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Human FGF8 Protein expressed in Escherichia coli (E. coli) - ABIN2667402
Gemel, Gorry, Ehrlich, MacArthur: Structure and sequence of human FGF8. in Genomics 1996
Show all 6 references for ABIN2667402
Human FGF8 Protein expressed in Escherichia coli (E. coli) - ABIN935347
Borello, Cobos, Long, McWhirter, Murre, Rubenstein: FGF15 promotes neurogenesis and opposes FGF8 function during neocortical development. in Neural development 2008
FGF-8 was revealed to suppress BMP-induced osteoblast differentiation through the ERK (show EPHB2 Proteins) pathway and the effects were enhanced by TNF-alpha (show TNF Proteins).
Fgf8 expression is required for the continued postnatal development/maturation of the Vasopressin (show AVP Proteins) and CRH (show CRH Proteins) neurons in the Paraventricular nucleus.
Deregulated FGF8 and Otx2 (show OTX2 Proteins)/Gbx2 (show GBX2 Proteins) gene expression underlies cerebellar vermis hypoplasia in mouse model of CHARGE syndrome.
Cre fate mapping in Fgf8 mutant embryos revealed novel functions of this gene in rostral patterning center progenitor development. Disruption resulted in aberrant progenitor number and distribution in the rostral telencephalon.
Tfap2a (show TFAP2A Proteins)-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosage
Results show that DLX5 (show DLX5 Proteins), p63 (show CKAP4 Proteins), Pin1 (show PIN1 Proteins) and FGF8 participate to the same time- and location-restricted regulatory loop essential for apical ectodermal ridge stratification, hence for normal patterning and skeletal morphogenesis of the limb buds.
This study demonistrated that Fgf8- and Fgfr1 (show FGFR1 Proteins)/Fgf8-deficient mice diplay increased anxiety-like behavior and reductions in specific populations of serotonergic neurons in the brain.
Scube3 may be a critical upstream regulator of fast fiber myogenesis by modulating fgf8 signaling during zebrafish embryogenesis
Retinoic acid directly represses Fgf8 through a retinoic acid response element-mediated mechanism that promotes repressive chromatin
Together our data demonstrates that Foxc1 (show FOXC1 Proteins) - Fgf8 signaling regulates mammalian jaw patterning and provides a mechanistic basis for the pathogenesis of syngnathia
Regulation of neurogenesis by Fgf8a requires Cdc42 (show CDC42 Proteins) signaling and a novel Cdc42 effector (show FNBP1L Proteins) protein
Our results link FGF8, c-Abl (show ABL1 Proteins) and p300 (show EP300 Proteins) in a regulatory pathway that controls DeltaNp63alpha protein stability and transcriptional activity.
Data indicate that overexpression of fibroblast growth factor 8 (FGF8) correlates with lymph node metastasis and poor prognosis in colorectal cancer (CRC (show CALR Proteins)).
FGF8 mutations (p.Gly29_Arg34dup and p.Pro26Leu) contribute to the formation of the VATER/VACTERL association.
Together, these data demonstrate that FGF (FGFR-2 (show FGFR2 Proteins) and Fgf8)signaling regulates cell proliferation and cell polarity and that these cell processes contribute to facial morphogenesis.
The oncoprotein HBXIP enhances angiogenesis and growth of breast cancer through modulating FGF8 and VEGF.
genetic association study in population in Massachusetts: Data suggest that clinical features in Kallmann syndrome (KS) are associated with genetic causes: dental agenesis/digital bony abnormalities are associated with variations/mutations in FGF8.
A novel FGF8b-binding peptide (show HP Proteins) with anti-tumor effect on prostate cancer.
genetic association studies in 103 patients from US and UK: Mutations in FGF8, FGFR1 (show FGFR1 Proteins), or PROKR2 (show PROKR2 Proteins) contributed to 7.8% of patients with combined pituitary hormone (show CGA Proteins) deficiency or septo-optic dysplasia. Data suggest genetic overlap with Kallmann syndrome.
FGF8 and FGF18 (show FGF18 Proteins) signal through divergent pathways in ovarian granulosa cells, despite reportedly similar receptor activation patterns.
These results suggest that polymorphisms discovered in DECR1 (show DECR1 Proteins), CBFA2T1 (show RUNX1T1 Proteins), and FGF8 may play a role in the lipid metabolism pathway affecting carcass quality traits in beef cattle.
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 protein is known to be a factor that supports androgen and anchorage independent growth of mammary tumor cells. Overexpression of this gene has been shown to increase tumor growth and angiogensis. The adult expression of this gene is restricted to testes and ovaries. Temporal and spatial pattern of this gene expression suggests its function as an embryonic epithelial factor. Studies of the mouse and chick homologs revealed roles in midbrain and limb development, organogenesis, embryo gastrulation and left-right axis determination. The alternative splicing of this gene results in four transcript variants.
, androgen-induced growth factor
, heparin-binding growth factor 8
, fibroblast growth factor 8 (androgen-induced)
, fibroblast growth factor 8
, fibroblast growth factor-8
, fibroblast growth factor 8 (androgen-induced) isoform 1
, fibroblast growth factor 8 (androgen-induced) isoform 2
, fibroblast growth factor 8 (androgen-induced) isoform 3