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The protein encoded by FGF13 is a member of the fibroblast growth factor (FGF) family. Additionally we are shipping FGF13 Antibodies (120) and FGF13 Kits (16) and many more products for this protein.
Showing 9 out of 11 products:
Human FGF13 Protein expressed in Wheat germ - ABIN1354001
Chan, Li, Hsueh, Lee, Chen, Hwang, Chen, Shih, Hsieh: Fibroblast growth factor-10 promotes cardiomyocyte differentiation from embryonic and induced pluripotent stem cells. in PLoS ONE 2011
for PCa (show FLVCR1 Proteins) patients after RP, FGF13 serves as a potential novel prognostic marker that improves prediction of BCR (show BCR Proteins)-free survival, in particular if combined with other clinical parameters.
The findings of this study reveal a novel cause of this syndrome and underscore the powerful role of FGF13 in control of neuronal excitability.
X-chromosome deletions may be a cause of WS with larger deletions being lethal to males and that FGF13 mutations may be a cause of Wildervanck Syndrome (WS).
Upregulated expression of FGF13/FHF2 mediates resistance to platinum drugs in cervical cancer cells
FGF13 has a role in hair follicle growth and in the hair cycle as shown in a family with X-linked congenital generalized hypertrichosis
FGF13 down-regulated Spry1 protein expression, activating the ERK1/2 pathway by phosphorylation and leading to C2C12 cell differentiation inhibition.
Fibroblast growth factor homologous factors (FGF11 (show FGF11 Proteins)-14) modulate cardiac calcium channels.
FGF13 has a role in hair follicle growth and in the hair cycle
Genetic deletion of FGF13 in mice results in neuronal migration defects in both the neocortex and the hippocampus. FGF13-deficient mice also exhibit weakened learning and memory.
FGF-13 may play a role in regulating the function of cells in the bulge region and basal layer of the epidermis.
The protein encoded by this gene 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. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini.
, fibroblast growth factor 13
, Fibroblast growth factor 13
, fibroblast growth factor homologous factor 2