ITB8 Polyclonal Antibody, 50ul sgRNA Oligos Mutations in the winged-helix transcription

Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia

with the second SH3 domain of the adapter protein NCK1

Alternatively spliced transcript variants have been found for STAT5A

Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

belongs to the protein kinase superfamily

ITB8 Polyclonal Antibody, 50ul sgRNA Oligos Mutations in the winged-helix transcriptionThis gene is a member of the integrin beta chain family and encodes a single pass type I membrane protein with a VWFA domain and four cysteine rich repeats. This protein noncovalently binds to an alpha subunit to form a heterodimeric integrin complex. In general, integrin complexes mediate cell cell and cell extracellular matrix interactions and this complex plays a role in human airway epithelial proliferation. Alternatively spliced variants which