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Degrees of the Future 2022: Genetics – Gizmodo

Posted: August 14, 2022 at 2:24 am

Genetics is the study of inheritancefrom someones brown eyes to their inability to eat dairy. Taken together with genomicsthe study of the entire genome of an organismresearchers get better at understanding overall human health, and how to fight diseases.

Genetics and genomics will pave the way for innovations in health and better understanding of human origins. Theres just no question that 30 years ago, if you would have told me how far genomics would be in 2022, I would have just said, youre out of your mind, theres no way, said Eric Green, director of the National Human Genome Research Institute at the U.S. National Institutes of Health. Back then, I have to admit, I think most of us never thought half the things that are happening now would have happened in our lifetime, let alone within our career. As costs of genetic testing and sequencing go down, the application of genomics across the life sciences will become ubiquitous.

The Degrees of the Future 2022 top Genetics programs are:

How did Gizmodo determine this years honorees? Check out the methodology or return to the full Degrees of the Future 2022 list.

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U of U Health-Led Research Awarded $28 Million to Explore HIV’s Inner Workings and Vulnerabilities – University of Utah Health Care

Posted: August 14, 2022 at 2:24 am

Media Contacts Julie Kiefer

Associate Director, Science Communications, University of Utah HealthEmail: julie.kiefer@hsc.utah.eduPhone: 801-587-1293

Aug 08, 2022 10:00 AM

A University of Utah Health-led multi-institutional research center that studies the inner workings and vulnerabilities of HIV, the human immunodeficieny virus that causes AIDS, recently received a five-year, $28 million grant renewal from the National Institutes of Health.

Since its founding in 2007, the CHEETAH Center for Structural Biology of HIV Infection Restriction and Viral Dynamics has published more than 300 research papers that have led to a better understanding of HIV and its potential treatments.

Wesley Sundquist, Ph.D., the centers director and professor and chair of the Department of Biochemistry at U of U Health, is leading 20 research teams from 12 institutions. With the grant renewal, the researchers will focus on:

The outstanding science stemming from this program is changing an understanding of HIV/AIDS, other viral diseases, and cellular biology, enabling the development of novel therapeutics such as lenacapavir and D-peptide inhibitors, says Rachel Hess, M.D., associate vice president for research at U of U Health, referring to two investigational drugs with roots in CHEETAH.

From deep understanding to investigational drugs

Just a half-century ago, HIV infection almost inevitably led to serious illness and death. Todays antiretroviral therapies can suppress the virus and prevent symptoms, but improvement is still needed. If these drugs arent taken daily, the virus can rebound and acquire drug resistance. The medicines can also cause difficult side effects. The underpinnings for two new investigational drugs that could help circumvent these issues are based on years of research by CHEETAH scientists.

Research from Sundquist; Christopher Hill, D.Phil, distinguished biochemistry professor at U of U Health; and other CHEETAH Center labs on the HIV capsida structure they found is vital for different steps of the HIV life cyclelaid the groundwork that led the pharmaceutical company Gilead Sciences to identify the capsid inhibitor, lenacapavir. This investigational drug is now in phase 3 clinical trials and is already showing great promise as a potent, long-acting treatment.

Taking a different approach, Michael Kay, M.D., Ph.D., CHEETAH investigator and biochemistry professor, and Debra Eckert, Ph.D., biochemistry research assistant professor, used synthetic chemistry to design a D-peptide inhibitor called CPT31 that jams HIVs infection machinery. The molecule is now in phase 1 clinical trials sponsored by Navigen, Inc.

Often people forget that drug development builds from basic research, Sundquist says. These are two more cases where that has happened, and it is very satisfying.

Learning lessons from HIV

CHEETAH continues to bring an understanding of HIV, related viruses, and host biology in new directions through collaborations between its scientists, who come from a variety of disciplines. "The CHEETAH Center is doing exciting, interdisciplinary science in a collaborative environment that allows us to accomplish projects that wouldn't otherwise be possible in any single lab," says Pamela Bjorkman, Ph.D., a professor of biology and biological engineering at Caltech.

NelsElde, Ph.D., professor of human genetics at U of U Health, turns to evolution for inspiration, noting that many animals are not as susceptible as humans to disease caused by HIV. He is collaborating with fellow CHEETAH scientists to explore whether a gene found in mice and squirrel monkeys that prevents HIV from exiting cells after replicating could become the basis for anew type of antiviral.

Nature has done seemingly countless billions of experiments that got us to where we are today, Elde says. Can we learn from whats happened and borrow and deploy them in ways that are useful?

By contrast, Owen Pornillos, Ph.D., a CHEETAH investigator from the University of Virginia who received his doctorate from the U, takes advantage of his biochemistry expertise to take a different approach. In a collaborative project with several CHEETAH Center members, he is removing the virus from the complex environment of the host cell and bringing it to the test tube. By adding back specific ingredients a few at a time, the team is identifying key virus and host cell components that are essential for early stages of viral infection and replication. Combining this approach with new microscope technologies is allowing them to visualize these steps with unprecedented clarity.

CHEETAH is committed to doing excellent science and is always planning for where we envision the field will be five years from now, Pornillos says. Its exciting to be a part of it.

These diverse tactics are providing valuable insights into virology and biology, and uncovering targets for new types of therapeutic intervention.

# # #

Research News iii

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Revisiting Companies That Had Their IPO in 2018 – Investment U

Posted: August 14, 2022 at 2:24 am

2018 was a historic year for initial public offerings (IPOs) on the stock market. In fact, there are many successful companies that had their IPO in 2018. And as an investor, there is much to learn from and reflect on. Therefore, lets take a closer look at some of the standout IPOs that made their public debuts in 2018.

2018 was full of newsworthy events around the globe. In the United States, there was marijuana reform, gun control protests and a partial government shutdown in December.

There were many monumental moments in other parts of the world as well. In sports, there was the Winter Olympics in February and the World Cup in July. Meghan Markle became the first woman of color to join the British Royal Family. Cuba ended the 59-year reign of Castro leadership, announcing Miguel Diaz-Canel as its new President. And North and South Korea vowed to formally end the Korean War.

