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Category Archives: Transhuman News
Money on the Move: May 5 – 11 – BioSpace
Posted: May 14, 2021 at 6:24 am
Catch up on the investment news quickly with BioSpace'sbrief overview of the biotech companies hitting the Nasdaq and raking in fresh cash the past week.
GingkoBioworks
Going public is all the rage in the biotech space, and GingkoBioworksis taking the fast train via special acquisition company (SPAC) Soaring Eagle Acquisition Corp.Theorganism company has its hand in a variety of markets, starting in fragrance, then food and agriculture and since expanding into antibiotics, vaccines, therapeutics and enzymes. The company landed a$1.1 billion loan for COVID-19 testing and to manufacture raw materials forpotentialtherapies last year. This SPAC deal isone of the biggest,expectingto raise$2.5 billioninproceedsandvaluing the combined company at $17.5 billion.
Science 37
Also jumping aboard the SPAC train isclinical trial companyScience 37. Merging withLifeSciAcquisitions II Corp to hit the Nasdaq, the deal will raise$280 million in gross proceedsand leave the company with a valuation of over $1 billion.Science 37 conducts decentralized clinical studies for clients and has 95 trials under its belt since itsinception in 2014. Funds from the merger will be usedto finance its decentralized trial technology platform, extend into new adjacencies, and power the next generation in clinical research.Science 37 intends to establish a Diversity in Clinical Research Foundation to make clinical trial research more accessible to underserved patient populations.
NuvalentInc.
Less than four months afteremerging from stealth modewith $50 million in the pocket, cancer startupNuvalentcompleted another financing round, this time in a$135 million Series B.The sole investor in the companys launch, Deerfield Management, participated with round leader Bain Capital Life Sciences and some new investors.Funds are funneling into the companys lead programs: NVL-520 and NVL-655. Each a potentially best-in-class kinase inhibitor, the first targets ROS1-driven tumors and the other ALK-driven. Both drugs are in IND enabling studies and are designed to address the identified clinical needs of kinase selectivity, brain penetrance, and activity against drug resistance.
Aetion
Using technology to understand the safety, efficacy, and value of drugs in the real world, RWE leaderAetionscooped up a$110 million Series Cto advance its Evidence Platform.Having raised $212 million to date,Aetionclose to doubled revenue last year while retaining 100% of current customers and adding new. The New York-based health care company landed the first collaboration agreement with the FDA to study COVID-19 research. In addition to growing the capabilities of theAetionEvidence Platform, the company will also expand its European and Asian-Pacific footprint and increase its commercial team to meet growing demand from the majority of top global biopharma firms and leading regulatory agencies.
Jasper Therapeutics
Taking the SPAC route to the Nasdaq, Jasper iscombining with Amplitude Health Acquisition Corp.The deal keeps up to $100million in a trust at Amplitude along with a public investment in private equity financing of another $100million. Leadprogram, JSP191is currently in an early-stage safety trial for patients withacute myeloid leukemia and myelodysplastic syndromes and severe combined immunodeficiency.Cash from the deal will advance JSP191 through clinical developmentand also advance the companys preclinical Engineered Hematopoietic Stem Cell (eHSCs) platform. Using mRNA or DNA editing, the platform is designed to overcome the biggest limitations ofallogeneic and autologous gene-edited stem cell grafts.
Dyno Therapeutics
Sinceemerging from stealth modein 2020 with multiple collaborations in place with big pharma companies, Dyno Therapeutics now bolstered its research with$100 millionraised in a Series A financing round.The Cambridge companyis advancing itsCapsidMapplatform, which leverages the power of artificial intelligence to improve the design of gene therapies and make them safer, more effectiveand applicable to more diseases.Funds from the Series A will be used to expand theCapsidMapplatform to broaden the functionality and improve the therapeutic impact of the gene therapies developed by its partners, Novartis, Roche and Sarepta Therapeutics.
Day One Biopharmaceuticals
San Francisco-basedDay One Biopharmaceuticalsis taking the more traditional route tothe market with a$100 million IPO.Founded in 2018, the biotech hasraised $190 million in the last 12 monthsalone.Its first drug, aimed at pediatric cancer in the brain, isa brain-penetrating,highly selective type II pan-rapidly accelerated fibrosarcoma kinase inhibitor designed to fight brain and spine cancers. A Phase II trial is anticipated soon forchildrenwithrelapsed or progressivelow-gradeglioma, the most common brain tumor for kids.The hope is for an NDAfilingin 2023.
Valneva
French vaccine developer Valneva went public this week, completing a$93.5 million IPO.Valnevahas a COVID-19 vaccine in the pipeline. Its stock prices were bolstered recently as big-name Moderna andBioNTechfell amidstPresident Bidens announcement insupport of waivingthe intellectual propertyprotections for COVID-19 vaccines in an effort to stop the pandemic.Valnevaplans to use the proceeds to developits COVID-19 vaccine candidate, VLA2001, andtwo additional vaccines one to prevent Lyme disease and another to fight chikungunya virus, usually spread by mosquitos.
