A&B could become premier stem cell producer – Antigua …

ByRobert A. Emmanuel

Officials at the StemCell Medical Center believe that Antigua and Barbuda could become the leadingnation for stem cell export and research.

The centers Chairman,Dr. Bruce Murphy made the disclosure during a press conference on Tuesday.

There is certainlythe potential that, because of the sophisticated nature of the scientificprocesses that we are using, Antigua and Barbuda could be the source of stemcells for a lot of different countries.

Dr. Murphy noted that,for the time being, the facility will be importing stem cells from the UnitedStates.

These stem cells aregoing to be derived from fetal cord blood, which is the part of the umbilicalcord attached to the placenta that is thrown away; it is full of young,healthy stem cells.

It will be sourced inthe US; there are multiple companies right now that take a healthy [young]woman who is pregnant, test her to be sure that she is absolutely healthy and,at the time of an elective caesarean section,get the placenta and the cord blood.

He noted that theimported stem cells will be incubated and stored on island once the clean roomhas been completed in July.

The chairman furtherexplained that the facility will be working with pluripotent stem cells, whichcan develop into bone, cartilage, muscle, an organ tissueliver, kidneyandskin and nervous tissue.

He added that thepluripotent stem cells are looking for a signal from a place in the body thatis generally inflamed and sending out inflammatory signals for them to go toand repair or call in other cells to make new tissue.

He said that everyperson is made out of stem cells and you depend on stem cells every day, yourblood everyday has to depend on stem cells out of your bone marrow to make newred blood cells, new white blood cells, new platelets.

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A&B could become premier stem cell producer - Antigua ...

Be The Match Appoints Amy Ronneberg as Chief Executive Officer – Southernminn.com

MINNEAPOLIS, June 10, 2020 /PRNewswire/ -- Be The Matchtoday announced the appointment of Amy Ronneberg as chief executive officer (CEO)the first female CEO for the organization. Ronneberg joined Be The Match in 2013 as chief financial officer (CFO) and chief of staff, and has served as acting CEO since February.

Be The Match is a non-profit organization that delivers cures to patients in need of life-saving blood stem cell therapy. The organization operates the national Be The Match Registry,the world's largest and most diverse listing of potential stem cell donors. As trusted leaders in advancing stem cell therapy, Be The Match also provides ground-breaking research, innovative technologies, patient support, and education so even more lives can be saved.

Around the same time Ronneberg joined Be The Match as CFO, she was diagnosed with breast cancer. Now cancer-free, she brings unique passion and perspective to her work.

"As a cancer survivor, I have personally felt what many other cancer patients and their loved ones encounter every day. My experience, the patients we serve, and our outstanding, dedicated employees are my motivation," Ronneberg said. "I am deeply honored to be selected to lead this organization and look forward to further advancing our commitment to providing equal outcomes for all. The recent pandemic has put a spotlight on healthcare inequalities, and we are uniquely positioned to address one glaring disparity that is affecting ethnically diverse patientsthat is the ability to find a matching donor. I look forward to leading our team in diversifying the registry and delivering more life-saving treatments to patients of all backgrounds."

After the Affordable Care Act was implemented, Ronneberg led a Be The Match budget restructure that netted a sustainable $50 million cost reduction and made marrow transplants more affordable. Those efforts and more earned her one of the Minneapolis/St. Paul Business Journal's 2016 CFO of the Year awards. Ronneberg also played a pivotal role in establishing Be The Match's operations in Mexico.

This spring, the Be The Match Board of Directors worked with an outside firm to identify the qualities needed in its next CEO and unanimously agreed that Ronneberg possesses all of them.

"Amy has the perfect blend of business experience, passion and health care expertise to lead Be The Match," said Chair of the Board David L. Porter, M.D. "She likes to say, 'patients first, employees always.' I applaud her commitment to carrying out our mission and putting people first."

Ronneberg is also responsible for Be The Match BioTherapies, which partners with global cell and gene therapy industry leaders to deliver high-quality, consistent and compliant therapies to patients in need. Under her guidance, Be The Match BioTherapies has invested in several therapeutics companies and launched an integrated supply chain platform called MatchSource.

Prior to joining Be The Match, Ronneberg spent 12 years at Capella Education Company where she served as chief accounting officer, vice president of finance and led enterprise-wide operations and customer service. She also worked for Ernst & Young as an audit manager.

Ronneberg has served on several boards and is currently on the board of Magenta Therapeutics (MGTA) and the Finance Committee for Allina Healthcare and the World Marrow Donor Association.

Ronneberg earned a Master of Business Administration from Capella University, Minneapolis, Minn. and a Bachelor of Business Administration in Accounting from University of Wisconsin-Eau Claire.

"Going through treatment with my husband and young children at my side made me a much stronger person, leader and decision maker," Ronneberg said. "Cancer is an unfortunate reality that millions of people have to face, but with support, hope and the right medical tools, it can be overcome."