However, the stock market had one of its worst years in over a decade. Specifically, the S&P 500 was down 6.2%. The Dow fell 5.6% and the Nasdaq dropped 4%. But there were many companies that had their IPO in 2018 nonetheless. And some have brought in massive returns since their offering dates. For example, five of the best IPOs in 2018 include:

Each of these stocks is flourishing on the market since making its public debut in 2018. And this comes despite the recent stock market downturn, recession fears and high inflation. Thats why I consider them a few of the best companies that had their IPO in 2018. Therefore, lets dig into their stock performances a little further.

Americold provides supply chain services and infrastructure for food service providers, retailers, producers and direct-to-consumer. In addition, Americold has 249 facilities around the globe.

COLD stock made its debut on the New York Stock Exchange (NYSE) on January 19, 2018 for $724.8 million at $17 per share. In just four years time, its now trading around $30 a share with an all-time high closing of $39.21 in July of 2021. Since its offering date, Americold stock is up more than 70%.

BJs is a popular membership-only warehouse club chain that operates on the East Coast of the United States with plans to expand in the near future. Its main competitors includeCostco (Nasdaq: COST) and Sams Club, which is owned and operated by Walmart (NYSE: WMT).

While BJs is much smaller, it has become a stock market darling since its debut. The IPO came on June 28, 2018 for $733.13 million at $17 a share. The stock is now trading around $70 for an increase of more than 300% since its IPO. Furthermore, its one of the few companies that is up year-to-date (YTD) at close to 7% despite the bear market. BJs is clearly one of the best companies that had their IPO in 2018 based on performance alone.

Moderna is a pioneer in delivering transformative medicines and vaccines via mRNA science. And as you may know, it produces one of the most prominent COVID-19 vaccines and booster shots. Moderna has played a major role in the fight against COVID-19 and will continue to do so moving forward.

Before the pandemic, Moderna went public on December 7, 2018 for $23.00 a share. Its now trading for more than $170! Thats an increase of close to 630% since its IPO.

Nio is an electric vehicle company out of China. Its currently producing six EV car models, home charging equipment, battery swaps and mobile charging services. The ES6, a five-seater mid-size SUV, seems to be its flagship model with close to half of its sales in a record-breaking June.

Nio launched on the NYSE for $6.26 per share on September 12, 2018. Its now trading just below $20 a share, though it hit an all-time high of $66.90 in January of 2021. As you can see, Nio has the potential as one of the best companies that had their IPO in 2018.

Twist Bioscience is a biotech company in San Francisco that manufactures synthetic DNA and DNA products for various industries. These DNA tools help research in human genetics, drug discovery, infectious diseases, animal health and more.

The Twist Bioscience IPO hit the market on October 30, 2018 for $14 per share. In 2022, TWST stock is pushing $50. However, it was trading close to $200 per share in 2021 before a drastic decline that winter.

While 2018 wasnt the best of years in terms of the overall stock market, many businesses shined in their debuts. The five stocks above continue to impress in difficult circumstances as volatility continues to rise.

As the market fights to recover, its important that you continue to do your due diligence and expand your research even further. Consider signing up for one of the best investment newsletters. These daily e-letters give readers stock insights, chart analysis and trends that may help you make better investment decisions.

Its also wise to learn more about the IPO process before investing in new offerings. This step-by-step guide breaks down everything you need to know.

You may have missed out on the massive returns of some of the best companies that had their IPO in 2018. However, you can position yourself to take advantage of future gains by staying on top of the market and scouring news feeds, analyzing chart patterns and doing extensive research.

Corey Mann is the Content Manager of Investment U. He has more than 10 years of experience as a journalist and content creator. Since 2012, Coreys work has been featured in major publications such as The Virginian-Pilot, The Washington Post, CNN, MSNBC and more. When Corey isnt focusing on Investment U, he enjoys traveling with his wife, going to Yankees games and spending time with his family.

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Monkeypox Myth Busting: Here’s What You Need to Know – The Mighty

Posted: August 14, 2022 at 2:24 am

This interview took place on August 4, 2022. As scientists are still learning about this virus, this information could have shifted and changed. Please do your due diligence when it comes to information about any viral disease.

On August 5, 2022, the United States government declared monkeypox a public health emergency.

As someone who (sadly) lives on the internet, ever since monkeypox was announced Ive been seeing different peoples thoughts, opinions, and fears when it comes to this disease. Generally speaking, theres been a lot of good information and threads on the virus; however, theres also been a lot of fear-based misinformation that, even if well-intentioned, can ultimately cause more harm than good.

Its for this reason that I connected with Emma Crowley. Emma is a public health professional and rare disease advocate with over a decade of paired experience and advocacy. In addition to public health, Emma has previously worked in human genetics, clinical trials, and global health. Her broad experience has allowed her to speak to physician groups, pharmaceutical companies, and the Food and Drug Administration. She is skilled at breaking down complicated scientific concepts into accessible content.

Emma: Monkeypox is a pustule virus that is related to smallpox and to chickenpox, and what they have in common is those little bumps all over your skin.

Emma: Before this outbreak, there were two different clades [of this virus]. One that was found in the Congo is called the Congo Basin clade, and then the other one is called the West African clade.

Traditionally the one found in the Congo was more transmissible and more deadly. The West African one was less transmissible and less deadly. At this point, we believe the virus were seeing now is genetically different than those two, but we believe its come from or has mutated from the West African one. Its existed in those regions since the 1970s, and we know that it transmits from animals to humans. It lives in monkeys, of course, but also in rodents, squirrels, moles, and things like that. Its remained quiet for decades, but in the past 10-15 years there has been some growth.

Emma: When it comes to it possibly being a sexually transmitted infection (STI), it can be spread by sexual contact, but it doesnt mean its exclusively an STI. It can live on surfaces, which is called a fomite, but touching a table or trying on clothes at a store likely wont give it to you. You do need likely close contact sharing bed linens or cups, but obviously, youre close with that individual. Sex can be part of that transmission, but its not exclusive.

