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OPINION: What would happen if Roe v. Wade is overturned? – Westside Eagle Observer

So, what would happen if Roe v. Wade was overturned?

Should the Supreme Court overturn the Roe v. Wade decision of 1973, the issue would go back to the states, where it was prior to the 1973 decision -- where it constitutionally belongs -- and the federal government would, as before, have no jurisdiction over the issue.

It was taken from the states in violation of Amendment 10, which reserves powers not given to the federal government in Article I, Section 8, to the states or to the people, as described in the recent column, "The Word Abortion has never been in the Constitution."

Planned Parenthood would receive no federal allocations, so their extermination centers would largely disappear.

According to the Guttmacher Institute, there are 13 states that have banned most or all abortions. These are Arkansas, Idaho, Kentucky, Louisiana, Mississippi, Missouri, North Dakota, Oklahoma, South Dakota, Tennessee, Texas, Utah and Wyoming. Five additional states have a preexisting Roe v. Wade abortion ban on the books that would probably be reactivated. These are Alabama, Arizona, Michigan, West Virginia and Wisconsin. Yet another four states currently have laws banning abortion after the six-week mark which are currently ruled unconstitutional but probably would be reversed if Roe was overturned. Finally, another four states, Florida, Indiana, Montana and Nebraska, appear likely to ban or severely restrict abortion if Roe is overturned "based upon current legislative effort" (X22 Reports, Ep. 2767B -- Much to be Revealed Renegade Panicking, The Deal Keeps Iran Quiet, Control lost. May 4, 2022).

Twenty-six states, over half of the United States, would be likely to abandon abortion as an acceptable alternative to birth control. It is increasingly difficult to make babies pay for their right to exist when they have a heartbeat at six weeks old. The stain and stench of innocent blood are in the practice and cannot be hidden anymore.

Then too, revelations of genocide by Planned Parenthood in Idaho against black babies turn the stomachs of Christian and moral people. Project Veritas caught on tape a caller's question, "What about abortions for under-aged minority groups? The Planned Parenthood employee: "Certainly, and showed a willingness to accept larger donations to abort black babies!" "Caller: We just think ... You know ... the less black kids out there the better. Planned Parenthood employee: (laughs) Understandable! Understandable!"

Abortion is the Democrat Party's sacred cow. Virtually all Democrats look the other way (a form of approval) of the genocide of their own unwanted or inconvenient humankind. If racism and eugenics have merged with the party, as appears so in the conversation above to "kill off segments of the population," such is unacceptable in any society. Reportedly 79% of Planned Parenthood clinics are in minority neighborhoods (X22 Reports, Ep. 2767B, May 4, 2022, 27:00). Planned Parenthood founder Margaret Sanger certainly supported the eugenics of black babies.

This prompted Candace Owens to say, "If it wasn't for the abortion industry, the black population would be virtually doubled today" (Tucker Carlson). Let that sink in. If blacks ever come to recognize that they have been the targeted race of white Democrats for black eugenics, the Democratic Party would cease to exist overnight and Planned Parenthood facilities would likely be burned to the ground nationwide.

Another dark secret seems to be festering in Ukraine, already seen as the Deep State laundering capital of the world for dark money, bioweapons labs, illegal drugs, etc. JuliansRum posed the question, "Where do all these aborted-baby body parts go? And follows up with Ukraine as a "baby maker" operation. He asks: "Why is Ukraine at the world's forefront of fetal stem cell therapies? -- The first fetal stem cell treatment in humans occurred at the National Medical University of Ukraine. -- The world's first center to use fetal stem cells for therapeutic purposes in humans was founded in Kyiv, Ukraine. -- The world's first-ever fully licensed fetal stem cell bank was in Ukraine. -- The world's largest fetal stem cell therapy clinic (EmCell) is in Ukraine. Stem cell anti-aging therapy is big biz there." He ends with the observation that "Ukraine has become the self-styled stem cell capital of the world" (X22 Reports, Ep. 2767B -- May 4, 2022).

BBC News was the first news outlet to focus on Ukrainian research in the area ("Ukraine Babies in Stem cell probe," BBC News, by Matthew Hill, BBC Health Correspondent, Dec. 12, 2006). The column hypothesized, "There is heated debate about the ethics of using stem cells. Healthy newborn babies may have been killed in Ukraine to feed a flourishing international trade in stem cells, evidence obtained by BBC suggests." The report "describes a general culture of trafficking of children snatched at birth and a wall of silence from hospital staff upwards."

Why Ukraine? For the same reason 13 bioweapons labs existed there. The Deep State is the Ukrainian government and is unregulated in its dark science and dark money. Ukraine appears to be the world's Deep State playground for activities that civilized nations would never permit, such as "gain of function research" on human killer diseases and/or stem cell "research on live human cells." Far-fetched? Perhaps, but that is what they said about the "nonexistent" bioweapons labs before Putin took them out -- something no longer seriously disputed. Conspiracy theories have a history of becoming conspiracy realities when enough money is attached.

So what would happen to abortion if Roe v. Wade was overturned? Almost anything from returning the issue to the states in accordance with Amendment 10 to deeper revelations about eugenics on blacks in America to even darker revelations of stem cell research to preserve the youth of rich, old people -- all positive for ending the darkest chapter in the world's history.

Frankly, I believe America is tired of the guilt and shame which always accompany the practice.

Harold W. Pease, Ph.D., is an expert on the United States Consitution and a syndicated columnist. He has dedicated his career to studying the writings of the Founding Fathers and applying that knowledge to current events. He taught history and political science from this perspective for more than 30 years. To read more of his weekly articles, visit http://www.LibertyUnderFire.org. The opinions expressed are those of the author.

