing the market based on its segments like applications and major regions. The report tracks the latest trends in the industry and studies their impact on the overall market. It also assesses the market dynamics, covering the key demand and price indicators, along with analysing the market based on the SWOT and Porters Five Forces models.

Get a Free Sample Report with Table of Contents:https://www.expertmarketresearch.com/reports/human-embryonic-stem-cell-market/requestsample

The key highlights of the report include:

Market Overview (2017-2027)

Historical Market Size (2020): USD 0.7 billion Forecast CAGR (2022-2027): 10%

The human embryonic stem cell market is being driven by the thriving medical sector. The rising demand for embryonic stem cells can be attributed to the increasing prevalence of chronic diseases around the world owing to the rising adoption of unhealthy and sedentary lifestyle among the youth and middle-class population. The increased risk of premature death as a result of chronic diseases is a growing concern. Therefore, human embryonic stem cells are gaining popularity in the medical sector. Furthermore, the increase in research grants and private as well as public funding for the development of effective and safe stem cell therapy products is further aiding the market growth. The rising investments from key players towards enhancing human embryonic cell therapy is expected to aid the market growth in the forecast period. In post-COVID days, as the various sectors recover from the negative impacts of the pandemic, human embryonic stem cells are likely to witness a rise in demand.

Industry Definition and Major Segments

Human embryonic stem cells, also known as human embryonic stem cells are self-replicating cells derived from human fetal tissue or human embryos that develop into tissues and cells of 3 primary layers. Furthermore, human embryonic stem cells are pluripotent and are roughly 3-5 days old. It is highly versatile, as it may split into new stem cells and even transform into any type of cell in the human body, allowing it to regenerate or repair any diseased organ or tissue.

Read Full Report with Table of Contents:https://www.expertmarketresearch.com/reports/human-embryonic-stem-cell-market

The human embryonic stem cell market, on the basis of application, can be segmented into:

Regenerative Medicine Stem Cell Biology Research Tissue Engineering Toxicology Testing

The regional markets for human embryonic stem cell include:

North America Europe Asia Pacific Latin America Middle East and Africa

Among these, North America represents a significant share of the human embryonic stem cell market.

Market Trends

The rising population along with the rapidly evolving medical infrastructure of emerging economies like India and China is expected to provide an impetus to the human embryonic stem cell market. Furthermore, technological advancements and increasing research and development investments and initiatives are expected to generate opportunities in the market. Researchers and scientists are increasingly leaning toward the transformation of human embryonic stem cells into a number of mature cell types that represent various tissues and organs in the body, as embryonic cells provide unequalled data relating to a variety of disorders. The increasing efforts by the governments of various nations towards enhancing human embryonic stem cell therapy is likely to be another key trend bolstering the market growth in the forecast period.

Key Market Players

The major players in the market Astellas Pharma Inc, Stemcell Technologies Inc., Biotime INC, Thermo Fisher Scientific, Inc., among others. The report covers the market shares, capacities, plant turnarounds, expansions, investments and mergers and acquisitions, among other latest developments of these market players.

About Us:

Expert Market Research (EMR) is a leading market research and business intelligence company, ensuring its clients remain at the vanguard of their industries by providing them with exhaustive and actionable market data through its syndicated and custom market reports, covering over 15 major industry domains. The companys expansive and ever-growing database of reports, which are constantly updated, includes reports from industry verticals like chemicals and materials, food and beverages, energy and mining, technology and media, consumer goods, pharmaceuticals, agriculture, and packaging.

EMR leverages its state-of-the-art technological and analytical tools, along with the expertise of its highly skilled team of over 100 analysts and more than 3000 consultants, to help its clients, ranging from Fortune 1,000 companies to small and medium-sized enterprises, easily grasp the expansive industry data and help them in formulating market and business strategies, which ensure that they remain ahead of the curve.

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Global Human Embryonic Stem Cell Market To Be Driven By The Rapid Technological Advancements In The Forecast Period Of 2022-2027 - Digital Journal

Stem Cells Market by Type (Umbilical Cord Blood Stem Cell, Embryonic Stem Cell, Adult Stem Cell, Other), Application (Diseases Therapy, Healthcare),…

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Dhirtek Business Research and Consulting most recent study on the stem cells market provides a comprehensive view of the entire market. The research report delves deeply into the global stem cells markets drivers and restraints. Analysts have extensively researched the global stem cells markets milestones and the current trends that are expected to determine its future. Primary and secondary research methods were used to create an in-depth report on the topic. Analysts have provided clients with unbiased perspectives on the global stem cells industry to assist them in making well-informed business decisions.

The comprehensive research study employs Porters five forces analysis and SWOT analysis to provide readers with a clear picture of the global stem cells markets expected direction. The SWOT analysis focuses on defining the global stem cells markets strengths, weaknesses, opportunities, and threats, whereas Porters five forces analysis emphasizes competitive competition. The research report goes into great detail about the trends and consumer behavior patterns expected to shape the global stem cells markets evolution.

Request a Sample of this Report at: https://www.dhirtekbusinessresearch.com/market-report/Stem-Cells-Market/request-for-sample-report

The global stem cells market research studys type, application, and region components are divided into three parts. Each segmentation is divided into chapters that go over the various details. The chapters include graphs that show year-over-year growth and segment-specific drivers and constraints. Furthermore, the study provides government forecasts for regional markets that affect the global stem cells sector.

Stem Cells Market Segments

Regions Covered in the Global Stem Cells Market:

In the report on the stem cells market, a detailed chapter on company profiles is included. The leading players in the global stem cells market are examined in this chapter. It contains a synopsis of the companys strategic goals and a description of its primary goods and services. An overall analysis of the organizations strategic initiatives reveals the trends that they are expected to pursue and their R&D statuses and financial outlooks. This research aims to provide readers with a thorough understanding of the global stem cells markets anticipated trajectory.

