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Exclusive Research on Stem Cell Therapy Products Market 2020 Segments, Regions, Strategy Analysis: Mesoblast, TiGenix, Osiris – LionLowdown

A research report on Stem Cell Therapy Products Market compiled byWorldwide Market Reports features a succinct analysis of the latest market trends. The report also includes detailed abstracts about statistics, revenue forecasts, and market valuation, which additionally highlights its status in the competitive landscape and growth trends accepted by major industry players.

Stem Cell Therapy Products Market reports provide a comprehensive overview of the global market size and share. Stem Cell Therapy Products market data reports also provide a 5 year pre-historic and forecast for the sector and include data on socio-economic data of global. Key stakeholders can consider statistics, tables & figures mentioned in this report for strategic planning which leads to the success of the organization.

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The major players profiled in this report include

New business opportunities and rising demand for Stem Cell Therapy Products market activities are the primary factors expected to drive the growth of the Stem Cell Therapy Products market in the United States, EU, Japan, China, India, Africa, Southeast Asia are the major region leading the Stem Cell Therapy Products market.

Impact of COVID-19:

Stem Cell Therapy Products Market report analyses the impact of Coronavirus (COVID-19) on the Stem Cell Therapy Products industry. Since the COVID-19 virus outbreak in December 2019, the disease has spread to almost 180+ countries around the globe with the World Health Organization declaring it a public health emergency. The global impacts of the coronavirus disease 2019 (COVID-19) are already starting to be felt, and will significantly affect the Stem Cell Therapy Products market in 2020.

COVID-19 can affect the global economy in 3 main ways: by directly affecting production and demand, by creating supply chain and market disturbance, and by its financial impact on firms and financial markets.

Further in the Stem Cell Therapy Products Market research reports, following points are included along with in-depth study of each point:

Production Analysis: Production of the Stem Cell Therapy Products is analyzed with respect to different regions, types, and applications. Here, price analysis of various Stem Cell Therapy Products Market key players is also covered.

Supply and Consumption: In continuation with sales, this section studies supply and consumption for the Stem Cell Therapy Products Market. This part also sheds light on the gap between supply and consumption. Import and export figures are also given in this report.

Key Strategic Developments: The study also includes the key strategic developments of the Stem Cell Therapy Products market, comprising R&D, new product launch, M&A, agreements, collaborations, partnerships, joint ventures, Global and regional growth of the leading competitors operating in the market on a global and regional scale.

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In this report, the global Stem Cell Therapy Products market is valued at USD XX million in 2019 and is expected to reach USD XX million by the end of 2026, growing at a CAGR of XX% between 2019 and 2026.

History Year: 2013-2019

Base Year:2020

Estimated Year:2021

Forecast Year 2020to2026

The report provides an in-detail list of drivers and restraints in the market, which are influencing the market growth. Additionally, provides expected opportunities and emerging trends in the market.

The report includes a detailed study of Porters Five Forces model to analyze the different factors affecting the growth of the market. Moreover, the study also covers a market attractiveness analysis, PESTLE analysis, Value Chain Analysis, and SWOT analysis.

The report is a collection of first-hand information, qualitative assessment by industry analysts, and inputs from industry experts. Moreover, the report also maps the qualitative impact of various market factors on market segments and geographies. The major factor driving the adoption of Stem Cell Therapy Products is the formation of the major industry changing factors for the market segments are explored in this report. This report also covers the growth factors of the global market based on end-users.

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This report includes the estimation of market size for value (million US$) and volume (K Units). Both top-down and bottom-up approaches have been used to estimate and validate the market size of Stem Cell Therapy Products market, to estimate the size of various other dependent submarkets in the overall market. Key players in the market have been identified through secondary research, and their market shares have been determined through primary and secondary research. All percentage shares split, and breakdowns have been determined using secondary sources and verified primary sources.

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About WMR

Worldwide Market Reports is your one-stop repository of detailed and in-depth market research reports compiled by an extensive list of publishers from across the globe. We offer reports across virtually all domains and an exhaustive list of sub-domains under the sun. The in-depth market analysis by some of the most vastly experienced analysts provide our diverse range of clients from across all industries with vital decision making insights to plan and align their market strategies in line with current market trends.

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Exclusive Research on Stem Cell Therapy Products Market 2020 Segments, Regions, Strategy Analysis: Mesoblast, TiGenix, Osiris - LionLowdown

Heterogenous Nature of MDS Warrants Further Research, Review Finds – AJMC.com Managed Markets Network

MDS is a complex disease with a fascinating origin. A plethora of molecular pathway disruptions have been postulated to explain the heterogeneity of the disease phenotype, but no exclusive genetic drivers are capable of recapitulating all its aspects, wrote the researchers, noting the heterogeneity of MDS introduces challenges when trying to fully understand the pathogenesis of the group of disorders.