CellaresCorporation
Automating cell therapy manufacturing,Cellaresraked in an$82 million Series Alast week, bringingfunding to $100 million to date.The fresh dollars will support the development of the companys factory-in-a-box.Cellaris Cell Shuttle enables complete automation ofhighly individualized cell therapies, including the increasingly popular CAR-T therapies which use the patients own immune system to attack blood cancer cells.This automated solution would cut costs forautologous celltherapies by up to 75%and can produce 10 patient doses simultaneously, significantly reducing the time from initial cell extraction to treatment.
Esker Therapeutics
Focused on precision therapies for autoimmune diseases, thisForesite-labs incubated company launched last week with a$70 million Series A.The companys precision analyticsplatform is made up of high-quality curated genetic, clinical and medical record data, a systems immunology approach for prospective data collections and tools for building patient registries. Its lead product ESK-001, a highly selective TYK2 inhibitor with greater selectivity for TYK2 over JAK1, is currently in a Phase I trial for psoriasis.
AlebundPharmaceuticals
Renal disease-focusedAlebundscooped up$60 million in a Series Bround this week. The fresh funds will be harnessed to further drive the companys focus on renal disease, a health condition with a fairly high prevalence in China. The raised funding represents a record for financing raised during a single round by any other Chinese nephrology-related biopharmaceutical company.Current pipeline candidates target renal chronic kidney disease (CKD)/dialysis complications, IgA nephropathy, diabetic kidney disease, and autosomal dominant polycystic kidney disease.
AppioBio
Jumping into the cell therapy fray this week is newcomer Appia Bio. Backed by a$52 million Series A, thecompanyhopes to bringcelltherapy to more peoplewith moreoff-the-shelf treatments, which are typically far more affordable.Appia is developing engineered allogeneic cell therapies from hematopoietic stem cells (HSCs) for cancer patients. Its ACUA platform utilizes the biology of lymphocyte development with CAR and TCR gene engineering to produce CAR-engineered invariant natural killer T (CAR-iNKT) cells from HSCs.
Adaptive Phage Therapeutics
Every year 35,000 Americans die from antibiotic-resistant superbugs.Adaptive Phage Therapeuticsis fighting back with bacteriophage therapies, and landed a$40.75 million Series Bto fund the war. Deerfield Management took the lead on this round, joined by existing investor Mayo Clinic.Funds from this round will be used to advance clinical-stage programs in prosthetic joint infection and diabetic foot osteomyelitis. Further development of thePhageBankSusceptibility Test, a tool to rapidly identify which phage therapy is needed for a specific condition, is also moving ahead.
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Money on the Move: May 5 - 11 - BioSpace
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NZ scientists warned about danger of GE viruses and microbes – Voxy
Posted: at 6:24 am
New Zealand scientists interviewed on Newshub [1] calling for loosening regulatory controls on Genetic Engineering must heed warnings from overseas, and international standards of regulation need to be strengthened against the risks of genetically engineered (GE) viruses and microbes.
A new report by the Institute for Responsible Technology [2] is an alert for government regulators and scientists that GE technologies like CRISPR- of viruses and microbes urgently requires stronger controls in the US and globally.
This contradicts the views of The Malaghan Institute scientists calling for changes to New Zealands Hazardous Substances and New Organisms (HSNO) Act that would exempt regulation of GE techniques like CRISPR for medical trials.
"The need for regulation is increasing with the ease and power of emerging gene technologies. In an emergency like Covid-19 the rules have helped provide safety of vaccines approved for emergency use and trials are continuing. This must not be used to justify deregulation of Gene Editing in food and the wider environment," said Jon Carapiet, spokesman for GE-Free NZ in Food and Environment
"Regulation is vital for public confidence. The IRT report reveals the need for regulation of GE viruses and microbes in non-medical as well as medical uses."
In New Zealand The Environmental Protection Agency (EPA) evaluates all applications for live GE products using the stipulations set out by the HSNO Act. The HSNO Act is an environmental law that is in place to protect the environment from the introduction of unknown risks of pesticides and new organisms.
"This requires applicants to show safety of their products by conducting contained trials, indoors or outdoors, in the New Zealand environment," said Claire Bleakley, president of GE Free NZ in food and environment.
"If the HSNO Act is changed and GE organisms are exempted, the level of pesticide use will increase in both the environment and food crops".
GE regulatory exemptions are dangerous as they remove the need for proof of safety. Already, in the six years CRISPR technology has existed, research has shown that mutations, unintended effects, and off target effects are common.
