The team used these newly generated stem cells to help form a living, breathing mouse from a developing embryo.

Scientists have engineered a hybrid mouse with a gene that predates all animal life. The team replaced a single gene in the ...

Genes make up the blueprints and outline the process of building every living organism. To ensure that the right genes are ...

Scientists have reprogrammed mouse cells into pluripotent stem cells using a gene from choanoflagellates, single-celled ...

UCSF Benioff Children's Hospital Oakland is enrolling patients in an innovative clinical trial that seeks to cure sickle cell disease. The trial is the first in the U.S. to apply non-viral CRISPR-Cas9 ...

Efforts to develop a gene therapy for Diamond-Blackfan anemia (DBA) — a rare, life-threatening disorder in which bone marrow ...

In a significant move towards the liberalization of the healthcare sector, Shanghai's Pudong New Area witnessed the first ...

In another sign of biopharma's waning interest in the traditional ex vivo gene therapy approach, CSL Behring is shutti | CSL ...

Campus Chemical Instrument Center, Mass Spectrometry & Proteomics Facility, The Ohio State University, Columbus, USA ...

This study presents important findings on the role of CXXC-finger protein 1 in regulatory T cell gene regulation and function. The evidence supporting the authors' claims is solid, with mostly ...