Researchers have revealed new details about the CRISPR-Cas5-HNH/Cascade complex, a variant of the type I-E CRISPR-Cas system, ...

Recent research from Michigan Medicine takes aim at the a variant in gene SCN1B, which causes a severe form of developmental epileptic encephalopathy.

Feb. 06, 2025 (GLOBE NEWSWIRE) -- Denali Therapeutics Inc. (NASDAQ: DNLI), today announced the primary analysis of the Phase 1/2 study in 47 participants with Hunter syndrome (MPS II) in the 24-week ...

LIG4 syndrome is an exceptionally rare disorder caused by a genetic mutation that prevents the body from repairing damaged ...

This foundation is dedicated to significantly improving the lives of people with down syndrome through research, medical care, education. Parents of children wi ...

Hereditary cancer risk can be passed down among generations, just like physical characteristics that we can identify in our ...

Genetics significantly impact cancer risk, particularly in inherited mutations like BRCA1/BRCA2, which increase ...

CHICAGO (Reuters) — Scientists have characterized the role of thousands of mutations in the BRCA2 cancer gene, findings that may help reassure worried patients about their cancer risk or guide doctors ...

Advancements in gene therapy and molecular research have opened pathways to target cognitive and developmental challenges associated with down syndrome. Stem cell therapy is being explored for ...

What is Zollinger-Ellison syndrome? Zollinger-Ellison syndrome (ZES ... Stomach acid is needed to break down food. But too much acid can cause painful peptic ulcers. In ZES, the ulcers are usually in ...

Viralgen and Axovia Therapeutics are set to form a partnership to progress the development and manufacturing of an adeno-associated virus vector serotype 9 (AAV9)-based gene therapy for retinal ...