New Zealand has had a range of GM field trials on a variety of onion species, brassica, and canola in the last 22 years, all engineered to tolerate either herbicides or produce insecticides. All these have failed due to poor performance, disease susceptibility, and negligence. However, persistence of the GE canola weeds meant that the field trials had to be monitored for 10 years. [3]
AgResearch has trialled GM ryegrass in the US at a cost of $25 million over the last 5 years, but has been left behind. In the meantime, conventionally bred high performance rye grass is being sold in New Zealand with excellent performance outcomes. NZ is leading the research in animal methane reduction in cattle feed trials [4] and cross-bred sheep that produce less methane emissions. [5]
Animal welfare issues also require that outcomes of Gene Editing be regulated. GM Animals have suffered horrifying problems, including sterility and deformities, while viable production of pharmaceutical proteins in the milk has failed. [6]
The International trial in which NZ participated; on the GE drug Pexa Vec, was withdrawn early due to a high level of risks to patient health. [7]
"Clinical trials are important to understand the risks that GE poses," said Claire Bleakley "It appears that frustration at slow commercialisation and failure of GE organisms to perform in trials is clouding the judgment of GE proponents."
The Government must ensure that regulation and public consultation on issues that affect the New Zealand publics wellbeing are enshrined in law.
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NZ scientists warned about danger of GE viruses and microbes - Voxy
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5 Things to Watch for at the ATS 2021 International Conference – AJMC.com Managed Markets Network
Posted: at 6:20 am
This year, vaping and other key respiratory issues join COVID-19 on the agenda for the ATS 2021 International Conference.
Vaping really fell under the radar. And I actually think it would be worth mentioning that it hasn't gone away, said Andrew J. Halayko, PhD, ATSF, FCAHS, professor of physiology and pathophysiology and internal medicine at the University of Manitoba, in Canada, and chair of the international conference.
The conference begins Friday, May 14, formally opening with a keynote address on Saturday from Anthony Fauci, MD, titled, COVID-19 in 2021: Lessons Learned and Remaining Challenges. Fauci is President Joe Biden's medical adviser and head of the National Institute of Allergy and Infectious Diseases.
In an interview with The American Journal of Managed Care, Halayko gave a broad overview of what attendees can expect to hear during the meeting.
Asthma management guidelines
This session, called Three in One: Updates on Asthma Management From 3 Guidelines Committees, was postponed from last year, Halayko said, to ensure that it received due attention. It will highlight the most recent recommendations from the US National Asthma Education and Prevention Program and the Global Initiative for Asthma, as well as guidelines from the European Respiratory Society and the ATS.
Biologics and biomarkers
A number of presentations and posters will focus on various aspects of biologics and biomarkers for severe asthma, which affects about 10% of patients.
What we're learning is that a really good antibody therapy for asthma doesn't fit all, and it's really important to endotype or phenotype the patient, Halayko said. Given the expense of newer therapies, its vital to know which subset of patients they will help the most, he added.
COPD
Every talk in the chronic obstructive pulmonary disease (COPD) section is starred as a hot topic, Halayko said, partly in recognition of the fact that it's time to move forward with a better understanding of disease pathology, but also therapies where we really have not made significant progress. And we are starting to get to the point where precision medicine and large data studies, omics studies, are coming forward.
Vaping and cannabis
There are more than 2 dozen posters on vaping and cannabis, the long-term pulmonary effects of which are not known. Previous studies have linked vaping to more severe effects from COVID-19. The 2019 e-cigarette or vaping-associated lung injury epidemic is continuing, and various presentations and posters will discuss the types of injuries seen, the chemicals involved, recovery trajectories, and more.
Racism and health equity
The president of ATS, Juan C. Celedn, MD, DrPH, division director, Pulmonology; the Niels K. Jerne Professor of Pediatrics; and professor of medicine, epidemiology, and human genetics, chairs a symposium asking if racial and ethnic disparities in respiratory health can be eliminated. Social determinants of health, universal health care, improving access to lung cancer screening, and other areas are up for discussion by the panel.
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5 Things to Watch for at the ATS 2021 International Conference - AJMC.com Managed Markets Network
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Third Rock Ventures Launches Flare Therapeutics With $82 Million Series A – BioSpace
Posted: at 6:20 am
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Third Rock Ventures has closed a Series A financing round thatraised $82 million, funding which will be used to launchFlare Therapeutics, a new biotech startup focused on developing precision treatments for cancer and other diseases. Significant contributions were made to the Series A by Boxer Capital, Nextech Invest, Casdin Capital, Invus Financial Advisors, and Eventide Asset Management.
Flare uses a switch-site based drug discovery approach, which helped the company develop a pipeline of therapeutic programs that target pivotal cancer drivers such as transcription factor dysregulation and mutations. The new financing from the Series A will support its ability to advance its lead precision oncology program toward the clinic.
Flare currently has three lead precision oncology programs. The first program is expected to move into the clinic in 2023 or 2024, while the following two programs are expected to enter the clinic in the two years following.
Abbie Celniker, Ph.D., Flares interim Chief Executive Officer, and Third Rock Ventures partner, said in a statement that the new startup company was created to pursue the mission of conquering transcription factors which have been one of the most sought-after targets of drug developers based on the central role they play in cancer and other diseases.
Transcription factors appear to play a central role in cancer, among other diseases, according to emerging data and scientific discoveries published over the past ten years. Yet, transcription factors have continued to be elusive for finding targetable sites for drug discovery, with less than 1% of transcription factors successfully targeted for medicines, according to a statement made by Flares Scientific Co-Founder, Fraydoon Rastinejad, Ph.D., a professor of biochemistry and structural biology at the University of Oxford.