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OPINION: What would happen if Roe v. Wade is overturned? - Westside Eagle Observer

Hunting for the immune cells that predispose people to severe COVID-19 – EurekAlert

Some macrophages help the human body fight SARS-CoV-2 without systemic inflammation. But an aggressive subset of these immune molecules instead starts a cascade of events that can lead to multi-organ failure, researchers have discovered

image:Asst. Prof. Huanhuan Joyce Chen of Pritzker Molecular Engineering lead a new study showing that the type of macrophages present in a persons body might determine how likely they are to develop severe inflammation in response to COVID-19. view more

Credit: John Zich

When a virus makes its way into a persons body, one of the immune systems first responders is a set of pathogen-removal cells called macrophages. But macrophages are diverse; they dont all target viruses in the same way.

Researchers at the University of Chicagos Pritzker School of Molecular Engineering (PME) have discovered that the type of macrophages present in a persons body might determine how likely they are to develop severe inflammation in response to COVID-19. Their study has been published inNature Communications.

Clinicians know that COVID-19 can cause a spectrum of disease severity from mild to severe symptoms. Why some people, and not others, develop very severe disease has been a mystery, said Asst. Prof.Huanhuan Joyce Chen, who led the research with Qizhou Lian of the University of Hong Kong.This is the first time anyone has linked the variation in symptoms to macrophages.

A better model for COVID-19 infection Studying the cellular and molecular effects of the SARS-CoV-2 virus has been challenging for researchers who usually turn to model organisms to mimic human diseases; mice, rats, and many other animals dont develop the same COVID-19 symptoms as people. Thats why, shortly after the COVID-19 pandemic began, Chens group harnessed human stem cells to study the virus.

As reported previously in Nature, Chen and her colleagues grew stem cells into functioning mini-lungs and colonscalled lung and colon organoidsto probe the effects of SARS-CoV-2 on those organs and screen drugs to treat the virus.

In the new study, the researchers first analyzed lung biopsies from COVID-19 patients and discovered that they had especially high levels of macrophages. To better understand the role of macrophages during a COVID-19 infection, Chens team developed an approach that could exploit the same line of human stem cells to become both lung cells and macrophages simultaneously. The fact that they arose from the same initial stem cells was important to prevent the immune cells from attacking the lung cells.

This model system provides a perfect way to decode, step by step, how these three componentsthe immune system, the lungs, and the virusinteract, said Chen.

A cascade of inflammation When Chens lab infected the stem cell-derived lungs and macrophages with SARS-CoV-2, they found that not all macrophages responded in the same way. One subset, dubbed M2 macrophages, eliminate the virus by physically engulfing virus and virus-infected cells in a process known as phagocytosis, while releasing anti-inflammatory molecules.

M1 macrophages behaved in an opposite way: these cells released a plethora of inflammatory chemical signals that not only fight SARS-CoV-2, but cause a more widespread immune response. These same inflammatory factors have been shown to be present in the blood of people with severe COVID-19 symptoms.

Our results suggest that people who already have M1 macrophages activated in the lungs when infected with COVID-19 might be more likely to develop very severe inflammation from the virus, said Chen.

Elderly people and those with certain conditions like hypertension or diabetesalready known to be prone to more severe COVID-19 symptomsmay have higher levels of the M1 macrophages, she added.

Her team went on to show that antibodiessimilar to those already used clinically to treat COVID-19helped M2 macrophages clear the SARS-CoV-2 virus. More work is needed to show whether the observations hold true in humans, but the findings could help inform the prevention or treatment of severe COVID-19 in the most at-risk patients. And Chen is already thinking ahead to her next experiments with the stem cell-derived organoids.

This model system is useful for decoding the molecular mechanisms behind not only COVID-19, but other infectious diseases, said Chen.

In the future, her group hopes to make more complex mini-organs that include not only lung and immune cells, but blood vessels, nerves and other supporting cell types.

##

Differential effects of macrophage subtypes on SARS-CoV-2 infection in a human pluripotent stem cell-derived model

Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.

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Hunting for the immune cells that predispose people to severe COVID-19 - EurekAlert

Data at the 2022 ASCO Annual Meeting Highlight Genentech’s Continued Commitment to Innovation in Oncology and Personalized Healthcare – BioSpace

SOUTH SAN FRANCISCO, Calif.--(BUSINESS WIRE)-- Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), today announced that new data from clinical trials of 18 approved and investigational medicines across more than 20 cancer types will be presented at the 2022 American Society of Clinical Oncology (ASCO) Annual Meeting, which will be held June 3-7, 2022. Genentech and its partners will present clinical studies across medicines, comprehensive genomic tests, and real-world data at this years meeting.

At ASCO this year, progress from our portfolio, partnerships and collaborations showcase our commitment to advance innovation in cancer care, said Levi Garraway, M.D., Ph.D., chief medical officer and head of Global Product Development. Were especially pleased to present data from our broad hematology portfolio, including pivotal data for glofitamab, a potential first-in-class bispecific antibody that may improve the lives of people with heavily pre-treated aggressive lymphoma.