They added, Seminal experimental studies have clarified the role of diverse gene mutations in the context of disease phenotypes, but the lack of faithful murine models and/or cell lines spontaneously carrying certain gene mutations have hampered the knowledge on how and why specific pathways are associated with MDS pathogenesis.

Recently, a gene expression-based classification was applied to RNA-sequencing data from CD34+ cells of 100 patients with MDS, resulting in the identification of 2 subcellular populations. The populations were associated and characterized by increased expression of genes related to erythroid/megakaryocytic lineages and those related to immature progenitor cells.

In addition, several genes in the iron pathway have been implicated in the pathogenesis of MDS, including:

Other recent research involved identifying differences in downstream pathways, particularly for genes of the spliceosomal complex, with all studies showing convergent functions in the 3 splice site. Some studies have shown that splicing factor mutations could result in the build-up of R-loops, including one that showed an increase in R-loops in an induced pluripotent stem cell clone harboring a SF3B1 mutation compared with a clone lacking SF3B1 mutations from a patient with MDS.

For patients with an SF3B1 mutation, luspatercept has been shown to improve response in low-grade MDS through its ability to increase erythroid maturation and hemoglobin levels.

More recently, splicing factor mutations were found to lead to the activation of inflammation and innate immunity pathways (e.g., NF-kB) or indirectly by deregulating histone acetylase (e.g., sirtuins), detailed the researchers. In fact, sirtuin 1 (SIRT1) was found to be involved in HSPC maintenance. U2AF1 mutant patients had IRAK4, a serine/threonine that activates NF-kB in the Toll-like receptor and T-cell receptor signaling pathways, that is aberrantly spliced.

Treatments targeting splicing factor mutations have mainly included developing pan-splicing modulators, including bacterially derived products and analogs that have been shown to bind the SF3B complex and disrupt spliceosome assembly.

Research focused on novel treatments for mutant p53 has also found that PRIMA-1Met, an investigational small molecule, restores the conformation of p53 and rescues p53 function. Another treatment, APR-246, has shown promise either as monotherapy or in combination with 5-azacitidine in reactivating p53 and inducing apoptosis in MDS cases carrying TP53 mutations.

Reference: Awada H, Thapa B, and Visconte V. The genomics of myelodysplastic syndrome: origins of disease evolution, biological pathways, and prognostic implications. Cells.2020;9(11):2512. doi:10.3390/cells9112512

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Heterogenous Nature of MDS Warrants Further Research, Review Finds - AJMC.com Managed Markets Network

Research Assistant – Department of Obstetrics and Gynaecology job with NATIONAL UNIVERSITY OF SINGAPORE | 239606 – Times Higher Education (THE)

Roles & Responsibilities

Job description: A Research Assistant (RA) position is available in a leading stem cell research team in the Department of Obstetrics and Gynaecology, NUS Yong Loo Lin School of Medicine, NUHS, National University of Singapore. The job entails work in a laboratory and hospital setting. The successful candidate will work with a team undertaking laboratory research and clinical trials on human umbilical cord Whartons jelly stem cells for the treatment of surgical and diabetic wounds, keloids, bed-sores and blood cancers. The team is currently developing cGMP clinical-grade Whartons jelly stem cells for these applications.

Required skills

Job responsibilities:

Employment type: Medical research

Minimum qualifications: The applicant should possess at least a Bachelors degree in the biological, biomedical, biotechnology, pharmaceutical or allied sciences.

Working hours: 8.30 am to 6 pm on week days. A few additional hours on week-ends or after office hours if experiments require this.

Address of workplace: Department of Obstetrics and Gynaecology Research Laboratories, MD11 Clinical Research Centre, NUS Campus, Kent Ridge, Singapore. Only shortlisted applicants will be notified and interviewed.

Originally posted here:
Research Assistant - Department of Obstetrics and Gynaecology job with NATIONAL UNIVERSITY OF SINGAPORE | 239606 - Times Higher Education (THE)

Getting to the root of why hair goes gray – messenger-inquirer

Marco Kaltofen was 11 when he noticed his first white hairs. As his hair grew whiter, his middle-school friends started calling him the professor. By his mid-30s, it was completely white, as it had been for three of his grandparents. His parents went white in their 40s, so I had no chance of avoiding this, Kaltofen says.

Now 61, he is a civil engineer who lives in Boston. He wears his white hair in a ponytail. White hair is part of my identity, and I am completely at peace with it, he says.

Then there is Joe Rees, 75, a retired customs attache who lives in Washington. He is balding, but the hair that remains on the sides and in the back is the same dark brown it always has been. He jokingly attributes this to clean living and a pure heart, although, like Kaltofen, it probably is genetic. His mothers black hair didnt start to go gray until she was in her 70s, and was 50/50 when she died at 88, he says.