The novel drug discovery paradigm established by Flare uses an approach that targets transcription factors. According to the company, this strategy is based primarily on a broader understanding of the cooperative communication and allosteric interaction among the elements of the transcriptional molecular complex, in contrast to the previous scientific focus on only single, isolated transcription factor domains.
Recent work by the companys Scientific Co-Founders has helped Flare gain a greater understanding of the molecular mechanisms involved in targeting transcription factors. This understanding, according to Flare, has helped its research team to recognize the broad potential to generalize these principles to the switch site as a focal point for drugging transcription factors in a new way.
Scientific Co-Founder of Flare, Steven McKnight, Ph.D., a professor at the University of Texas, Southwestern, noted, Maturation of the fields of human genetics and the biochemistry of gene regulation now point us towards opportunities for therapeutic intervention using conventional, small molecule drugs.
Likely, Flare will also plan to use the new Series A funding to grow its staff to 25 employees. Currently, the company employs 12 to 15 full-time staffers, mainly relying on contractors and partners to fulfill its operational needs.
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Third Rock Ventures Launches Flare Therapeutics With $82 Million Series A - BioSpace
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National Coordinating Center for the Regional Genetics Network (NCC) Announces the Second Annual Public Health Genetics Week, May 24-28, 2021 -…
Posted: at 6:20 am
BETHESDA, Md., May 13, 2021 /PRNewswire/ --The National Coordinating Center for the Regional Genetics Network (NCC) is excited to announce the second annual Public Health Genetics Week from May 24-28, 2021. The goal of Public Health Genetics Week is to increase awareness and to celebrate the field of public health genetics.
Each day of Public Health Genetics Week will have a different theme:
Individuals and organizations are encouraged to participate in the week by using the hashtags #PHGW and #PublicHealthGenetics across their social media platforms.
The following events will also occur throughout the week:
Ken Burns Presents The Gene: An Intimate HistoryVirtual Screening
In collaboration with WETA Washington, D.C., virtual daily screenings of Ken Burns Presents The Gene: An Intimate History ("THE GENE") will be held to celebrate Public Health Genetics Week. The landmark four-hour documentary seriesweaves together science, history, and personal stories to present a historical biography of the human genome, while also exploring groundbreaking breakthroughs for diagnosis and treatment of genetic diseases, and the complex web of moral, ethical and scientific questions raised by developments in genetics.
Listed below is the virtual screening schedule. More information, including registration information, can be found at https://phgw.org/thegene.
For more information about the film, visit https://pbs.org/thegene.
Social Media Events
Other Activities
OnPHGW.org, everyone can find more information about the daily themes, social media events, and social media tools (such as daily social media images, GIFs, social media banners, and more).
For questions or comments about Public Health Genetics Week, please contact [emailprotected]and be sure to follow NCC (@nccrcg) onFacebook,Instagram,LinkedIn,TikTok, andTwitterfor the latest updates on the week.
About the National Coordinating Center for the Regional Genetics Networks (NCC)
Funded since 2004 by the Health Resources and Services Administration/Maternal and Child Health Bureau (MCHB) to the American College of Medical Genetics and Genomics (ACMG), NCC's mission is to improve access to genetic services for underserved populations. In collaboration with the seven Regional Genetics Network (RGNs) and the National Genetics Education and Family Support Center (NGEFSC), NCC achieves this mission by working in the following focus areas: genetics and genomics education; genetics policy education; telemedicine; and data collection and evaluation. Learn more about the efforts of the NCC athttps://nccrcg.org.
NCC Funding Acknowledgement
This project is supported by the Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services (HHS) under Cooperative Agreement #UH9MC30770-01-00 from June 2020 to May 2024 for $800,000 per award year.
This information or content and conclusions are those of the author and should not be construed as the official position or policy of, nor should any endorsements be inferred by HRSA, HHS or the U.S. government.
About Ken Burns Presents The Gene: An Intimate History
Ken Burns Presents The Gene: An Intimate Historyis a production of Florentine Films and WETA Washington, D.C., in association with Ark Media. Executive Producer and Senior Creative Consultant: Ken Burns. Written by Geoffrey C. Ward; and Barak Goodman & David Blistein. Based on the book "The Gene: An Intimate History" by Dr. Siddhartha Mukherjee. Narrator: David Costabile. Senior Producer: Barak Goodman. Directors: Chris Durrance and Jack Youngelson. Executive Producers: Dr. Siddhartha Mukherjee, Dalton Delan, Tom Chiodo, John F. Wilson and Anne Harrington. Production funding has been provided by Genentech, 23andMe, Cancer Treatment Centers of America, Alfred P. Sloan Foundation, Gray Foundation, American Society of Clinical Oncology (ASCO) & Conquer Cancer Foundation, Judy and Peter Blum Kovler Foundation, Craig and Susan McCaw Foundation, and the Corporation for Public Broadcasting. The Outreach and Education Partner is National Institutes of Health, National Human Genome Research Institute. Outreach support is provided by Foundation Medicine.