The following Companies as the Key Players in the Global Stem Cells Market Research Report:

Beikebiotech, Boyalife, CCBC, Vcanbio

Dhirtek Business Research and Consulting conducted this study using primary and secondary sources. As primary sources, industry experts from core and adjacent industries and those involved in the market. All primary sources were interviewed to obtain and verify critical qualitative and quantitative data and gain access to prospects. Secondary sources include directories, white papers, blogs, and databases.

The market size for stem cells was estimated and validated using a top-down approach. Secondary research was conducted to identify key players in the industrial value chain, and primary and secondary research was conducted to determine these companies market revenues. This includes analyzing yearly business and financial reports from major industry players and conducting in-depth interviews with CEOs, directors, vice presidents, and marketing executives.

Secondary sources were used to gather geographic market estimates, which were then cross-checked with primary sources. Variables such as key players, sales partners, and distribution networks have an impact on them. The investigation also looks into the scope of each areas research efforts. The total market size for stem cells was computed and validated using revenue and revenue share data from market businesses. The market size of each category was calculated using a top-down approach based on the total market size.

This study provides critical information on the global markets current size and projected growth for stem cells and its related industries. It also discusses geographys market characteristics, significant suppliers, consumer preference trends, and market prospects. As many countries are in a recession, firms are attempting to weather the storm by limiting unanticipated losses and spending related to the stem cells market.

Introduction

Market Overview

Market Segmentation

Regional Analysis

Competitive Analysis

Company Profiles

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Dhirtek Business Research & Consulting Pvt Ltd is a global market research and consulting services provider headquartered in India. We offer our customers syndicated research reports, customized research reports, and consulting services. Our objective is to enable our clientele to achieve transformational progress and help them to make better strategic business decisions and enhance their global presence.

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Stem Cells Market by Type (Umbilical Cord Blood Stem Cell, Embryonic Stem Cell, Adult Stem Cell, Other), Application (Diseases Therapy, Healthcare),...

Why haven’t we cloned a human yet? – Livescience.com

In 1996, Dolly the sheep made headlines around the world after becoming the first mammal to be successfully cloned from an adult cell. Many commentators thought this would catalyze a golden age of cloning, with numerous voices speculating that the first human clone must surely be just a few years away.

Some people suggested that human clones could play a role in eradicating genetic diseases, while others considered that the cloning process could, eventually, eliminate birth defects (despite research by a group of French scientists in 1999 finding that cloning may actually increase the risk of birth defects).

There have been various claims all unfounded, it is important to add of successful human cloning progams since the success of Dolly. In 2002, Brigitte Boisselier, a French chemist and devout supporter of Ralism a UFO religion based on the idea that aliens created humanity claimed that she and a team of scientists had successfully delivered the first cloned human, whom she named Eve.

However, Boisselier was unwilling or indeed unable to provide any evidence, and so it is widely believed to be a hoax.

So why, almost 30 years on from Dolly, haven't humans been cloned yet? Is it primarily for ethical reasons, are there technological barriers, or is it simply not worth doing?

Related: What are the alternatives to animal testing?

"Cloning" is a broad term, given it can be used to describe a range of processes and approaches, but the aim is always to produce "genetically identical copies of a biological entity," according to the National Human Genome Research Institute (NHGRI).

Any attempted human cloning would most likely utilize "reproductive cloning" techniques an approach in which a "mature somatic cell," most probably a skin cell, would be used, according to NHGRI. The DNA extracted from this cell would be placed into the egg cell of a donor that has "had its own DNA-containing nucleus removed."

The egg would then begin to develop in a test tube before being "implanted into the womb of an adult female," according to NHGRI.

However, while scientists have cloned many mammals, including cattle, goats, rabbits and cats, humans have not made the list.

"I think there is no good reason to make [human] clones," Hank Greely, a professor of law and genetics at Stanford University who specializes in ethical, legal and social issues arising from advances in the biosciences, told Live Science in an email.

"Human cloning is a particularly dramatic action, and was one of the topics that helped launch American bioethics," Greely added.

The ethical concerns around human cloning are many and varied. According to Britannica, the potential issues encompass "psychological, social and physiological risks." These include the idea that cloning could lead to a "very high likelihood" of loss of life, as well as concerns around cloning being used by supporters of eugenics. Furthermore, according to Britannica, cloning could be deemed to violate "principles of human dignity, freedom and equality."

In addition, the cloning of mammals has historically resulted in extremely high rates of death and developmental abnormalities in the clones, Live Science previously reported.

Another core issue with human cloning is that, rather than creating a carbon copy of the original person, it would produce an individual with their own thoughts and opinions.

"We've all known clones identical twins are clones of each other and thus we all know that clones aren't the same person," Greely explained.

A human clone, Greely continued, would only have the same genetic makeup as someone else they would not share other things such as personality, morals or sense of humor: these would be unique to both parties.

People are, as we well know, far more than simply a product of their DNA. While it is possible to reproduce genetic material, it is not possible to exactly replicate living environments, create an identical upbringing, or have two people encounter the same life experiences.

So, if scientists were to clone a human, would there be any benefits, scientific or otherwise?

"There are none that we should be willing to consider," Greely said, emphasizing that the ethical concerns would be impossible to overlook.

However, if moral considerations were removed entirely from the equation, then "one theoretical benefit would be to create genetically identical humans for research purposes," Greely said, though he was keen to reaffirm his view that this should be thought of as "an ethical non-starter."

