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Displaying Results 326-350 of 2510 "'GENE'"

Apr 29, 2026, 09:00 ET Kytopen, T-CURX, and the Fraunhofer IZI Establish Center of Excellence to Develop Advanced, Non-viral Cell Therapies

therapies.T-CURX, a clinical-stage biotech company developing personalized immunotherapies, will contribute its expertise and proprietary transposon-based gene transfer technology.Process development through manufacturing scale-up will be led by teams at Fraunhofer IZI.The CoE aims to develop

More news about: Kytopen


Apr 29, 2026, 08:56 ET NanoMosaic to Showcase the FDA/CBER AMT Designated Analytics Platform at ASGCT 2026

/PRNewswire/ -- NanoMosaic, Inc., a leader in advanced analytical technologies for cell and gene therapy development and manufacturing, today announced its strong scientific and commercial presence at the American Society of Gene & Cell Therapy Annual Meeting, taking place May 11-15, 2026, in Boston, Massachusetts.

More news about: NanoMosaic


Apr 29, 2026, 05:00 ET Biohub Launches the Virtual Biology Initiative to Galvanize a Global Effort to Create the Open Data Foundation for AI-Accelerated Biology

diseases."The Billion Cells Project is a landmark single-cell sequencing project to advance researchers' understanding of cellular behavior and gene function. Launched in 2025 to break through the data bottleneck limiting biological AI models, the Billion Cells Project coordinates 17 projects across

More news about: Biohub


Apr 28, 2026, 16:05 ET PTC Therapeutics Reports Positive Topline Results from Month 24 Interim Analysis of PIVOT-HD Extension Study of Votoplam

disorder of the central nervous system.1 It is caused by a defective gene. This gene produces a protein, called Huntingtin (HTT), which is involved in the functioning of the nerve cells in the brain (neurons). When the gene is defective, it produces an abnormal (or mutated) HTT protein that is toxic

More news about: PTC Therapeutics, Inc.


Apr 28, 2026, 12:21 ET CIRM Awards AcuraStem $7.5 Million in Grant Funding to Advance AS-241 Toward a First-in-Human Trial for ALS and FTD

consequence of ALS and FTD driven by dysfunction of the protein TDP–43. Pathological  loss of nuclear TDP–43 leads to cryptic splicing of the UNC13A gene, resulting in loss of a protein that is essential for healthy synaptic communication. TDP-43 pathology is observed in approximately 97% of ALS patients,

More news about: AcuraStem - Patient-Based Therapeutics


Apr 28, 2026, 10:15 ET Environmental DNA Market worth $5.61 billion by 2031- Exclusive Report by MarketsandMarkets™

(Luxembourg), SGS Société Générale de Surveillance SA (Switzerland), NatureMetrics (UK), EnviroDNA (Australia), EDNAtec (Canada), SPYGEN (France), ID-GENE ecodiagnostics Ltd. (France), Takara Bio Inc. (Japan), Stantec (Canada), Applied Genomics (UK), AllGenetics (Spain), and Jonah Ventures (US).Get

More news about: MarketsandMarkets


Apr 28, 2026, 10:00 ET ACROBiosystems Showcases AI-Driven Innovation at AACR 2026, Empowering Next-Generation Biologics Discovery

Box" Protein Engineering Toolkit autonomously optimizes multiple key properties like binding affinity, stability, and solubility. Focused on cell and gene therapy, it has been used to develop essential GMP-grade materials such as the Salt Active GENIUS™ Nuclease, Human FGF basic Superior Stable Mutant

More news about: ACROBiosystems Inc.; ACROBiosystems Group


Apr 28, 2026, 09:47 ET Lupus Research Alliance Announces New Lupus Innovation Award Recipients to Advance Understanding of Lupus

PhD, Sloan Kettering InstituteToll-like receptor (TLR7) signaling plays a major role in lupus. However, many different gene mutations – not only those affecting TLR7 – can cause lupus, and it is unclear whether a shared mechanism ties these mutations together. Dr. Gitlin

More news about: Lupus Research Alliance


Apr 28, 2026, 09:28 ET PTC Therapeutics to Report Results from PIVOT-HD Long Term Extension Study

disorder of the central nervous system.1 It is caused by a defective gene. This gene produces a protein, called Huntingtin (HTT), which is involved in the functioning of the nerve cells in the brain (neurons). When the gene is defective, it produces an abnormal (or mutated) HTT protein that is toxic

More news about: PTC Therapeutics, Inc.


Apr 28, 2026, 09:13 ET Introducing TIES™: A Foundational Men's Fertility and Performance Brand, Backed by $1.5M Seed Round Led by HumanCo and Jason H. Karp

Review and Network Meta-Analysis of Randomized Controlled Trials. 2022 — China Academy of Chinese Medical SciencesThe Effect of Vitamin C on the Gene Expression Profile of Sperm Protamines in the Male Partners of Couples with Recurrent Pregnancy Loss: A Randomized Clinical Trial. 2020 — Clinical and

More news about: HumanCo Investments


Apr 28, 2026, 09:05 ET Nuevocor Appoints Dr. Monica Shah as Chief Medical Officer

clinical programs spanning rare disease, gene therapy, and cardiovascular indications. Prior to CTI, she was Senior Vice President and AAV Global Program Head at Rocket Pharmaceuticals, where she launched and led pivotal clinical programs in cardiovascular gene therapy. She previously served as Vice President

More news about: Nuevocor


Apr 28, 2026, 08:02 ET Azitra, Inc. Announces Poster Presentation at ASGCT 2026 Highlighting ATR-01 Program for Ichthyosis Vulgaris

dermatology, today announced the presentation of new preclinical data from its ATR-01 program at the 2026 Annual Meeting of the American Society of Gene & Cell Therapy ("ASGCT 2026").

More news about: Azitra, Inc.


Apr 28, 2026, 08:00 ET Genezen and The Charlotte & Gwenyth Gray Foundation to Cure Batten Disease Announce Manufacturing Partnership for CLN6 Gene Therapy Clinical Trial

April 28, 2026 /PRNewswire/ -- Genezen, a gene therapy contract development and manufacturing organization (CDMO), and The Charlotte & Gwenyth Gray Foundation to Cure Batten Disease today announced a manufacturing partnership to advance a CLN6 gene therapy into a Phase 1/2 clinical trial.

More news about: Genezen


Apr 28, 2026, 08:00 ET Argo Biopharma Announces First Subject Dosed in Phase I Study of siRNA Therapeutic BW-50218

BW-50218BW-50218 is an siRNA therapeutic developed from Argo Biopharma's proprietary RADS™ platform, and is designed to enable potent, durable gene silencing with differentiated safety and delivery characteristics through hepatic delivery. Argo Biopharma continues to advance a cardiovascular and

More news about: Argo Biopharmaceutical Co., Ltd


Apr 28, 2026, 07:57 ET U.S. FDA Grants Breakthrough Device Designation to Laguna Diagnostics' mRNA Gene Biomarker Test to Aid in Differentiation of Schizophrenia and Bipolar I Disorder

Diagnostics, LLC today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation to the company's mRNA Gene Biomarker Test, a novel blood-based test designed to aid in the differentiation of schizophrenia and bipolar I disorder in symptomatic patients.

More news about: Laguna Diagnostics, LLC


Apr 28, 2026, 07:37 ET Arcera Life Sciences and Fosun Pharma launch long-term collaboration framework

foster sovereign R&D capabilities in the UAE across small molecules, biologics, radiopharmaceuticals, small interfering RNA therapies, and cell and gene therapies.Strategic collaboration in neuroscience: The neuroscience collaboration will focus particularly on neurodegenerative diseases,

More news about: Fosun Pharma


Apr 28, 2026, 07:00 ET Genprex Collaborators to Present Positive Preclinical Data on Diabetes Gene Therapy for Type 2 Diabetes at the 2026 American Society of Gene and Cell Therapy Annual Meeting

clinical-stage gene therapy company focused on developing life-changing therapies for patients with cancer and diabetes, today announced that its research collaborators will present positive preclinical data on the Company's diabetes gene therapy drug candidate at the upcoming 2026 American Society of Gene and

More news about: Genprex, Inc.


Apr 28, 2026, 07:00 ET Ascidian to Highlight Progress of Lead Program in Stargardt and Platform Advancements Across Therapeutic Areas at ASGCT 2026 Annual Meeting

treat human diseases by rewriting RNA, today announced it will present two oral presentations and one poster presentation at the American Society of Gene & Cell Therapy (ASGCT) annual meeting in Boston, MA, May 11-15, 2026.

More news about: Ascidian Therapeutics


Apr 28, 2026, 07:00 ET Triquetra Health Launches BioActive B-Complex™ Liquid--First Formula with Five Active B-Vitamin Form Upgrades and Tri-Form B12 in Liquid Delivery

folate form, requires the MTHFR enzyme to convert to active L-5-MTHF before the methylation cycle can use it. An estimated 40–60% of adults carry MTHFR gene variants that reduce this enzyme's activity by 35–70%. Meanwhile, standard thiamine HCl relies on saturable carrier proteins that limit tissue delivery

More news about: Triquetra Health LLC


Apr 28, 2026, 06:00 ET Economic Pressure Makes Boomerang Living a New Normal, Annual Thrivent Survey Finds

"Adult children moving back in with their parents has shifted from stigma to strategy – for both parents and kids," says Thrivent Financial Consultant Gene Elder. "Five years into Thrivent's survey, we've found that boomerang living is not a blip; it's becoming a lasting part of how families plan their

More news about: Thrivent


Apr 28, 2026, 04:07 ET Ivonescimab Receives Major Recommendations Across Multiple Therapies in the 2026 CSCO NSCLC Guideline

Class I recommendation.First-line treatment for advanced driver gene-negative squamous NSCLC with PD-L1 TPS ≥1%: Ivonescimab monotherapy upgraded to Class I recommendation.First-line treatment for advanced driver gene-negative non-squamous NSCLC with PD-L1 TPS ≥1%: Ivonescimab monotherapy

More news about: Akeso, Inc.


Apr 27, 2026, 16:30 ET Apertura Gene Therapy and Scientists from the Broad Institute to Share Data on TfR1 CapX™, a Novel Capsid Targeting the Central Nervous System (CNS), at the American Society of Gene and Cell Therapy (ASGCT) Annual Meeting

Science.About Apertura Gene Therapy Apertura Gene Therapy develops genetic medicines and next-generation AAV capsids that engage human-relevant receptors, aiming to enable more effective and selective gene delivery. The company's lead capsid, TfR1 CapX™, leverages human

More news about: Apertura Gene Therapy


Apr 27, 2026, 11:30 ET Avirmax Biopharma Inc. Proudly Presents at the 2026 ARVO Annual Meeting in Denver, Colorado

Session Title: Gene Editing and Gene Therapy II Session Date/Time: May 5, 2026, from 8:30 AM to 10:15 AM MDTDr. Shengjiang Liu, Ph.D. Chief Executive and Scientific Officer will present "From Bench to Clinic: CMC and Preclinical Development of ABI-110 Gene Therapy for Ocular Neovascularized

More news about: Avirmax


Apr 27, 2026, 08:44 ET BioMarin Completes Acquisition of Amicus Therapeutics

pharmacological chaperone of alpha-Galactosidase A (alpha-Gal A) for the treatment of Fabry disease in adults who have amenable galactosidase alpha gene (GLA) variants. In these patients, Galafold works by stabilizing the body's own dysfunctional enzyme so that it can clear the accumulation of disease

More news about: BioMarin Pharmaceutical Inc.


Apr 27, 2026, 08:30 ET Greenland Mines Appoints SLR Consulting as Geological Consultant and Qualified Person for Skaergaard

of the Skaergaard Project in Southeast Greenland, one of the largest undeveloped palladium, gold, and platinum deposits in the world; and 2) Cell and Gene Therapy, including Klotho's KLTO-202 primary indication for ALS. The Company holds, through its recent acquisition of Greenland Mines Corp., an 80%

More news about: Greenland Mines Ltd


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