Focusing on improving outcomes in non-Hodgkin lymphoma

New and updated data in non-Hodgkin lymphoma will be presented at ASCO. This includes pivotal data from the Phase II NP30179 study investigating glofitamab, an investigational CD20xCD3 T-cell engaging bispecific antibody, in heavily pre-treated patients with diffuse large B-cell lymphoma (DLBCL). DLBCL is an aggressive form of lymphoma, where as many as 40% of patients will relapse, at which point treatment options are limited and survival is shortened. Glofitamab is part of Genentechs broad bispecific antibody development program, which may offer a new immunotherapy-based approach to tackle a range of blood cancers. It is being investigated in several clinical trials including the STARGLO Phase III study, evaluating glofitamab in combination with gemcitabine and oxaliplatin (GemOx) versus MabThera/Rituxan (rituximab) in combination with GemOx in autologous stem-cell transplant ineligible relapsed or refractory DLBCL. In addition, key findings from an analysis of the Asia subpopulation from the pivotal Phase III POLARIX study investigating Polivy (polatuzumab vedotin) in combination with MabThera/Rituxan plus cyclophosphamide, doxorubicin and prednisone (R-CHP) in people with newly diagnosed DLBCL will be featured. Polivy plus R-CHP is the first treatment regimen to significantly improve outcomes in previously untreated DLBCL in more than 20 years, potentially transforming treatment for people with this disease.

Driving innovation in personalized cancer care

More than 20 new pieces of research from partnerships with Foundation Medicine will be presented, which continue to support innovation as well as progress in personalized cancer care. This includes new data from the Phase II Profiler02 study,* which investigates the use of a comprehensive genomic profiling testing panel from Foundation Medicine, with the aim of informing possible treatment decisions for patients based on their tumors unique genomic information.

Data from the imCORE network

Additionally, three abstracts from the Immunotherapy Centers Of Research Excellence (imCORE) Network will be presented at ASCO: a Phase I study** investigating autogene cevumeran (an mRNA-based individualized neoantigen-specific immunotherapy [iNeST]***) in the adjuvant setting of pancreatic ductal adenocarcinoma; a data mining study** evaluating intermediate endpoints for survival in metastatic breast cancer in the real-world setting; and a study identifying mechanisms of acquired resistance to immune checkpoint blockade.**

imCORE is an academic-industry network for scientific collaboration. Established by Genentech and connecting experts from 26 leading institutions around the globe, imCORE is committed to advancing and accelerating cancer immunotherapy research. imCORE is an example of Genentechs dedication to collaborating with the global cancer community to further understand cancer biology and immunology, help inform the development of potential future treatment, and transform patients lives.

Genentechs data presented at ASCO will feature its efforts to drive innovation and commitment to health equity through delivery of pioneering medicines and personalized cancer care that together improve outcomes for every patient while reducing the cost to society, inclusive clinical trials that remove barriers to participation, partnerships that multiply our ability to address challenges in cancer care, and bringing innovation into earlier stages of disease to maximize a chance of cure.

Overview of key presentations featuring Genentech medicines

Medicine

Abstract title

Abstract number

Blood cancer

Glofitamab

Glofitamab in patients (pts) with relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) and 2 prior therapies: Pivotal Phase II expansion results

#7500

Mosunetuzumab

CELESTIMO: a Phase III trial evaluating the efficacy and safety of mosunetuzumab plus lenalidomide versus rituximab plus lenalidomide in patients with relapsed or refractory follicular lymphoma who have received 1 line of systemic therapy

#TPS7588

Polivy

Asia subpopulation analysis from the Phase III POLARIX trial

#7558

Initial safety run-in results of the Phase III POLARGO trial: polatuzumab vedotin plus rituximab, gemcitabine, and oxaliplatin in patients (pts) with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL)

#7551

Lung cancer

Tiragolumab

SKYSCRAPER-02: primary results of a Phase III, randomized, double-blind, placebo-controlled study of atezolizumab (atezo) plus carboplatin plus etoposide (CE) with or without tiragolumab (tira) in patients (pts) with untreated extensive-stage small cell lung cancer (ES-SCLC)

#LBA8507

Breast cancer

Giredestrant

Neoadjuvant giredestrant (GDC-9545) plus palbociclib (P) versus anastrozole (A) plus P in postmenopausal women with estrogen receptor-positive, HER2-negative, untreated early breast cancer (ER+/HER2 eBC): final analysis of the randomized, open-label, international Phase 2 coopERA BC study

#589

Inavolisib

Long-term safety of inavolisib (GDC-0077) in an ongoing Phase 1/1b study evaluating monotherapy and in combination (combo) with palbociclib (palbo) and/or endocrine therapy in patients (pts) with PIK3CA-mutated, hormone receptor-positive/HER2-negative (HR+/HER2) metastatic breast cancer (BC)

#1052

Tumor agnostic treatment and personalized healthcare

Rozlytrek

Efficacy/safety of entrectinib in patients (pts) with ROS1-positive (ROS1+) advanced/metastatic NSCLC from the Blood First Assay Screening Trial (BFAST)

#LBA9023

Rozlytrek

Trial in progress: a randomized Phase 3 study of entrectinib vs crizotinib in patients (pts) with locally advanced/metastatic ROS1 fusion-positive (fp) NSCLC with or without baseline CNS metastases (mets)

#TPS9141

Comprehensive genomic profiling

(IIS, Centre Lon Brard)

Increasing targeted therapy options for patients with relapsed cancer with broader somatic gene panel analysis from the primary tumor: The Profiler02 randomized Phase II trial*

#3130

Comprehensive genomic profiling

Clinical and genomic characteristics of patients with durable benefit from immune checkpoint inhibitors (ICI) in advanced non-small cell lung cancer (aNSCLC)