Greely also stated that, regardless of his own personal opinion, some of the potential benefits associated with cloning humans have, to a certain degree, been made redundant by other scientific developments.

"The idea of using cloned embryos for purposes other than making babies, for example producing human embryonic stem cells identical to a donor's cells, was widely discussed in the early 2000s," he said, but this line of research became irrelevant and has subsequently not been expanded upon post-2006, the year so-called induced pluripotent stem cells (iPSCs) were discovered. These are "adult" cells that have been reprogrammed to resemble cells in early development.

Shinya Yamanaka, a Japanese stem cell researcher and 2012 Nobel Prize winner, made the discovery when he "worked out how to return adult mouse cells to an embryonic-like state using just four genetic factors," according to an article in Nature. The following year, Yamanaka, alongside renowned American biologist James Thompson, managed to do the same with human cells.

When iPSCs are "reprogrammed back into an embryonic-like pluripotent state," they enable the "development of an unlimited source of any type of human cell needed for therapeutic purposes," according to the Center of Regenerative Medicine and Stem Cell Research at the University of California, Los Angeles.

Therefore, instead of using embryos, "we can effectively do the same thing with skin cells," Greely said.

This development in iPSC technology essentially rendered the concept of using cloned embryos both unnecessary and scientifically inferior.

Related: What is the most genetically diverse species?

Nowadays, iPSCs can be used for research in disease modeling, medicinal drug discovery and regenerative medicine, according to a 2015 paper published in the journal Frontiers in Cell and Developmental Biology.

Additionally, Greely also suggested that human cloning may simply no longer be a "sexy" area of scientific study, which could also explain why it has seen very little development in recent years.

He pointed out that human germline genome editing is now a more interesting topic in the public's mind, with many curious about the concept of creating "super babies," for example. Germline editing, or germline engineering, is a process, or series of processes, that create permanent changes to an individuals genome. These alterations, when introduced effectively, become heritable, meaning they will be handed down from parent to child.

Such editing is controversial and yet to be fully understood. In 2018, the Council of Europe Committee on Bioethics, which represents 47 European states, released a statement saying that "ethics and human rights must guide any use of genome editing technologies in human beings," adding that "the application of genome editing technologies to human embryos raises many ethical, social and safety issues, particularly from any modification of the human genome which could be passed on to future generations."

However, the council also noted that there is "strong support" for using such engineering and editing technologies to better understand "the causes of diseases and their future treatment," noting that they offer "considerable potential for research in this field and to improve human health."

George Church, a geneticist and molecular engineer at Harvard University, supports Greely's assertion that germline editing is likely to garner more scientific interest in the future, especially when compared with "conventional" cloning.

"Cloning-based germline editing is typically more precise, can involve more genes, and has more efficient delivery to all cells than somatic genome editing," he told Live Science.

However, Church was keen to urge caution, and admitted that such editing has not yet been mastered.

"Potential drawbacks to address include safety, efficacy and equitable access for all," he concluded.

Originally published on Live Science.

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Why haven't we cloned a human yet? - Livescience.com

Cell Isolation/Cell Separation Market Research Report by Product, Cell Type, Cell Source, Technique, Application, End User, Region – Global Forecast…

New York, May 06, 2022 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Cell Isolation/Cell Separation Market Research Report by Product, Cell Type, Cell Source, Technique, Application, End User, Region - Global Forecast to 2027 - Cumulative Impact of COVID-19" - https://www.reportlinker.com/p06260219/?utm_source=GNW

The Global Cell Isolation/Cell Separation Market size was estimated at USD 8,638.55 million in 2021 and expected to reach USD 9,976.06 million in 2022, and is projected to grow at a CAGR 15.66% to reach USD 20,679.59 million by 2027.

Market Statistics: The report provides market sizing and forecast across five major currencies - USD, EUR, JPY, GBP, AUD, CAD, and CHF. It helps organization leaders make better decisions when currency exchange data is readily available. In this report, the years 2019 and 2020 are considered historical years, 2021 as the base year, 2022 as the estimated year, and years from 2023 to 2027 are considered the forecast period.

Market Segmentation & Coverage: This research report categorizes the Cell Isolation/Cell Separation to forecast the revenues and analyze the trends in each of the following sub-markets:

Based on Product, the market was studied across Consumables and Instruments. The Consumables is further studied across Beads, Disposables, and Reagents, Kits, Media, and Sera. The Instruments is further studied across Centrifuges, Filtration Systems, Flow Cytometers, and Magnetic-Activated Cell Separator Systems.

Based on Cell Type, the market was studied across Animal Cells and Human Cells. The Human Cells is further studied across Differentiated Cells and Stem Cells.

Based on Cell Source, the market was studied across Adipose Tissue, Bone Marrow, and Cord Blood/Embryonic Stem Cells.

Based on Technique, the market was studied across Centrifugation-Based Cell Isolation, Filtration-Based Cell Isolation, and Surface Marker-Based Cell Isolation.

Based on Application, the market was studied across Biomolecule Isolation, Cancer Research, In Vitro Diagnostics, Stem Cell Research, and Tissue Regeneration & Regenerative Medicine.

Based on End User, the market was studied across Biotechnology & Biopharmaceutical Companies, Hospitals & Diagnostic Laboratories, and Research Laboratories & Institutes.

Based on Region, the market was studied across Americas, Asia-Pacific, and Europe, Middle East & Africa. The Americas is further studied across Argentina, Brazil, Canada, Mexico, and United States. The United States is further studied across California, Florida, Illinois, New York, Ohio, Pennsylvania, and Texas. The Asia-Pacific is further studied across Australia, China, India, Indonesia, Japan, Malaysia, Philippines, Singapore, South Korea, Taiwan, and Thailand. The Europe, Middle East & Africa is further studied across France, Germany, Italy, Netherlands, Qatar, Russia, Saudi Arabia, South Africa, Spain, United Arab Emirates, and United Kingdom.