Still, Id rather be gray than bald, he says. That way, I wouldnt have to worry about wearing a hat all the time.

To be sure, Rees and Kaltofen are exceptions, since most people start graying in their 50s and 60s. Nevertheless, their experiences are among the many mysteries of gray, white or silver-looking hair that scientists are exploring to learn more about aging. They want to know why some people turn gray early and others late or not at all and what this might signal about their health. They also want to understand the factors that hasten graying, and even whether gray hair is reversible which could be a boon to those allergic to hair dye, or who hate spending money to keep the gray away.

Most important, studying gray hair could point to new approaches in promoting healthier aging, says Candace Kerr, health scientist administrator in the National Institute on Agings Division of Aging Biology.

While graying is one of the markers of aging aging is the ultimate risk factor for why hair goes gray it highlights the need for better understanding of the mechanisms that drive aging and age-related diseases, she says. To be able to target these pathways will be critically important for our aging population to live longer and happier lives.

Hair that looks gray, white or silver actually is colorless. Hair color comes from melanin, a pigment produced by cells in the hair follicles. Over time, these cells suffer damage and become depleted, losing their ability to make melanin. This results in new hair without pigment meaning, no color.

People use gray, white and silver interchangeably to describe hair that is turning or has turned. Its appearance whether it looks, gray, white or silver depends on how much natural color, or pigment, remains, experts say. Hair that has lost all its color typically appears white.

Studies have identified a number of factors that also may speed up gray hair, including smoking, diet, stress and genetics.

Our hair color depends on a set of specialized stem cells called melanocyte stem cells, and every time a new hair grows, these melanocyte stem cells have to divide in two and make a new melanocyte, [or] pigment cells, explains Melissa Harris, assistant professor of biology at the University of Alabama at Birmingham. These pigment cells stay in the base of your hair and their job is to produce pigment. These melanocytes reach out skinny arms, called dendritic processes, that shuttle the pigment to the hair shaft as it grows. So if all your melanocyte stem cells disappear, so do your melanocytes and so does your hair pigment. Thus gray hair.

Because stem cells directly influence hair color, studying gray hair can provide insights about why stem cells age and ultimately fail, offering important clues about the workings of other stem cells in the body for example, those found in muscles, bones and organs. In turn, these ultimately could point to whether gray hair could be a marker for disease, or the opposite, a longer life. Previous studies have not shown a relationship between life span and gray hair, including whether late onset of gray hair predicts longevity. Some research, however, indicates that gray or white hair can be a sign of early heart disease, regardless of age.

In some people, gray hair could potentially serve as indication of their health for instance when caused by stress, or a signal for those who may be developing cardiovascular disease, Kerr says. We still need to learn more about whether and, if so, how late onset of gray hair can signal better health and longevity in some people under certain circumstances, as well as whether early graying means stem cells might be aging.

There are many different stem cells in our body which may or may not age by different means, she says. How stem cells mark aging overall and how they could interact to promote aging is an important question.

This is why scientists who study gray hair regard it as a valuable research tool.

As gray hair researchers, we often have to defend why we study a cosmetic characteristic, rather than a life-threatening disease, Harris says. But what is very cool about gray hair from a scientific point of view is that we can see it with our own eyes, meaning we dont have to take invasive biopsies, and it doesnt kill you. We have asked a lot of important and interesting questions about stem cells by studying gray hair in mice. And, we are constantly on the lookout for gray-haired mice so we can use our scientific skills to find out what makes them gray.

A 2018 mouse study by Team Hair-Us (Harris nickname for her lab colleagues) found a connection between MITF (microphthalmia), a transcription factor (a protein involved in gene expression) important in managing pigment production, and the innate immune system, suggesting that some peoples hair may turn gray in response to serious illness or chronic stress. They discovered a relationship between genes involved in hair color and those that trigger an immune response to a viral infection, suggesting this interaction could increase the chances of developing gray hair.

MITF, in a sense, shields melanocyte stem cells from our own immune system, she says. Normally our immune system protects our bodies from infection. But for melanocyte stem cells, too much immune response is bad for their health, and this leads to their loss and to gray hair. Why melanocyte stem cells are so sensitive to our own natural means for protection, we still dont know.

Im very curious to see whether we see an uptick in individuals with gray hair due to coronavirus infection, she says. Unfortunately, we probably wont know because gray hair is rarely documented clinically, unless it is very extreme.

Scientists still dont know why some people turn gray early, late, or not at all, although they suspect genes, nutrients and possibly the immune system play a role in depleting melanocyte stem cells.

There is still much to learn about what regulates these stem cells and what may contribute to their loss, says Ya-Chieh Hsu, associate professor of stem cell and regenerative biology at Harvard University and principal faculty member of the Harvard Stem Cell Institute.