#9048

Comprehensive genomic profiling

ctDNA Shed as a Tool to Select Immune Checkpoint Inhibitors (ICPI) with or without Chemotherapy for Patients (pts) with advanced Non-small Cell Lung Cancer (aNSCLC)

#9045

Comprehensive genomic profiling

Trial in progress: LCMC LEADER Neoadjuvant Screening Trial: LCMC4 Evaluation of Actionable Drivers in Early Stage Lung Cancers

#TPS8596

Real world data

A real world (rw) evidence study quantifying the clinical value of multi-gene testing in early-stage lung adenocarcinoma (LUAD)

#8525

Real world data

Real world analysis of quantitative MET copy number (CN) as a biomarker in advanced NSCLC (aNSCLC)

#9123

Real world data

Ancestry-based differences in gene alterations in non-small cell lung cancer: real-world data using genetic ancestry analysis

#9125

imCORE,

ISR, Genentech

Identifying mechanisms of acquired immune escape from sequential, paired biopsies**

#2519

imCORE

ISR, Dana-Farber Cancer Institute

Real-World Progression-Free Survival (rwPFS) and Time to Next Line of Therapy (TTNT) as Intermediate Endpoints for Survival in Metastatic Breast Cancer: A Real World Experience**

#6520

imCORE

ISR, Memorial Sloan Kettering Cancer Center

Phase I Trial of Adjuvant Autogene Cevumeran, an Individualized mRNA Neoantigen Vaccine, for Pancreatic Ductal Adenocarcinoma**

#2516

* IIS, investigator-initiated study

** ISR, institution-sponsored research

*** jointly developed by Genentech and BioNTech

About Polivy (polatuzumab vedotin-piiq)

Polivy is a first-in-class anti-CD79b antibody-drug conjugate (ADC). The CD79b protein is expressed specifically in the majority of B cells, an immune cell impacted in some types of non-Hodgkins lymphoma (NHL), making it a promising target for the development of new therapies. Polivy binds to CD79b and destroys these B cells through the delivery of an anti-cancer agent, which is thought to minimize the effects on normal cells. Polivy is being developed by Genentech using Seagen ADC technology and is currently being investigated for the treatment of several types of NHL.

Polivy U.S. Indication

Polivy is a prescription medicine used with other medicines, bendamustine and a rituximab product, to treat diffuse large B-cell lymphoma in adults who have progressed after at least two prior therapies.

The accelerated approval of Polivy is based on a type of response rate. There are ongoing studies to confirm the clinical benefit of Polivy.

Important Safety Information

Possible serious side effects

Everyone reacts differently to Polivy therapy, so its important to know what the side effects are. Some people who have been treated with Polivy have experienced serious to fatal side effects. A patients doctor may stop or adjust a patients treatment if any serious side effects occur. Patients must contact their healthcare team if there are any signs of these side effects.

Nerve problems in arms and legs: This may happen as early as after the first dose and may worsen with every dose. If a patient already has nerve pain, Polivy may make it worse. The patients doctor will monitor for signs and symptoms, such as changes in sense of touch, numbness or tingling in hands or feet, nerve pain, burning sensation, any muscle weakness, or changes to walking patterns

Side effects seen most often

The most common side effects during treatment were:

Polivy may not be for everyone. A patient should talk to their doctor if they are:

These may not be all the side effects. Patients should talk to their healthcare provider for more information about the benefits and risks of Polivy treatment.

Report side effects to the FDA at (800) FDA-1088 or http://www.fda.gov/medwatch. Report side effects to Genentech at (888) 835-2555.

Please visit http://www.Polivy.com for the full Prescribing Information for additional Important Safety Information.

About Tecentriq (atezolizumab)

Tecentriq is a monoclonal antibody designed to bind with a protein called PD-L1. Tecentriq is designed to bind to PD-L1 expressed on tumor cells and tumor-infiltrating immune cells, blocking its interactions with both PD-1 and B7.1 receptors. By inhibiting PD-L1, Tecentriq may enable the re-activation of T cells. Tecentriq may also affect normal cells.

Tecentriq U.S. Indications

Tecentriq is a prescription medicine used to treat adults with:

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Data at the 2022 ASCO Annual Meeting Highlight Genentech's Continued Commitment to Innovation in Oncology and Personalized Healthcare - BioSpace

How the Metaverse Will Reshape Mental Health Therapy – Entrepreneur

Opinions expressed by Entrepreneur contributors are their own.

The tech industry has seen a seismic shift in awareness around the metaverse following Facebook's rebranding to Meta and announcements about its development from other tech leaders like Microsoft, AMD, Nvidia and Epic Games. However, it's true potential lies beyond gaming, social media and consumer technology. For one thing, therapy in this new format, could soon become the standard way to get and provide mental health care.

In this digital age of interconnectedness, our society has become more cut-off than ever before. A recent report by Harvard suggests that 36% of all Americans, including 61% of young adults, feel serious loneliness, which recent research indicates is a key risk factor for mental health conditions. One study by the American Cancer Society analyzed data from more than 580,000 adults and found that social isolation increases the risk of premature death for every race.

Unable to access face-to-face care during the pandemic, many people are turning to support online. As VR headsets grow in popularity, that same technology could soon become an essential tool for therapy that is more engaging than traditional telemedicine or mobile apps.

Related:Into theMetaverse: How Digital Twins Can Change the Business Landscape

Many healthcare companies are developing innovative new business models in the metaverse to solve current challenges. Companies that make therapy sessions more human will be the ones that will make the greatest impact on therapy in the metaverse.

