c-Abl Monoclonal Antibody, 50ul Petri Dishes Mutations in DLX3 have been

Mutations in DLX3 have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism

This member is a delayed rectifier potassium channel and its activity is modulated by some other family members

a zinc-binding B-box motif

and thus the BARK/beta-arrestin system is believed to play a major role in regulating receptor-mediated immune functions

members of the TNF receptor superfamily

c-Abl Monoclonal Antibody, 50ul Petri Dishes Mutations in DLX3 have beenThis gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes, including cell division, adhesion, differentiation, and response to stress. The activity of the protein is negatively regulated by its SH3 domain, whereby deletion of the region encoding this domain results in an oncogene. The ubiquitously expressed protein has DNA binding activity that is regulated by CDC2 mediated phosphorylation,