About Be The MatchFor people with life-threatening blood cancerslike leukemia and lymphomaor other diseases, a cure exists. Be The Match connects patients with their donor match for a life-saving marrow or umbilical cord blood transplant. People can contribute to the cure as a member of the Be The Match Registry, financial contributor or volunteer. Be The Match provides patients and their families one-on-one support, education, and guidancebefore, during and after transplant.

Be The Match is operated by the National Marrow Donor Program (NMDP), a nonprofit organization that matches patients with donors, educates health care professionals and conducts research through its research program, CIBMTR (Center for International Blood and Marrow Transplant Research), so more lives can be saved. To learn more about the cure, visit BeTheMatch.orgor call 1 (800) MARROW-2.

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Be The Match Appoints Amy Ronneberg as Chief Executive Officer - Southernminn.com

Nick Cordero Had a ‘Rocky Night’ After He ‘Spiked a Fever’ During His Hospitalization, Wife Says – PopCulture.com

Blue Bloods actor Nick Cordero suffered a "little blip" amid his recovery from coronavirus complications after he recently "spiked a fever," his wife, Amanda Kloots, said in a health update. Taking to her Instagram Story on Tuesday, Kloots opened up about the "bit of a rocky night" her husband experienced as he remains hospitalized in the ICU at Los Angeles' Cedars-Sinai Medical Center.

Addressing fans, who have continued to rally their support around Cordero, Kloots assured that "everything is back to normal today and that was just a little blip that can happen in ICU," PEOPLE reports. She added that her husband is "stable" and "things are going, I think, good." According to Kloots, Cordero had "spiked a fever" overnight, forcing doctors "to do a little bit of fixing of that and antibiotics." She said that they will likely be "looking at doing another, hopefully, CT scan of his lungs to see what kind of progress or if there's further damage in his lungs." Throughout his more than two-month hospitalization, Cordero has suffered a number of setbacks, including lung infections.

Kloots also revealed that doctors will "maybe do another round of stem cells" treatment to help repair and strengthen his lungs. Sharing "exciting news" over the weekend, Kloots had revealed on Sunday that her husband had started stem-cell treatment, expressing her hopes that it would "help repair, strengthen Nick's lungs and get him any better" and possibly bridge "us to the next level in healing for him."

In her Tuesday update, Kloots also opened up about the difficulty of her husband being unable to celebrate and be there as their son, Elvis, turned one. She said that "it breaks my heart" and she "literally can't even talk about it because it makes me so sad." Kloots said that while her husband may not be able to be there with them, she planned "on FaceTiming so he can see Elvis." She admitted that "it's going to be really hard."

Kloots also opened up about her sons birthday in an Instagram post, in which she shared a number of photos from shortly after Elvis was born. Following his birth, Kloots said, Elvis was immediately taken to the ICU "because there was fluid in his lungs." During his two-night stay there, she and her husband "visited him all day" and they "couldn't stop staring at him and eventually holding him." Kloots concluded the post by writing, "My two Cordero men: last June Elvis is in the NICU. This June Nick is in the ICU," adding, "these guys are really trying to take me down."

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Nick Cordero Had a 'Rocky Night' After He 'Spiked a Fever' During His Hospitalization, Wife Says - PopCulture.com

Magenta Therapeutics Provides Portfolio Update: Stem Cell Mobilization and Conditioning Programs Prioritized and Advancing Toward Clinical Milestones…

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Magenta Therapeutics (NASDAQ: MGTA), a clinical-stage biotechnology company developing novel medicines to bring the curative power of stem cell transplant to more patients, today provided a portfolio update, highlighting progress and recent updates across its most advanced programs.

Magenta has multiple high-priority medicines in our portfolio, including the mobilization and targeted conditioning programs, which have the potential to benefit many patients with genetic diseases, blood cancers and autoimmune diseases. We believe that these new medicines will provide patients with life-saving treatments and we are focusing our resources to move these programs forward as efficiently as possible, said Jason Gardner, D.Phil., President and Chief Executive Officer, Magenta Therapeutics. We have made the strategic decision based on patient benefit, emerging new results, collaborations and regulatory input to prioritize these programs as they advance through clinical development. As part of this strategic decision, we will discontinue enrollment in the Phase 2 study of MGTA-456 cell therapy in patients with inherited metabolic disorders. We thank the brave patients and their families who participated in the trial, as well as the dedicated investigators and team members at the clinical trial sites.

Portfolio Updates

Magenta will participate in a fireside chat at the 41st annual Goldman Sachs Healthcare Conference today at 8:50 a.m. ET. A live webcast of the fireside chat can be accessed on the Magenta Therapeutics website at https://investor.magentatx.com/events-and-presentations. The webcast replay will be available for 90 days following the event.

About Magenta TherapeuticsHeadquartered in Cambridge, Mass., Magenta Therapeutics is a clinical-stage biotechnology company developing novel medicines for patients with autoimmune diseases, blood cancers and genetic diseases. By creating a platform focused on critical areas of unmet need, Magenta Therapeutics is pioneering an integrated approach to allow more patients to receive one-time, curative therapies by making the process more effective, safer and easier.