Most people still prefer in-person care, as evidenced by a recent survey by The Harris Poll finding that 80% of US patients always prefer face-to-face visits. This is mainly because sessions that take place in a therapist's office provide a space away from everyday life, and can increase trust when compared to digital therapy.

Conversely,a recent pollconducted byBetterHelp, found that 35% of those surveyed claimed that their opinion of how a therapy session went, wasdependent on which day of the week the appointment took place, the weather outside (31%) or by recent current events (30%).

Thats why the metaverse care model has the potential to radically change how digital therapy is delivered. Simply put, its as close to being in-person as you can get.

Being able to access support without geographical limitations from the comfort of your home has already taken off with telemedicine, but the metaverse provides a much more life-like experience.

This new increased depth of immersion can create greater engagement, focus, and connectedness compared to other digital therapy solutions. The natural environments and the intuitive nature of the design can also lead to a greater bond between patients and providers. There is a possibility that treatment outcomes can be improved due to these potential benefits but more research is needed to find out the best way to deliver therapy through VR.

My company, Rocket VR Health, is getting ready to launch a clinical trial exploring the use of mental health therapy delivered via virtual reality in patients undergoing stem cell transplantation. We have partnered with Massachusetts General Hospital in Boston to take a well-researched conventional therapy program and transform it into an immersive VR treatment.

We hypothesize that the result will be a more effective, accessible, and data-driven approach to therapy, which could be invaluable not just for the participants in the trial, but also for countless individuals suffering from mental health conditions for years to come.

Related:The 3 Biggest Challenges to Marketing in theMetaverse

Despite all the Facebook and Web3 metaverse hype, the reality is VR headsets are expensive, and though usage is growing, its estimated that only 12.5 millionwere sold in 2021. The majority of the metaverses that currently exist are for entertainment and healthcare is typically much slower to catch on.

For starters, healthcare providers must ensure that they properly manage patient data and provide security that meets the highest standards of mental healthcare.

In addition, further research needs to be done to prove the efficacy of VR therapy and convince insurance companies to cover this new treatment delivery method. Were hoping that research like our study with Massachusetts General will help make the case. Previous research findings are positive, and the FDA approved the first VR software as a medical device to treat pain management. Meanwhile, insurance companies are already covering VR-based telemedicine.

Lastly, the most compelling therapy offerings will provide headsets to patients directly, so that access to the most well-researched, cutting-edge treatments isnt dependent upon individual purchases of VR technology by consumers.

The exciting news is that a small but growing group of researchers, technologists and investors are already beginning to overcome these challenges. Slowly but surely, the metaverse will be a bigger part of all of our lives, and given the proper attention mental health may prove to be one of its best use cases in due time.

Related:Why Intellectual Property Will Dominate NFTs

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How the Metaverse Will Reshape Mental Health Therapy - Entrepreneur

Premature Ovarian Failure Treatment Market Size 2022 Share, New Trends, Industry News, Business Growth, Top Key Players Analysis to 2028 The Daily…

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Continued

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Premature Ovarian Failure Treatment Market Size 2022 Share, New Trends, Industry News, Business Growth, Top Key Players Analysis to 2028 The Daily...

Precision Cancer Therapies Market Size And Forecast | Abbott Laboratories, Bayer HealthCare, GlaxoSmithKline, OncoGenex Pharmaceuticals, Hospira,…

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Precision Cancer Therapies Market Types Outlook (Revenue, USD Million, 2017 2029)

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North America (United States, Canada, and Mexico) Europe (Germany, France, UK, Russia, and Italy) Asia-Pacific (China, Japan, Korea, India, and Southeast Asia) South America (Brazil, Argentina, Colombia, etc.) Middle East and Africa (Saudi Arabia, UAE, Egypt, Nigeria, and South Africa)

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Precision Cancer Therapies fragmentation on the basis of product type, end-use, and region Comprehensive assessment of upstream starting materials, downstream demand, and present market landscape Collaborations, R&D projects, acquisitions, and product launches of each Precision Cancer Therapies player Various regulations imposed by the governments on the consumption of Precision Cancer Therapies in detail Impact of modern technologies, such as big data & analytics, artificial intelligence, and social media platforms on the Precision Cancer Therapies

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Precision Cancer Therapies Market Size And Forecast | Abbott Laboratories, Bayer HealthCare, GlaxoSmithKline, OncoGenex Pharmaceuticals, Hospira,...

Cystinuria Treatment Market indication by Industry Dynamics, Regional breakdown and Forecast 2022- 2027 The Daily Vale – The Daily Vale

New York, United States: The Cystinuria Treatment Market research report crafted by DECISIVE MARKETS INSIGHTS delineates a list of the latest upgrades of the different business plans including several units and collaborations embraced by the significant global market leaders. It elucidates a crystal-clear scenario regarding the adoption of upgraded technologies for expansion of the customer base as well as enlarging the current competitive global market. The most possible CAGR percentage over the forecasted period of 2020-2027 has been thoroughly incorporated.

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Cystinuria Treatment Market Segmentation- By Type : Gene Therapy, Copper Injection Therapy By Application : Hospitals, Homecare, Specialty Clinics and Others By Key Players : Retrophin, Inc, Mission Pharmacal Company, Revive Therapeutics Ltd, Teva Pharmaceutical Industries Ltd, Amerigen Pharmaceuticals Limited, Mylan N.V., Bausch Health, Zhejiang Huahai Pharmaceutical Co., Ltd, WOCKHARDT

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Cystinuria Treatment Market indication by Industry Dynamics, Regional breakdown and Forecast 2022- 2027 The Daily Vale - The Daily Vale

Chronic Granulomatous Disease Treatment Market New Report 2027: Research Methodology Focuses On Exploring Major Factors Influencing The Industry…

Chronic Granulomatous Disease Treatment Market is expected to grow at a CAGR of 8.46% .