Cumulative Impact of COVID-19: COVID-19 is an incomparable global public health emergency that has affected almost every industry, and the long-term effects are projected to impact the industry growth during the forecast period. Our ongoing research amplifies our research framework to ensure the inclusion of underlying COVID-19 issues and potential paths forward. The report delivers insights on COVID-19 considering the changes in consumer behavior and demand, purchasing patterns, re-routing of the supply chain, dynamics of current market forces, and the significant interventions of governments. The updated study provides insights, analysis, estimations, and forecasts, considering the COVID-19 impact on the market.

Cumulative Impact of 2022 Russia Ukraine Conflict: We continuously monitor and update reports on political and economic uncertainty due to the Russian invasion of Ukraine. Negative impacts are significantly foreseen globally, especially across Eastern Europe, European Union, Eastern & Central Asia, and the United States. This contention has severely affected lives and livelihoods and represents far-reaching disruptions in trade dynamics. The potential effects of ongoing war and uncertainty in Eastern Europe are expected to have an adverse impact on the world economy, with especially long-term harsh effects on Russia.

This report uncovers the impact of demand & supply, pricing variants, strategic uptake of vendors, and recommendations for Cell Isolation/Cell Separation market considering the current update on the conflict and its global response.

Competitive Strategic Window: The Competitive Strategic Window analyses the competitive landscape in terms of markets, applications, and geographies to help the vendor define an alignment or fit between their capabilities and opportunities for future growth prospects. It describes the optimal or favorable fit for the vendors to adopt successive merger and acquisition strategies, geography expansion, research & development, and new product introduction strategies to execute further business expansion and growth during a forecast period.

FPNV Positioning Matrix: The FPNV Positioning Matrix evaluates and categorizes the vendors in the Cell Isolation/Cell Separation Market based on Business Strategy (Business Growth, Industry Coverage, Financial Viability, and Channel Support) and Product Satisfaction (Value for Money, Ease of Use, Product Features, and Customer Support) that aids businesses in better decision making and understanding the competitive landscape.

Market Share Analysis: The Market Share Analysis offers the analysis of vendors considering their contribution to the overall market. It provides the idea of its revenue generation into the overall market compared to other vendors in the space. It provides insights into how vendors are performing in terms of revenue generation and customer base compared to others. Knowing market share offers an idea of the size and competitiveness of the vendors for the base year. It reveals the market characteristics in terms of accumulation, fragmentation, dominance, and amalgamation traits.

Competitive Scenario: The Competitive Scenario provides an outlook analysis of the various business growth strategies adopted by the vendors. The news covered in this section deliver valuable thoughts at the different stage while keeping up-to-date with the business and engage stakeholders in the economic debate. The competitive scenario represents press releases or news of the companies categorized into Merger & Acquisition, Agreement, Collaboration, & Partnership, New Product Launch & Enhancement, Investment & Funding, and Award, Recognition, & Expansion. All the news collected help vendor to understand the gaps in the marketplace and competitors strength and weakness thereby, providing insights to enhance product and service.

Company Usability Profiles: The report profoundly explores the recent significant developments by the leading vendors and innovation profiles in the Global Cell Isolation/Cell Separation Market, including Akadeum Life Sciences, Inc., Alfa Laval, Beckman Coulter Inc., Becton, Dickinson and Company, Bio Legend, Bio- Techne, Bio-Rad Laboratories, Inc., Cell Biologics, Inc. A, Cell Microsystems, cellenion SASU, Corning Inc., GE Healthcare, Invent Biotechnologies, Lonza, Merck KGaA, Miltenyl Biotech, Omega Bio-tek, Inc., pluriSelect Life Science, Pluriselect Life Science Ug (Haftungsbeschrnkt) & Co. Kg, REPROCELL Inc., Roche Diagnostics, Stemcell Technologies, Inc., Terumo Bct, and Thermo Fisher Scientific, Inc..

The report provides insights on the following pointers: 1. Market Penetration: Provides comprehensive information on the market offered by the key players 2. Market Development: Provides in-depth information about lucrative emerging markets and analyze penetration across mature segments of the markets 3. Market Diversification: Provides detailed information about new product launches, untapped geographies, recent developments, and investments 4. Competitive Assessment & Intelligence: Provides an exhaustive assessment of market shares, strategies, products, certification, regulatory approvals, patent landscape, and manufacturing capabilities of the leading players 5. Product Development & Innovation: Provides intelligent insights on future technologies, R&D activities, and breakthrough product developments

The report answers questions such as: 1. What is the market size and forecast of the Global Cell Isolation/Cell Separation Market? 2. What are the inhibiting factors and impact of COVID-19 shaping the Global Cell Isolation/Cell Separation Market during the forecast period? 3. Which are the products/segments/applications/areas to invest in over the forecast period in the Global Cell Isolation/Cell Separation Market? 4. What is the competitive strategic window for opportunities in the Global Cell Isolation/Cell Separation Market? 5. What are the technology trends and regulatory frameworks in the Global Cell Isolation/Cell Separation Market? 6. What is the market share of the leading vendors in the Global Cell Isolation/Cell Separation Market? 7. What modes and strategic moves are considered suitable for entering the Global Cell Isolation/Cell Separation Market? Read the full report: https://www.reportlinker.com/p06260219/?utm_source=GNW

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Cell Isolation/Cell Separation Market Research Report by Product, Cell Type, Cell Source, Technique, Application, End User, Region - Global Forecast...