About WETA Washington, D.C.
WETA Washington, D.C., is a leading producer of new content for public television in the United States. WETA productions and co-productions include PBS NewsHour; Washington Week; documentaries by filmmaker Ken Burns, including Ken Burns Presents The Gene: An Intimate History, Cancer: The Emperor of all Maladies, Hemingway and the forthcoming MuhammadAli;and series and specials by scholar Henry Louis Gates, Jr., including Finding Your Roots, Reconstruction: America After the Civil War and The Black Church: This Is Our Story, This Is Our Song. WETA's multi-year campaign Well Beings addresses the critical health needs of Americans. More information on WETA and its programs and services is available at weta.org. On social media, visit facebook.com/wetatvfmon Facebook and follow @WETAtvfmon Twitter.
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Genes responsible for high blood pressure discovered in the human kidney – British Heart Foundation
Posted: at 6:20 am
Research that we have part-funded has led to the discovery of 179 kidney genes responsible for high blood pressure.
Scientists who led the study, which has been published in Nature Genetics, say that this sheds new light on our understanding of genes associated with the condition.
High blood pressure is a key risk factor for heart and circulatory diseases, such as heart attack and stroke, and can run in families. However, the exact ways in which genes can cause people to inherit the condition is not clear.
The study found how certain information inherited in DNA can translate into an increased likelihood of high blood pressure, through changes in the activity of certain kidney genes.
The research, led by Professor Maciej Tomaszewski at The University of Manchester, was possible through access to huge datasets of human DNA and biological material known as RNA from possibly the worlds largest source of human kidney tissue samples.
Around 80 per cent of the 179 genes discovered by the team have never been associated with high blood pressure before. Some of these genes can be targeted by existing medicines, creating new opportunities to treat the condition.
Professor James Leiper, our Associate Medical Director, said: We have known for many years that the kidney is a major regulator of blood pressure, but our understanding of precisely how the kidney controls blood pressure is incomplete.
The identification of this large set of genes that appear to directly affect blood pressure fills in an important missing piece of that puzzle. The researchers have also found a subset of these genes that are a potential new target for the treatment of hypertension.
This is important because many people taking existing medications still struggle to control their blood pressure. If doctors have more tools to work with then it will help stop thousands of lives being lost each year from this potentially preventable condition.
The study was also supported by Kidney Research UK.
OUR RESEARCH INTO HIGH BLOOD PRESSURE
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Genes responsible for high blood pressure discovered in the human kidney - British Heart Foundation
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NeuBase Therapeutics Appoints Gerald J. McDougall to Board of Directors – BioSpace
Posted: at 6:20 am
PITTSBURGH, May 12, 2021 (GLOBE NEWSWIRE) -- NeuBase Therapeutics, Inc. (Nasdaq: NBSE) ("NeuBase" or the "Company"), a biotechnology company accelerating the genetic revolution with a new class of precision genetic medicines, announced today the appointment of Gerald (Gerry) J. McDougall to the Company's Board of Directors. For more than 25 years, Mr. McDougall has been the driving force behind large-scale strategic alliances, joint ventures, and industry partnerships across the healthcare industry to advance innovations in precision medicine and cancer.
"Gerry's deep expertise, passionate commitment to improve the human condition, and vast network have been the foundation for numerous transformational alliances in life sciences and healthcare, and his ability to create synergistic combinations of people, ideas, and resources is exceptional," said Dietrich A. Stephan, Ph.D., Founder, CEO and Chairman of NeuBase. "The Board and I look forward to working closely with Gerry as we advance NeuBase's comprehensive approach to precision genetic medicine to address previously untreatable diseases."
"Genetics are the foundation for understanding and treating rare and common diseases including cancers, and the ability to precisely modulate gene function is key to developing new medicines for the many diseases that still have no treatment options," said Mr. McDougall. "I have dedicated my career to coalescing divergent approaches to achieve precision care, and I believe NeuBase can unify the field of precision genetic medicine with its PATrOL technology platform."
Mr. McDougall spent almost his entire career as a senior partner at PwC where he built and led the firm's Global Health Science consulting practice before retiring. He has worked across the entire ecosystem of the healthcare industry and advised an array of Fortune 500 companies, including leading global pharmaceutical companies. Mr. McDougall has been instrumental around the globe in building public-private partnerships to address human health imperatives. These include the creation and maturation of the Translational Genomics Research Institute (TGen), Arizona's renowned bio-cluster; the design and launch of the Multiple Myeloma Research Consortium (MMRC); the strategic plan for the California Institute of Regenerative Medicine (CIRM) and the Country of Luxemburg's biotechnology commercialization ecosystem.
About NeuBase Therapeutics, Inc.NeuBase is accelerating the genetic revolution by developing a new class of precision genetic medicines which can be designed to increase, decrease, or change gene function, as appropriate, to resolve genetic defects that drive disease. NeuBase's targeted PATrOL therapies are centered around its proprietary drug scaffold to address genetic diseases at the DNA or RNA level by combining the highly targeted approach of traditional genetic therapies with the broad organ distribution capabilities of small molecules. With an initial focus on silencing disease-causing mutations in debilitating neurological, neuromuscular, and oncologic disorders, NeuBase is committed to redefining medicine for the millions of patients with both common and rare conditions. To learn more, visit http://www.neubasetherapeutics.com.