Forward-Looking StatementThis press release may contain forward-looking statements, including express or implied statements regarding Magentas future expectations, plans and prospects, including, without limitation, statements regarding expectations and plans for presenting pre-clinical and clinical data, the anticipated timing of our clinical trials and regulatory filings, the development of our product candidates and advancement of our preclinical programs, as well as other statements containing the words anticipate, believe, continue, could, estimate, expect, intend, may, might, plan, potential, project, should, target, will or would and similar expressions that constitute forward-looking statements under the Private Securities Litigation Reform Act of 1995. The express or implied forward-looking statements included in this press release are only predictions and are subject to a number of risks, uncertainties and assumptions, including, without limitation: uncertainties inherent in preclinical and clinical studies and in the availability and timing of data from ongoing preclinical and clinical studies; whether interim results from a clinical trial will be predictive of the final results of the trial; whether results from preclinical studies or earlier clinical studies will be predictive of the results of future trials; the expected timing of submissions for regulatory approval or review by governmental authorities, including review under accelerated approval processes; orphan drug designation eligibility; regulatory approvals to conduct trials or to market products; whether Magenta's cash resources will be sufficient to fund Magenta's foreseeable and unforeseeable operating expenses and capital expenditure requirements; risks, uncertainties and assumptions regarding the impact of the COVID-19 pandemic on Magentas business, operations, strategy, goals and anticipated timelines; the timing, progress and success of the Magentas collaborations with NMDP/Be the Match and AVROBIO; and other risks concerning Magenta's programs and operations are described in additional detail in its Annual Report on Form 10-K filed on March 3, 2020, as updated by its most recent Quarterly Report on Form 10-Q and its other filings made with the Securities and Exchange Commission from time to time. Although Magenta's forward-looking statements reflect the good faith judgment of its management, these statements are based only on facts and factors currently known by Magenta. As a result, you are cautioned not to rely on these forward-looking statements. Any forward-looking statement made in this press release speaks only as of the date on which it is made. Magenta undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future developments or otherwise.

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Magenta Therapeutics Provides Portfolio Update: Stem Cell Mobilization and Conditioning Programs Prioritized and Advancing Toward Clinical Milestones...

R3 Stem Cell International Now Offering Full Program for Rheumatoid Arthritis in Mexico – PR Web

Stem Cell Therapy for Rheumatoid Arthritis in Mexico (888) 988-0515

SAN DIEGO (PRWEB) June 11, 2020

R3 Stem Cell International is now offering a full treatment program for rheumatoid arthritis that includes upward of 200 million stem cells. All inclusive treatment starts at only $8975 and has shown immense effectiveness for RA and other autoimmune disorders.

Rheumatoid arthritis affects millions of individuals, with traditional treatment options often not working well and containing numerous side effects. For instance, Methotrexate is used often for RA patients and while it can help, it has significant toxic effects.

Stem cell therapy for rheumatoid arthritis in Mexico, on the other hand, offers excellent outcomes while being extremely safe. R3's Center in Tijuana has successfully performed hundreds of regenerative cases for arthritis, neuropathy, stroke, dementia, COPD, organ failure and autoimmune diseases.

According to R3 Founder David Greene, MD, MBA, "Our new stem cell therapy program for RA includes upwards of 200 million stem cells. Numbers matter when it comes to outcomes for autoimmune disease, so we've made sure that patients receive what's needed in a safe manner with expert providers!"

The process is not only straightforward, but also easy for patients. Starting with a free phone consultation, patients will find out if they are a candidate. Then there are two programs to choose from, one involves a five day treatment, and the other one involves four treatments over a year.

R3 International offers VIP escort transportation from San Diego to and from the treatment center. The biologics used are exceptionally safe, with the lab quality assurance standards exceeding FDA standards in the US. In addition, no preservative is necessary which means cell viability exceeds 95%!

When it comes to pricing, Dr. Greene added, "I created R3 International so we could offer effective treatment with very large cell numbers for a fraction of the cost in the US or Panama. The quality of care is phenomenal, cost effective and very safe!"

To learn more about R3 International, conditions treated, the process and getting set up for a free consultation, call (888) 988-0515 or visit https://stemcelltreatmentclinic.com for more information.

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Saanich father dies of leukemia after battle to find mixed-race stem cell donor – Saanich News

A Saanich father who fought to grow the data bank of mixed-race stem cell donors has died of leukemia.

Jeremy Chow was diagnosed with acute myeloid leukemia in November 2018. While chemotherapy treatment worked and Jeremy entered remission, doctors advised that stem cell therapy would be the best possible treatment to eradicate the risk of returning cancer cells.

But when Jeremy and his wife Evelyn Chow began their quest to find a match, they learned there were virtually no donors in the national or worldwide registry who matched Jeremys genetic makeup a requirement for a successful stem cell transplant.

READ ALSO: In a fight against cancer, Victoria mans only stem cell match was his own donation

Ironically, Jeremy had applied to become a stem cell donor years earlier. When doctors searched the database they found one unusable match: his own donation. Shocked and saddened by the lack of options, the family spearheaded the Match4Jeremy campaign, organizing stem cell drives and raising awareness of the dire need for mixed race and Asian donors.