Decisive Markets Insights Global Chronic Granulomatous Disease Treatment Market research report on Global market growth (Status and Outlook) 2020-2026 provides detailed information and an overview of the critical factors required to make a sound business decision. Global Market Sizing: A Comprehensive Analysis of Global, Regional, and Country Markets features a detailed examination of market factors, including competitive analysis, market size, market share, opportunities, and sales analysis, along with value chain analysis, and value chain optimization. There are nine market segments within the report, each addressing applications, types, regional outlooks, market demands, latest trends, and industry shares and revenue by manufacturers, company profiles, and growth forecasts.

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Chronic Granulomatous Disease Treatment Market Segmentation- By Type : Medication, Bone Marrow Transplant, Gene Therapy, Others By Application : Hospitals, Homecare, Specialty Clinics, Others By Key Players : Clinigen Group plc, Orchard Therapeutics plc, Gnthon, Horizon Therapeutics plc, ViroMed. Co.Ltd, Bellicum Pharmaceuticals, Inc., Pfizer Inc., F. Hoffmann-La Roche Ltd, Novartis AG, Lonza, GlaxoSmithKline plc., Eli Lilly and Company, Johnson & Johnson Services, Inc., Merck KGaA, Smith & Nephew, JCR Pharmaceuticals Co.Ltd, MaxCyte, Inc., Fresenius Kabi AG, Sun Pharmaceutical Industries Ltd., Antares Pharma

This report is wide in concept and content right from Chronic Granulomatous Disease Treatment market The Global Market Report is important because: By providing an overall view of the global market, the Chronic Granulomatous Disease Treatment Market report provides significant insights into the global market. Market segments are categorized into sub-segments and geography. To provide a more detailed analysis and understanding of the market, the key segments have been further categorized into sub-segments. This Chronic Granulomatous Disease Treatment Market report covers a comprehensive analysis of market trends and factors impacting the global industry. According to the report, market concentration rate, price trends, growth opportunities, and raw material expenditure graph are used to summarize the market.The report covers several vendors operating in the global market. There are also complete statistics for numbers, divisions, revenue, and shares, and an analysis of current trends, opportunities, and industry news.

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Answers to the following questions about the market are discussed in the report: Which companies dominate the global market? In what ways will a variety of factors affect market growth? In the global market, what mergers and acquisitions, product launches, and collaborations have taken place recently? How would you classify the market? How do major players formulate their strategies? Where will the fastest growth occur in the application segment? In what way is the market expected to grow? What is the most likely regional market to emerge as the winner in the next few years? Which growth strategies are employed by the companies to maintain their position on the global market?

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The reports objectives are as follows: A projection of sales volume and value for key market segments is required. In addition to defining, describing, and analysing the sales volumes, values, market shares, and competitive landscape of key companies. A new product launch, an acquisition, or an expansion in the market will be assessed based on the competitive environment. By identifying its various sub-segments, you can gain an understanding of the structure of the market. Detailed information will be provided regarding the key factors influencing the market growth (growth potential, opportunities, challenges, and risks). To study and analyse the market size, key regions, products, end-user and forecast to 2026.

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Chronic Granulomatous Disease Treatment Market New Report 2027: Research Methodology Focuses On Exploring Major Factors Influencing The Industry...

StageZero Life Sciences Partners with DiagnoseAtHome to Offer Aristotle(R) Multi-Cancer Blood Test in Canada and USA – Digital Journal

First-ever mRNA gene expression, multi-cancer panel simultaneously screens for multiple cancers from a single sample of blood

TORONTO, ON and RICHMOND, VA / ACCESSWIRE / May 25, 2022 / StageZero Life Sciences, Ltd. (TSX:SZLS) (OTCQB:SZLSF) (StageZero or the Company), a vertically integrated healthcare company devoted to improving the early detection and management of cancer and other chronic diseases through leading-edge molecular diagnostics and clinical interventions, today announced that it has partnered with DiagnoseAtHome (DAH) to make the Companys multi-cancer blood test, Aristotle, available to DiagnoseAtHomes patients in Canada and the USA. Built on StageZeros proprietary mRNA gene expression technology platform, Aristotle is a next-generation test which simultaneously screens for multiple cancers from a single sample of blood.

DiagnoseAtHome offers accessible at-home health and lab testing solutions, allowing businesses, organizations, and healthcare providers to offer safe, accurate and discreet lab testing to patients as an alternative to in-person laboratory visits. Powered by a proprietary technology platform, DAH partners with telehealth organizations, assisted living, long-term care facilities, corporations, self-insured employers, healthcare providers, and clinics.

Our partnership with DiagnoseAtHome allows greater access to early cancer screening for their many clients and broadens the availability of Aristotle in Canada and the USA, said James Howard-Tripp, Chairman and CEO of StageZero Life Sciences. Growing our patient base and expanding the availability of our early cancer test is a key pillar in our Growth Strategy. We look forward to working with DiagnoseAtHome and their patients and clients.

Our partnership with StageZero Life Sciences furthers our mission to provide accessible cutting edge diagnostic solutions to patients and providers at scale said Dr Ian Plener, founder of DiagnoseAtHome. By onboarding Aristotle to the DAH platform, we are better able to provide our patients and providers with a novel approach to early cancer screening. Growing our laboratory network will further enhance the breadth of curated laboratory solutions available to our growing patient and provider base. We look forward to working with the entire StageZero Life Sciences team.

