Finnish researchers have been the first to determine the cause for the nonsyndromic early-onset hereditary canine hearing loss in Rottweilers.
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Scientists discover gene signature responsible for plaque-eating microglia in Alzheimer’s disease
Alzheimer’s disease is the most common form of dementia and is characterized by the build-up of amyloid plaques in the
Read moreGene therapy restores immune function in children with rare immunodeficiency
An investigational gene therapy can safely restore the immune systems of infants and children who have a rare, life-threatening inherited
Read moreHigh-throughput system can regulate gene expression for treating sickle cell disease, beta thalassemia
St. Jude Children's Research Hospital scientists have developed an integrated, high-throughput system to better understand and possibly manipulate gene expression
Read moreNew gene editing strategies developed for Duchenne muscular dystrophy
UT Southwestern scientists successfully employed a new type of gene therapy to treat mice with Duchenne muscular dystrophy (DMD), uniquely
Read moreCRISPR/Cas technology helped revolutionize diagnostics and gene therapy
Announcing a new article publication for BIO Integration journal. In this mini review article the authors Meiyu Qiu and Pei
Read moreStudy links muscle gene to type 2 diabetes
People with type 2 diabetes tend to have poorer muscle function than others. Now a research team at Lund University
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Almost 80% of South Africans speak one of the SEB family languages as their first language. Their origins can be
Read moreResearchers identify ‘instigator’ gene associated with Alzheimer’s disease
In a new paper published in Nature Communications, Mayo Clinic researchers and collaborators report the protein-coding gene SERPINA5 may worsen
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Findings of a study by the Translational Genomics Research Institute (TGen), an affiliate of City of Hope, suggest that increasing
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