BT3A3 Rabbit Polyclonal Antibody, 100ul Variant Libraries Hearing impairment is a heterogeneous

Hearing impairment is a heterogeneous condition with over 40 loci described

Mutations have been identified in patients with Parkinson disease and chronic obstructive pulmonary disease

Enhances the transcriptional repressor activity of NR1D1 through stabilization of NR1D1 protein levels by preventing its ubiquitination and subsequent degradation (PubMed: 18235501

breast cancer

similarity:Contains 1 protein kinase domain

BT3A3 Rabbit Polyclonal Antibody, 100ul Variant Libraries Hearing impairment is a heterogeneousThe butyrophilin (BTN) genes are a group of major histocompatibility complex (MHC) associated genes that encode type I membrane proteins with 2 extracellular immunoglobulin (Ig) domains and an intracellular B30. 2 (PRYSPRY) domain. Three subfamilies of human BTN genes are located in the MHC class I region: the single copy BTN1A1 gene (MIM 601610) and the BTN2 (e. g., BTN2A1; MIM 613590) and BTN3 (e. g., BNT3A3) genes, which have undergone tandem