On Aug. 8, 2019, the family learned that Jeremys cancer had returned. But the Chows battle to find a match didnt slow down. They worked with the Otherhalf-Chinese Stem Cell Initiative to host an emergency stem cell drive in Vancouver that month.

Despite their tireless efforts, Jeremy did not recover from the second round of cancer. The father of two died on May 30 with his wife at his side.

On a GoFundMe page aimed at raising money for his daughters educations, family friend Jenny Leung says Jeremy fought hard and did it with grace, humour and a positive attitude.

READ ALSO: Stem cell donor with rare genetic makeup needed to save Saanich man after cancer returns

Jeremys priority was always being able to provide and take care of his family, Leung writes. He was so involved with his girls lives, from driving them to their extracurricular activities to attending school fairs, to braiding their hair and explaining to them the importance of a good education.

He was always looking for a way to care for those around him whether it meant sharing knowledge, offering a helping hand, or just being there in any way he could, she added. Jeremy was truly someone to look up to and although he was always supporting others, he rarely asked for anything in return.

While the Chow family fought for a match for Jeremy, their crusade for stem cell donors gained momentum when they realized just how dire the situation was for mixed-race and Asian Canadians. Only three per cent of the Canadian Blood Services stem cell registry is mixed race.

In March 2019, Jeremy spoke with Black Press Media.

If all of this goes well [and] I stay in remission, and the awareness is out there and other people sign up to be donors and other people are getting the help they need, then thats a win, he said.

Donations are being accepted via GoFundMe to support Jeremys family and his daughters future education.

READ ALSO: Victoria couple continues fight for increased diversity in Canadian stem cell registry

Do you have something to add to this story, or something else we should report on? Email:nina.grossman@blackpress.ca

@NinaGrossmanLike us on Facebook and follow us on Twitter

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Saanich father dies of leukemia after battle to find mixed-race stem cell donor - Saanich News

Study finds little evidence to back cord-blood therapy for autism – Spectrum

Infusion in question: Cord-blood therapies have failed to ease autism traits in a series of ongoing clinical trials.

Burger / Science Photo Library

An infusion of umbilical cord blood does not improve social skills in autistic children, according to results from the largest clinical trial of the therapys effectiveness for autism to date1.

Independent experts say the findings are unfortunate but not unexpected. Doubts have surrounded the trial since its start at Duke University in Durham, North Carolina, in 2014.

Its not a surprise; it is nonetheless a disappointment, says Arnold Kriegstein, professor of neurology at the University of California, San Francisco, who was not involved in the study. Ive been skeptical of this kind of treatment from the beginning.

The new study took a rigorous approach: The Duke team randomly assigned 180 autistic children aged 2 to 7 to receive a single infusion of cord blood or a placebo. Neither the researchers nor caregivers knew which children had received cord blood when the team evaluated them six months later. But at that point, the participants traits remained largely unchanged. The results were published in May in the The Journal of Pediatrics.

The work is very good quality, and they are honest in their results, says Michael Chez, a pediatric neurologist at the Sutter Institute for Medical Research in Sacramento, California, who conducted a small trial in 2018 showing cord-blood therapy was safe in children with autism2.

Despite the new trials failure, the Duke researchers are moving ahead with a study using cells derived from umbilical cords, building on the observation that the treatment may have improved social behavior among the participants with the highest intellectual abilities.

I feel encouraged by the results, says co-lead investigator Joanne Kurtzberg, director of Dukes Marcus Center for Cellular Cures. It wasnt a home run, but there are reasons why we gained valuable information.

Umbilical cord blood contains a wide variety of cells, including immune cells known as monocytes and blood-producing stem cells involved in proven therapies for blood cancers.

The researchers theorize that molecules released by the monocytes quell brain inflammation. Studies show that inflammation in the womb can shape brain development and may boost the odds of autism. Some researchers have proposed that an overactive immune response might ease autism traits in some children.

Longtime skeptics of the Duke study, including Kriegstein, point out that a single infusion of these cells is unlikely to have a lasting impact or reverse damage already done.

In response to rising demand from parents for unproven stem-cell therapies, Kurtzberg, who is a cord-blood pioneer, launched the trial together with Geraldine Dawson, director of Duke Universitys Center for Autism and Brain Development, with funding from the Marcus Foundation.

The researchers tested two types of cord blood: 56 children received cord blood banked at their own birth, and 63 received cord blood from an unrelated donor. The analyses found no statistically significant differences between the groups six months later. The children who had injections were comparable to controls in terms of social skills, as reported by their parents, and overall autism traits, measured in a clinical evaluation.

The treatment may have had a small effect in some individuals, particularly those receiving donated cord blood, the researchers say. Children with the highest intelligence quotient (IQ) scores appeared to show some improvements in social skills following the infusions.

The results are, at best, only suggestive in a subgroup of patients, says Gahan Pandina, an autism researcher at Janssen Research and Development in New Jersey.

