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Animal Stem Cell Therapy Market: Challenges and Opportunities Report 2017 2025 Bulletin Line – Bulletin Line

The comprehensive report published by Persistence Market Research offers an in-depth intelligence related to the various factors that are likely to impact the demand, revenue generation, and sales of the Animal Stem Cell Therapy Market. In addition, the report singles out the different parameters that are expected to influence the overall dynamics of the Animal Stem Cell Therapy Market during the forecast period 2017 2025.

As per the findings of the presented study, the Animal Stem Cell Therapy Market is poised to surpass the value of ~US$ XX by the end of 2029 growing at a CAGR of ~XX% over the assessment period. The report includes a thorough analysis of the upstream raw materials, supply-demand ratio of the Animal Stem Cell Therapy in different regions, import-export trends and more to provide readers a fair understanding of the global market scenario.

ThisPress Release will help you to understand the Volume, growth with Impacting Trends. Click HERE To get SAMPLE PDF (Including Full TOC, Table & Figures) athttps://www.persistencemarketresearch.co/samples/14941

The report segregates the Animal Stem Cell Therapy Market into different segments to provide a detailed understanding of the various aspects of the market. The competitive analysis of the Animal Stem Cell Therapy Market includes valuable insights based on which, market players can formulate impactful growth strategies to enhance their presence in the Animal Stem Cell Therapy Market.

Key findings of the report:

The report aims to eliminate the following doubts related to the Animal Stem Cell Therapy Market:

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Key Participants

The key participants in the animal stem cell therapy market are Magellan Stem Cells, ANIMAL CELL THERAPIES, Abbott Animal Hospital, VETSTEM BIOPHARMA, Veterinary Hospital and Clinic Frisco, CO, etc. The companies are entering into the collaboration and partnership to keep up the pace of the innovations.

The report covers exhaustive analysis on:

Regional analysis for Market includes

Report Highlights:

In order to get a strategic overview of the market,Access Research Methodology Prepared By Experts athttps://www.persistencemarketresearch.co/methodology/14941

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Animal Stem Cell Therapy Market: Challenges and Opportunities Report 2017 2025 Bulletin Line - Bulletin Line

Don’t throw food in the trash in Vermont, or ask about salary history in New Jersey. Here are 7 state law changes for 2020 – USA TODAY

A slew of state laws take effect in 2020 ranging from mandatory compostingto child abuse registriesto access to diaper changing stations. One state will even begin banning expiration dates for gift certificates.

A few of the more notable changes:

Food scraps can't goin Vermont landfillsbeginningJuly 1. Residents will have four ways to handle rotten leftovers anditems such aspeels, eggshells, seeds, pits, coffee grounds and oils, according to the state's environmental conservation department.

Vermonters can use a household compost bin, buy a Green Cone solar digester to break down the scraps, feed scraps to pigs or leave it to the composting professionals.Theuniversal recycling lawwillrequiretrucking companies to provide food scrap collection services to nonresidential customers and multi-unit apartment complexes, the Burlington Free Press reported.

Restaurants, supermarkets and cafeteriasmust alsocomply with the law, which is the firststate law of its kind. The state hopes to reach a 60% recycling rate through mandatory composting.

Citing a need to respect human life, Arkansas will not allowpublic funding for human cloning or"destructive embryo research," which the statedefinesas medical procedures or investigations that kill or injure developing humans. ACT 653 also blocks state funds from stem cell research involving embryos, the stage lasting to eight weeks after fertilization.

Under the law effective Jan. 1, no state educational institutions can do human cloning for scientific research, either.It does not block state funds frominvitro fertilization.

Businesses in Washington state will be prohibited from putting expiration dates on gift cards beginning July 1.HB1727 will also prevent gift certificate users from being hit by inactivity or service charges.

However, ifa gift card is part of rewards orloyalty program, itcan still expire. The law will also not apply to gift certificates given to charitable organizations as a donation.

