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抗Human WNT9B 抗体:
抗Rat (Rattus) WNT9B 抗体:
抗Mouse (Murine) WNT9B 抗体:
Cow (Bovine) Polyclonal WNT9B Primary Antibody for WB - ABIN2776703
Chiquet, Blanton, Burt, Ma, Stal, Mulliken, Hecht: Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate. in Human molecular genetics 2008
Our study further supports the involvement of WNT9B as a cleft susceptibility gene in Brazilian families experiencing NSCL (显示 NHLH1 抗体)+/-P. Although additional studies are still necessary to unveil the exact mechanism by which WNT (显示 WNT2 抗体) genes would contribute to NSCL (显示 NHLH1 抗体)+/-P, allelic polymorphisms in these genes and their interactions may partly explain the variance of individual susceptibility to NSCL (显示 NHLH1 抗体)+/-P.
Multi-layered mutation in hedgehog (显示 SHH 抗体)-related genes in Gorlin syndrome may affect the phenotype
This association study successfully identified two susceptibility Single Nucleotide Polymorphisms, (WNT9B and PBX1 (显示 PBX1 抗体)) associated with Mayer-Rokitansky-Kuster-Hauser syndrome risk, both separately and interactively.
Genome association study shows a highly conserved 32 kb intergenic region containing regulatory elements between WNT3 (显示 WNT3 抗体) and WNT9B in patients with classic bladder exstrophy.
results indicate that mutations in the coding sequence of WNT9B are not responsible for Mullerian duct abnormalities in the Chinese population
Two novel mutations (a missense mutation in exon 1, and one in the 3-UTR (显示 UTS2R 抗体)) may be pathogenic variants in Mayer-Rokitansky-Kuster-Hauser syndrome patients and warrant further functional study.
secretion of WNT2B (显示 WNT2B 抗体) and WNT9B and stabilization of beta-catenin (CTNNB1 (显示 CTNNB1 抗体)) upon virus infection negatively regulate expression of representative inducible genes IFNB1 (显示 IFNB1 抗体), IFIT1 (显示 IFIT1 抗体) and TNF (显示 TNF 抗体) in a CTNNB1 (显示 CTNNB1 抗体)-dependent effector mechanism
The signals from the stromal fibroblasts cooperate with Wnt9b to promote differentiation of the progenitor cells.
Mutations in the coding sequence of WNT4 (显示 WNT4 抗体), WNT5A (显示 WNT5A 抗体), WNT7A (显示 WNT7A 抗体), and WNT9B are not responsible for the Mayer-Rokitansky-Kuster-Hauser syndrome.
These analyses suggest that in zebrafish, as in humans, wnt9b plays distinct roles in directing morphogenetic movements of developing branchial arch elements.
Data indicate that mutations in wingless-type MMTV integration site family, member 9B protein (WNT9B) were frequently associated with Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS).
Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain.
Expression of Wnt9b in Six2 (显示 SIX2 抗体)-positive cells disrupts cell fate decisions in the kidney and the gastrointestinal tract.
Epithelial Wnt7b (显示 WNT7B 抗体) and Wnt9b as possible ligands of Fzd1 (显示 Fzd1 抗体)-mediated beta-catenin (Ctnnb1 (显示 CTNNB1 抗体))-dependent (canonical) Wnt (显示 WNT2 抗体) signaling in the undifferentiated ureteric mesenchyme
Study has identified a previously unknown regulatory link between WNT9B and FGF signaling during lip and upper jaw development.
Notch (显示 NOTCH1 抗体) pathway activation can replace the requirement for Wnt4 (显示 WNT4 抗体) and Wnt9b in mesenchymal-to-epithelial transition of nephron stem cells
wnt9b signaling regulates stem cell proliferation and differention in the developing kidney depending on the activity of the transcription factor Six2 (显示 SIX2 抗体) in the responding cell.
transgenic overexpression of Wnt9b in the ureteric bud causes reduced branching in multiple founder lines.
expression in most but not all tissues of the 16.5-day embryo; no significant elevation of Wnt9b expression was detected in 29 mouse mammary tumor virus-induced tumors
Wnt9b is a common organizing signal regulating diverse components of the mammalian urogenital system.
Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. May be a signaling molecule which affects the development of discrete regions of tissues. Is likely to signal over only few cell diameters (By similarity).
, protein Wnt-9b
, wingless-type MMTV integration site family, member 15
, wnt9b protein
, wingless related MMTV integration site 9B
, wingless-type MMTV integration site 9B
, wingless-type MMTV integration site family, member 9B
, wingless-type MMTV integration site 15