One shortcoming of the study is that it includes too few autistic children without intellectual disability, Dawson and Kurtzberg say. They used medical records and video to screen participants before they were enrolled and then invited them to travel to Duke for on-site evaluations. But this strategy meant they initially overlooked intellectual disability in some children, particularly in the younger ones, and so they ended up with fewer high-IQ participants than expected.

In the new trial they have launched, dubbed the Duke IMPACT trial, they are enrolling a slightly older cohort to improve their ability to track participants without intellectual disability, and they are conducting all evaluations on site prior to recruitment. They will also use mesenchymal stromal cells (MSC) grown from donated cord tissue rather than monocyte-containing cord blood. Like monocytes, MSCs release molecules that might decrease inflammation, the researchers say.

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Study finds little evidence to back cord-blood therapy for autism - Spectrum

‘Schumacher will be in surgeory again’ – GPblog

Since his skiing accident at the end of 2013, there has been speculation about Michael Schumacher's state of health for over six years. The family has released some information about this, but has never really gone into detail. That leaves room for rumours, this time about a new operation that the seven-time world champion may undergo.

Last September it was already known that Schumacher had been transferred to the Georges-Pompidou hospital in Paris for a 'secret' operation. There he would have received an experimental stem cell treatment. According to the Italian Contro Copertina, he now probaby get a second stem cell transplant.

This operation will be performed by the same doctor. Philippe Menasche is his name and he has previously stated that the purpose of the operation is to 'repair Michael's nervous system'. It is still unclear to what extent this was achieved during the first operation. The science behind this is still in its infancy.

"Over the past 20 years, science has made tremendous progress in stem cell treatment, but that doesn't change the fact that we still know little about the human brain. We are not able to say what results it will bring," said neurosurgeon Nicola Acciari, who says that Schumacher suffers from muscle atrophy and osteoporosis.

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'Schumacher will be in surgeory again' - GPblog

HMGA1 Regulates the Stem Cell-Like Properties of Circulating Tumor Cel | OTT – Dove Medical Press

Ming Chen,1,2,* Kangjing Xu,1,2,* Bowen Li,1,2,* Nuofan Wang,1,2 Qiang Zhang,3 Liang Chen,4 Diancai Zhang,1,2 Li Yang,1,2 Zekuan Xu,1,2,* Hao Xu1,2,*

1Department of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, Peoples Republic of China; 2Jiangsu Key Laboratory of Cancer Biomarkers, Prevention and Treatment, Jiangsu Collaborative Innovation Center for Cancer Personalized Medical University, Nanjing, Jiangsu 211166, Peoples Republic of China; 3Department of Gastrointestinal Surgery, The Second Peoples Hospital of Lianyungang, Lianyungang, Jiangsu 222000, Peoples Republic of China; 4Department of General Surgery, Jiangsu Cancer Hospital, Jiangsu Institute of Cancer Research, The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, Jiangsu 210009, Peoples Republic of China

*These authors contributed equally to this work.

Correspondence: Hao Xu; Zekuan XuDepartment of General Surgery, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu Province 210029, Peoples Republic of ChinaTel +86 25 68306863Fax +86 25 83781992Email hxu@njmu.edu.cn; xuzekuan@njmu.edu.cn

Background: Gastrointestinal stromal tumor (GIST) is the most common sarcoma of the digestive system. Circulating tumor cells (CTCs) have been proven to be critical in the recurrence and metastasis of diseases; however, the characteristics of CTCs of GIST are still unclear.Methods: We sorted out and verified the validity of CTCs from peripheral blood of gastrointestinal stromal tumor (GIST) patients with or without heterochronous liver metastasis using flow cytometry (FCM). Differential genes were analyzed between the GIST patients with and without liver metastasis using next-generation sequencing (NGS).Results: The preliminary study on the characteristics of CTCs revealed that CTCs of GIST patients with heterochronous liver metastasis had stronger stem cell-like properties (SC-like properties) than CTCs of those without liver metastasis. Furthermore, NGS followed with a series of assays revealed that HMGA1 played a critical role in regulating the SC-like properties of CTCs. Mechanistically, HMGA1 could activate Wnt/-catenin pathway in vitro and vivo. Moreover, we found that the expression level of HMGA1 in CTCs was an independent risk factor probably influencing the prognosis of GIST patients.Conclusion: Our findings indicate the significant role of HMGA1 in SC-like properties, IM resistance and eventually hepatic metastasis formation of CTCs. Targeting HMGA1 in CTCs may be a therapeutic strategy for GIST patients with hepatic metastasis.

Keywords: circulating tumor cells, gastrointestinal stromal tumor, stem cell-like properties, heterochronous liver metastasis, HMGA1, Wnt/-catenin

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License.By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.

