Scientists have identified mutations in the CPD gene as a key cause of a rare congenital hearing loss, revealing how ...

Deciphering how the GR forms oligomers—through the binding of several subunits—opens a crucial avenue for developing more ...

Mutations in a gene called CPD have been found to play a key role in a rare inherited form of hearing loss, according to an international research ...

A new study has revealed the mechanism of multimerization — the association of different molecules to form complex structures ...

All primary and secondary interim analysis endpoints in FORTIFY Phase 3 study successfully achieved with well-tolerated safety profile ...

Up to 60% of congenital and early-onset hearing loss is caused by genetic mutations in an inherited gene, and gene therapy ...

Village Caregiving reports that frontotemporal dementia is a progressive brain disease affecting behavior, speech, and memory ...

Drugs to treat inflammatory and autoimmune diseases - such as asthma, psoriasis, rheumatoid arthritis or Chrousos syndrome - ...

With Eli Lilly's recent acquisition of Verve Therapeutics and its PCSK9 candidate, delve into what the target represents.

Scientists have discovered a CPD gene mutation that causes congenital hearing loss. The study reveals how arginine and nitric ...

Chinese scientists have analyzed the genomes and physical characteristics of nearly 1,000 macaques to provide domestic ...

Aurigene Oncology Limited, a clinical-stage biopharmaceutical company developing novel therapies in oncology, today announced ...