Scientists Reverse Signs of Aging By 30 Years | What Are Yamanaka Factors? – Popular Mechanics

Stefania Pelfini, La Waziya PhotographyGetty Images

Fifteen years ago, scientists made a stirring discovery when they demonstrated that they could reverse the process of aging in cells. By activating a set of four factors in the DNA, they reset the cells clock to zero, reverting adult cells to their embryonic state. The factors were named Yamanaka factors after their discoverer, Shinya Yamanaka, and a few years later, they earned him a Nobel Prize. For the first time, scientists saw a glimmer of hope that aging could be reversed.

Its quite amazing if you think about it, Wolf Reik, a molecular biologist at the Babraham Institute in the United Kingdom, tells Popular Mechanics. You can potentially reset the age of human cells back to zero.

Scientists hoped that these cells, stripped of the tell-tale signs of aging, could be used to repair and rejuvenate damaged organs. Younger, healthier nerve cells, for example, could take over for brain cells killed by a stroke, or collagen-boosting skin cells could be injected directly into stubborn wounds. The only problem is that the Yamanaka factors reset the cells too far. A cell that is zero days old cant send an electrical nervous signal or produce collagen, nor carry on any other function. Like a stem cell, it is nothing more than a blob of potential.

To overcome this, scientists have been tinkering with the timing and looking for ways to halt the reverse-aging process at the precise moment before the cell reverts to its embryonic form. Previous efforts in mice have shown some promise, but the gains have been modest, reversing the clock only three years or so.

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But now, a group of scientists led by Reik showed that they could turn back the clock by up to 30 years. It is the farthest back anyone has gone without going too far. In April, they published the results in eLife.

Whats new and interesting in this study is that they push the cells into reprogramming in a time-controlled way, Manuel Serranoa molecular biologist at Barcelona, Italys Institute for Research in Biomedicine, who was not involved in the studytells Popular Mechanics. Serrano says that up until now, scientists were not really able to control the Yamanaka factors with much certainty.

To start, researchers collected skin cells from middle-aged adults between 38 and 53 years old. They specifically collected skin fibroblast cells, which are essential for wound healing and whose effectiveness declines with age. Using viral vectors, they injected the Yamanaka factors (a set of four genes) into the cells and turned them on. Previous research showed that it takes a total of 50 days for the Yamanaka factors to reset the clock to zero, and that between Day 10 and Day 17, the cells were roughly 20 to 40 years old, respectively. The researchers decided to halt the action of the Yamanaka factors during this period, looking at the effects on the cells between Day 10 and Day 17.

Ed ReschkeGetty Images

At each pause, researchers evaluated the biological age of the cells using molecular aging clocks. Changes to the DNA that cause cancer, called epigenetic changes, were measured. They also measured collagen production because this protein imbues young skin with its characteristic firm and plump texture, but it declines with age. They even measured the cells mobility. When the skin is damaged, fibroblasts physically migrate into the wound to kick-start collagen production and initiate the repair process. As they age, fibroblasts become noticeably slower, which explains why older skin takes longer to heal.

The scientists found the sweet spot after just 13 days. The cells were youthful, but still retained their ability to produce collagen and move quickly into damaged areas. Understanding that we could rejuvenate cells was amazing, Ins Milagrea researcher at the Gulbenkian Institute of Science in Portugal, and an author on the new studytells Popular Mechanics. But the most exciting thing was to see that the cells were functionally younger, she says.

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According to Milagre, the work is an important milestone and proof that the Yamanaka factors can be fine-tuned. However, she says that we should not expect the technique to be available in the clinic anytime soon. The activation of the Yamanaka factors can cause cancer, and it is still unclear whether this process will work in other cell types. There are still so many unknowns, she says.

Reik echoes these concerns and has plans to develop safer strategies. He thinks by better pinpointing how Yamanaka factors work, he will be able to find downstream molecules that are turned on by the genetic factors. By identifying those factors, which may be RNA or protein, he could develop therapeutics that dont require messing with the genes in the cell, therefore lowering the risk of cancer and other side effects.

We could call them rejuvenation factors, and they would provide a safer way of rejuvenating cells, Reik says.

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Scientists Reverse Signs of Aging By 30 Years | What Are Yamanaka Factors? - Popular Mechanics

Alzheimer’s Drugs Market Size worth US$ ~9.67 billion by 2031: Exclusive Report by Growth Plus Reports – PR Newswire

NEW YORK, May 10, 2022 /PRNewswire/ --The Global Alzheimer's Drugs Market Size is expected to clock US$ ~9.67 billion by 2031, according to the latest report published by Growth Plus Reports. Owing to the rising prevalence of Alzheimer's disease coupled with a strong product pipeline.

Growth Factor

The prominent players are progressively implementing collaborative initiatives with several organizations, research centers, and companies in order to encourage R&D of Alzheimer's treatment. For instance, in February 2020, Biogen Inc. and Sangamo Therapeutics, Inc. entered into a global licensing collaboration agreement to develop and commercialize ST-501 for tauopathies including Alzheimer's disease.

The global Alzheimer's drugs market has been analyzed from three different perspectivesDrug Type, Distribution Channel, and Region.

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Government bodies and numerous organizations across the globe are taking initiatives to fast-track the development of Alzheimer's drug by providing the necessary funding and approvals. For instance, federal funding for USC's research on Alzheimer's disease and related dementias grew by more than 400% between 2015 and 2018. USC's NIH funding for Alzheimer's was $13.3 million in 2015 and it increased to $68.3 million in 2018.