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New Trends: Covid-19 impact on Stem Cell Therapy Market Regional Outlook, Analysis and Competitive Analysis by 2026 – 3rd Watch News

Stem Cell Therapy Industry Amid Global COVID-19 Crisis: Report Hive Viewpoint

Los Angeles, United States, June 2020: The Stem Cell Therapy market has been garnering remarkable momentum in the recent years. The steadily escalating demand due to improving purchasing power is projected to bode well for the market. Report Hives latest publication, Titled [Stem Cell Therapy Market Research Report 2020], offers an insightful take on the drivers and restraints present in the market. It assesses the historical data pertaining to the Stem Cell Therapy market and compares it to the current market trends to give the readers a detailed analysis of the trajectory of the market. A team subject-matter experts have provided the readers a qualitative and quantitative data about the market and the various elements associated with it. Additionally, this report encompasses an accurate competitive analysis of major market players and their strategies during the projection timeline.

The research study includes the latest updates about the COVID-19 impact on the Stem Cell Therapy sector. The outbreak has broadly influenced the global economic landscape. The report contains a complete breakdown of the current situation in the ever-evolving business sector and estimates the aftereffects of the outbreak on the overall economy. Key players in this market are Osiris Therapeutics, NuVasive, Chiesi Pharmaceuticals, JCRPharmaceutical, Pharmicell, Medi-post, Anterogen, Molmed, Takeda (TiGenix), etc.

>>> To know How COVID-19 Pandemic Will Impact This Market/Industry | Request a sample copy of the Stem Cell Therapy Market report:

There are 10 Chapters to deeply display the Stem Cell Therapy market:

Chapter 1, is executive summary of Stem Cell Therapy Market; Chapter 2, is definition and segment of Stem Cell Therapy; Chapter 3, to show info and data comparison of Stem Cell Therapy Players; Chapter 4, to explain the industry chain of Stem Cell Therapy; Chapter 5, to show comparison of regions and courtiers(or sub-regions); Chapter 6, to show competition and trade situation of Stem Cell Therapy Market; Chapter 7, to show comparison of applications; Chapter 8, to show comparison of types; Chapter 9, to show investment of Stem Cell Therapy Market; Chapter 10, to forecast Stem Cell Therapy market in the next years.

Global Stem Cell Therapy Market is estimated to reach xxx million USD in 2020 and projected to grow at the CAGR of xx% during 2020-2026. According to the latest report added to the online repository of Report Hive Research the Stem Cell Therapy market has witnessed an unprecedented growth till 2020. The report also emphasizes the initiatives undertaken by the companies operating in the market including product innovation, product launches, and technological development to help their organization offer more effective products in the market. It also studies notable business events, including corporate deals, mergers and acquisitions, joint ventures, partnerships, product launches, and brand promotions.

The Stem Cell Therapy Market study address the following queries:

How has the Stem Cell Therapy Market evolved during the historic period 2014-2019? What proprietary technologies are the players using in the Stem Cell Therapy Market? What are the factors hindering the growth of the Stem Cell Therapy Market? Why region remains the top consumer of Stem Cell Therapy ? By end use, which segment currently leads the Stem Cell Therapy Market?

Global Stem Cell Therapy Market: Competitive Rivalry

The segmentation is used to decide the target market into smaller sections or segments like product type, application, and geographical regions to optimize marketing strategies, advertising techniques, and global as well as regional sales efforts of Global Stem Cell Therapy Market. Common characteristics are being considered for segmentation such as global market share, common interests, global demand and access control unit supply. Moreover, the report compares the production value and growth rate of the Global Stem Cell Therapy market across different geographies.

On the basis on the end users/applications, this report focuses on the status and outlook for major applications/end users, shipments, revenue (Million USD), price, and market share and growth rate for each application.

Autologous, Allogeneic

On the basis of product type, this report displays the shipments, revenue (Million USD), price, and market share and growth rate of each type.

Musculoskeletal Disorder, Wounds & Injuries, Cornea, Cardiovascular Diseases, Others

Stem Cell Therapy Market Regional Analysis Includes:

Asia-Pacific (Vietnam, China, Malaysia, Japan, Philippines, Korea, Thailand, India, Indonesia, and Australia) Europe (Turkey, Germany, Russia UK, Italy, France, etc.) North America (the United States, Mexico, and Canada.) South America (Brazil etc.) The Middle East and Africa (GCC Countries and Egypt.)

Our exploration specialists acutely ascertain the significant aspects of the global Stem Cell Therapy market report. It also provides an in-depth valuation in regards to the future advancements relying on the past data and present circumstance of Stem Cell Therapy market situation. In this Stem Cell Therapy report, we have investigated the principals, players in the market, geological regions, product type, and market end-client applications. The global Stem Cell Therapy report comprises of primary and secondary data which is exemplified in the form of pie outlines, Stem Cell Therapy tables, analytical figures, and reference diagrams. The Stem Cell Therapy report is presented in an efficient way that involves basic dialect, basic Stem Cell Therapy outline, agreements, and certain facts as per solace and comprehension.

