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Mutations in EDA and EDAR genes cause dominant syndromic tooth agenesis
Choline transporter-like proteins 1 and 2 are newly identified plasma membrane and mitochondrial ethanolamine transporters
Familial Alzheimer’s disease mutations in amyloid protein precursor alter proteolysis by γ-secretase to increase amyloid β-peptides of ≥45 residues
TMF1- A novel mediator of the Insulin regulated glucose homeostasis and normal glycemic level
T cell-derived extracellular vesicles are elevated in essential Hypertension
Skeletal muscle mitochondrial fragmentation and impaired bioenergetics from nutrient overload are prevented by carbon monoxide
CAPS2 Deficiency in Autism Impairs the Release of the Social Peptide Oxytocin
Role of Kalirin and mouse strain in retention of spatial memory training in an Alzheimer’s disease model mouse line
Dysregulation of TRPV4, eNOS and caveolin-1 contribute to endothelial dysfunction