Alzheimer's is the fifth-leading cause of death among those aged 65 & older and is also a leading cause of disability & poor health. An estimated 5.8 million Americans aged 65 and older were living with Alzheimer's dementia in 2020. 80% of this population was aged 75 or older. This number is expected to increase to 13.5 million by 2050. Among people of age 70, 61% of those with Alzheimer's dementia are expected to die before the age of 80 compared with 30% of people without Alzheimer's. The rising prevalence of Alzheimer's disease has increased the demand for the treatment, which in turn is expected to boost the market growth.

Restraints:

Alzheimer's drug development is considered to have the highest failure rates of all drug research, at 99.6% compared to 81% for cancer, according to Scientific American. The drug development process includes high capital investments, therefore, failures in drug research may prove to be huge loss for companies, thereby discouraging the companies to invest and participate in the clinical trials. In January 2018, Pfizer, announced to end its R&D on new drugs for Alzheimer's and Parkinson's diseases and reallocate the funding to areas where the company has strong scientific leadership. Pfizer is among the first companies to research Alzheimer's. Such instances are expected to slow down the growth of the market.

Excerpts from 'By Drug Type Segmentation'

The global Alzheimer's drugs market has been segmented majorly into three distinct categories depending on drug type, viz.

The NMDA receptor antagonists segment consists of Memantine drug. Whereas cholinesterase inhibitors consists of Galantamine, Rivastigmine, and Donepezil drugs. The cholinesterase inhibitors segment dominated the market with the largest share in 2020. The growth of the segment can be attributed to the use of cholinesterase inhibitors as a first line treatment for mild to moderate Alzheimer's condition.

Excerpts from 'By Region Segmentation'

The global Alzheimer's drugs market has been segmented into North America, Europe, Asia Pacific, and the Rest of the World (RoW).

North America is expected to command the largest share in the global Alzheimer's Drugs market in 2020, followed by the Asia Pacific, Europe and Rest of the World (RoW). Factors such as rising prevalence of Alzheimer's among geriatric population, rising initiatives by various public and private organizations, and presence of the prominent players coupled with large number of drugs present in pipeline are attributed for the large share of the region in the global market.

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Excerpts from 'Competitive Landscape'

The prominent players operating in the global Alzheimer's drugs market are: -

Alzheimer's DrugsMarket Segmentation

Growth Plus Reports has segmented the global Alzheimer's Drugs market on the basis Drug Type, Distribution Channel, and Region:

Drug Type Outlook:

Distribution Channel Outlook:

Region Outlook:

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Check out more healthcare related studies published by Growth Plus Reports:

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Alzheimer's Drugs Market Size worth US$ ~9.67 billion by 2031: Exclusive Report by Growth Plus Reports - PR Newswire

Christian leaders and controversies: The case of Francis Collins – The Christian Post

National Institutes of Health Director Francis Collins speaks at the 2019 BioLogos Conference in Baltimore, Maryland on March 27, 2019. | THE CHRISTIAN POST

There is always a dilemma for Christians in best handling and reacting to the positions and counsel of Christian leaders. Often these are people we have grown to trust and respect as followers of Christ.

Their convictions at times are consistent with Christian principles and biblical wisdom. They champion appropriate positions and defend causes from a historically Christian perspective. They gain traction and respect even among cultural, political, and religious opponents because of the internally consistent strength of their arguments and their winsome and gracious demeanor.

And yet, it is impossible for any fallen and sinful person to be right all the time. Similarly, it is quite possible and regularly demonstrated that the unregenerate are not always wrong.

As a case in point, contrast Dr. Francis Collins and President Donald Trump.

Trump, not convincingly a born-again Christian, became president in large measure because he promised to represent conservative Christians and their concerns. His appointing of originalist judges to federal courts and the U.S. Supreme Court, as well as his attendance at events like the annual March for Life while he was in office (this was unprecedented for a president), were encouragements to many Christians. Yet his demeanor was consistently characterized as non-Christian. Such may well have cost him re-election. Christians and conservative political analysts will debate for decades whether he was a net positive or negative influence on America. Clearly, both cases can be made. Different Christian voices have weighed in on the matter. Many Christians, even conservatives, felt that Trump used them for his personal gain and prestige.

In certain notable ways, a case could be made that the Francis Collins situation at times echoes the debate over Donald Trump among Christians.

Dr. Francis Collins, the famous geneticist, was and is vocally Christian. He has clearly identified as such, and he has taken heat for it. For example, in the summer of 2009, after his nomination as director of NIH by President Barack Obama, outspoken atheist Sam Harris attacked Collins in theNew York Timesas unfit for the job because of his religious convictions.

Collins became known to many Americans during his direction of the Human Genome Project through the 1990s. In February 1998,Scientific Americanprofiled Dr. Collins with the headline Where Science and Religion meet: The U.S. head of the Human Genome Project, Francis S. Collins, stives to keep his Christianity from interfering with his science and politics. That article quoted Dr. Collins saying he is intensely uncomfortable with abortion. He said that he does not advocate changing the law and is very careful to ensure his personal feelings on abortion do not affect his political stance.

The article went on to say: researchers and academics familiar with Collins work agree that he has separated his private religious views from his professional life. He shows no influence of religious beliefs on his work other than a generalized sensitivity to ethics issues in genetics.

In essence, what these people were saying is that Francis Collins is such a good scientist because you can hardly tell he is a Christian from his work.

As a much younger biology professor at the time, I was aghast at this. A Christian has separated his religious views from his professional life. Why is that a good thing?

I emailed Dr. Collins at the time, asking him ifScientific Americanhad it right. Maybe the article misunderstood Collins? My email was never answered. Not that I expected that it would be, given my obscurity and his standing and responsibilities. Still, the article troubled me, as I was always left with the lingering question.