Among other things, Hsu studies the effect of stress on graying. Most of us are familiar with those before-and-after photographs of U.S. presidents most recently Barack Obama showing a striking increase in gray hair during their terms, even in relatively young presidents. Its known as the Marie Antoinette Syndrome, after the 18th-century French queen whose hair allegedly turned white overnight before she went to the guillotine and her death at age 38 during the French Revolution.

With the aging process, we gradually lose melanocyte stem cells one-by-one over a very long period of time, Hsu says. What we found in our research was that the stress can accelerate that process.

Hsu and her colleagues found that stress stimulates the same nerves that trigger the fight-or-flight response, which in turn causes permanent damage to the pigment-producing cells in hair follicles. The fight or flight response is thought to be a good thing in stressful situations because it can drive us and other organisms to respond to danger rapidly, Hsu says. This activation causes a spike in the neurotransmitter norepinephrine. Norepinephrine raises our heartbeat and allows us to react quickly to danger without having to think about it.

But norepinephrine also tells melanocyte stem cells to pump up their activity and proliferate, and too much norepinephrine, in this case triggered by stress, causes the melanocyte stem cells to burst into so much activity it leads to rapid depletion of the stem cell reservoir, she says. If all the stem cells are depleted, no more pigment-producing cells can be produced anymore, and the hair turns gray.

Other stress hormones, ACTH (adrenocorticotropic hormone) for example, can cause melanocyte stem cells to migrate away from the hair follicle before they can produce the melanocytes needed for hair and skin color, according to research. Such hormones are known to increase in the body after stress, and may have the potential to promote the loss of these cells, regardless of age, says study author Mayumi Ito, associate professor in the departments of cell biology and dermatology at the New York University Grossman School of Medicine.

Hsu believes the connection between stress and hair color could reveal additional information about how stress affects other biological processes. How stress affects our tissues is still poorly understood, and one of the powerful aspects about the melanocyte is that it provides a visible and highly trackable system to study stress, she says.

Ito also found that certain cell signaling proteins called endothelins (substances known to constrict blood vessels and raise blood pressure) bind to melanocyte stem cells and, in doing so, keep them healthy. Interrupting the process causes cell loss and early graying in mice. They are studying whether the same happens in human hair follicles, hoping to find ways to preserve or regenerate the key stem cells that give hair its color.

All of this raises the intriguing possibility that scientists could discover ways to prevent or reverse gray hair.

Team Hair-Us recently published a paper describing a topical drug combination that increased melanocyte stem cells in gray mice, ridding them of their gray and restoring their original fur color perhaps for good. Because the treatment originally developed to regrow hair replenished pigment-producing stem cells, the effects could be long-lasting, Harris says.

We didnt keep the mice forever so we dont know, says Harris, who plans more studies. This has made us very interested in whether gray hair really is permanent, and if we can do something about it. We really want to know and so does everyone else we talk to is whether and when we can bring this to humans.

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Getting to the root of why hair goes gray - messenger-inquirer

How the COVID Virus Induces Inflammation, Cytokine Storm and Stress in Infected Lung Cells – SciTechDaily

The coronavirus SARS-CoV-2 docks with its spike protein onto the receptor-ACE2 found on the surface of lung cells. The levels of co-expressed genes with the human receptor-ACE2 were calculated from several publicly available datasets pertaining to lung epithelial cells infected with SARS-CoV-2. The resulting gene-signature consisted of members from the Trans-Membrane-Serine-Protease (TMPRSS) gene family which prime the virus spike protein for cell entry. Other genes from the gene-signature are associated with reduced immune responses and activated inflammation, Reactive Oxygen Species (ROS) and cellular stress. Credit: WruckW /AdjayeJ, HHU Duesseldorf, Germany

The researchers Wasco Wruck and Prof. James Adjaye from the Institute of Stem Cell Research and Regenerative Medicine, Medical Faculty of Heinrich-Heine-University Duesseldorf, Germany, employed a bioinformatic approach on transcriptome data pertaining to human lung epithelial cells infected with SARS-CoV-2. The meta-analysis unveiled several adversely affected biological processes in the lung which no doubt also applies to other infected organs such as the heart and kidney. Their study is published in Scientific Reports.

With a current estimation of more than 60 Mio. infected people and more than 1.4 Mio. recorded deaths worldwide, COVID-19 the disease caused by the coronavirus SARS-CoV-2 and is classified as a pandemic by the WHO poses a threat to public health, national economies, and society as a whole. Although effective vaccines are becoming available, we still need a better understanding of the molecular mechanisms underlying the etiology of COVID-19 to enable more effective therapies in the future.