Restaurants, stores and other buildings with public restrooms in Illinois musthave at least one babydiaper changing stationunderHB 3711. Effective Jan. 1, the law requires buildings either have a station in both a women's and men's restroom, or a station in a unisex restroom. Building owners must also display a sign near restroom entrances to show that a sanitary andsafe changing station is inside.

Public buildings in New York must now have changing tables in bathrooms for both genders.(Photo: Wittayayut, Getty Images/iStockphoto)

Diaper duty: John Legend speaks out about why he changes diapers

Exceptions to the law include bars and nightclubs that don't allow minors, as well as cases where adding a station isn't feasible or would prevent people with disabilities from navigating the restroom.

In federal buildings, theBathrooms Accessible in Every Situation (BABIES) act already requires diaper changing stations in men's and women's restrooms. California has a law similar to Illinois, whileNew Yorkrequires stations in new or renovated public restrooms.

At the beginning of the new year, Nevada will joina dozenother states inpreventinginsurers from denying coverage to patients because ofpreexisting conditions. The federal Affordable Care Act currently protectspeople with preexisting conditions from that and higher coverage costs, but the act is facing legal challenges. A federal appeals court struck down a major partof the ACA last week, which could lead to a Supreme Court case.

'Unconstitutional': Federal appeals court strikes down key part of Affordable Care Act

Democratic Gov. Steve Sisolak said Nevada'sAB 170will keep health care protections in place if the ACA is eliminated. States with similar protectionsin placefor preexisting conditionsinclude Delaware, Hawaii, Indiana, Maine, New Hampshire, New Mexico, Oregon, Vermont and Washington,according to the Commonwealth Fund.

In Georgia, HB 478 will create stricter requirements to list a person on the state's child abuse registry, upping the age from 13 to 18.Previously, the state entered offenders who were minors into the database and didn't remove them until they turned 18,could prove they had been rehabilitated or more than a year passed since the date of the act that prompted the last case.

Effective Jan. 1, the law also updates theprocess to get a name expunged from the state registry. If a judge refuses to remove an offender from the registry after a hearing, the offender can request another three years later.

The state established the registry, which the public cannot view,in 2016. Each year, the state receives about 140,000 reports of child maltreatment, according to theGeorgia Division of Family and Children Services.

Employers cannot screen applicants based ontheir salary history under a New Jersey law effective Jan. 1.AB 1094also prevents hiring managers from requiring that an applicant's salary history falls within a minimum or maximum criteria.

If a worker voluntarily provideshis or her previous salaries, wages or benefits, employers can use the information to determine compensation, however. More than 15 other states, including California, Hawaii and Maine, have similar bans on salary history screening, HR Dive reported.

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Don't throw food in the trash in Vermont, or ask about salary history in New Jersey. Here are 7 state law changes for 2020 - USA TODAY

From the image of a black hole to ‘artificial embryos’, 2019 was the year of many firsts in science – Economic Times

NEW DELHI: An image of the black hole, the stuff of science fiction down the decades, was at the centre of a year that saw science breaching new frontiers with exciting firsts such as the development of a quantum computer that can outperform its classical counterparts and artificial embryos.

Cutting edge innovations in research and technology celebrated science and forwarded humankind's understanding of complex realities of the universe. The year will also be remembered as the year of testing biological and ethical limits in the laboratory, helping researchers find new avenues in the treatment of critical diseases.

In April, the International Event Horizon Telescope collaboration, consisting of a global network of radio telescopes, unveiled the first actual image of a black hole, a place in space where gravity pulls so much that even light cannot escape.

To produce the image, the researchers combined data from a network of radio telescopes to take simultaneous readings from around the world.

Science magazine named the image of the supermassive black hole situated at the centre of the Messier 87 galaxy, 54 million light years away, as the 2019 Breakthrough of the Year.

The imaging of the black hole is a fantastic revelation that is simultaneously a validation and a celebration of science, Ayan Banerjee, from the Indian Institute of Science Education and Research (IISER) in Kolkata, told PTI.

