SHAN3 Polyclonal Antibody, 50ul Bacterial Expression Mutations in NR3C are associated

Mutations in NR3C are associated with generalized glucocorticoid resistance

Recently| patients with an unusual autosomal-dominant bleeding disorder (factor V Quebec) were found to have a deficiency of platelet multimerin

RPS13 is co-transcribed with two U14 small nucleolar RNA genes

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SHAN3 Polyclonal Antibody, 50ul Bacterial Expression Mutations in NR3C are associatedThis gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G protein coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized