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Human FGF8 ELISA Kit für Sandwich ELISA - ABIN418595
Amable, Teixeira, Carias, Granjeiro, Borojevic: Mesenchymal stromal cell proliferation, gene expression and protein production in human platelet-rich plasma-supplemented media. in PLoS ONE 2014
Results indicate that perinatal fibroblast growth factor 8 (FGF8) signaling is important for the timing of the onset of anterior-dorsal glial fibrillary acidic protein (zeige GFAP ELISA Kits) expression in midline glial cells suggesting that FGF8 function regulates midline GFAP (zeige GFAP ELISA Kits)-IR glial cell development, which when disrupted by Fgf8 deficiency prevents the formation of the corpus callosum.
The FBLN1 (zeige FBLN1 ELISA Kits)/FGF8 interaction may also be involved in the survival of neural crest cell population during development.
These results indicate that the modulatory effects of SHH (zeige SHH ELISA Kits) on BALB/c mouse metanephric explant cultures may involve the regulation of Fgf8 expression but not Fgf10 (zeige FGF10 ELISA Kits) expression, which provides evidence for the functional role of Fgf proteins in renal morphogenesis.
FGF-8 was revealed to suppress BMP-induced osteoblast differentiation through the ERK (zeige EPHB2 ELISA Kits) pathway and the effects were enhanced by TNF-alpha (zeige TNF ELISA Kits).
Fgf8 expression is required for the continued postnatal development/maturation of the Vasopressin (zeige AVP ELISA Kits) and CRH (zeige CRH ELISA Kits) neurons in the Paraventricular nucleus.
Deregulated FGF8 and Otx2 (zeige OTX2 ELISA Kits)/Gbx2 (zeige GBX2 ELISA Kits) 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 (zeige TFAP2A ELISA Kits)-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosage
Results show that DLX5 (zeige DLX5 ELISA Kits), p63 (zeige CKAP4 ELISA Kits), Pin1 (zeige PIN1 ELISA Kits) 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 (zeige FGFR1 ELISA Kits)/Fgf8-deficient mice diplay increased anxiety-like behavior and reductions in specific populations of serotonergic neurons in the brain.
in one holoprosencephaly (HPE) family, a deleterious FGFR1 (zeige FGFR1 ELISA Kits) allele was transmitted from one parent and a loss-of-function allele in FGF8 from the other parent to both affected daughters. This family is one of the clearest examples to date of gene:gene synergistic interactions causing HPE in humans.
Fgf8 activates Ras-ERK (zeige EPHB2 ELISA Kits) pathway to specify hindbrain. Downstream of ERK (zeige EPHB2 ELISA Kits), Pea3 (zeige ETV4 ELISA Kits) specifies isthmus (rhombomere 0, r0), and Irx2 (zeige IRX2 ELISA Kits) may specify r1, where the cerebellum is formed.
Regulation of neurogenesis by Fgf8a requires Cdc42 (zeige CDC42 ELISA Kits) signaling and a novel Cdc42 effector (zeige FNBP1L ELISA Kits) protein
Our results link FGF8, c-Abl (zeige ABL1 ELISA Kits) and p300 (zeige EP300 ELISA Kits) 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 (zeige CALR ELISA Kits)).
FGF8 mutations (p.Gly29_Arg34dup and p.Pro26Leu) contribute to the formation of the VATER/VACTERL association.
Scube3 may be a critical upstream regulator of fast fiber myogenesis by modulating fgf8 signaling during zebrafish embryogenesis
Together, these data demonstrate that FGF (FGFR-2 (zeige FGFR2 ELISA Kits) 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.
FGF8 and FGF18 (zeige FGF18 ELISA Kits) signal through divergent pathways in ovarian granulosa cells, despite reportedly similar receptor activation patterns.
These results suggest that polymorphisms discovered in DECR1, CBFA2T1 (zeige RUNX1T1 ELISA Kits), 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