Although it does not uncover something that we did not know earlier, it does convert science fiction into science -- which is crucial for the acceptance of science in the daily lives of human beings, and the generation of future scientists, Banerjee said.

In a year that marked the 50th anniversary of the Apollo Moon landings, lunar exploration was high on the agendas of space agencies.

In January, China's Chang'e-4 probe became the first spacecraft to land safely on the far side of the Moon. Its rover Yutu-2 continues to roll across the dusty soils of Von Karman crater on the lunar body.

Other attempts to explore the Earth's natural satellite were not so successful.

To produce the image, the researchers combined data from a network of radio telescopes to take simultaneous readings from around the world. In April, an Israeli-led effort to put the first private spacecraft on the Moon's surface ended in a crash landing. The same fate was met by India's ambitious Chandrayaan-2 Vikram lander in September.

The ongoing Mars missions returned a host of results. In April, NASA announced that its robotic Mars InSight lander had recorded a marsquake for the first time ever.

The marsquake' is the first recorded trembling that appears to have come from inside the planet, as opposed to being caused by the forces above the surface, such as wind.

There were many firsts in the micro world of laboratories too.

US researchers restored cellular function in 32 pig brains that had been dead for hours, opening up a new avenue in treating brain disease -- and shaking our definition of brain death to its core.

Announced in April in the journal Nature, the researchers at the Yale University School of Medicine devised a system roughly analogous to a dialysis machine, called BrainEx, that restores circulation and oxygen flow to a dead brain.

In another out-of-body experiment, scientists grew monkey embryos in a dish for nearly three weeks -- longer than primate embryos have ever been grown in the laboratory before.

The advance raised ethical concerns of whether lab-grown human embryos should be allowed to develop beyond 14 days, a restriction imposed in most countries.

In September, researchers at the University of Michigan in the US provided a possible circumvention of the 14-day limit by using human stem cells to make artificial embryos' that mimic the early development of a real human embryo.

Our stem cell structures that mimic embryos can help fill critical gaps in knowledge about early human development, and that could lead to a lot of good, Jianping Fu, an associate professor at Michigan, who led the study, said in a statement.

In October, Google took a quantum leap in computer science. Using its state-of-the-art quantum computer, called Sycamore, the tech giant claimed "quantum supremacy" over the most powerful supercomputers in the world by solving a problem considered virtually impossible for normal machines.

The quantum computer completed the complex computation in 200 seconds. That same calculation would take even the most powerful supercomputer approximately 10,000 years to finish, according to researchers from the University of California, Santa Barbara, who published their results in the journal Nature.

A fantastic discovery has been that of Google's 53 qubit quantum computer ('quantum supremacy), Banerjee said.

And for the first time in July, an artificial intelligence (AI) bot beat human champions at multiplayer poker.

The AI programme developed by Carnegie Mellon University in the US in collaboration with Facebook AI defeated leading professionals in six-player no-limit Texas hold'em poker, the world's most popular form of poker.

The AI, called Pluribus, defeated poker professional Darren Elias, who holds the record for most World Poker Tour titles, and Chris Ferguson, winner of six World Series of Poker events.

In August, researchers from Oxford University and IBM Research made the first-ever ring-shaped molecule of pure carbon in the lab by using an atomic-force microscope to manipulate individual molecules.

Carbon can be arranged in a number of configurations. For example when each of its atoms is bonded to three other carbon atoms, it's relatively soft graphite.

A ring of carbon atoms, where each atom is bonded to just two others, and nothing else has eluded scientists for 50 years. Their best attempts have resulted in a gaseous carbon ring that quickly dissipated.

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From the image of a black hole to 'artificial embryos', 2019 was the year of many firsts in science - Economic Times

What is HLH, and what role did it play in the death of a healthy 34-year-old ESPN reporter? – 11Alive.com WXIA

ATLANTA How does a healthy 34-year-old die after being diagnosed with pneumonia?

That's the question at the heart of the tragic and sudden death of an ESPN reporter earlier this week.