Scientists are still looking into if there is a bodily fluid transfer that makes it more transmissible in the men who have sex with men, or MSM, community. But it does seem unusual that a majority of cases have been men who have sex with men when according to statistics, we should be seeing more women and children exposed. It could be because of superspreader events, Or, ever since the HIV/AIDS epidemic, the MSM community has really developed close ties to their local health departments and have really close health relationships with people that they have sex with. So it could just be that they were the ones who brought it to our attention first.

The isolation period is long: about three to four weeks. You are contagious until your lesions drop; they kinda scab over and drop and are replaced with new skin. You are contagious until that new skin has formed.

Because its in the pox virus family, the smallpox vaccine is protective. I do believe that the CDC is still recommending people who are high risk in the gay community, in the MSM community to get a vaccine anyway, but its very interesting when you look at the data because you can see that as smallpox vaccines decline which, in the United States, we stopped vaccinating for smallpox in 1973 and we declared officially eradicated from the world in 1980 monkeypox has increased because theres an unvaccinated population. This has allowed the virus to spread.

Also, the mortality rate for the African clades is about 1-10%, but were seeing very few deaths for how many cases there are. Its not always presenting the same way as those pustules. People are also getting rashes, or they may look like a bunch of little pimples and bumps instead of the traditional pox that you think of. Its also making it difficult for doctors to feel comfortable with diagnosing, so the word from the CDC is if you see something just test it, which is probably the right thing to do at this point.

Its kind of unfortunate, but its really important for at-risk communities to decrease their sexual partners. This isnt just for transmission, but it also buys time for public health officials to vaccinate as many people as possible.

The vaccines that people are using are called Jynneos. It comes from a company called Bavarian Nordic and they produce it in Copenhagen, and it was really only approved for people with the monkeypox virus, or if you were on assignment for a specific job in an African nation that sees it more often. Part of the difficulty is that weve never needed this many, but whats important is that its safe for individuals who are HIV positive. So it doesnt pose a big risk, there are very few side effects, and its a great safe vaccine. You do need two doses, and if you are exposed, it is recommended that you get vaccinated within four days. If you do, you may be able to stop the onset of illness, and if you stop the onset, you stop the transmission.

There is still some research going on to see if you can spread [the virus] asymptomatically, but thats still being researched.

The ACAM2000 was left over from our old-school smallpox vaccine. It was developed for smallpox and we just happened to have a bunch on hand in case there was biological terrorism, but the rate of people having adverse reactions was relatively high, like a couple per thousand, and its a live virus that has the ability to replicate, whereas Jynneos does not. So youre exposing yourself to a tiny amount of the live virus, which for those who are immunocompromised (such as those who are HIV positive) isnt safe.

Hopefully, thatll just be a backup. It looks like the federal government is working to procure as many doses as possible and will be implementing the Defense Production Act to engage other pharmaceutical companies to support them in their production, so hopefully, we get ahead of it but its unfortunate how widespread it got so quickly.

Doctors are still learning about this. Were all learning in real-time, but I would recommend people contact their local health departments. We can make sure to get you in contact with the resources that you need and ensure that you have some funding so you can stay home and isolate, yourself because the isolation period is long: about three to four weeks. You are contagious until your lesions drop; they kinda scab over and drop and are replaced with new skin. You are contagious until that new skin has formed.

Its important that we stay properly informed about Monkeypox so we know how to both protect ourselves and our community. Make sure you stay up to date with the latest news from the CDC as they help advise the country through this public health crisis. Youre not alone, and together were going to get through this.

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Stem Cell Clinic in Mexico That Successfully Treated Gordie Howe …

Posted: August 14, 2022 at 2:23 am

SAN DIEGO, July 12, 2022 /CNW/ -- Novastem, the largest stem cell clinic in Mexico, has launched a brand new protocol aimed at American and Canadian stroke patients. The stem cell protocol accelerates physical recovery after a stroke, and in some cases, when applied early enough, may stop the advancement of all sorts of damage.

Novastem in Tijuana Mexico helps stroke patients with breakthrough stem cell protocol, led by Dr Vanessa Felix.

Novastem's unique stem cell protocol is not FDA-approved which is why patients must travel to Mexico to receive it.

Back in December of 2014, Novastem administered their stem cells to Canadian hockey legend Gordie Howe after he suffered a series of strokes earlier that year.

Howe had several small strokes in the summer of 2014, and in October, he suffered a serious one. At 86, his right side was paralyzed and he could not remember the names of his children, New York magazine reported.

The stem cells migrated to his brain where they multiplied, ultimately helping his brain recover from the damage caused by the stroke; Howe's condition improved within 24 hours and Howe was finally able to walk.

The treatment was not FDA-approved, which is why Howe had to go to Tijuana, Mexico for the treatment.

"To my mind, the relationship between his stem cell treatment and his response was very clear," Murray Howe told USA TODAY Sports on Feb. 26, 2015. "It was literally eight hours. I've been a practicing physician for 28 years now, and I've taken care of many stroke patients. All of his caregivers all of them had taken care of stroke patients. None of them had ever seen anything like this."

Now, as of July 2022, Dr Vanessa Felix, the clinical director at Novastem, has developed a protocol that is widely available for patients, specially the ones that have been told by their primary care physicians that there's no hope left for their case.

"With the growing demand for alternative stroke treatments, Novastem has been receiving more and more patients looking for the exact same treatment Gordie Howe received in 2015. We have since then evolved into a different, more stable and replicable protocol that can help patients suffering from the stroke symptoms." comments Dr Felix.

Story continues

Novastem's unique stem cell protocol is not FDA-approved which is why patients interested in receiving it must travel to Tijuana, Mexico. Novastem is located twenty five minutes south of San Diego International Airport, which makes it an ideal location for travelers worldwide. To learn more, please visit novastem.com.