Use of Forward-Looking StatementsThis press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act. These forward-looking statements are distinguished by use of words such as "will," "would," "anticipate," "expect," "believe," "designed," "plan," or "intend," the negative of these terms, and similar references to future periods. Forward-looking statements include, among others, those related to the anticipated strategic guidance and assistance that the Company's new director will provide to support the Company's comprehensive approach to precision genetic medicine to address previously untreatable diseases. These views involve risks and uncertainties that are difficult to predict and, accordingly, our actual results may differ materially from the results discussed in our forward-looking statements. Our forward-looking statements contained herein speak only as of the date of this press release. Factors or events that we cannot predict, including those risk factors contained in our filings with the U.S. Securities and Exchange Commission (the SEC), may cause our actual results to differ from those expressed in forward-looking statements. The Company may not actually achieve the plans, carry out the intentions or meet the expectations or projections disclosed in the forward-looking statements, and you should not place undue reliance on these forward-looking statements. Because such statements deal with future events and are based on the Company's current expectations, they are subject to various risks and uncertainties, and actual results, performance or achievements of the Company could differ materially from those described in or implied by the statements in this press release, including: the Company's plans to develop and commercialize its product candidates; the timing of initiation of the Company's planned clinical trials; the timing of the availability of data from the Company's clinical trials; the timing of any planned investigational new drug application or new drug application; the Company's plans to research, develop and commercialize its current and future product candidates; the clinical utility, potential benefits and market acceptance of the Company's product candidates; the Company's commercialization, marketing and manufacturing capabilities and strategy; global health conditions, including the impact of COVID-19; the Company's ability to protect its intellectual property position; and the requirement for additional capital to continue to advance these product candidates, which may not be available on favorable terms or at all, as well as those risk factors contained in our filings with the SEC. Except as otherwise required by law, the Company disclaims any intention or obligation to update or revise any forward-looking statements, which speak only as of the date hereof, whether as a result of new information, future events or circumstances or otherwise.
NeuBase Investor Contact:Dan FerryManaging DirectorLifeSci Advisors, LLCdaniel@lifesciadvisors.comOP: (617) 430-7576
NeuBase Media Contact:Jessica Yingling, Ph.D.Little Dog Communications Inc.jessica@litldog.com+1 (858) 344-8091
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Eczema On The Eyes: Causes, Symptoms, and Treatment – Greatist
Posted: at 6:14 am
Eczema is a group of skin conditions that 31 million people in the United States live with, according to the National Eczema Association. Patches of dry, leathery, or blistered-covered skin anywhere on your body are eczemas deal and its not pleasant.
Types of eczema that affect your eyes
Here are the types of eczema most likely to appear near your eyes:
Many types of eczema can form around your eyes. Youll sometimes hear them referred to as eyelid dermatitis, although eyelids arent your only eye-adjacent face spaces at risk.
We break down what types of eczema can affect your eyelids and the types of treatments that may work for you.
Super flaky eyelids? We can help you work out whether its eczema or not.
Eczema is defined as dry, red or discolored, itchy, and scaly skin. It can occur around your eyes.
When discussing eczema around your eyes, there are three noteworthy types of eczema:
Doctors sometimes refer to all three as eyelid dermatitis (when they pop up on your eyelids, obvs).
This is the most common eczema around. According to the Asthma and Allergy Foundation of America, around 16.5 million of 31 million folks with eczema in the United States have the atopic variety, and around 20 percent of kids are thought to have it, according to a 2010 research review. So yeah, super common.
Atopic eczema is what most people mean when they say eczema. Its rough patches of skin that itch, like, a lot. Obviously, theres more to atopic eczema than that but thats the tl;dr version.
Your flimsy, sensitive eyelid skin is prone to atopic eczema. It can appear anywhere though, and atopic eczema can also develop on your cheeks, nose, eyebrows, and whatever that bit of your face is called where crows feet develop.
Seborrhoeic dermatitis mainly happens on your scalp. You know the cradle cap that babies get? Thats seborrhoeic dermatitis. It presents as dry flaky skin that appears in patches.
As scalp-associated as it is, seborrhoeic dermatitis around your eyes isnt uncommon. Patches of seborrhoeic dermatitis or seborrhoeic eczema can appear anywhere around your eyes but are most common where your eyelids and eyes meet.
Also called contact dermatitis, this is an irritation caused by touching something that your skin takes a severe disliking to. There are two types.
Irritant contact eczema is from substances that negatively affect your skin no matter who you are. Poisonous plants and irritant chemicals are the most common catalysts.
Allergic contact eczema is when a flare-up happens because of something that your skin shouldnt have an issue with. The clue is in the name, but allergic contact eczema is a fancier medical term for your common-or-garden allergic skin reaction.