Dr. Collins went on to launch the BioLogos Foundation, a Christian/science interface organization that advocates for the reconciliation of modern science and Christianity. The idea is that nature and Scripture are both from God and ultimately are not in conflict. This reflects Dr. Collins Christian convictions and his love of science, the study of Gods physical world. Give Dr. Collins credit for leveraging his popularity, leadership qualities, and obvious pastoral instincts for the noble cause.

Ultimately, I met Dr. Collins several years ago at a conference and heard him speak. There is no reason he would remember our quick contact in an elevator any more than he would remember my email. However, one cannot help but be impressed by his genuine humility and his concern for the spiritual health of the people around him. He has made it clear that he believes that Jesus Christ is incarnate and divine and that humans are made in the image of God (although he rejects the historic Adam), and that salvation is real.

Yet, inconsistencies remain. Dr. Collins seems to allow his science to inordinately arbitrate over biblical truth, or at least when the two are portrayed as in conflict. As his professional life has unfolded, it has become clear that theScientific Americanarticle had gotten a lot right. It is fair to say that he has remained uncertain about when human life begins. He concedes that the fertilized egg is alive at conception, but believes that maybe it is not quite human. Consequently, in his 2010 book,The Language of Life,he advocated for experimentation using excess human embryos fromin vitro fertilization(IVF) that are stuck in cryo-storage with uncertain futures, so that some good could come from them. He has never publicly disavowed human embryonic research because he sees its potential fruitfulness. In fact, as late as last summer, experiments involving human embryonic cells and mice was supported by NIH funding at the University of Pittsburgh.

There are ongoing ramifications of Dr. Collins acceptance of abortion as the law of the land. TheScientific Americanarticle in 1998 mentioned that Dr. Collins was concerned that embryonic genetic testing might lead to abortions of fetuses that have conditions that are less than disastrous. The article did not suggest what he would consider less than disastrous. For instance, would my great-nephews Downs syndrome condition be considered less than a disaster?

Princeton bioethicist and legal scholar, Dr. Robert George, made a clearer case in his 1998 address to the American Political Science Association Convention, stating, once I was a child, once I was an infant, once I was an embryo, I cannot say I was once an egg or a sperm. However, it is clear that the viable sperm and egg are quite alive. Also, it is good to remember what we say in the Apostles Creed. He was conceived born suffered died and rose again.

What human is not on that trajectory of life and death? The Bible teaches that we all are.

This leaves many conservative Christians convinced that Dr. Collins would rather come down on the side of a quote from his old boss, President Barack Obama. In March 2009, Obama signed an executive order that lifted President George W. Bushs 2001 ban on federal funding of human embryonic research. Today we will lift the ban on federal funding for promising embryonic stem cell research, stated Obama. We will vigorously support scientists who pursue this research. And we will aim for America to lead the world in the discoveries it one day may yield. Obama continued, Promoting science isnt just about providing resources it is also about protecting free and open inquiry. It is about letting scientists like those here today do their jobs, free from manipulation or coercion, and that we make scientific decisions based on facts, not ideology.

Obama insisted that Im going to let scientists do science. Im going to remove politics, religion, and ideology from that.

Of course, the reality is that such a thing cannot be done. The presidents own politics and ideology were clearly stated and inserted.

One would hope that Dr. Collins would be more comfortable with the principles articulated in President George W. Bushs 2006 State of the Union Address. A hopeful society has institutions of science and medicine that do not cut ethical corners, and that recognize the matchless value of every life, stated Bush. Tonight, I ask you to pass legislation to prohibit the most egregious abuses of medical research human cloning in all its forms creating or implanting embryos for experiments creating human-animal hybrids and buying, selling, or patenting human embryos. Human life is a gift from our Creatorand that gift should never be discarded, devalued, or put up for sale.

These are all ethical issues that have confronted Dr. Francis Collins as a man of science and of faith. The issues more recently included COVID mask and vaccine mandates. To many in the evangelical community, the pro-life appeals he made for the mandates have rung increasingly hollow, and his seeming inconsistencies have been bothersome.

Os Guinness, in his book,The Magna Carta of Humanity, brings out a principle that every intentional Christian should keep in mind: The notion of arguing on behalf of the true, the right, and the good lies behind the biblical principle of corrigibility. Guinness quotes Jewish Hebrew scholar Jonathan Sacks, We are all open to challenge. No one is above criticism, no one is too junior to administer it, if done with due grace and humility.

This requires knowing scripture and applying its logical conclusions, consistently. Otherwise, our ability to be salt and light is diminished, and we can be played. Francis Collins needs to add salt and light. Many of us have admired him, and we expect more from him in his Christian witness to science.

Dr. Jan Dudt is a professor of biology at Grove City College and fellow for medical ethics with the Institute for Faith & Freedom. He teaches as part of colleges required core course Studies in Science, Faith and Technology wherein students, among other things, study all the major origins theories and are asked to measure them in the light of biblical authority.

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Christian leaders and controversies: The case of Francis Collins - The Christian Post

Google relaxes ban on stem cell therapy ads – The Verge

Google will allow ads for stem cell treatments that are approved by the US Food and Drug Administration a change from its previous policy, which banned all ads for this experimental category of medical care. The policy update was first reported by Gizmodo and will go into effect in July.

The company said in the policy update that it will also allow cell or gene therapy ads that are exclusively educational or informational in nature, even if they reference products or applications that are not approved by the FDA. Its not clear how Google would define educational or informational or what type of advertisements would be allowed under that umbrella.

