10h
MyChesCo on MSNCMTA Invests $300,000 in Groundbreaking Gene Editing Therapy for CMT2AThe Charcot-Marie-Tooth Association (CMTA) has announced a $300,000 investment in a groundbreaking gene editing project aimed ...
Marek’s disease can be pervasive in chicken houses. Chickens infected by this highly contagious viral disease often develop ...
Mpox, once a rare virus mainly confined to parts of Central Africa, is rapidly evolving into a more serious global health ...
Deep-sea fish adapt to some of the most extreme conditions on Earth. New research analyzing their evolution finds the same ...
By analyzing huge amounts of biological data, the use of machine learning accelerates the identification of critical control ...
Scientists identify mutation patterns in healthy stomach lining, offering new insights into the earliest steps of cancer ...
5h
News Medical on MSNNovel ARPC1B mutation identified in a patient with recurrent eosinophiliaImmunodeficiency disorders linked to cytoskeleton defects are rare and complex, often presenting with diverse clinical features.
A surprising mix of inherited and de novo mutations in 60 genes contribute to 10 percent of CHD cases. Many of these same ...
Inherited retinal degeneration (IRD) encompasses various disorders characterized by progressive loss of retinal photoreceptor ...
AIRNA’s lead candidate AIR-001 works by correcting the most common pathologic mutation driving the rare disease alpha-1 ...
Although cystic fibrosis is a single gene mutation, there are more than 1,000 different ways the CFTR gene can mutate in ...
A comparison of patients with and without BRCA gene mutations receiving prophylactic risk-reduction surgery suggest ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results