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The protein encoded by GATA5 is a transcription factor that contains two GATA-type zinc fingers. 再加上，我们可以发GATA5 试剂盒 (30) 和 GATA5 蛋白 (6)和数多这个蛋白质的别的产品。
Showing 10 out of 65 products:
Human Monoclonal GATA5 Primary Antibody for ELISA, WB - ABIN969170
Hellebrekers, Lentjes, van den Bosch, Melotte, Wouters, Daenen, Smits, Akiyama, Yuasa, Sanduleanu, Khalid-de Bakker, Jonkers, Weijenberg, Louwagie, van Criekinge, Carvalho, Meijer, Baylin, Herman et al.: GATA4 and GATA5 are potential tumor suppressors and biomarkers in colorectal cancer. ... in Clinical cancer research : an official journal of the American Association for Cancer Research 2009
Human Polyclonal GATA5 Primary Antibody for ELISA, WB - ABIN188675
Belinsky, Liechty, Gentry, Wolf, Rogers, Vu, Haney, Kennedy, Hirsch, Miller, Franklin, Herman, Baylin, Bunn, Byers: Promoter hypermethylation of multiple genes in sputum precedes lung cancer incidence in a high-risk cohort. in Cancer research 2006
findings show that GATA5 mutations, in addition to heart diseases, can result in congenital abnormalities of the female genitourinary tract in humans
A multivariate regression model revealed that the effects of both the promoter methylation and the exonic SNPs in GATA5 were independent.This interaction between GATA5 variants and GATA5 promoter methylation indicates that the association of either factor with gastric disease progression is modified by the other
These results suggest that the induction of GATA-6 (显示 GATA6 抗体) dysfunction may be more effective for chemotherapy for colorectal cancer, although the mechanism underlying the synergistic effect of 5-FU and anisomycin remains unknown.
The Correlation between GATA5, WT1 (显示 WT1 抗体) and PAX5 (显示 PAX5 抗体) methylation and clinical/histological parameters is suggestive of applicability of these markers in non-invasive (epi (显示 TFPI 抗体))genetic testing in hepatocellular carcinoma (HCC (显示 FAM126A 抗体)).
we identified gene promoter methylation signatures (WT1 (显示 WT1 抗体), MSH6 (显示 MSH6 抗体), GATA5 and PAX5 (显示 PAX5 抗体)) that are strongly correlated to, and can have a predictive value for the clinical outcome of oral squamous cell carcinoma patients
Evidence supporting a genetic basis includes the autosomal dominance of Bicuspid aortic valve inheritance patterns, and the identification of mutations in GATA binding protein 5 transcription factor.
Transcriptomic analysis of human microvascular endothelial cells with GATA5 knockdown reveals that GATA5 affects several genes and pathways critical for endothelial function.
This study firstly links GATA5 mutation to DCM, which provides novel insight into the molecular mechanisms of DCM, suggesting a potential molecular target for the prenatal prophylaxis and allele-specific treatment of DCM.
Promoter hypermethylation is an important mechanism of the transcriptional inactivation of GATA5 in invasive ductal breast carcinoma.
A combination of GATA5 and SFRP2 (显示 SFRP2 抗体) methylation could be promising as a marker for the detection and diagnosis of colorectal cancers and adenomas.
GATA5 is expressed in microvascular endothelial cells and its inactivation in mice leads to vascular endothelial dysfunction and hypertension.
GATA (显示 QRSL1 抗体) transcription factors are repressors of hedgehog (显示 SHH 抗体) signaling, and NKX3.2 (显示 NKX3-2 抗体) maintains the ability of sclerotomal cells to express SHH (显示 SHH 抗体) transcriptional targets in the presence of BMP signals by repressing the induction of Gata4 (显示 GATA4 抗体)/5/6
Gata5 deficiency induces airway hyperresponsiveness, at least in part, by blunting apoE (显示 APOE 抗体) and increasing IL-13 (显示 IL13 抗体) expression.
Expression of Gata5 very efficiently promotes cardiomyocyte fate from murine embryonic stem cells.
USF1 transactivates GATA5 expression by binding to the E-box in its promoter
compound Gata4 (显示 GATA4 抗体)/Gata5 and Gata5/Gata6 (显示 GATA6 抗体) mutants die embryonically or perinatally due to severe congenital heart defects
Results unravel a critical cell-autonomous role for endocardial Gata5 in aortic valve formation and identify GATA5 as a potential gene responsible for congenital heart disease in humans.
These results demonstrate functional redundancy between Gata4 and Gata5 during cardiac development and implicate Gata5 as a candidate modifier gene for congenital heart disease.
data reveal that transcription factor GATA5 is required for differentiation of cardiogenic precursors into endothelial endocardial cells
collaboration between GATA-6 (显示 GATA6 抗体) and GATA-4 (显示 GATA4 抗体), or GATA-6 (显示 GATA6 抗体) and GATA-5 which can substitute for GATA-4 (显示 GATA4 抗体), is involved in the perception of differentiation cues by embryonic stem cells in their determination of endoderm lineage
Data show that GATA4 or 6 regulate both cardiogenic potential and subsequent cardiomyocyte differentiation but that GATA5 is involved in regulating cardiomyocyte differentiation.
identified GATA5 as a SUMO substrate, and lysine 324 (K324) and lysine 360 (K360) as two major modification sites
specification of cardiac fate downstream of gata5 (显示 GATA6 抗体)/6 involves activation of the tmem88a gene to constrain WNT (显示 WNT2 抗体) signaling and expand the number of cardiac progenitors.
Overexpression of smarcd3b and gata5 in zebrafish results in an enlarged heart, whereas combinatorial loss of cBAF components inhibits cardiac differentiation, demonstrating that Smarcd3b and Gata5 can induce a primitive, progenitor cell-like state.
First evidence for a regulatory function for gata5 in the formation of Kupffer's vesicle and left-right patterning.
Grl forms a complex with Gata5 through the carboxyl region and can repress Gata5-mediated transcription.
Data show that GATA4 (显示 GATA4 抗体) knockdown only affects cardiac marker expression in the absence of either GATA5 (显示 GATA6 抗体) or GATA6 (显示 GATA6 抗体), suggesting redundancy in this family during myocardial development.
the gata5 genes are redundant for specification of cardiomyocytes.
The protein encoded by this gene is a transcription factor that contains two GATA-type zinc fingers. The encoded protein is known to bind to hepatocyte nuclear factor-1alpha (HNF-1alpha), and this interaction is essential for cooperative activation of the intestinal lactase-phlorizin hydrolase promoter. In other organisms, similar proteins may be involved in the establishment of cardiac smooth muscle cell diversity.
GATA binding factor-5
, GATA-binding factor 5
, GATA-binding protein 5
, transcription factor GATA-5
, Transcription factor GATA-5 (GATA binding factor-5)
, GATA-5 transcription factor
, GATA binding protein 5
, GATA-binding factor 5-A
, transcription factor xGATA-5a