Media Contact: Rafael Cuadras619-617-7884rcuadras@patronusdigitalventures.com

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The Worldwide Biobanking Industry is Expected to Reach $3.6 Billion by 2027 – Yahoo Finance

Posted: August 14, 2022 at 2:23 am

Company Logo

Global Biobanking Market

Global Biobanking Market

Dublin, Aug. 12, 2022 (GLOBE NEWSWIRE) -- The "Global Biobanking Market (2022-2027) by Product & Service, Sample, Storage, Application, Geography, Competitive Analysis and the Impact of Covid-19 with Ansoff Analysis" report has been added to ResearchAndMarkets.com's offering.

The Global Biobanking Market is estimated to be USD 2.52 Bn in 2022 and is expected to reach USD 3.65 Bn by 2027, growing at a CAGR of 7.71%.

Market Dynamics

Market dynamics are forces that impact the prices and behaviors of the stakeholders. These forces create pricing signals which result from the changes in the supply and demand curves for a given product or service. Forces of Market Dynamics may be related to macro-economic and micro-economic factors.

There are dynamic market forces other than price, demand, and supply. Human emotions can also drive decisions, influence the market, and create price signals. As the market dynamics impact the supply and demand curves, decision-makers aim to determine the best way to use various financial tools to stem various strategies for speeding the growth and reducing the risks.

Company Profiles

The report provides a detailed analysis of the competitors in the market. It covers the financial performance analysis for the publicly listed companies in the market. The report also offers detailed information on the companies' recent development and competitive scenario. Some of the companies covered in this report are AMS Biotechnology, Bay Biosciences, Becton, Dickinson and Company, Bioivt & Elevating Science, Boca Biolistics, etc.

Countries Studied

America (Argentina, Brazil, Canada, Chile, Colombia, Mexico, Peru, United States, Rest of Americas)

Europe (Austria, Belgium, Denmark, Finland, France, Germany, Italy, Netherlands, Norway, Poland, Russia, Spain, Sweden, Switzerland, United Kingdom, Rest of Europe)

Middle-East and Africa (Egypt, Israel, Qatar, Saudi Arabia, South Africa, United Arab Emirates, Rest of MEA)

Asia-Pacific (Australia, Bangladesh, China, India, Indonesia, Japan, Malaysia, Philippines, Singapore, South Korea, Sri Lanka, Thailand, Taiwan, Rest of Asia-Pacific)

Story continues

Competitive Quadrant

The report includes Competitive Quadrant, a proprietary tool to analyze and evaluate the position of companies based on their Industry Position score and Market Performance score. The tool uses various factors for categorizing the players into four categories. Some of these factors considered for analysis are financial performance over the last 3 years, growth strategies, innovation score, new product launches, investments, growth in market share, etc.

Ansoff Analysis

The report presents a detailed Ansoff matrix analysis for the Global Biobanking Market. Ansoff Matrix, also known as Product/Market Expansion Grid, is a strategic tool used to design strategies for the growth of the company. The matrix can be used to evaluate approaches in four strategies viz. Market Development, Market Penetration, Product Development and Diversification. The matrix is also used for risk analysis to understand the risk involved with each approach.

The analyst analyses the Global Biobanking Market using the Ansoff Matrix to provide the best approaches a company can take to improve its market position. Based on the SWOT analysis conducted on the industry and industry players, the analyst has devised suitable strategies for market growth.

Why buy this report?

The report offers a comprehensive evaluation of the Global Biobanking Market. The report includes in-depth qualitative analysis, verifiable data from authentic sources, and projections about market size. The projections are calculated using proven research methodologies.

The report has been compiled through extensive primary and secondary research. The primary research is done through interviews, surveys, and observation of renowned personnel in the industry.

The report includes an in-depth market analysis using Porter's 5 forces model and the Ansoff Matrix. In addition, the impact of Covid-19 on the market is also featured in the report.

The report also includes the regulatory scenario in the industry, which will help you make a well-informed decision. The report discusses major regulatory bodies and major rules and regulations imposed on this sector across various geographies.

The report also contains the competitive analysis using Positioning Quadrants, the analyst's Proprietary competitive positioning tool.

Key Topics Covered:

1 Report Description

2 Research Methodology

3 Executive Summary

4 Market Dynamics4.1 Drivers4.1.1 Growing Cost-Effective Drug Discovery and Development and 4.1.2 Genomic Research Activities 4.1.3 Advances in Biobanking and Growing Trend of Conserving Cord Blood Stem Cells of Newborns 4.1.4 Government and Private Funding to Support Regenerative Medicine Research4.2 Restraints4.2.1 High Cost of Automation4.2.2 Issues Related to Biospecimen Sample Procurement4.3 Opportunities4.3.1 Emerging Countries 4.3.2 Growing Focus on the R&D of Cell Therapies4.4 Challenges4.4.1 Long-Term Sustainability of Biobanks

5 Market Analysis5.1 Regulatory Scenario5.2 Porter's Five Forces Analysis5.3 Impact of COVID-195.4 Ansoff Matrix Analysis

6 Global Biobanking Market, By Product & Service6.1 Introduction6.2 Equipment6.2.1 Storage Equipment6.2.2 Sample Analysis Equipment6.2.3 Sample Processing Equipment6.2.4 Sample Transport Equipment6.3 Consumables6.3.1 Storage Consumables6.3.2 Analysis Consumables6.3.3 Processing Consumables6.3.4 Collection Consumables6.4 Services6.4.1 Storage Services6.4.2 Processing Services6.4.3 Transport Services6.4.4 Supply Services

7 Global Biobanking Market, By Sample7.1 Introduction7.2 Blood Products7.3 Human Tissues7.4 Cell Lines7.5 Nucleic Acids7.6 Biological Fluids7.7 Human Waste Products

8 Global Biobanking Market, By Storage8.1 Introduction8.2 Manual Storage8.3 Automated Storage

9 Global Biobanking Market, By Application9.1 Introduction9.2 Regenerative Medicine 9.3 Life Science Research 9.4 Clinical Research

10 Americas Biobanking Market10.1 Introduction10.2 Argentina10.3 Brazil10.4 Canada10.5 Chile10.6 Colombia10.7 Mexico10.8 Peru10.9 United States10.10 Rest of Americas