Wasco Wruck, first author of the study, says: We initially viewed the results of the analysis in an unbiased manner. To our surprise, we noticed that several Transmembrane Serine Proteases besides the already known TMPRSS2 were highly correlated with ACE2 expression. Furthermore, in a more in-depth analysis, the gene-signature could be annotated with numerous biological processes. Among these were regulation of viral life cycle, immune responses, pro-inflammatory responses, several interleukins such as IL6, IL1, IL20 and IL33, IFI16 regulating the interferon response to a virus, chemo-attraction of macrophages, and cellular stress resulting from activated Reactive Oxygen Species.

Prof. James Adjaye, senior author of the study, summarizes: We have shown that not having access or the necessary infrastructure to carry out research with the deadly coronavirus SARS-CoV-2 should not preclude progress in dissecting the etiology underlying COVID-19. There are currently numerous transcriptome-based datasets related to experiments carried out on numerous cell types infected with SARS-CoV-2 which can be retrieved and analyzed to identify adversely affected biological processes with the hope of identifying putative druggable targets that can be used to better manage COVID-19 in the future.

Reference: SARS-CoV-2 receptor ACE2 is co-expressed with genes related to transmembrane serine proteases, viral entry, immunity and cellular stress by Wasco Wruck and James Adjaye, 8 December 2020, Scientific Reports. DOI: 10.1038/s41598-020-78402-2

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How the COVID Virus Induces Inflammation, Cytokine Storm and Stress in Infected Lung Cells - SciTechDaily

Four years after devastating spinal injury, former St. Paul’s football player reunites with caregivers – NOLA.com

Michael Doherty was just 17 when he lost the ability to walk, but the former St. Paul's studenthasn't lost his determination to regain the mobility taken from him when he suffered a spinal cord injury during a 2016 football game at the Covington school.

Now a junior at LSU, Doherty is quick to say that he's gained something in the years since his injurythe realization that nothing should be taken for granted and a deep gratitude for those who've helped him, including doctors, nurses and therapists, as well as family and friends.

During a recent visit to Lakeview Regional Medical Center, the 21-year-old said thank you in person to some of the staff members who cared for him when he arrived at the Covington areahospital's emergency department on that fateful November night, a stay that stretched to 17 days.

Michael Doherty, center, heads to his truck after visiting with the medical team at Lakeview Regional Medical Center near Covington that helped him during surgery and recovery following a spinal injury he suffered while playing high school football in November 2016. Doherty uses a wheelchair to get around but he and his doctors hope he'll be able to walk again in the future. (Photo by Chris Granger | The Times-Picayune | The New Orleans Advocate)

"He could hardly raise his arms," said Holly Leonhard, then a critical care nurse and now a nurse practitioner, as she marveled at her former patient's progress.

This time, Doherty arrived at the hospital on his own steam, driving a modified truck that uses hand controls and a platform that slides out so he can maneuver his wheelchair without assistance.

Many people on his team of caregivers 27 in all had not seen him since he left the hospital four years ago. But they hadn't forgotten his determination to recover, something that they say was evident from the outset.

Sharon Resmondo, who was a night nurse then, choked up a bit as she recalled those days.

"The beginning was very hard," she said. "But he rallied every day."

"I have children his age," critical care nurse Melanie Norris added. "It was his resolve: he was going to get through it. Your heart went out to him. He hasn't proven us wrong yet."

Hospital staffers remember lighter moments, too, particularly the unending stream of visitors, mostly his classmates, and their gentle bending of the rules to allow them to be there for their friend. His hospital room was rearranged to bring in a big-screen TV, and some friends even slept over.

Nurse Practitioner Sharon Resmondo, center, holds up her phone so that other medical staff who couldn't see Michael Doherty in person could visit with him in a video chat on Wednesday, December 9, 2020 at Lakeview Regional Medical Center near Covington. Doherty wanted to thank the medical staff that helped him during surgery and in his recovery following a spinal injury suffered during a high school football game in November 2016. (Photo by Chris Granger | The Times-Picayune | The New Orleans Advocate)

Dr. Marco Hidalgo, medical director of the hospital's trauma program, said there was a train of people bringing food just for the visitors.

"I kept asking, 'Don't these kids have to go to school?' There was never a day when there were not at least a dozen," Hidalgo said. "He had more visitors in a day than the whole hospital has now."

Because of COVID-19, he pointed out, such attention isn't possible.

Doherty, at the time a junior defensive back, was injured in what appeared to be a routine play in a November 2016 playoff game against Archbishop Shaw. But after the play, Doherty couldn't pick himself up.

Michael Doherty, center, is surrounded by some of the medical team that helped him during surgery and recovery at Lakeview Regional Medical Center near Covington back in November 2016 following a spinal injury he suffered at a high school football game. On Wednesday, December 9, 2020, Doherty drove to the hospital using a modified truck to thank the staff. (Photo by Chris Granger | The Times-Picayune | The New Orleans Advocate)

Dr. Justin Owen, a neurosurgeon, got the phone call from the football field that night about an injured player who couldn't feel his legs. While those on the scene were focused on his thoracic spine, Owen said he was much more concerned about his neck, and that is where his spinal cord was compressed, at the C5-6 vertebrae. Doctors were also worried about a possible clot in one of the arteries that supplies blood to the brain.

