Chromosome

Michael F. Roizen, MD to Increase Activities with Telomir Pharmaceuticals as Special Advisor on Age Reversal

Retrieved on: 
Martedì, Marzo 5, 2024

BALTIMORE, March 05, 2024 (GLOBE NEWSWIRE) -- Telomir Pharmaceuticals, Inc. (Nasdaq: TELO) (“Telomir” or the “Company”), a pre-clinical-stage pharmaceutical company focused on the development and commercialization of Telomir-1 as the first novel small molecule to lengthen the DNA’s protective telomere caps in order to affect age reversal, today announced that Michael F. Roizen, MD, a leader in age-related medicine and an existing advisor to the Company, will be increasing his role in the coming months as a Special Advisor on Age Reversal.

Key Points: 
  • A board-certified internist and anesthesiologist, Dr. Roizen has been instrumental in the development of many successful ventures.
  • He also served 16 years on Food and Drug Administration (FDA) advisory committee and chaired one for two years.
  • Chris Chapman, MD, co-founder, chairman, chief executive officer and president of Telomir, stated, “Telomir's groundbreaking work has captured the attention and imagination of the industry.
  • We look forward to his continued contributions to our efforts.”
    To be included in the Telomir Pharmaceuticals email distribution list, please email [email protected] with TELO in the subject line.

PRISM MarketView Highlights Work of Emerging Companies on Rare Disease Day

Retrieved on: 
Giovedì, Febbraio 29, 2024

All areas of medicine, and all organs and body systems, are impacted by rare diseases, including rare neurological and neuromuscular diseases, metabolic, skin and bone diseases, and chromosomal disorders.

Key Points: 
  • All areas of medicine, and all organs and body systems, are impacted by rare diseases, including rare neurological and neuromuscular diseases, metabolic, skin and bone diseases, and chromosomal disorders.
  • Today on Rare Disease Day, PRISM MarketView highlights emerging companies working to deliver life changing treatments for those living with rare diseases.
  • RDEB is a severe rare disease characterized by extremely fragile, and extensive blistering and wounds.
  • Capricor is a biotechnology company dedicated to advancing transformative cell and exosome-based therapeutics to redefine the treatment landscape for rare diseases.

Nabsys Opens a Distribution Channel for the OhmX™ Platform in Canada

Retrieved on: 
Giovedì, Marzo 7, 2024

PROVIDENCE, R.I., March 7, 2024 /PRNewswire/ -- Next generation genomic tools company, Nabsys®, has executed a nonexclusive agreement with Canadian distributor, DMark Biosciences ("DMark"), for sales of its OhmX™ platform.

Key Points: 
  • PROVIDENCE, R.I., March 7, 2024 /PRNewswire/ -- Next generation genomic tools company, Nabsys®, has executed a nonexclusive agreement with Canadian distributor, DMark Biosciences ("DMark"), for sales of its OhmX™ platform.
  • OhmX is Nabsys' first commercially available product and was released in October 2023.
  • DMark will be responsible for distributing both the Nabsys OhmX™ Analyzer and consumables into both public and private research core labs and institutions in the Canadian market.
  • "With growing demand for the OhmX platform in the US, this distribution agreement marks an important step towards establishing a strong global distribution network," Nabsys' Chief Commercial Officer, Justin Bingham, remarked.

From crop to cup – a new genetic map could make your morning coffee more climate resilient

Retrieved on: 
Mercoledì, Febbraio 14, 2024

With their superior smooth taste and many fine varieties, arabica coffee beans make up around 60%-70% of global coffee production.

Key Points: 
  • With their superior smooth taste and many fine varieties, arabica coffee beans make up around 60%-70% of global coffee production.
  • Coffee cultivation also directly supports the livelihoods of 25 million family farmers with another 100 million people involved in coffee processing and retailing.
  • This study could help produce coffee varieties with higher yields and more resilience to climate change.
  • With more detailed information about the genetic makeup of coffee, researchers can begin to use these methods to improve coffee varieties.

Synthetic human embryos let researchers study early development while sidestepping ethical and logistical hurdles

Retrieved on: 
Mercoledì, Febbraio 7, 2024

This has made it difficult for scientists to understand early human development.

Key Points: 
  • This has made it difficult for scientists to understand early human development.
  • By offering new tools to explore the enigmatic earliest stages of human development, synthetic embryology can help researchers overcome the challenges of using real human embryos.
  • With these new models, researchers can also better understand conditions that affect human reproduction and development as well as maternal-fetal health, potentially leading to new therapies.

Making human embryos from stem cells

  • This triggers the egg to rapidly divide into embryonic cells that soon form an inner cell mass that eventually develops into the fetus and a outer layer of cells that will give rise to the placenta.
  • Synthetic embryology artificially recreates these developmental stages using human pluripotent stem cells derived from human embryos or induced from adult human cells.
  • Like early embryonic cells, these cells have the ability to develop into any type of cell in the human body.
  • Researchers created the first human embryo model from embryonic stem cells in 2014.
  • This pioneering model, also called a gastruloid, captured key aspects of early human development and showed that scientists can drive pluripotent stem cells to form patterned layers echoing the three germ layers and the outer layers of the embryo.

Advancements in human embryo models

  • Over the years, various models have been able to replicate different facets of human embryogenesis, such as amniotic sac development, germ layer formation and body plan organization.
  • However, none of these models fully captures the entire process of a single cell type developing into the complete structure of a whole embryo.
  • Blastoids form in a similar way to human embryos, starting from just a few cells that proliferate and organize themselves.
  • Recently, researchers have successfully created more complex models in the lab that mimic what happens after embryos attach to the womb.

Choosing the right models

  • This goal underscores the importance of carefully choosing the model best suited to the specific research objectives at hand.
  • Creating embryo models from a patient’s own cells could also allow researchers to study the genetics of development and aid in personalizing treatments.
  • The International Society for Stem Cell Research strictly prohibits transferring these embryo models into the uterus of a human or an animal.
  • Although these models mimic certain features of early developmental stages, they cannot and will not develop into the equivalent of a human baby after birth.


Min (Mia) Yang receives funding from University of Washington

Singleron launches the AccuraSCOPE® Single Cell Transcriptome

Retrieved on: 
Martedì, Gennaio 30, 2024

COLOGNE, Germany, Jan. 30, 2024 /PRNewswire/ -- Singleron Biotechnologies, a leader in single cell multi-omic solutions for precision medicine, announced two new commercial product launches : AccuraSCOPE® Single Cell Transcriptome and Genome Library Kit and the AccuraSCOPE® Single Cell Full-Length Transcriptome Library Kit.

Key Points: 
  • COLOGNE, Germany, Jan. 30, 2024 /PRNewswire/ -- Singleron Biotechnologies, a leader in single cell multi-omic solutions for precision medicine, announced two new commercial product launches : AccuraSCOPE® Single Cell Transcriptome and Genome Library Kit and the AccuraSCOPE® Single Cell Full-Length Transcriptome Library Kit.
  • AccuraSCOPE  Single Cell Transcriptome and Genome Library Kit opens new possibilities for single cell multi-omic analysis by profiling the entire genome and transcriptome simultaneously.
  • In addition to single cell RNA sequencing, this method enables deep single cell genome sequencing, amplifying ultra-low quantities of DNA from individual cells.
  • It enables the detection of alternative splicing at the single cell level, substantially reducing hands-on time compared to existing full-length single cell RNAseq methods.

Crnic Institute Awarded Anschutz Acceleration Initiative Grant for Pioneering Research Aimed at Improving the Health of Children with Down Syndrome

Retrieved on: 
Giovedì, Gennaio 18, 2024

“Receiving this grant is deeply gratifying,” says Dr. Joaquín Espinosa, Professor in Pharmacology and Executive Director of the Crnic Institute.

Key Points: 
  • “Receiving this grant is deeply gratifying,” says Dr. Joaquín Espinosa, Professor in Pharmacology and Executive Director of the Crnic Institute.
  • “Everyone at the Crnic Institute, GLOBAL and all our Affiliates have worked so hard in the last ten years to take our remarkable findings from the Petri dish and parlay that into benefit for people with Down syndrome.
  • Key outstanding questions specific to individuals with Down syndrome will be addressed:
    What are the impacts of interferon hyperactivity during early childhood?
  • From over 165 letters of intent and ultimately 56 full proposals, 9 research projects were funded.

Gattaca Genomics Unveils State-of-the-Art Genetic Testing Services to Transform Family Planning

Retrieved on: 
Giovedì, Gennaio 18, 2024

Fort Lauderdale, FL, Jan. 18, 2024 (GLOBE NEWSWIRE) -- Gattaca Genomics, a pioneering next generation company innovating solutions for reproductive health, is set to revolutionize family planning with its advanced genetic testing services.

Key Points: 
  • Fort Lauderdale, FL, Jan. 18, 2024 (GLOBE NEWSWIRE) -- Gattaca Genomics, a pioneering next generation company innovating solutions for reproductive health, is set to revolutionize family planning with its advanced genetic testing services.
  • Specializing in Preimplantation Genetic Testing (PGT), Gattaca Genomics employs state-of-the-art techniques to enhance pregnancy success rates, identify chromosomal abnormalities, and reduce the risk of genetic disorders.
  • Whole Genome Sequencing (WGS): Gattaca Genomics introduces a breakthrough in genetic testing with Whole Genome Sequencing, offering a comprehensive analysis of an individual's entire genome.
  • Gattaca Genomics invites prospective parents, healthcare providers, and clinicians to explore the possibilities that genetic testing can offer.

Molecular Diagnostics in Oncology, Genetic/Inherited Diseases and NIPT 2023-2028 - ResearchAndMarkets.com

Retrieved on: 
Lunedì, Gennaio 29, 2024

The "Molecular Diagnostics in Oncology, Genetic/Inherited Diseases, and NIPT, 2023-2028" report has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Molecular Diagnostics in Oncology, Genetic/Inherited Diseases, and NIPT, 2023-2028" report has been added to ResearchAndMarkets.com's offering.
  • In addition, the fields of rare inherited/ genetic diseases and NIPT have become areas of new breakthroughs in healthcare.
  • These and other technologies and applications in oncology, rare inherited/ genetic disease, and NIPT molecular diagnostic testing are covered in the report.
  • The report contains detailed market data on the following IVD segments for their use in molecular testing:
    Molecular Diagnostics in Oncology Market by Segment, 2023-2028

deCODE genetics: A sequence variant that increases risk of pregnancy loss

Retrieved on: 
Lunedì, Gennaio 29, 2024

Over 114 thousand women from Iceland, Denmark, the UK, USA, and Finland who have experienced pregnancy loss participated in a genome-wide association study, testing 50 million sequence variants.

Key Points: 
  • Over 114 thousand women from Iceland, Denmark, the UK, USA, and Finland who have experienced pregnancy loss participated in a genome-wide association study, testing 50 million sequence variants.
  • A low-frequency missense variant in the SYCE2 gene was found to increase the risk of pregnancy loss by 22%.
  • The association with pregnancy loss does not account for embryos lost in early gestation before pregnancy has been detected so the effect of the variant on pregnancy success may be underestimated.
  • The findings reported in this study demonstrate that a variant with a substantial effect on recombinations can be maintained in the population despite increasing the risk of pregnancy loss.