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Table of Content

1 Study Coverage1.1 Stem Cell Therapy Product Introduction1.2 Key Market Segments in This Study1.3 Key Manufacturers Covered: Ranking of Global Top Stem Cell Therapy Manufacturers by Revenue in 20191.4 Market by Type1.4.1 Global Stem Cell Therapy Market Size Growth Rate by Type1.4.2 Autologous, Allogeneic1.5 Market by Application1.5.1 Global Stem Cell Therapy Market Size Growth Rate by Application1.5.2 Musculoskeletal Disorder, Wounds & Injuries, Cornea, Cardiovascular Diseases, Others1.5.4 Others1.6 Coronavirus Disease 2019 (Covid-19): Stem Cell Therapy Industry Impact1.6.1 How the Covid-19 is Affecting the Stem Cell Therapy Industry1.6.1.1 Stem Cell Therapy Business Impact Assessment Covid-191.6.1.2 Supply Chain Challenges1.6.1.3 COVID-19s Impact On Crude Oil and Refined Products1.6.2 Market Trends and Stem Cell Therapy Potential Opportunities in the COVID-19 Landscape1.6.3 Measures / Proposal against Covid-191.6.3.1 Government Measures to Combat Covid-19 Impact1.6.3.2 Proposal for Stem Cell Therapy Players to Combat Covid-19 Impact1.7 Study Objectives1.8 Years Considered

2 Executive Summary2.1 Global Stem Cell Therapy Market Size Estimates and Forecasts2.1.1 Global Stem Cell Therapy Revenue Estimates and Forecasts 2015-20262.1.2 Global Stem Cell Therapy Production Capacity Estimates and Forecasts 2015-20262.1.3 Global Stem Cell Therapy Production Estimates and Forecasts 2015-20262.2 Global Stem Cell Therapy Market Size by Producing Regions: 2015 VS 2020 VS 20262.3 Analysis of Competitive Landscape2.3.1 Manufacturers Market Concentration Ratio (CR5 and HHI)2.3.2 Global Stem Cell Therapy Market Share by Company Type (Tier 1, Tier 2 and Tier 3)2.3.3 Global Stem Cell Therapy Manufacturers Geographical Distribution2.4 Key Trends for Stem Cell Therapy Markets & Products2.5 Primary Interviews with Key Stem Cell Therapy Players (Opinion Leaders)

3 Market Size by Manufacturers3.1 Global Top Stem Cell Therapy Manufacturers by Production Capacity3.1.1 Global Top Stem Cell Therapy Manufacturers by Production Capacity (2015-2020)3.1.2 Global Top Stem Cell Therapy Manufacturers by Production (2015-2020)3.1.3 Global Top Stem Cell Therapy Manufacturers Market Share by Production3.2 Global Top Stem Cell Therapy Manufacturers by Revenue3.2.1 Global Top Stem Cell Therapy Manufacturers by Revenue (2015-2020)3.2.2 Global Top Stem Cell Therapy Manufacturers Market Share by Revenue (2015-2020)3.2.3 Global Top 10 and Top 5 Companies by Stem Cell Therapy Revenue in 20193.3 Global Stem Cell Therapy Price by Manufacturers3.4 Mergers & Acquisitions, Expansion Plans

4 Stem Cell Therapy Production by Regions4.1 Global Stem Cell Therapy Historic Market Facts & Figures by Regions4.1.1 Global Top Stem Cell Therapy Regions by Production (2015-2020)4.1.2 Global Top Stem Cell Therapy Regions by Revenue (2015-2020)4.2 North America4.2.1 North America Stem Cell Therapy Production (2015-2020)4.2.2 North America Stem Cell Therapy Revenue (2015-2020)4.2.3 Key Players in North America4.2.4 North America Stem Cell Therapy Import & Export (2015-2020)4.3 Europe4.3.1 Europe Stem Cell Therapy Production (2015-2020)4.3.2 Europe Stem Cell Therapy Revenue (2015-2020)4.3.3 Key Players in Europe4.3.4 Europe Stem Cell Therapy Import & Export (2015-2020)4.4 China4.4.1 China Stem Cell Therapy Production (2015-2020)4.4.2 China Stem Cell Therapy Revenue (2015-2020)4.4.3 Key Players in China4.4.4 China Stem Cell Therapy Import & Export (2015-2020)4.5 Japan4.5.1 Japan Stem Cell Therapy Production (2015-2020)4.5.2 Japan Stem Cell Therapy Revenue (2015-2020)4.5.3 Key Players in Japan4.5.4 Japan Stem Cell Therapy Import & Export (2015-2020)