Owen and the others operated on Doherty deep into the next morning and the plan was to transfer him to New Orleans afterward. But Owen said the south shore hospital "got cold feet." So Lakeview reevaluated him and kept a very close eye on him, he said.

His caregivers agree that the presence of so many people was a key to Doherty's recovery, which wouldn't have been possible if he had been moved. "The fact that he was closer meant that family and friends could be there," Hidalgo said.

Doherty left Lakeview Regional to go the Shepherd Center in Atlanta, where he worked hard at rehabilitation, returning to St. Paul's in March of 2017 to finish his junior year. He has returned to the Shepherd Center since, and also works on his own.

He has some feeling in his legs and has regained enough arm movement to handle a cellphone, cups and the all-important hand controls for his truck.

"It gives me a lot of independence," he said. "I had to rely on other people for rides."

Michael Doherty visits with the medical team that helped him during surgery and recovery at Lakeview Regional Medical Center near Covington on Wednesday, December 9, 2020. In November 2016, Doherty suffered a spinal injury during a high school football game. (Photo by Chris Granger | The Times-Picayune | The New Orleans Advocate)

As for school, he jokingly told Owen, "It's fun, but the school part sucks." He's looking forward to life after college, when he hopes to have a career in sports administration.

His love of football hasn't diminished, and his on-campus job is working in the player personnel office for the LSU football program, which handles recruitment.

"It was a great year last year, then 2020 came," Doherty said with a smile.

But his biggest goal remains to walk again. Owen and Hidalgo believe he will.

"You're going to walk again, I know it's going to happen," Hidalgo told Doherty. The reason, he said, is Doherty's spirit. "I really would not tell that to a lot of patients."

The steering wheel on the modified truck that Michael Doherty drives. Doherty recently visited with the team at Lakeview Regional Medical Center near Covington that helped him during surgery and recovery following a spinal injury he suffered while playing high school football in November 2016. Doherty uses a wheelchair to get around but he and his doctors hope he'll be able to walk again in the future. (Photo by Chris Granger | The Times-Picayune | The New Orleans Advocate)

Owen pointed to advances in research, including stem cell therapy and robotics, and Doherty's youth. Statistically, those most likely to succeed are often athletes, he said, because they understand the demands that must be met to do something like winning a two-minute race.

For Doherty, the race is more of a marathon, but one he intends to win.

He found himself in a reflective mood after watching a football game at his alma mater before Thanksgiving, prompting him to make a rare post on social media. "Four years ago, I played my last football game and my life was forever changed," he wrote. "I miss playing football, and I wish I could play one more game."

But he also stressed the positives in his life. "I want to thank every doctor, nurse and therapist that has helped me along the way," he wrote. "I appreciate everything you had done for me. This journey will not stop until I reach my final goal of walking again."

"I wouldn't be where I am today without them."

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Four years after devastating spinal injury, former St. Paul's football player reunites with caregivers - NOLA.com

New Combination Therapy Tested By Children’s May Offer Hope For Leukemia Patients – WVXU

Cancer cells pose an uncanny ability to make new cells and dodge drugs, "somewhat like would-be robbers hacking the bank's alarm code," one doctor explains. But researchers at Cincinnati Children's Hospital Medical Center have figured out how cancer cells rewire themselves and, in turn, how to possibly overcome drug resistance.

This drug resistance may explain why some acute myeloid leukemia (AML) and other cancer patients suffer fatal relapses despite many improvements in leukemia outcomes over the years, according to a Children's news release.

"Overcoming resistance to therapy remains a holy grail of leukemia treatment," says Yi Zheng, Ph.D., director, experimental hematology and cancer biology at Cincinnati Children's. Zheng and his colleagues have now discovered a way to boost the effectiveness ofmTOR inhibitors, which prohibit unwanted cell proliferation.

"While the latest study is based on mouse models, building upon the findingspublished Dec. 21, 2020, in PNASeventually could improve outcomes for people with AML, and possibly other forms of cancer," a release says.

What Happens When Treatments Target mTOR?

"Using a novel mouse model, we have learned that deleting the mTOR gene prompts blood stem cells to multiply rapidly to open other pathways to continue producing new blood cells," says Zheng, the study's senior author. "We also found that leukemia cells use a similar response to continue multiplying despite mTOR-inhibiting treatments."