Aristotle is the first-ever mRNA multi-cancer panel for simultaneously screening for multiple cancers from a single sample of blood with high sensitivity and specificity for each cancer. The Aristotle test works by interrogating mRNA from a sample of whole blood and detecting gene expression profiles indicative of specific cancers. Aristotle screens for the molecular signatures associated with multiple, individual cancers, including breast, ovarian, endometrial, colorectal, liver, stomach, prostate, and others.

To learn more, please visit https://www.stagezerolifesciences.com/aristotle-test.html.

About StageZero Life Sciences, Ltd.

StageZero Life Sciences, Ltd. is a vertically integrated healthcare company dedicated to improving the early detection and management of cancer and other chronic diseases through next-generation diagnostics and unique telehealth programs that provide clinical interventions to assist patients who currently have cancer (COC Protocol) as well as help patients reduce the risk of developing late-stage disease (AVRT).

The Companys next generation test, Aristotle, is the first ever mRNA multi-cancer panel for simultaneously screening for multiple cancers from a single sample of blood with high sensitivity and specificity for each cancer. Aristotle uses mRNA technology to identify the molecular signatures of multiple cancer types and is built on the Companys patented technology platform, the Sentinel Principle. This underlying technology has been validated in more than 9,000 patients and used by more than 100,000 patients in North America.

The Care Oncology Clinic offers a supervised treatment regimen (the COC Protocol) for people diagnosed with cancer of any type or stage. Developed by scientists and oncologists, the COC Protocol is intended for adjunctive administration alongside standard-of-care cancer therapy. It is an individualized therapeutic approach which seeks to simultaneously target multiple metabolic cancer pathways. The aim is to restrict cancer cell energy supply and use, which may make it more difficult overall for cancer cells to survive, grow, and adapt to changing conditions in the body. As a result, such cells can potentially become more vulnerable to attack from cell-killing therapies such as radiotherapy and chemotherapy. The patented COC Protocol incorporates a multifaceted approach, supported by peer-reviewed scientific studies, which highlight the potential of certain treatments to target the specific energy requirements of cancer cells, impacting their ability to grow and multiply.

AVRT is a physician-Led, telehealth program for identifying and managing the early warning signs of cancer and chronic disease. Our program includes: a comprehensive online health evaluation; blood tests to measure markers of inflammation and metabolism; an in-depth initial physician consultation; regular physician follow-up appointments and interval screening.

Aristotle, as well as additional cancer diagnostics (ColonSentry, and the Prostate Health Index) are processed at the Companys clinical laboratory, StageZero Life Sciences, Inc., a CAP accredited and CLIA certified high-complexity reference laboratory in Richmond, Virginia. In addition, the Company is also leveraging its specialty in polymerase chain reaction (PCR) testing to provide COVID-19 PCR testing (swab and saliva) and Antibody Testing (blood analysis).

StageZero Life Sciences trades on the Toronto Stock exchange under the symbol SZLS and on the OTCQB under the symbol SZLSF.

About DiagnoseAtHome:

DiagnoseAtHome is a multichannel health technology company specializing in at-home health and laboratory testing solutions, allowing businesses, organizations and healthcare providers to offer safe, accurate and discreet lab testing to patients as an alternative to in-person laboratory visits. DiagnoseAtHome has partnered with leading virtual care organizations, corporations and healthcare providers to support modern and scalable accessibility to diagnostic testing. Harnessing a leading proprietary technology platform, DAH delivers the most comprehensive, affordable and efficient at-home lab testing platform with the most expansive test menu. DAHs propriety technology platform integrates with a broad network of ISO, CLIA and CAP-certified high complex laboratory partners, providing the most reliable, accurate and expansive at-home laboratory capabilities. DAHs logistics arm has perfected over-the-mail testing, providing best in class medical kitting, stability and results validation. With a focus on research and innovation, the DAH platform will continue to be at the forefront of health tech innovation.

Forward-Looking Statements

This press release contains forward-looking statements identified by words such as expects, will and similar expressions, which reflect the Companys current expectations regarding future events. The forward-looking statements involve risks and uncertainties that could cause the Companys actual events to differ materially from those projected herein. Investors should consult the Companys ongoing quarterly filings and annual reports for additional information on risks and uncertainties relating to these forward-looking statements. The reader is cautioned not to rely on these forward-looking statements. The Company disclaims any obligation to update these forward-looking statements, except as required by law.

Important Safety Information

The Aristotle, and ColonSentry tests were developed, and their performance characteristics determined, by Stage Zero Life Sciences, Inc. They have not been cleared or approved by the U.S. Food and Drug Administration. These tests are performed in a CLIA certified laboratory and are intended for clinical purposes. These tests must be ordered by and used only in consultation with a healthcare provider.