It can occur around your eyes because, as we all know, its embarrassingly easy to get stuff in your eyes. Makeup and swimming pool chlorine are common reasons for contact eczema in your eye region. So is jizz.
Each case of eczema is different. That being said, there are common symptoms that can appear across every type with varying degrees of severity.
Heres the eczema stuff that can happen around your eyes:
Eczema cant directly cause blindness. However, having eczema around your eyes increases your risk of eye conditions which can lead to blindness.
This risk increases the longer your eye eczema is left untreated. If youre experiencing an eczema flare-up around your eyes and start having vision problems you should consult your doctor ASAP.
Eczema isnt the only condition that can make your skin around your eyes red or discolored, swollen, and really sore.
There are a few other common ailments that present in a similar way (and in most cases develop as a result of eye eczema-based complications). Some of these are:
Theres not a definitive reason that some people develop eczema. Even with contact eczema, science hasnt discovered why some people have allergic reactions to the stuff others can touch no-problemo.
You can develop any kind of eczema due to a mix of genetic and environmental factors. There are strong hereditary links, stress can play a big part, and your immune system is also a catalyst for many eczema types.
Theres no way to test if youre at a high risk of developing eczema (aside from others in your family experiencing it). Avoiding it may be impossible for some people. There are, however, known triggers that folks at risk of eczema are advised to steer clear of where they can.
Here are some common eczema triggers to avoid if youve got sensitive skin around your peepers:
Diagnosing eczema anywhere is actually super easy. They dont need to do lab tests or anything.
Your doctor will ask you a bunch of questions if youve had eczema in other places or have had any irritants near your eyes.
Once they ask some questions, theyll tell you if its eczema or not. The only extra step is that your doctor may want to do a patch test, which exposes an area of skin to allergens, to check for a reaction.
Home remedies for eczema near your eyes
There are plenty of home remedies that can treat eczema around your eyes and take the edge off uncomfortable symptoms.
If youre prone to eczema flare-ups, there are steps you can take to manage this and reduce the risk.
There are plenty of over-the-counter (OTC) and off-the-shelf treatments for eczema available at pharmacies.
If you develop eczema due to an allergic reaction, antihistamines can help you manage the itching and swelling.
Corticosteroids can also treat eczema itching, but using them around your eyes is risky (it can lead to glaucoma, which is really serious and 100 percent worse for your eyes than eczema).
Consult your doctor before trying any OTC treatment (especially if youre already on other medications or undergoing treatment for another condition).
If home remedies and OTC medication dont do the job, your doctor can prescribe more intensive treatment. Severe and recurring eczema will probably require some kind of prescription medication.
Your eyes are pretty sensitive. This may limit the treatments your doc can offer because they want to protect your eyes condition from becoming more severe. Prescription eczema treatments that are safe to use near your eyes include:
Eczema around your eyes isnt always serious, but it can become serious without treatment. It can also lead to serious conditions, some of which can make you experience blindness.
Eye-based eczema also presents more of a risk than some other eczemas simply because of how sensitive your eyes are.
As eyes are prone to infections and protected only by a thin membrane, eczema near your eyes is more likely to cause complications than an eczema patch on your belly or butt cheek.
Theres no way to prevent eczema flare-ups completely. You can significantly reduce the risks of them developing though.
Most of the home remedies and treatments to treat flare-ups also prevent them. Steps to keep eczema flare-ups at bay include:
The three main types of eczema that mess with your eyes are atopic eczema, contact eczema, and seborrheic dermatitis. Theres no single cause: Eczema usually develops due to a mix of genetic and environmental factors.
You cant prevent eczema flare-ups around your eyes, but you can minimize the risk by avoiding known triggers.
Theres plenty of home remedies that can treat eczema around your eyes (and almost prevent it from happening again). If these dont work there are plenty of OTC and prescription treatments as next steps.
Eczema near your eyes isnt normally serious but can be without treatment so get it sorted straight away.
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What It’s Like to Be a Mom With Eczema – WebMD
Posted: at 6:14 am
Imagine youre a parent on a Saturday morning and its your turn to wake up early with the kids. Of course youre tired when you get up -- youve been tired since you became a parent!
You smile when you see them in their cute pajamas. You brush their teeth and head to the kitchen to make them breakfast while they watch cartoons. They start fighting and you go into mediator mode, while ensuring the pancakes on the skillet dont burn.
They eat happily and are messy -- as expected when you give little ones pancakes with syrup. Its time to change them out of sticky pajamas and into their outfits for the day.
Fast forward a few hours and youre tired and need a break, which you can take during nap time after you feed the kids lunch.
Fast forward more and its the evening, which means cooking dinner, feeding kids, bath time, bedtime, and the post-bedtime kid shenanigans that follow. At that point, you can finally relax until you go to bed and do it all again the next day.
Being a mom with atopic dermatitis (AD) or eczema is like that -- except youre doing it all while also being itchy. Although my daily routine and activities will change as my children grow, Ill likely always be itchy.
