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FGF12, RBFOX1 (show A2BP1 ELISA Kits), and MIR302F could be important in human heterotaxy, because they were noted in multiple cases. Further investigation into genes involved in the NODAL, BMP, and WNT (show WNT2 ELISA Kits) body patterning pathways and into the dosage effects of FGF12, RBFOX1 (show A2BP1 ELISA Kits), and MIR302F is warranted.
FGF12 strongly induced the quiescent and contractile vascular smooth muscle cell phenotype and directly promoted VSMC lineage differentiation.
Results demonstrate that gain-of-function FHF mutations can cause neurologic disorder, and expand the repertoire of genetic causes (FHF1) and mechanisms (altered Nav gating) underlying early-onset epileptic encephalopathies and cerebellar atrophy
Nine SNPs of the FGF12 gene were associated with Kashin-Beck disease.
Data indicate that SCN5A (show SCN5A ELISA Kits) variant (Nav1.5 (show SCN5A ELISA Kits)) p.H1849R affected interaction with fibroblast growth factor homologous factor (FHFs).
Q7R-FGF12 is a disease-associated BrS mutation. Moreover, these data suggest for the first time that FHF effects on Na(+) and Ca(2 (show CA2 ELISA Kits)+) channels are separable.
VAX1 (show VAX1 ELISA Kits) rs10787760, rs6585429 and rs1871345 polymorphisms may be involved in nonsyndromic cleft lip with or without cleft palate in Brazilian patients, but there is no association with polymorphisms in FGF12, VCL (show VCL ELISA Kits), or CX43 (show GJA1 ELISA Kits)
PHOX2B (show PHOX2B ELISA Kits), FGF12 and GAD2 (show GAD2 ELISA Kits) genes are hypermethylated in colorectal neoplastic tissue
exogenous FGF12 can play a role in tissues by translocating into cells through the plasma membrane
Fibroblast growth factor homologous factor 1B (FHF1B) modulated the cardiac sodium channel Nav1.5 (show SCN5A ELISA Kits).
FGF21 (show FGF21 ELISA Kits) does not appear necessary for exercise-induced systemic and hepatic mitochondrial adaptations, but the increased adiposity, hyperinsulinemia, and impairments in hepatic mitochondrial function induced by FGF21 (show FGF21 ELISA Kits) deficiency can be partially rescued by daily wheel running exercise.
x-ray crystal structure of FHF1b
results argue strongly against the possibility that FHF1 has a modulatory effect on the Na(v)1.9 sodium channel isoform in cRet (show RET ELISA Kits)+/IB4+ neurons, but FHF1 could play a role in a distinct subset of TrkA (show NTRK1 ELISA Kits)+/CGRP (show CALCA ELISA Kits)+ nociceptors.
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 growth factor lacks the N-terminal signal sequence present in most of the FGF family members, but it contains clusters of basic residues that have been demonstrated to act as a nuclear localization signal. When transfected into mammalian cells, this protein accumulated in the nucleus, but was not secreted. The specific function of this gene has not yet been determined. Two alternatively spliced transcript variants encoding distinct isoforms have been reported.
fibroblast growth factor 12
, Fibroblast growth factor 12
, fibroblast growth factor 12B
, fibroblast growth factor FGF-12b
, fibroblast growth factor homologous factor 1
, myocyte-activating factor
, fibroblast growth factor homologous factor 1b