According to college football reporter Edward Aschoff's fiance, Katy Berteau, about a week after being diagnosed with a severe form of pneumonia, he began treatment for a "presumed diagnosed" of hemophagocytic lymphohistiocytosis (HLH). Three days after being moved to the ICU, Berteau tweeted from Aschoff's account on Thursday night, he died.

RELATED: Edward Aschoff's fiance releases new information about ESPN reporter's sudden death, memorable life

HLH is a rare and complicated condition that's not entirely well-understood by researchers, but it basically stems from your immune system severely overreacting to an infection (such as pneumonia) or another illness.

"It just gets overworked and starts fighting regular tissues, so usually those tissues are organs, like your spleen or your liver," Atlanta area doctor Will Epps said. "So it can result in liver failure or organ failure and unfortunately end up expiring from it."

Here's a general outline:

According to the Genetic and Rare Diseases Information Center at the National Institutes of Health, HLH comes in two forms: A genetic form and an acquired form.

St. Jude Children's Research Hospital says the genetic form is more common in young children, while the acquired form, sometimes called the secondary form, usually affects older children and adults, such as Aschoff.

What happens, broadly, is this: Faced with a severe infection, such as pneumonia (or other severe conditions like cancer), a person's immune system overreacts and, as the Johns Hopkins School of Medicine describes it, certain while blood cells called histiocytes and lymphocytes "attack your other blood cells."

"These abnormal blood cells collect in your spleen and liver, causing these organs to enlarge," Johns Hopkins says.

(According to the NIH, HLH may also be associated with a separate genetic condition X-linked lymphoproliferative disease - XLP - when it results from an inappropriate immune response.)

It can cause death in a matter of weeks, according to researchers.

A 2012 paper in the medical journal "Clinical Advances in Hematology & Oncology,"outlines adult HLH extensively.

"It is useful to think of HLH as the severe end of a spectrum of hyperinflammatory diseases in which the immune system causes damage to host tissues," the paper's authors, Dr. Roman Leonid Kleynberg and Dr Gary J. Schiller, wrote.

That paper estimated HLH occurs in only 1.2 cases per one million individuals every year, making it extremely rare.

Specifically amongst children, St. Jude estimates HLH is diagnosed in fewer than 1 out of every 50,000 - 100,000 children per year.

The condition's mortality rate is difficult to pin down because it can fluctuate based on what caused it. Many sources say a common cause is Epstein-Barr virus, for example, and the 2012 paper reported the mortality rate associated with that 18-24 percent. Other causes can have lower mortality rates.

Generally, doctors try both to treat the underlying trigger for HLH and address the immune response.

"Treating that is tamping that down, either through steroids or with a chemotherapeutic agent which tends to attack or lower that immune system," Epps said.

John Hopkins Medicine also details antibiotic and antiviral drugs being used, or if drug treatment fails doctors may turn to stem cell transplants.

There is no known way to prevent HLH.

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What is HLH, and what role did it play in the death of a healthy 34-year-old ESPN reporter? - 11Alive.com WXIA

New technology being used to heal serious wounds – WWLTV.com

NEW ORLEANS Nancy Van Den Akker went through a difficult time.

Compressed discs caused pain shooting down her leg. In May, she had surgery to fix that. Then there was another problem.

"Was about ready to start physical therapy when apparently some of the stitches in the side opened up. I had kind of these gaping holes there," said Nancy Van Den Akker.

It's harder for diabetics like Nancy to heal, so even with standard wound medicine the incision stayed open for three months. Then Tulane reconstructive plastic surgeon Dr. Abigail Chaffin asked Nancy to try new technology.

"What we're talking about today is living tissue. These are donated placentas from healthy mothers, undergoing planned C-sections, that give consent to donate tissue that would otherwise be discarded," explained Dr. Abigail Chaffin, a reconstructive plastic surgeon specializing in wound medicine who is the Medical Director of the MedCentris Wound Healing Institute at Tulane.

The tissue comes in many sizes. Dr. Chaffin spreads it out over the wound, then it's bandaged for a week. The tissue bathes the wound in growth factors and stem cells helping regenerate your own tissue, faster.

