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Displaying Results 1126-1150 of 2507 "'GENE'"

Jan 06, 2026, 08:00 ET Chromatin Bioscience, Mediphage Bioceuticals, and Entos Pharmaceuticals, collaborate on Genetic Medicines Project with support from UKRI Innovate UK and Canadian R&D Funding

focused on the design and development of synthetic promoters for targeted eukaryotic gene control systems. Its proprietary platform, chromatinLENS TM, enables precise, cell-type-selective, and durable gene expression, which is key to advancing the next generation of genetic medicines. Chromatin's

More news about: CHROMATIN BIOSCIENCE LTD


Jan 06, 2026, 08:00 ET Unchained Labs Cracks the Code on ADC Characterization

Calif., Jan. 6, 2026 /PRNewswire/ -- Unchained Labs, the life sciences company that's all about getting biologics and gene therapy researchers the right tool for the job, just launched a brand-new application on Stunner today that delivers rapid, low-volume antibody-drug

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Jan 06, 2026, 08:00 ET Unchained Labs Cracks the Code on ADC Characterization

Calif., Jan. 6, 2026 /PRNewswire/ -- Unchained Labs, the life sciences company that's all about getting biologics and gene therapy researchers the right tool for the job, just launched a brand-new application on Stunner today that delivers rapid, low-volume antibody-drug

More news about: Unchained Labs


Jan 06, 2026, 07:17 ET Federal Appeals Court Sides With Natural Grocers® in GMO Labeling Case

in 2014. The company prohibits most GMO ingredients in the grocery products it sells, including those produced using new genetic techniques such as gene-editing and cell culture.Natural Grocers' philosophy is simple: food should come from real sources and undergo as few modifications as possible.

More news about: Natural Grocers by Vitamin Cottage, Inc.


Jan 06, 2026, 07:03 ET Variant Bio Launches Inference, the World's First Agentic AI Genomic Drug Discovery Platform

available for dynamic downstream analyses. A proprietary application programming interface (API) powers the entire platform, enabling instant retrieval of gene and variant-level data across hundreds of millions of data points in seconds."With Inference, we built the tool we wished existed

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Jan 06, 2026, 07:00 ET Genprex Announces Positive Preliminary Preclinical Data from Study of GPX-002 in Type 2 Diabetic Animal Studies

(NASDAQ: GNPX), a clinical-stage gene therapy company focused on developing life-changing therapies for patients with cancer and diabetes, today announced preliminary in vivo preclinical proof-of-concept data for GPX-002, the Company's diabetes gene therapy drug candidate which may have the

More news about: Genprex, Inc.


Jan 05, 2026, 21:08 ET The Inner Circle acknowledges, Sinisa Dovat, MD, Ph.D. as a Pinnacle Lifetime Member

Pediatric Experimental Therapeutics Program. He plays a pivotal role in the Four Diamonds Pediatric Cancer Research Center, leading research on the Ikaros gene and its implications in high-risk childhood leukemia. Dr. Dovat's work includes developing novel drug designs and targeted therapies to combat pediatric

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Jan 05, 2026, 17:31 ET Castration-sensitive Prostate Cancer Market Projected to Grow at a 13.2% CAGR (2020-2034), Driven by Expanded Approval and Wider Commercialization Opportunity in nmCSPC Segment | DelveInsight

TherapiesThe development of therapies targeting specific mutations is expected to perform better in the future, such as AKEEGA (HRR gene-mutated mCSPC), TALZENNA (DDR-deficient mCSPC), TRUQAP (de novo PTEN-deficient mHSPC), and others.Radioligand and PARP Inhibitors

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Jan 05, 2026, 11:15 ET GenEditBio Receives FDA Clearance of IND Application for Its Lead In Vivo Genome-Editing Program GEB-101 for TGFBI Corneal Dystrophy

GenEditBio.About TGFBI Corneal DystrophyTGFBI corneal dystrophy is a group of genetic eye disorders caused by mutations in the TGFBI gene, resulting in progressive abnormal protein buildup and deposits in the cornea. Symptoms include photophobia, gradual vision loss and recurrent corneal

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Jan 05, 2026, 10:30 ET Cell Culture Vessels Market worth $8.03 billion by 2030 | MarketsandMarkets™

https://www.marketsandmarkets.com/pdfdownloadNew.asp?id=75000041 The cell culture vessels market is growing rapidly, driven by advancements in biologics, vaccines, and cell and gene therapies, which require efficient and scalable cell expansion platforms. The use of advanced cell culture methods for drug discovery and toxicity testing

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Jan 05, 2026, 09:30 ET Mira Precision Health, Based in Mason, Ohio, Announces U.S. Launch of ToxNav® Advantage™ at the 2026 ASCO® GI Cancers Symposium

treatment with fluoropyrimidines.Key features of ToxNav® Advantage™ include:Comprehensive analysis of 23 DPYD gene variantsInclusion of DGLUCY and ENOSF1/TYMS variants predictive of fluoropyrimidine-associated cardiotoxicity (CTRCD) and Hand-Foot Syndrome

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Jan 05, 2026, 09:00 ET Morrison Foerster Elects 17 Partners

and biotechnology sectors. She has significant experience representing leading innovators in matters involving biologics, antibody-drug conjugates, gene therapy, and bio-manufacturing technologies. Sumaiya has litigated across multiple forums, including federal district courts, the Patent Trial and Appeal

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Jan 05, 2026, 08:00 ET Kenai Therapeutics Receives $8M Grant from California Institute for Regenerative Medicine (CIRM) to Advance RNDP-001 for Treatment of Idiopathic Parkinson's Disease