11 Europe's Biobanking Market11.1 Introduction11.2 Austria11.3 Belgium11.4 Denmark11.5 Finland11.6 France11.7 Germany11.8 Italy11.9 Netherlands11.10 Norway11.11 Poland11.12 Russia11.13 Spain11.14 Sweden11.15 Switzerland11.16 United Kingdom11.17 Rest of Europe

12 Middle East and Africa's Biobanking Market12.1 Introduction12.2 Egypt12.3 Israel12.4 Qatar12.5 Saudi Arabia12.6 South Africa12.7 United Arab Emirates12.8 Rest of MEA

13 APAC's Biobanking Market13.1 Introduction13.2 Australia13.3 Bangladesh13.4 China13.5 India13.6 Indonesia13.7 Japan13.8 Malaysia13.9 Philippines13.10 Singapore13.11 South Korea13.12 Sri Lanka13.13 Thailand13.14 Taiwan13.15 Rest of Asia-Pacific

14 Competitive Landscape14.1 Competitive Quadrant14.2 Market Share Analysis14.3 Strategic Initiatives14.3.1 M&A and Investments14.3.2 Partnerships and Collaborations14.3.3 Product Developments and Improvements

15 Company Profiles15.1 AMS Biotechnology15.2 Bay Biosciences15.3 Becton, Dickinson and Company 15.4 Bioivt & Elevating Science15.5 Boca Biolistics15.6 CTI Biotech15.7 Cureline15.8 Cureline15.9 Firalis 15.10 Geneticist 15.11 Greiner Holding AG 15.12 Hamilton Company 15.13 Merck KGaA 15.14 Panasonic Healthcare Holdings 15.15 Promega 15.16 Proteogenex15.17 Qiagen N.V. 15.18 Tecan Trading 15.19 Thermo Fisher Scientific 15.20 US Biolab Corp15.21 VWR International

16 Appendix

For more information about this report visit https://www.researchandmarkets.com/r/wsjf7c

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Century Therapeutics Reports Second Quarter 2022 Financial Results and Provides Business Updates – KULR-TV

Posted: August 14, 2022 at 2:22 am

- Following the recent submission of the IND application for CNTY-101 and pending FDA clearance, the Phase 1 ELiPSE-1 trial in relapsed/refractory lymphoma is on track to commence in the second half of 2022 -

- Ended second quarter 2022 with cash, cash equivalents, and investments of $429.4; Expected cash runway into 2025 -

PHILADELPHIA, Aug. 11, 2022 (GLOBE NEWSWIRE) -- Century Therapeutics, Inc., (NASDAQ: IPSC), an innovative biotechnology company developing induced pluripotent stem cell (iPSC)-derived cell therapies in immuno-oncology, today reported financial results and business highlights for the second quarter ended June 30, 2022.

We are excited about our recent IND submission for our lead candidate, CNTY-101, and pending FDA clearance, are looking forward to initiating the Phase 1 ELiPSE-1 trial in relapsed/refractory lymphoma, said Lalo Flores, Chief Executive Officer, Century Therapeutics. We continue to make steady progress in building a best-in-class allogeneic cell therapy platform and achieved a key milestone this quarter in establishing the iNK 3.0 Common Progenitor, which we believe will accelerate new candidate selection. Additionally, we look forward to providing updates on our gamma delta iT platform and other program advancements in the coming months.

Business Highlights

The Company

preclinical data on MAD7, a novel CRISPR nuclease used to enable the genetic engineering of iPSC-derived NK and T cell product candidates, during a poster presentation at the American Society of Gene and Cell Therapy (ASGCT) 25th Annual Meeting held on May 16-19, 2022 in Washington, D.C. A copy of the presentation is available in the Posters section of Centurys website. During a Research and Development Event in June, Centurys management team discussed CNTY-103, the Companys first solid tumor candidate for glioblastoma, the establishment of the Common Progenitor iNK 3.0, and progress on the Companys next-generation iPSC-based cell therapy platform. Century expects to submit an Investigational New Drug (IND) application for CNTY-103 in 2024. The Companys current Good Manufacturing Practice (cGMP) manufacturing facility in Branchburg, New Jersey is operational and undergoing qualification.Century was added to the Russell Microcap Index in June 2022.

Subsequent Events and Upcoming Milestones

Following the recent submission of the IND application for CNTY-101, the Company remains on track to initiate its Phase 1 ELiPSE-1 clinical trial in the second half of 2022, subject to U.S. Food and Drug Administration (FDA) clearance of the application. ELiPSE-1 will assess CNTY-101 in patients with relapsed/refractory CD19 positive aggressive lymphoma or indolent lymphoma after at least two prior lines of therapy, including patients who have received prior CAR-T cell therapy.

Second Quarter 2022 Financial Results

Cash Position:Cash, cash equivalents, and investments were $429.4 million as of June 30, 2022, as compared to $358.8 million as of December 31, 2021. Net cash provided by operations was $61.2 million for the six months ended June 30, 2022 (which includes deferred revenue from the Bristol-Myers Squibb (BMS) collaboration of $120.7M) compared to net cash used in operations of $40.7 million for the six months ended June 30, 2021.Collaboration Revenue: Collaboration revenue was $1.4 million for the three months ended June 30, 2022, generated through the Companys collaboration, option and license agreement with BMS.Research and Development (R&D) expenses: R&D expenses were $24.5 million for the three months ended June 30, 2022, compared to $18.9 million for the same period in 2021. The increase in R&D expenses was primarily due to an increase in personnel expenses related to increased headcount to expand the Companys R&D capabilities, costs for pre-clinical studies, costs for laboratory supplies and facility costs, offset by a decrease in collaboration expenses with FUJIFILM Cellular Dynamics, Inc. (FCDI) as the scope of work with FCDI has narrowed down to primarily manufacturing CNTY-101 clinical supply. General and Administrative (G&A) expenses: G&A expenses were $8.3 million for the three months ended June 30, 2022, compared to $4.1 million for the same period in 2021. The increase was primarily due to an increase in employee headcount, an increase in directors and officers insurance expense and an increase in the Companys professional fees as a result of expanded operations to support the Companys infrastructure as well as additional costs to operate as a public company, and increased information technology and facility costs. Net loss: Net loss was $31.0 million for the three months ended June 30, 2022, compared to $23.3 million for the same period in 2021.