"These can be used for many different type of wounds, from diabetic ulcers, venous ulcers, non-healing surgical wounds, over any area of the body," said Dr. Chaffin.

This can keep people out of the operating room with anesthesia and from having a painful skin graft that leaves a big scar. It can also help prevent infection and limb amputation. She even used it successfully before surgery on a young patient whose wound did not heal for 10 years.

Nancy healed in four weeks with the treatment.

"It's all healed up. I don't even feel it. Within just a couple of weeks, I was able to start physical therapy," said Nancy Van Den Akker.

Every time someone is finished with the treatment the medical team rings a big bell hanging in the center.

Now that her medical team has declared Nancy healed, she can't wait to take the senior dog she rescued out for walks again.

Here are more before and after pictures:

The MedCentris Wound Healing Institute is doing a study at Tulane on the effectiveness of the new technology.

It's for any child or adult who has an open wound for at least four weeks.It is through your insurance and co-pay.

For more call 504-399-3605 or toll free, 1-855-HEAL-DAT.

Get breaking news from your neighborhood delivered directly to you by downloading the new FREE WWL-TV News app now in theIOS App StoreorGoogle Play.

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New technology being used to heal serious wounds - WWLTV.com

Five hot topics in autism research in 2019 – Spectrum

This year, researchers unearthed clues to the causes of autism and how to treat it from a variety of sources.

Advances in tiny models of the human brain bared new details about the biology of autism and provided possible platforms for testing therapies. Studies of heart rate put a spotlight on the autonomic nervous system as a potential wellspring of autism traits. And others forged a controversial connection between the gut microbiome and autism.

A few studies revealed important information about the time points at which different forms of autism are amenable to therapy. This year also saw scrutiny of tests used for screening and diagnosis, revealing gaps and limitations in the system for identifying autistic children.

Here are the years top five topics in autism research.

Brain organoids start as mere clusters of stem cells, which then are coaxed to mature into brain cells. This year, the life span of these brains-in-a-dish grew to one year and then nearly two, enabling them to mature and mimic some aspects of the human brain. In the longest-lived organoids, researchers tracked changes in the expression of autism genes. Organoids derived from the skin cells of autistic people have a shortage of cells that suppress brain activity, they found. The finding supports the signaling imbalance theory of autism, which holds that the brains of autistic people are hyper-excitable.

This year, scientists also built tiny replicas of two brain areas bridged by a long fiber tract that might reveal how long-range connections are altered in the brains of people with autism.

Brain organoids spun from people with fragile X syndrome may help explain why some experimental fragile X drugs work in mice but not in people and generate leads for effective therapies. Organoids could provide a platform for testing treatments, too, as researchers can now churn out hundreds of these brain-like blobs in parallel and make them uniform in shape and composition.

More distant applications include studies of consciousness and the effects of microgravity on the brain. In a fledgling sign of the former, brain organoids showed synchronized neuronal firing patterns, some aspects of which look like those in preterm infants.

New evidence emerged tying autism to the workings of the autonomic nervous system, which controls breathing, heart rate and digestion. Differences in the system could explain a range of autism traits, including social difficulties and sensory sensitivity, as well as heart problems and digestive issues.

Many of these differences show up in the heart rate. Heart rate remains steady in autistic people as they breathe instead of the typical pattern of slowing slightly on exhale and quickening on inhale. This discrepancy arises after 18 months of age, around the same time that the conditions core traits emerge. Children with Rett syndrome also have unusual heart-rate patterns.

These differences may persist beyond childhood. One study showed that autistic adults resting heart rates rarely vary; an even heart rate suggests a lack of flexibility in responding to environmental changes.

Autistic children are unusually prone to gastrointestinal problems. This association may not be a coincidence: Certain genetic mutations or alterations in the microbiome the mix of microbes in the intestines may contribute to both autism and gut problems.