Eczema Can Scare Children
My children are Nico Atlas, 2, and Nina Sol, 4. I cant hide my eczema from my children. Their experience with my eczema will evolve as they get older.
Nina was a baby when she and my husband joined me at my allergists office for an allergy skin prick test on my back. This test should instead be called the skin stabbing test, because its painful! But with my baby girl next to me, I knew I had to be extra tolerant and calm to not scare her.
Throughout the years, Ive been careful to not bleed in front of her because blood can be scary for kids. Most important, Ive been open with my children about my eczema. Nina knows that I have eczema, because when she was younger she asked me why I had polka dots on my body (so cute!). I told her it was my eczema.
When Nico gets older, Ill tell him, too. Eczema shouldnt be scary, but it can seem that way to kids when theyre confused or uninformed.
Eczema Affects Your Family Activities
Chronic eczema affects my daily life. As a parent, this means my family may be affected by my condition. Do the kids want to walk outside on a sizzling hot day when my eczema is flared? Maybe well do something indoors instead.
How about getting in the pool with the children? Some days, its best to not get wet. But its OK. We just do a different fun activity that wont worsen my skin. The kids will be just as giddy.
There are, however, some activities that eczema fighters must do even if it will hurt a bit. For example, even if my forearms are flared, Im still going to give my kids a bath. This means my arms will hurt as I dip them in the water. Stinging arms arent a big deal to me when I get to enjoy watching my babies play in a bubble bath. Now, if my eczema is severe, Ill ask my husband to do the bath.
Childrens Compassion Helps
One of the wonderful perks of being a parent to little kids is being showered by their unconditional love and affection. Since my daughter was almost 3, she showed deep empathy and support for me when I was itchy.
At a very young age, she began telling me that I shouldnt scratch and should tap instead. (Only my adorable toddler can tell me not to scratch!) Last year, my back was unbearably itchy during an allergy patch test and Nina was especially supportive, checking in on me and asking when the test would be over. My 4-year-old helped me get through gruesomely itchy 4 days.
Having chronic eczema can be hard as a mom, but the support from my adorable cheerleaders makes me stronger. I also keep things in perspective with gratitude. I focus on the special moments with my children. Ultimately, Im most grateful that its my body with eczema and not my childrens skin. I am, after all, a mother above all and want the best for my babies.
What Ive Learned
Choose products like shampoo, soaps, and moisturizes for your children that you can tolerate. That way youll avoid flare-ups on your skin when you use them on the kids.
Photo credit: Anastasia Malachi/iStock via Getty Images
WebMD Blog
Helen Pia has lived with chronic atopic dermatitis (eczema) and skin allergies for most of her life. Shes committed to offering support, advice, and compassion to fellow eczema fighters through her Itchy Pineapple blog. Pia is married with two young children and is a marketing leader in the B2B tech industry. She lives in Houston, TX.
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Kentucky Derby Winner Tests Positive for Betamethasone The Horse – TheHorse.com
Posted: at 6:14 am
Medina Spirits win in the 147th running of the Kentucky Derby presented by Woodford Reserve remains in question after a postrace blood test indicated the presence of betamethasone, a corticosteroid prohibited in horse racing.
Medina Spirit, a 3-year-old colt trained by Bob Baffert for owner Amr Zedans Zedan Racing Stables, went wire to wire under jockey John Valazquez to win the Kentucky Derby on May 1 at Churchill Downs, in Louisville, Kentucky. The Derby win, a record seventh for Baffert, could be overturned if a second round of testing, known as a split sample, also shows the presence of betamethasone.
The Racing Medication and Testing Consortium states that betamethasone is widely used in equine veterinary medicine as a steroidal anti-inflammatory. Several equine products approved by the U.S. Food and Drug Administration include betamethasone for intra-articular use in joints to control pain associated with inflammation and osteoarthritis.
According to the Kentucky Horse Racing Commissions April 2020 drug withdrawal time guidelines, betamethasone may be administered intra-articularly up to 14 days prior to a race. The acceptable threshold level was reduced from 10 picograms per milliliter (mL) in serum or plasma to zero in August 2020. Medina Spirits test showed 21 picograms per mL.
Reactions to the positive test were swift.
The Jockey Club, the breed registry for the Thoroughbred in the United States and Canada, also issued a statement that read in part: We sincerely hope justice is swift, sure, fair, and uniform. Bettors and fans need to have unshakable confidence in the integrity of the sport. The passage of the Horseracing Integrity and Safety Act (HISA) undeniably will give our sport a far better level of regulation.
On May 11 Baffert issued a statement through his lawyer, Craig Robertson III, stating that Medina Spirit had been treated for a skin condition with Otomax, a topical ointment labeled for dogs containing betamethasone, for dermatitis. Physicians often prescribe betamethasone topically to treat a variety of skin conditions including eczema, dermatitis, rash and allergies in people.
Baffert is currently suspended from Churchill Downs pending the results of the split sample. Medina Spirit has moved on to Pimlico Race Course, in Maryland, where he will be allowed to compete in the Preakness Stakes on Saturday, May 16, as long as a prerace drug test is negative.
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