Financial Guidance

The Company expects full year GAAP Operating Expenses to be between $155 million and $165 million including non-cash stock-based compensation expense of $10 million to $15 million. The Company expects its cash, cash equivalents, and investments will support operations into 2025.

About Century Therapeutics

Century Therapeutics, Inc. (NASDAQ: IPSC) is harnessing the power of adult stem cells to develop curative cell therapy products for cancer that we believe will allow us to overcome the limitations of first-generation cell therapies. Our genetically engineered, iPSC-derived iNK and iT cell product candidates are designed to specifically target hematologic and solid tumor cancers. We are leveraging our expertise in cellular reprogramming, genetic engineering, and manufacturing to develop therapies with the potential to overcome many of the challenges inherent to cell therapy and provide a significant advantage over existing cell therapy technologies. We believe our commitment to developing off-the-shelf cell therapies will expand patient access and provide an unparalleled opportunity to advance the course of cancer care. For more information on Century Therapeutics please visit https://www.centurytx.com/.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of, and made pursuant to the safe harbor provisions of, The Private Securities Litigation Reform Act of 1995. All statements contained in this press release, other than statements of historical facts or statements that relate to present facts or current conditions, including but not limited to, statements regarding our cash, financial resources, and estimated expenses, our clinical development plans and timelines, and the development of our U.S. manufacturing facility are forward-looking statements. These statements involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance, or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. In some cases, you can identify forward-looking statements by terms such as may, might, will, should, expect, plan, aim, seek, anticipate, could, intend, target, project, contemplate, believe, estimate, predict, forecast, potential or continue or the negative of these terms or other similar expressions. The forward-looking statements in this presentation are only predictions. We have based these forward-looking statements largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition, and results of operations. These forward-looking statements speak only as of the date of this press release and are subject to a number of risks, uncertainties and assumptions, some of which cannot be predicted or quantified and some of which are beyond our control, including, among others: our ability to successfully advance our current and future product candidates through development activities, preclinical studies, and clinical trials; our ability to obtain FDA acceptance for our IND submissions and commence clinical trials on expected timelines, or at all; our reliance on the maintenance of certain key collaborative relationships for the manufacturing and development of our product candidates; the timing, scope and likelihood of regulatory filings and approvals, including final regulatory approval of our product candidates; the impact of the COVID-19 pandemic, geopolitical issues and inflation on our business and operations, supply chain and labor force; the performance of third parties in connection with the development of our product candidates, including third parties conducting our future clinical trials as well as third-party suppliers and manufacturers; our ability to successfully commercialize our product candidates and develop sales and marketing capabilities, if our product candidates are approved; and our ability to maintain and successfully enforce adequate intellectual property protection. These and other risks and uncertainties are described more fully in the Risk Factors section of our most recent filings with the Securities and Exchange Commission and available at http://www.sec.gov. You should not rely on these forward-looking statements as predictions of future events. The events and circumstances reflected in our forward-looking statements may not be achieved or occur, and actual results could differ materially from those projected in the forward-looking statements. Moreover, we operate in a dynamic industry and economy. New risk factors and uncertainties may emerge from time to time, and it is not possible for management to predict all risk factors and uncertainties that we may face. Except as required by applicable law, we do not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.

For More Information:

Company: Elizabeth Krutoholow investor.relations@centurytx.com

Investors: Melissa Forst/Maghan Meyers century@argotpartners.com

Media: Joshua R. Mansbach century@argotpartners.com

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Century Therapeutics Reports Second Quarter 2022 Financial Results and Provides Business Updates - KULR-TV

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See-through zebrafish, new imaging method put blood stem cells in high-resolution spotlight – University of Wisconsin-Madison

Posted: August 14, 2022 at 2:20 am

Tracing features in a large 3D electron microscopy dataset reveals a zebrafish blood stem cell (in green) and its surrounding niche support cells, a group photo method that will help researchers understand factors that contribute to blood stem cell health which could in turn help develop therapies for blood diseases and cancers. Image by Keunyoung Kim.

MADISON For the first time, researchers can get a high-resolution view of single blood stem cells thanks to a little help from microscopy and zebrafish.

Researchers at the University of WisconsinMadison and the University of California San Diego have developed a method for scientists to track a single blood stem cell in a live organism and then describe the ultrastructure, or architecture, of that same cell using electron microscopy. This new technique will aid researchers as they develop therapies for blood diseases and cancers.

Currently, we look at stem cells in tissues with a limited number of markers and at low resolution, but we are missing so much information, says Owen Tamplin, an assistant professor in UWMadisons Department of Cell & Regenerative Biology, a member of the Stem Cell & Regenerative Medicine Center, and a co-author on the new study, which was published Aug. 9 in eLife. Using our new techniques, we can now see not only the stem cell, but also all the surrounding niche cells that are in contact.

The niche is a microenvironment found within tissues like the bone marrow that contain the blood stem cells that support the blood system. The niche is where specialized interactions between blood stem cells and their neighboring cells occur every second, but these interactions are hard to track and not clearly understood.

As a part of the new study, Tamplin and his co-lead author, Mark Ellisman, a professor of neuroscience at UC San Diego, identified a way to integrate multiple types of microscopic imaging to investigate a cells niche. With the newly developed technique that uses confocal microscopy, X-ray microscopy, and serial block-face scanningelectron microscopy, researchers will now be able to track the once elusive cell-cell interactions occurring in this space.

This has allowed us to identify cell types in the microenvironment that we didnt even know interacted with stem cells, which is opening new research directions, Tamplin says.