He says attacking mTOR essentially sets off alarms among hemopoietic stem cells (HSCs), which act like blood cell factories deep in bone marrow. Then the cells themselves produce a flood of new, re-wired blood cells. These re-wired stem cells, treated with mTOR inhibitors, can begin multiplying, rendering mTOR inhibitor drugs useless.

The co-authors say mTOR treatment resistance can be counteracted by inhibiting activity of the MNK, CDK9 or c-Myc genes. So-called BET inhibitors can act against c-Myc activity. Other inhibitors that are in clinical trials can act against CDK9.

Next Steps

Scientists at Cincinnati Childrens have already launched some of the research needed to prepare the combination therapies for in vivo test leading to human clinical trials, the news release says. That process will take time, but since mTOR inhibitors have been widely tested in clinical trials, investigators have a head start on exploring combination therapies.

Longer term, the findings may extend beyond AML, Zheng says, because mTOR has been a recognized target in most human cancers, including solid tumors like brain tumors.

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New Combination Therapy Tested By Children's May Offer Hope For Leukemia Patients - WVXU

Ashley Cain says over 80,000 people registered for stem cell donation in 48 hours after appeal to save baby – The Sun

ASHLEY Cain has revealed more than 80,000 have people joined the stem cell register after he pleaded for the public's help to save his baby daughter's life.

Little Azaylia was diagnosed with one of the rarest forms of leukaemia, AML [Acute Myeloid Leukaemia] , last month and needs a stem cell transplant to beat the disease.

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Ashley, 30, called upon his fans to help him and his partner Safiyya Vorajee find a donor - along with the charitable organisations DKMS and Anthony Nolan - for the four-month-old tot.

In a new interview, Ashley and Safiyya have spoken for the first time at their shock at the overwhelming amount of support they received and opened up about the turmoil they're going through as they watch their baby daughter fight for her life.

Former footballer Ashley said: "When Azaylia needed a donor the amount of people who came together straight away to order test kits, do the tests and then send them back, was crazy.

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"The DKMS and Anthony Nolan probably get around 30,000 to 40,000 registers a year. We got 80,000 people in a single weekend.

"It's now topping 100,000. And not only are they helping Azaylia, they are helping the thousands of people who also need donors.

"Social media can be such a cruel and cynical place at times but this has made me realise how beautiful it can be and how beautiful the people using it can be.

"For that support we will be forever grateful."

Ashley and Safiyya are currently living in a hotel next to Birmingham Children's Hospital to ensure they can be with their daughter around the clock.

Because of Covid-19 restrictions the couple can not be with their baby daughter together so spend 24 hours a day with her on rotation so they can both spend equal amounts of time with her.

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When they first discovered Azaylia was sick, Ashley said the couple were warned to expect the worst.

He explained: "When Azaylia first got diagnosed it looked really bleak.

"Me and you as normal people would have a white cell count of five. Someone with leukaemia, even an adult, would have a white cell count of 40.

"Azaylia had a white cell count of 200. Plus tumours in her lungs, kidneys and stomach.

"I am strong but having that news was something I never thought I would have to go through. It broke me. I was a broken man."

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Azaylia has since undergone two rounds of chemotherapy and is responding well to treatment.

However she will need a life-saving transplant in order to beat the disease once and for all.

Ashley added: "Its very rare to have leukaemia in babys as young as Azaylia, she is the only baby on the ward.

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"And she also has AML, the most aggressive type of leukaemia, which is even rarer.

"And what is even rarer again is the fact that she had tumours on her stomach, her lungs and her kidneys. And that her white blood cell count was so high.

"Realistically for her to have even got to this point is an absolute miracle."

Ashley and Safiyya also wanted to speak publicly to warn other parents about the signs to look out for after doctors repeatedly misdiagnosed Azaylia.

Ashley said: "We had back and forth to the doctors over the course of four weeks. She had cold type symptoms and we got told she had a blocked nose. At points we were pleading with the doctors to let us come in because we knew something wasnt right.

"Then we were told she had colic and then they told us she had constipation. We did all the things to treat that and then we noticed the mottling."

Going back to the beginning, Safiyya continued: There was an occasion four weeks after Azaylia was born when there was red spotting in her nappy.

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I went to the doctors and they told me to keep an eye on it. Then a little while after she had a really bloated stomach. I called up the doctor and then I took them in for her first course of injections.

Prior to her having her six week injection the doctor gave her a once over. I told the doctor about her stomach and that her chest was really heavy, it sounded like her chest was rattling it was like she couldnt breathe properly.

Her eyes were gunking up too, to the point where they were really swollen. It was making her face then swollen.

The tummy was so hard, it was like a hard ball, obviously now that was all the tumours. They gave her laxatives to try and sort it out, they gave us colic mixture, they gave us a spray for her nose

To know a doctor has felt over all the symptoms that were there, and there were two-three-four-five doctors we saw. The doctor I sent the picture of the mottling to was an on call doctor and he was the one who said take her immediately to A and E.