5 Stem Cell Therapy Consumption by Region5.1 Global Top Stem Cell Therapy Regions by Consumption5.1.1 Global Top Stem Cell Therapy Regions by Consumption (2015-2020)5.1.2 Global Top Stem Cell Therapy Regions Market Share by Consumption (2015-2020)5.2 North America5.2.1 North America Stem Cell Therapy Consumption by Application5.2.2 North America Stem Cell Therapy Consumption by Countries5.2.3 U.S.5.2.4 Canada5.3 Europe5.3.1 Europe Stem Cell Therapy Consumption by Application5.3.2 Europe Stem Cell Therapy Consumption by Countries5.3.3 Germany5.3.4 France5.3.5 U.K.5.3.6 Italy5.3.7 Russia5.4 Asia Pacific5.4.1 Asia Pacific Stem Cell Therapy Consumption by Application5.4.2 Asia Pacific Stem Cell Therapy Consumption by Regions5.4.3 China5.4.4 Japan5.4.5 South Korea5.4.6 India5.4.7 Australia5.4.8 Taiwan5.4.9 Indonesia5.4.10 Thailand5.4.11 Malaysia5.4.12 Philippines5.4.13 Vietnam5.5 Central & South America5.5.1 Central & South America Stem Cell Therapy Consumption by Application5.5.2 Central & South America Stem Cell Therapy Consumption by Country5.5.3 Mexico5.5.3 Brazil5.5.3 Argentina5.6 Middle East and Africa5.6.1 Middle East and Africa Stem Cell Therapy Consumption by Application5.6.2 Middle East and Africa Stem Cell Therapy Consumption by Countries5.6.3 Turkey5.6.4 Saudi Arabia5.6.5 U.A.E

6 Market Size by Type (2015-2026)6.1 Global Stem Cell Therapy Market Size by Type (2015-2020)6.1.1 Global Stem Cell Therapy Production by Type (2015-2020)6.1.2 Global Stem Cell Therapy Revenue by Type (2015-2020)6.1.3 Stem Cell Therapy Price by Type (2015-2020)6.2 Global Stem Cell Therapy Market Forecast by Type (2021-2026)6.2.1 Global Stem Cell Therapy Production Forecast by Type (2021-2026)6.2.2 Global Stem Cell Therapy Revenue Forecast by Type (2021-2026)6.2.3 Global Stem Cell Therapy Price Forecast by Type (2021-2026)6.3 Global Stem Cell Therapy Market Share by Price Tier (2015-2020): Low-End, Mid-Range and High-End

7 Market Size by Application (2015-2026)7.2.1 Global Stem Cell Therapy Consumption Historic Breakdown by Application (2015-2020)7.2.2 Global Stem Cell Therapy Consumption Forecast by Application (2021-2026)

8 Corporate Profiles8.1 Company18.1.1 Company1 Corporation Information8.1.2 Company1 Overview and Its Total Revenue8.1.3 Company1 Production Capacity and Supply, Price, Revenue and Gross Margin (2015-2020)8.1.4 Company1 Product Description8.1.5 Company1 Recent Development8.2 Company28.2.1 Company2 Corporation Information8.2.2 Company2 Overview and Its Total Revenue8.2.3 Company2 Production Capacity and Supply, Price, Revenue and Gross Margin (2015-2020)8.2.4 Company2 Product Description8.2.5 Company2 Recent Development8.3 Company38.3.1 Company3 Corporation Information8.3.2 Company3 Overview and Its Total Revenue8.3.3 Company3 Production Capacity and Supply, Price, Revenue and Gross Margin (2015-2020)8.3.4 Company3 Product Description8.3.5 Company3 Recent Development8.4 This Report Covers Leading Companies Associated in Worldwide Stem Cell Therapy Market (Osiris Therapeutics, NuVasive, Chiesi Pharmaceuticals, JCRPharmaceutical, Pharmicell, Medi-post, Anterogen, Molmed, Takeda (TiGenix).)

9 Production Forecasts by Regions9.1 Global Top Stem Cell Therapy Regions Forecast by Revenue (2021-2026)9.2 Global Top Stem Cell Therapy Regions Forecast by Production (2021-2026)9.3 Key Stem Cell Therapy Production Regions Forecast9.3.1 North America9.3.2 Europe9.3.3 China9.3.4 Japan

10 Stem Cell Therapy Consumption Forecast by Region10.1 Global Stem Cell Therapy Consumption Forecast by Region (2021-2026)10.2 North America Stem Cell Therapy Consumption Forecast by Region (2021-2026)10.3 Europe Stem Cell Therapy Consumption Forecast by Region (2021-2026)10.4 Asia Pacific Stem Cell Therapy Consumption Forecast by Region (2021-2026)10.5 Latin America Stem Cell Therapy Consumption Forecast by Region (2021-2026)10.6 Middle East and Africa Stem Cell Therapy Consumption Forecast by Region (2021-2026)11 Value Chain and Sales Channels Analysis11.1 Value Chain Analysis11.2 Sales Channels Analysis11.2.1 Stem Cell Therapy Sales Channels11.2.2 Stem Cell Therapy Distributors11.3 Stem Cell Therapy Customers12 Market Opportunities & Challenges, Risks and Influences Factors Analysis12.1 Market Opportunities and Drivers12.2 Market Challenges12.3 Market Risks/Restraints12.4 Porters Five Forces Analysis13 Key Finding in The Global Stem Cell Therapy Study14 Appendix14.1 Research Methodology14.1.1 Methodology/Research Approach14.1.2 Data Source14.2 Author Details14.3 Disclaimer

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New Trends: Covid-19 impact on Stem Cell Therapy Market Regional Outlook, Analysis and Competitive Analysis by 2026 - 3rd Watch News