As a part of this study, Tamplin, and his colleagues, including co-first authors Sobhika Agarwala and Keunyoung Kim, identified dopamine beta-hydroxylase positive ganglia cells, which were previously an uncharacterized cell type in the blood stem cell niche. This is crucial, as understanding the role of neurotransmitters like dopamine in regulating blood stem cells could lead to improved therapeutics.

Transplanted blood stem cells are used as a curative therapy for many blood diseases and cancers, but blood stem cells are very rare and difficult to locate in a living organism, Tamplin says. That makes it very challenging to characterize them and understand how they interact and connect with neighboring cells.

While blood stem cells are difficult to locate in most living organisms, the zebrafish larva, which is transparent, offers researchers a unique opportunity to view the inner workings of the blood stem cell niche more easily.

Thats the really nice thing about the zebrafish and being able to image the cells, Tamplin says of animals transparent quality. In mammals, blood stem cells develop in utero in the bone marrow, which makes it basically impossible to see those events happening in real time. But, with zebrafish you can actually watch the stem cell arrive through circulation, find the niche, attach to it, and then go in and lodge there.

While the zebrafish larva makes it easier to see blood stem cell development, specialized imaging is needed to find such small cells and then detail their ultrastructure. Tamplin and his colleagues spent over six years perfecting these imaging techniques. This allowed them to see and track the real-time development of a blood stem cell in the microenvironment of a live organism, then zoom in even further on the same cell using electron microscopy.

First, we identified single fluorescently labeledstem cells bylight sheet or confocal microscopy, Tamplin says. Next, we processed the same sample forserial block-face scanningelectron microscopy. We then aligned the 3D light and electron microscopy datasets. Byintersecting these different imaging techniques,we could see the ultrastructure of single rare cells deep inside a tissue. This also allowed us to find all the surrounding niche cellsthat contact a blood stem cell. We believe our approach will be broadly applicable for correlative light and electron microscopy in many systems.

Tamplin hopes that this approach can be used for many other types of stem cells, such as those in the gut, lung, and the tumor microenvironment, where rare cells need to be characterized at nanometer resolution. But, as a developmental biologist, Tamplin is especially excited to see how this work can improve researchers understanding of how the blood stem cell microenvironment forms.

I think this is really exciting because we generate all of our blood stem cells during embryonic development, and depending on what organism you are, a few hundred or maybe a few thousand of these stem cells will end up producing hundreds of billions of new blood cells every day throughout your life, Tamplin says. But we really dont know much about how stem cells first find their home in the niche where theyre going to be for the rest of the life of the organism. This research will really help us to understand how stem cells behave and function. A better understanding of stem cell behavior, and regulation by surrounding niche cells, could lead to improved stem cell-based therapies.

This research was supported by grants from the National Institutes of Health (R01HL142998, K01DK103908, 1U24NS120055-01, R24 GM137200) and the American Heart Association (19POST34380221).

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See-through zebrafish, new imaging method put blood stem cells in high-resolution spotlight - University of Wisconsin-Madison

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ISCT’s New Leader on the Future of Cell and Gene Therapy – The Medicine Maker

Posted: August 14, 2022 at 2:20 am

In the early nineties, Jacques Galipeau was outside his native Canada, training at the Tufts New England Medical Center in Boston. It was an exciting time to be a young hematologist. The dream of gene therapy was becoming a reality, and with it came the promise of potential cures for the likes of sickle cell disease and thalassemia.

Fast forward, and we find a man who has ascended to lofty heights. At the recent 2022 meeting of the International Society for Cell & Gene Therapy, Galipeau was crowned as its new president. Here, we quiz Galipeau about the present and future of advanced medicine.

Well, the field has matured since the early nineties. Its worth remembering that the proof-of-concept for applying cell and gene therapies in humans arrived more than 30 years ago. Now, we have approved products! The first live cell vaccine approved by the FDA was Provenge in 2010. More recently, weve had the whole CAR T story, and in Europe weve seen the approval of mesenchymal cells for Crohns-related skin complications. All in all, its a very nice buffet.

As Im university based, my work is in discovery understanding how cells tick and how to make a better mousetrap out of them. We also work more boldly, testing first-in-human studies that may grow legs and march toward further development. At the University of Wisconsin-Madison, we have a special interest in virus-specific T cells and the version 2.0 of mesenchymal cells. As a scholar, these are my particular specialisms.

While wearing my ISCT hat, on the other hand, Im like a kid locked in a candy shop! There are so many exciting, emerging, and improved platforms, especially in immunotherapy and regenerative medicine. For some, the latter term is a dirty word because it has so often been bandied about as a catch-all everything for everybody. But now, were hearing about ongoing works like the clinical trials of induced pluripotent stem (IPS) cell-derived dopaminergic neurons for Parkinson's disease an excellent example of a highly promising regenerative medicine.

Regenerative medicines are replacement therapies, but the definition has now broadened to include all somatic cell therapies. Historically, regenerative medicine was all about stem cells, but more recently we have realized that there are many cells and tissues that can be used as living therapeutics, while having nothing to do with stem cells. For example, lymphoid cells and live tumor cell vaccines.

Absolutely. We humans are gregarious simians. Chimps dont talk its all nonverbal. Humans deal in a great deal of nonverbal communication too, and that cant be replicated online. So much of the spontaneity and exchange is leached away through the virtual interface. Not to mention the drop in dopamine levels!

Offline serendipity cant be replicated either. Everybody has a story that proves it. You turn and say hello to the person behind you in a queue for lunch at an event, and the next thing you know youre launching a collaboration. That doesnt happen on Zoom, where everyone is just one rectangle in a grid of video feeds.

It was a bold bet. Between our CEO Queenie Jang, our outgoing president Bruce Levine, and myself, we knew that we would have to make the call by October 2021. Reading the signs, we made plans for an in person event, and the result was a smashing success the biggest turnout weve ever had at an international meeting. I also think it helped prove that in-person events should remain the gold standard, with virtual hybridity as a bonus that remains well worth considering. Recording events is another pandemic practice wed like to keep alive. Having those recordings for future reference and wider access is really valuable. We want these international events to be absolutely optimal because they only come once per year and attending them isnt cheap especially for our friends flying in from afar!