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The couple now credit Azaylia for giving them the strength to continue their appeal for donors.

Ashley added: We call Azaylia little lion, she has the face of an angel and the heart of a lion.

It is personally inspiring every day for us to see her sheer strength. Her waking up smiling every day, no matter what she is going through, gives us strength.

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We also have to thank Birmingham Childrens hospital. We heard a lot about them before and everything we had heard was right.

From the nurses to the cleaners to the doctors, everyone goes the extra mile. They do incredible work but they also make you feel so at home.

Its those little touches and the extra effort they put into helping you which they dont get paid for. They all go the extra mile. To everyone on ward 18, they are just incredible.

If you want to help, you can join the register here.

Originally posted here:
Ashley Cain says over 80,000 people registered for stem cell donation in 48 hours after appeal to save baby - The Sun

The 11 most mind-blowing, awe-inspiring health discoveries and innovations of 2020 – Business Insider – Business Insider

MSPhotographic/Getty Images

Most kids with peanut allergies do not outgrow them. But, with a little help, some might be able to better tolerate accidental exposures.

In January, the Food and Drug Administration approved Palforzia, a new drug designed to help kids who are allergic to peanuts react better, if they are accidentally exposed.

"Because there is no cure, allergic individuals must strictly avoid exposure to prevent severe and potentially life-threatening reactions," Dr. Peter Marks, director of the FDA's Center for Biologics Evaluation and Research said at the time in a news release. "When used in conjunction with peanut avoidance, Palforzia provides an FDA-approved treatment option to help reduce the risk of these allergic reactions."

Palforzia is not designed to be administered during an allergic reaction, instead it works as an allergy exposure therapy: children ages 4 through 17 receive daily doses of peanut powder under clinical supervision, and slowly up-dose it over time.

In clinical trials, the strategy worked well, but not perfectly. When peanut-allergic kids were fed 600 milligrams of peanut protein, 67.2% of Palforzia recipients who'd been using the medication for six months tolerated it, while only 4% of the control group did.

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The 11 most mind-blowing, awe-inspiring health discoveries and innovations of 2020 - Business Insider - Business Insider

Startups are racing to reproduce breast milk in the lab – MIT Technology Review

Biomilq was on the brink of shuttering when Strickland and Egger were promised $3.5 million in funding from a group of investors led by Breakthrough Energy Ventures, which Bill Gates had established to back technologies that could reduce carbon emissions. Upending the formula industry held the promise of doing just that. As the spring of 2020 gave way to summer, the money arrived in Biomilqs bank account.

Biomilq is not the only company aiming to make a new kind of baby formula. Using a broadly similar approach, TurtleTree Labs in Singapore eventually hopes to replace all milk currently on the market, according to cofounder Max Rye. In addition to other projects, the company is working to create fortifiers that can be added to formula to duplicate the properties of breast milk. Some formulas are already fortified with proteins and carbohydrates derived synthetically or from cows milk. Another cofounder, Fengru Lin, explains that, in contrast to Biomilq, TurtleTree plans to work with the formula industry and hopes to get its products to market in 2021.

Meanwhile, Helaina, a company based in New York, will emulate breast milk through fermentation. Laura Katz, the companys founder, plans to use microbes to synthesize the milks constituent compoundsproteins, carbohydrates, and fatsand then recombine them into a nutritious liquid. Since similar processes have already won approval from the US Food and Drug Administration for products like Impossible Burgers, which are made from fermented soy protein, she hopes to face fewer regulatory hurdles than her competitors. Like Strickland and Egger, she is motivated by indignation at the lack of options for new parents.

I think the best thing we can do is support women to breastfeed, Katz says. But if thats impossible, mothers deserve something better than current infant formula. She adds, I see all this innovation happening in cell-based meat production for people who just want to eat a burger, but the products that we feed babies have stayed static over the past 20, 30 years.

None of these propositions will be scientifically simple, in part because relatively little is known about breast milk. Most studies of human mammary epithelial cells tend to focus on their role in breast cancer rather than milk production.

As for the milk itself, its a rich and bewildering stew of thousands of chemicals. We know nutritionally about the proteins, the carbohydrates, and the fat in there. We know about some particular bioactive molecules in there, like oligosaccharides [complex sugars that feed healthy bacteria in a babys gut], IgA [the main antibody found in breast milk], bile-salt-stimulated lipase [an enzyme that aids in the digestion of fats]these things that people always bring up as being good in breast milk, says Tarah Colaizy, the research director of the Human Milk Banking Association of North America, who also teaches at the University of Iowa. But, she notes, breast milk also contains short strands of RNA, whose presence was only discovered in 2010, and whose role in infant development is not yet well understood.

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Startups are racing to reproduce breast milk in the lab - MIT Technology Review