Four mouse studies in 2019 offered up fresh evidence some of it controversial to support this idea. In one study, researchers replaced the gut microbes in mice with those from autistic boys. The mice have repetitive behaviors, make fewer vocalizations and spend less time socializing than controls do, providing the first evidence that gut microbes contribute to autism traits.

But within hours of the studys publication, several experts criticized its small sample size and highly variable results. Others found a possible statistical error.

In an unrelated study, researchers revealed that oral doses of Lactobacillus reuteri, a type of gut bacteria found in yogurt and breast milk, boost social behavior in three mouse models of autism. And two other sets of findings suggested that mutations in NLGN3, a high-confidence autism gene, alter gut function. One of them showed that a mutation in this gene disrupts the mices microbiome.

Drugs for autism may be most effective when given during a critical period of brain development. Researchers delineated the windows for treating autism traits in mouse and rat models of the condition.

One study revealed that by the time mice reach adulthood, they have lost their ability to learn from social experiences. Giving adult mice an injection of 3,4-methylenedioxymethamphetamine (MDMA), the active ingredient in ecstasy, reopens the critical window for learning.

In another study, researchers fed the cholesterol drug lovastatin to rat models of fragile X syndrome. The treatment, if given at 4 weeks of age (the rat equivalent of childhood), prevents cognitive problems, the researchers found.

The timing of treatments may be more important for some forms of autism than for others. A study of mice missing UBE3A, the gene mutated in Angelman syndrome, showed that the earlier in life the gene is restored, the more the mice improve.

By contrast, a mutation in the autism gene SCN2A has many of the same effects on neurons when introduced into adolescent mice as it does when it is present from conception. And unpublished results show that correcting an SCN2A mutation in adulthood reverses these problems.

A series of studies this year called into question the accuracy of early screening and revealed racial disparities in autism diagnoses.

Some studies cast doubt on the utility of a widely used screening tool, the Modified Checklist for Autism in Toddlers: The test identifies less than 40 percent of autistic children, and 85 percent of those it does flag do not have autism.

Of the toddlers the test flags, most do not receive follow-up evaluations. And for those who are seen again, a definitive diagnosis may not be possible right away. Some children who screen negative at age 3 meet the diagnostic criteria for autism only after age 5.

Not all children have equal access to autism evaluations, with black and Hispanic children at a disadvantage in several U.S. states. In New Jersey, black children are half as likely as white children to receive an autism assessment by age 3.

About 9 percent of autistic children may outgrow an autism diagnosis but still have other conditions that require support, highlighting the need for continued observation to adapt to their evolving needs.

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Five hot topics in autism research in 2019 - Spectrum

Humans may be Able to Regrow Teeth in the Future – NullTX

Scientific developments can have a major impact on society. It now appears that human teeth can simply be regrown through a relatively simple medical procedure.

When an adult human loses a tooth, it will never come back.

The only option to fill the gap is by using a fake tooth, or implant.

Unfortunately, those problems only grow bigger as humans grow older.

Addressing the loss of teeth has proven challenging, albeit a solution may have been discovered.

Gaining the ability to regrow teeth would certainly be beneficial to society as a whole.

Research into this matter is underway, resulting in some promising options to explore.

It appears the patients own stem cells can be used to regrow lost or damaged teeth.

That is the working theory, at least, as human trials have not been conducted yet.

When human trials will officially begin, has not been announced at this time.

A lot more research and development is needed to deem such trials safe.

Until then, tooth loss will need to be remedied with implants.

That solution has worked well for several decades, as they can serve as genuine teeth.

The downside is how the healing process associated with implants is rather lengthy, and the costs remain relatively high.

Link:
Humans may be Able to Regrow Teeth in the Future - NullTX

Gene Therapy Market 2019-2027 / Trends, Growth, Opportunities And Top Key – Market Research Sheets

The report covers the forecast and analysis of the gene therapy market on a global and regional level. The study provides historical data from 2015 to 2018 along with a forecast from 2019 to 2027 based on revenue (USD Million). The study includes drivers and restraints of the gene therapy market along with the impact they have on the demand over the forecast period. Additionally, the report includes the study of opportunities available in the gene therapy market on a global level.