California to fund stem cell and gene therapy research with the goal of accelerating treatments for patients with unmet medical needs. With $8.5 billion in funding allocated through both Proposition 71 in 2004 and Proposition 14 in 2020, CIRM supports stem cell and gene therapy discoveries from inception

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Jan 05, 2026, 03:15 ET GenEditBio Receives FDA Clearance of IND Application for Its Lead In Vivo Genome-Editing Program GEB-101 for TGFBI Corneal Dystrophy

TGFBI gene. GEB-101 is encapsulated as ribonucleoprotein in engineered protein delivery vehicle (PDV), a proprietary in vivo delivery system developed by GenEditBio.About GenEditBioEstablished in 2021 and headquartered in Hong Kong, China, GenEditBio is a clinical-stage gene therapy

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Jan 02, 2026, 13:29 ET Gene Therapy: 5 Biotech Stocks Chasing the $36B Prize

Equity Insider News Commentary – The gene therapy market is surging toward $36.55 billion by 2032, powered by rising demand for curative treatments that target genetic diseases at their source[1].

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Jan 02, 2026, 07:00 ET Insmed To Present at the 44th Annual J.P. Morgan Healthcare Conference

therapies to treat chronic, debilitating lung diseases. The Company's early-stage programs encompass a wide range of technologies and modalities, including gene therapy, AI-driven protein engineering, protein manufacturing, RNA end-joining, and synthetic rescue.Headquartered in Bridgewater, New Jersey,

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Jan 02, 2026, 01:00 ET Ecovyst Completes Sale of Advanced Materials & Catalysts Segment to Technip Energies

EBITDA from continuing operations of approximately $170 million provided in November 3, 2025 earnings release.For more information:Gene Shiels – Director of Investor Relations(484) 617 [email protected]

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Jan 01, 2026, 09:30 ET Columbus Marathon Set Fundraising Record for Nationwide Children's Hospital in 2025

Cell Ovarian Tumor, Pataskala, OHDon, 7, Spastic Quad Cerebral Palsy and Hereditary Spastic Paraplegia Type 4, Zanesville, OHFinn, 9, Gene Deletion, Adrenal Insufficiency and Hypothyroidism, Springfield, OHKaden, 9, SC Sickle Cell, Cystic Fibrosis, and Pancreatic Insufficiency,

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Dec 31, 2025, 02:00 ET The Uygur ethnic group: Atlas silk exhibits enduring glamour of cultural diversity, unity

characterized primarily by designing the pattern before weaving. The threads are dyed first, then woven into fabric.Its origin inherently embodies a gene of "integration."Over one thousand years ago, sericulture and silk reeling techniques from the Central Plains were introduced to the Western

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Dec 30, 2025, 16:00 ET AMERICA'S TIRE AMPLÍA SU PRESENCIA MINORISTA EN NUEVA JERSEY

están oficialmente abiertas, por lo que invitamos a todo el condado de Burlington a venir a saludar y revisar sus neumáticos de forma gratuita", dijo Gene Bailey, gerente de la tienda America's Tire. "America's Tire puede ser una marca desconocida para los conductores de Nueva Jersey, pero nuestro equipo

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Dec 30, 2025, 14:59 ET AMERICA'S TIRE EXPANDS RETAIL FOOTPRINT INTO NEW JERSEY

are officially open, so we invite all of Burlington County to come say hello and get their tires checked for free," said America's Tire store manager Gene Bailey. "America's Tire might be an unfamiliar brand to the drivers of New Jersey, but our team of tire experts is ready and trained to provide the

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Dec 29, 2025, 21:40 ET QURE Investigation Notice: Kessler Topaz Meltzer & Check, LLP Encourages uniQure N.V. (NASDAQ: QURE) Investors with Significant Losses to Contact the Firm

On November 3, 2025, uniQure issued a press release revealing that the FDA notified the company that data for its AMT-130, an investigational gene therapy for Huntington's disease, did not provide sufficient evidence to support uniQure's Biologics License Application ("BLA") submission. Specifically,

More news about: Kessler Topaz Meltzer & Check, LLP


Dec 29, 2025, 06:40 ET Cell and Gene Therapy Market to Exceed US$105B by 2033, Driving Strategic Value Across Healthcare Portfolios | According to DataM Intelligence

Cell and Gene Therapy Market Intelligence: https://www.datamintelligence.com/download-sample/cell-and-gene-therapy-market Market OverviewCell and gene therapies

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Dec 29, 2025, 02:49 ET Diamyd Medical accelerates primary efficacy readout by 9 months in type 1 diabetes Phase 3 trial following FDA alignment and guidance

antigen-specific immunomodulatory therapeutic for the preservation of endogenous insulin production specifically for individuals carrying an HLA DR3-DQ2 gene. Diamyd® has been granted Orphan Drug Designation in the U.S. as well as Fast Track Designation by the U.S. FDA for the treatment of Stage

More news about: Diamyd Medical AB


Dec 29, 2025, 02:45 ET Diamyd Medical accelerates primary efficacy readout by 9 months in type 1 diabetes Phase 3 trial following FDA alignment and guidance

antigen-specific immunomodulatory therapeutic for the preservation of endogenous insulin production specifically for individuals carrying an HLA DR3-DQ2 gene. Diamyd® has been granted Orphan Drug Designation in the U.S. as well as Fast Track Designation by the U.S. FDA for the treatment of Stage

More news about: Diamyd Medical AB


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