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University of Birmingham Supports New Tumour Organoid Biobank Revealing Genetic Weaknesses in Cancer

University of Birmingham Supports New Tumor Organoid Biobank Revealing Genetic Weaknesses in Cancer

Tumor organoid biobank: Researchers developed 256 patient-derived organoids representing five cancer types for biomedical research. Gene dependency mapping: CRISPR screening identified genes that...
Creative Biolabs Doubles Down on NHP Solutions Amid Biomedical Research Frenzy

Creative Biolabs Doubles Down on NHP Solutions Amid Biomedical Research Frenzy

Skyrocketing Demand Meets Critical Supply Crunch The biomedical world is riding a tidal wave of skyrocketing demand for non-human primate (NHP) biologicals, fueled by breakthroughs...
ATCC Awarded Two Projects from the USDA to Support its ARS Agency

ATCC Awarded Two Projects from the USDA Including the Creation of ARS Resources Collection...

ATCC, the world’s premier biological materials management and standards organization, today announced that it has been awarded two projects, with a combined value of...

Broad And Sanger Reproduce CRISPR-Cas9 Genetic Knock-Out Screens In 725 Cancer Cell Line Models

A comprehensive map of genes necessary for cancer survival is one step closer, following the validation of the two largest CRISPR-Cas9 genetic screens in 725 cancer...

CRISPR Therapeutics And Vertex Release Interim Phase I Data On CRISPR/Cas9 Gene-Editing Therapy

CRISPR Therapeutics and Vertex Pharmaceuticals Incorporated have announced positive, interim data from the first two patients with severe hemoglobinopathies treated with the investigational CRISPR/Cas9 gene-editing therapy CTX001...

Biobanking Science: CRISPR Gene Editing to Treat Human Disease

This year has seen a flurry of good news about CRISPR gene editing clinical trials in human patients. CRISPR-Cas 9 is a gene editing...

CRISPR Therapeutics And ViaCyte Collaborate To Create Universal Stem Cell Therapies For Diabetes

CRISPR Therapeutics and ViaCyte, Inc. have announced a collaboration focused on the discovery, development, and commercialization of gene-edited allogeneic stem cell therapies for the...

Cell Therapy – New Method To Reprogram T-cells Without Viral Vectors Developed At UCSF

  A new method has been developed, primarily by University of California San Francisco (UCSF) researcher Theo Roth of Alex Marson’s laboratory, to introduce gene...

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