In order to give the users of this report a comprehensive view of the gene therapy market, we have included a competitive landscape and an analysis of Porters Five Forces model for the market. The study encompasses a market attractiveness analysis, wherein all the segments are bench marked based on their market size, growth rate, and general attractiveness.

Download Sample of This Strategic Report:https://www.kennethresearch.com/sample-request-10170423

The report provides company market share analysis to give a broader overview of the key players in the market. In addition, the report also covers key strategic developments of the market including acquisitions & mergers, new service launches, agreements, partnerships, collaborations & joint ventures, research & development, and regional expansion of major participants involved in the market on a global and regional basis.

The study provides a decisive view of the gene therapy market by segmenting the market based on the type, vector type, therapy area, and regions. All the segments have been analyzed based on present and future trends and the market is estimated from 2019 to 2027. The regional segmentation includes the current and forecast demand for North America, Europe, Asia Pacific, Latin America, and the Middle East and Africa.

Gene therapy is utilized for treating neurodegenerative disorders like Alzheimer, amyotrophic lateral sclerosis, and spinal muscular atrophy. Gene therapy is one of the key treatment kinds that will propel the market growth over the forecast period. Moreover, gene therapy also finds lucrative applications in precision medicine. In addition to this, a rise in the occurrence of cancer is prompting the demand to treat the disease through gene therapy.

Based on the type, the market can be segregated into Germ Line Gene Therapy and Somatic Gene Therapy. In terms of vector type, the gene therapy industry can be divided into Viral Vectors, Non-Viral Vectors, and Human Artificial Chromosome. On the basis of therapy area, the market for gene therapy can be classified into Cancer, Neurological Diseases, Infectious Diseases, Genetic Disorders, Rheumatoid Arthritis, and Others.

Request For Full Report:https://www.kennethresearch.com/sample-request-10170423

The key players included in this market are Advanced Cell & Gene Therapy, Audentes Therapeutics, Benitec Biopharma, Biogen, Blubird Bio, Inc., Bristol-Myers Squibb Company, CHIESI Farmaceutici SPA, Eurofins Scientific, Geneta Science, Genzyme Corporation, Gilead, GlaxoSmithKline PLC, Human Stem Cells institute, Novartis AG, Orchard Therapeutics, Pfizer Inc., Sangamo therapeutics, Spark therapeutics, and Voyager Therapeutics.

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Gene Therapy Market 2019-2027 / Trends, Growth, Opportunities And Top Key - Market Research Sheets

AgeX Therapeutics Announces Drawdown of Second Tranche of Loan Facility from Juvenescence Ltd. – BioSpace

Juvenescence is pleased to continue its commitment to AgeX through this additional drawdown under the loan facility, commented Gregory Bailey, MD, Chairman of AgeX and CEO of Juvenescence. Juvenescence remains committed to funding the future development plans of AgeX through further advancements under the loan facility or otherwise. Since Juvenescences initial investment in AgeX in June 2018, AgeX has been an important element in the Juvenescence mission and strategy. Juvenescence is also investing its time and personnel to support AgeXs business development initiatives which have impressive potential. We look forward to AgeX announcing its plans for 2020 as it pursues tissue regeneration in Reverse Bioengineering, while advancing the development of BAT and VASC 1, the coupling of HLA-G with PureStem-derived cells for transplant therapies, and exploring partnerships with third parties.

This round of funding will allow us to continue to execute on our strategic plan to provide therapies for certain chronic and degenerative diseases through cellular regeneration and replacement, commented AgeXs founder and CEO Michael D. West, PhD.

As announced in the companys news release on August 14, 2019, AgeX has obtained a $2 million credit facility from Juvenescence to finance AgeXs operations and advance its product development programs.