Stem cell therapy is a broad term for medical treatments that use stem cells, which can develop into any cell type. There are some evidence-based applications for the cells, like to treat some cancers, and there are around two dozen FDA-approved cell- and gene-therapy products (which Googles new policy would allow ads for).

But most uses for stem cells are unproven, experimental, and can be dangerous. Clinics claim the cells, taken from donated umbilical cords or from patients fat, can treat things like joint pain or eye conditions. People have developed infections and died after getting those types of procedures. The FDA has tried to crack down on businesses offering these types of procedures, but theyve proliferated over the past few years.

Googles initial ban on stem cell ads hasnt done much to keep the clinics from popping up in search, Paul Knoepfler, a professor at the UC Davis School of Medicine, wrote in Stat in March. Even if they cant advertise, the companies have designed websites that appear at the top of search results for searches related to stem cells above more reputable medical resources, like the National Institutes of Health.

These companies are savvy and have been able to skirt policies to push out their products even in the face of a total ban. Now, that ban is set to relax, opening up new avenues for groups to distribute information. Googles continuing stem cell problem is emblematic of a serious, broader problem with unproven biomedical offerings the company needs to address, Knoepfler wrote.

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Google relaxes ban on stem cell therapy ads - The Verge

Stem cell therapy offers a new hope to repair brain damage in newborns – Yahoo News UK

A few hours after Tom (not his real name) was born, he became restless and did not want to be breastfed. His mother noticed that his left arm and leg were shaking rhythmically something was not right.

Tom was immediately transferred to the neonatal intensive care unit. An MRI scan revealed that he had suffered a severe stroke. Doctors told Toms parents that there was no treatment they could give the child. He would probably be disabled.

Most people think of stroke as something that mainly affects the elderly, but it can also occur in newborn babies. These perinatal strokes happen when one of the major arteries to the brain becomes blocked, leading to a lack of blood supply and hence oxygen to certain brain areas. About one in 5,000 newborns have a stroke. It usually happens in the first few days after they are born.

Most of the babies will have problems later in life, with the severity of the problems depending on which brain areas were injured. These problems can include muscle tightness in the arms and legs (cerebral palsy), behaviour problems, learning difficulties and epilepsy.

No therapy exists for newborns with stroke. Researchers, including our own team at University Medical Center Utrecht, have been working on new treatments, one of which involves stem cells.

Stem cells have the ability to turn into many different cells in the body, and they are little factories of several growth factors (proteins that stimulate the growth of specific tissues). The theory is that if we can get stem cells into the damaged part of a babys brain, the stem cells growth factors will stimulate the brain to repair itself.

Earlier studies in animals showed that injecting stem cells into the brains of newborn mice with stroke dramatically reduced the amount of brain damage and disability they suffered. The experiments showed that the treatment was safe and had no side-effects in the mice. These animal studies gave us hope that the treatment would work in newborn babies, too, preventing a lifetime of disability.

Story continues

But how do you deliver stem cells to a babys brain without having to use needles or surgery? We decided to try an intranasal route (through the nose), which was tested in mice. After we delivered the stem cells intranasally, the cells travelled rapidly and specifically to the injured brain areas. The injured brain area sends out alarm signals which guide the stem cells to the right spot in the brain.

Once the stem cells arrived at the damaged area, they secreted growth factors that boosted the repair systems of the mices brains. Within a few days, the stem cells were broken down and not traceable in the brain any longer. After several experiments with this method, we concluded that dripping stem cells in the nose is the safest and most efficient way to deliver them to the brain.

After many years of laboratory research, we have finally tested the treatment in babies. The results have been published in The Lancet Neurology.

Baby Tom, mentioned earlier, was the first baby to participate in the study and received stem cells within a week of being born. To ask parents to enrol in an experimental therapy in the first week of their newborn childs life is a very delicate process.

After we had a long conversation with his parents, they decided to let their son take part in the study. He received stem cells via nose droplets, a procedure that took only several minutes. Afterwards, Tom was monitored closely for a few days before he went home.

We treated ten newborns who were transferred from hospitals across the Netherlands to the University Medical Center Utrecht after suffering from a stroke. In all ten newborns, the stem cell droplets were administered without any complications. There was one baby who had a mild fever after the treatment, which quickly cleared up on its own.

A follow-up MRI scan of the brain made three months after the stroke showed less injury than expected, possibly because of the stem cells. At four months, the treated babies, including Tom, performed well when the quality of their movements was tested. When the children are two years old, we will check their development again.

We are now looking for opportunities to proceed with a randomised controlled trial (the gold standard for medical studies) to prove that stem cell therapy can effectively repair brain injury after perinatal stroke.

The discovery of a new and safe therapy with stem cells also opens up opportunities for other babies with brain injury, such as babies who are born too early, or babies that suffer from a lack of oxygen during birth (perinatal asphyxia). Stem cell therapy gives hope to the most vulnerable patient group, with possible lifelong benefits.

This article is republished from The Conversation under a Creative Commons license. Read the original article.

The Conversation

Nienke Wagenaar receives funding from Utrecht University, Wilhelmina Children's Hospital Research Fund, Royal Netherlands Academy of Arts and Sciences and the Research Training Centre of the Hospital for Sick Children. For previous work, including the PASSIoN study, she received funding from the Netherlands Organisation for Health Research and Development (ZonMW).

Lisanne Baak receives funding from the Netherlands Organisation for Health Research and Development (ZonMW).

Niek van der Aa receives funding from the Wilhelmina Children's Hospital Research Fund, Health Holland, Utrecht University and the Vaillant Fund.

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Stem cell therapy offers a new hope to repair brain damage in newborns - Yahoo News UK