For further information please contact:

Investor Relations

Rebecca Greco 1-855-420-7140 ext. 1838 [emailprotected]

Media Contact Kristin Villiotte SHIFT Communications [emailprotected]

SOURCE: StageZero Life Sciences Ltd

View source version on accesswire.com: https://www.accesswire.com/702700/StageZero-Life-Sciences-Partners-with-DiagnoseAtHome-to-Offer-AristotleR-Multi-Cancer-Blood-Test-in-Canada-and-USA

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StageZero Life Sciences Partners with DiagnoseAtHome to Offer Aristotle(R) Multi-Cancer Blood Test in Canada and USA - Digital Journal

Leigh Syndrome Treatment Market Research Study, Future Prospects and Growth Drivers to 2029 | Top Key Vendors GKS, Brother Enterprises, Huazhong The…

Overview of Global Leigh Syndrome Treatment Market:

An international Leigh Syndrome Treatment Market report is an excellent report that makes it possible to the Healthcare industry to take strategic decisions and achieve growth objectives. Such a great report has been prepared by a team of enthusiastic analysts, skilled researchers and experienced forecasters who work meticulously for the same. This report will act as a sure shot solution to the challenges and problems faced by Healthcare industry. The scope of Leigh Syndrome Treatment Market research report involves industry research, customer insights, market sizing and forecast, competitive analysis, market entry strategy, pricing trends, sustainability trends, innovation trends, technology evolution, and distribution channel assessment.

The Global Leigh Syndrome Treatment Market is expected to gain market growth in the forecast period of 2022 to 2029.

Available Exclusive Sample Copy of this Report @ https://www.databridgemarketresearch.com/request-a-sample/?dbmr=global-leigh-syndrome-treatment-market .

Leigh Syndrome Treatment Market report is a defined study of the Healthcare industry which explains what the market definition, classifications, applications, engagements, and global industry trends are. This global market report contains all the company profiles of the major players and brands. The market drivers and restraints have also been explained using SWOT analysis. The report exhibits important product developments and tracks recent acquisitions, mergers and research in the Healthcare industry by the key players. An influential Leigh Syndrome Treatment Market research report not only gives an advantage to grow business but also helps outshine the competition.

According to the market report analysis, Leigh Syndrome is a rare, genetic neurodegenerative disease which rarely occurs in teenagers or adults. Symptoms typically progress quickly. Early symptoms could include poor sucking ability, loss of head and motor skills, loss of appetite, vomiting and seizures. Symptoms may include weakness and lack of muscle tone, spasticity, movement disorders, cerebellar ataxia, and peripheral neuropathy, as the condition progresses.

Some of most important key factors driving the growth of the Global Leigh Syndrome Treatment Market are rising prevalence of treatment procedures such as gene therapy and RNA therapeutics.

Global Leigh Syndrome Treatment Market Segmentation:

Based on the Type, the Global Leigh Syndrome Treatment Market is segmented into mitochondrial DNA-associated leigh syndrome, and nuclear gene-encoded leigh syndrome.

Based on the Treatment, the leigh syndrome treatment market is segmented into magnetic resonance imaging (MRI), computed tomography (CT), laboratory test, and others.

Based on the Route of Administration, the leigh syndrome treatment market is segmented into oral, parenteral, and others.

Based on the End-Users, the leigh syndrome treatment market is segmented into hospitals, specialty clinics and others.

Regional analysis, Americas is expected to hold the largest share of the leigh syndrome treatment market for treating leigh syndrome due to the increasing mitochondrial disorders in the U.S. Leigh syndrome is much more prevalent in other groups, according to the National Center for Advancing Translational Science (NIH).

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Global Key Vendors:

GlaxoSmithKline Plc

Brother Enterprises

Huazhong

Zhejiang Tianxin

Stryker Corporation

Zimmer Biomet Holdings, Inc

Wright Medical Technology, Inc

Integra LifeSciences Holdings Corporation

Key questions answered in the report:

What will the market growth rate of Leigh Syndrome Treatment market in 2029? What are the key factors driving the global Leigh Syndrome Treatment market? What are sales, revenue, and price analysis of top manufacturers of Leigh Syndrome Treatment market? Who are the distributors, traders and dealers of Leigh Syndrome Treatment market? Who are the key manufacturers in Leigh Syndrome Treatment market space? What are the Leigh Syndrome Treatment market opportunities and threats faced by the vendors in the global Leigh Syndrome Treatment market? What are sales, revenue, and price analysis by types and applications of Leigh Syndrome Treatment market? What are sales, revenue, and price analysis by regions of Leigh Syndrome Treatment market? What are the market opportunities, market risk and market overview of the Leigh Syndrome Treatment market?

For More Insights Get FREE Detailed TOC of Global Leigh Syndrome Treatment Market Report 2022 @ https://www.databridgemarketresearch.com/toc/?dbmr=global-leigh-syndrome-treatment-market .

Major Highlights of TOC: Global Leigh Syndrome Treatment Market

1 Global Leigh Syndrome Treatment Market Overview

2 Global Leigh Syndrome Treatment Market Competitions by Manufacturers

3 Global Leigh Syndrome Treatment Capacity, Production, Revenue (Value) by Region (2022-2029

4 Global Leigh Syndrome Treatment Supply (Production), Consumption, Export, Import by Region (2022-2029)

5 Global Leigh Syndrome Treatment Production, Revenue (Value), Price Trend by Type

6 Global Leigh Syndrome Treatment Market Analysis by Application

7 Global Leigh Syndrome Treatment Manufacturers Profiles/Analysis

8 Leigh Syndrome Treatment Manufacturing Cost Analysis

9 Industrial Chain, Sourcing Strategy and Downstream Buyers

10 Marketing Strategy Analysis, Distributors/Traders

11 Market Effect Factors Analysis

12 Global Leigh Syndrome Treatment Market Forecast (2022-2029)

13 Research Findings and Conclusion

14 Appendix

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Leigh Syndrome Treatment Market Research Study, Future Prospects and Growth Drivers to 2029 | Top Key Vendors GKS, Brother Enterprises, Huazhong The...