About AgeX Therapeutics

AgeX Therapeutics, Inc. (NYSE American: AGE) is focused on developing and commercializing innovative therapeutics for human aging. Its PureStem and UniverCyte manufacturing and immunotolerance technologies are designed to work together to generate highly-defined, universal, allogeneic, off-the-shelf pluripotent stem cell-derived young cells of any type for application in a variety of diseases with a high unmet medical need. AgeX has two preclinical cell therapy programs: AGEX-VASC1 (vascular progenitor cells) for tissue ischemia and AGEX-BAT1 (brown fat cells) for Type II diabetes. AgeXs revolutionary longevity platform induced Tissue Regeneration (iTR) aims to unlock cellular immortality and regenerative capacity to reverse age-related changes within tissues. AGEX-iTR1547 is an iTR-based formulation in preclinical development. HyStem is AgeXs delivery technology to stably engraft PureStem cell therapies in the body. AgeX is developing its core product pipeline for use in the clinic to extend human healthspan and is seeking opportunities to establish licensing and collaboration agreements around its broad IP estate and proprietary technology platforms.

For more information, please visit http://www.agexinc.com or connect with the company on Twitter, LinkedIn, Facebook, and YouTube.

Forward-Looking Statements

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ESPN reporter diagnosed with pneumonia, HLH. What is HLH? – KXLY Spokane

Edward Aschoff, a college football reporter for ESPN, died Tuesday on his 34th birthday, according to ESPN Edward Aschoff, a college football reporter for ESPN, died Tuesday on his 34th birthday, according to ESPN Related stories

BRISTOL, Conn. - When ESPN reporter Edward Aschoff died, he had been diagnosed with multifocal pneumonia and a rare disease known as HLH, his fiance tweeted.

Aschoff was first admitted to the hospital and diagnosed with pneumonia in many parts of his lungs but was brought back to the emergency room when antibiotic treatment failed and he got worse, Katy Berteau said.

"After many tests - bone marrow and lung biopsies - treatment was started for a presumed diagnosis of HLH," she tweeted. "Within 3 days of being moved into the ICU, he passed."

HLH, hemophagocytic lymphohistiocytosis, is a rare disease that affects the immune system.

She did not provide any further details about the manner of Aschoff's death, which occurred on his 34th birthday.

Other people, including Aschoff himself, expressed surprise about the seriousness of the illness in a young man in apparently good health.

"Anyone ever had multifocal (bilateral) pneumonia in their early 30s as some who never gets sick and has a very good immune system? Asking for two friends ... my lungs," he tweeted on December 5.

More questions have come up about his second diagnosis, HLH. It is unclear if Aschoff had HLH or pneumonia first, if one came from the other, and exactly how he died so quickly.

Here is what we know about the diseases Aschoff's had:

Pneumonia is when air sacs in the lungs fill with fluid or pus. It can be caused by a virus, bacteria or a fungus, causing a fever and respiratory problems.

It can occur in one or both lungs, and multifocal means the pneumonia occurs in multiple places.

Thousands of people die around the world each year of pneumonia, but most healthy people can fight it off, especially with antibiotics and antiviral medications. The people most at risk are the young, elderly, frail or immune-compromised.

HLH is a rare disease that affects the immune system, making certain white blood cells attack other blood cells and enlarging the spleen and liver, according to Johns Hopkins Medicine.

It can be inherited or acquired, Johns Hopkins said. About a quarter of cases are passed down through families, and the rest come from infections, a weakened immune system and cancer.

Symptoms can include coughing, difficulty breathing, fever, headaches, rashes, swollen lymph nodes, jaundice and digestive problems, according to Johns Hopkins.

There is treatment for HLH, and acquired forms may clear when properly treated, Johns Hopkins said. If familial HLH goes untreated, it is usually fatal.

Treatments include chemotherapy, immunotherapy, steroids, antibiotic drugs and antiviral drugs. Stem cell transplants can cure HLH in most cases if drug treatments don't work, Johns Hopkins said.

There is no way to prevent HLH, the medical center said.

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ESPN reporter diagnosed with pneumonia, HLH. What is HLH? - KXLY Spokane