FGF-11 Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Naturally occurring read-through transcription also

Naturally occurring read-through transcription also exists between this gene and the downstream pentatricopeptide repeat domain 1 (PTCD1) gene

Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects

This gene is a member of the Bardet-Biedl syndrome (BBS) gene family

This MAGEA gene encodes a protein that is C-terminally truncated compared to other family members

and Rab (see MIM 179508) families

FGF-11 Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Naturally occurring read-through transcription alsoFibroblast growth factor 11 encoded by FGF11 is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The function of this gene has not yet been determined. The expression pattern of the mouse homolog implies a role in