We all know workforce development is an emerging topic, but I was surprised by just how strong the appetite for and imperative from stakeholders was. Had I not attended in person, I never would have got that impression.

From the perspective of platforms, I was surprised by the explosion of clinical-stage startups in cancer immunotherapy. Back in old school advanced therapy, the only way you could modify immune effector cells was using retroviral vectors. But now, we are seeing an explosion of emerging disruptive platforms that could be game changers as far as nimbleness is concerned.

Our societys focus on translational manufacturing, regulations, and first-in-human trials really sets us apart. In those areas, the technologists working in the field are really important. Theres a whole army of them. Thats why, at ISCT this year, we had a day for the technologists Saturday, to be precise.

It was standing room only! And it was great to see such a real uptick in attendance from people who are in neither business nor science. These are the people who really do the up-close work, and we learned that they have a real hunger for networking, change, and best practices. The ISCT is a knowledge-transfer organization, so we are more than happy to sate these appetites.

Last of all, Ill mention the real explosion of interest in exosomes as a therapeutic modality. Its lending a second life to the already popular interest in mesenchymal cells. Depending on how you tickle them in the petri dish, they spit out exosomes through which many of their functional attributes are transferred to tissues. This is a brand new development that is taking off in parallel with cancer immunotherapy, replacement therapy, and IPS.

I think the answer will be woven from different strands. In the case of established, approved, effective approaches that rinse, wash, and repeat 1000 times in a row, automation is your most obvious ally. But when youre still carrying out investigational development when youre building the plane as you fly it you may need some hands! Lab work can be a science in the same way cooking is a science. You need tactility, and more than a little artistry.

You really cannot underestimate the importance of having hands and being human! Take the analogy of baking a chocolate cake. I might give the exact same recipe to Bob and to Bert. Bob makes a beautiful cake, and Bert makes a burnt mess. Good hands and good instincts; some people have them, and some people just dont.

Compounding that, so many of our platforms are not set in stone. Disruptive technologies are loose in this field, and the task of incorporating and optimizing them is a hands-on affair. And thats where the workforce comes in. ISCT pays a great deal of attention here because we excel as a knowledge transfer and networking organization. Were not a university we cant confer diplomas but the way we pass on best practices and knowhow does make us serve as a sort of cooking school, if I may stretch my chocolate cake metaphor a little further.

We bring in domain experts that understand the obstacles and the friction points, and introduce them to newbies people who may well be very clever and have excellent degrees, but who still need to learn the ropes, and how to avoid beginners mistakes. Of course, you cant stop after initiation. This is an ever-evolving field of ever-evolving platforms. Penning a curriculum is not much use because it will likely be out of date by the time youve completed the first draft.

At ISCT events, we dont try to operate as a substitute for universities or technical colleges, as thats not our remit. Rather than disseminating knowledge through lecturing, we use a roundtable format. We set up a panel of experts, sit them down together, and let the audience listen to their back-and-forth in real time. Its an extremely valuable way to educate people on topics that wont appear in print for another year. In short, our attendees walk away as slightly more developed and informed professionals.

Right now, everybody is focusing on the highly impactful cell therapeutic platforms that have met marketing approval and are now commercially deployed. This is especially true in the case of cancer immunotherapy space, and even for Takedas mesenchymal product, Alofisel. The challenges here really hinge on the different regulatory environments that shape them.

In Europe, deployment and commercial success is dictated predominantly by universal payers and national entities. The US will be more of a wild west as far as pricing and reimbursement are concerned. I have no magic solutions for my commercial friends, but I do aim to help them understand the best practices that can ensure both ROI, as well as the sustainability and deployability necessary for distributive justice. Balancing ROI and access is not just a moral question; if one overtakes the other, the platform may collapse. Over time, competition ought to bring the current prices down. As more products are rolled out and sorted according to their effectiveness, potency, and ability to improve human outcomes, it is my hope and expectation that they will position themselves in a sustainable manner.

That said, I am currently very interested in another aspect that complements pharmas traditional central manufacturing, hub-and-spoke model: the democratization of advanced cell therapy, manufacture, and deployment. Bone marrow transplants serve as a good example. These are cell therapies, but since regulation does not define them as an advanced cell therapy, they do not require oversight by the EMA or FDA. Everything from cell collection and manipulation to re-administration is carried out in academic health centers. Industry had no direct involvement in the development of bone marrow transplants.

Now, with the explosion of cell therapies, the relevant technologies are becoming increasingly simple, and the prices are ever more robust. It is becoming easier to imagine that hospitals and other places of care could serve as a complement to large-scale manufacturing, especially for autologous cell therapies or one patient/one donor paradigms. There's a lot of new money in this space geared toward not only the traditional model, but also these complementary models of deployment. Thats something I think we need to face, as the future comes knocking.

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ISCT's New Leader on the Future of Cell and Gene Therapy - The Medicine Maker

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Epigenetics in Health and Disease – PubMed

Posted: August 14, 2022 at 2:17 am

Epigenetic mechanisms, which include DNA methylation, histone modification, and microRNA (miRNA), can produce heritable phenotypic changes without a change in DNA sequence. Disruption of gene expression patterns which are governed by epigenetics can result in autoimmune diseases, cancers, and various other maladies. Mechanisms of epigenetics include DNA methylation (and demethylation), histone modifications, and non-coding RNAs such as microRNAs. Compared to numerous studies that have focused on the field of genetics, research on epigenetics is fairly recent. In contrast to genetic changes, which are difficult to reverse, epigenetic aberrations can be pharmaceutically reversible. The emerging tools of epigenetics can be used as preventive, diagnostic, and therapeutic markers. With the development of drugs that target the specific epigenetic mechanisms involved in the regulation of gene expression, development and utilization of epigenetic tools are an appropriate and effective approach that can be clinically applied to the treatment of various diseases.

Keywords: Checkpoints; Cytokines; DNA methylation; Histone modification; Immune dysfunction; Signaling pathways; miRNA.

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Epigenetics in Health and Disease - PubMed

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