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FOXD3 belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. 再加上，我们可以发FOXD3 试剂盒 (12) 和 FOXD3 蛋白 (6)和数多这个蛋白质的别的产品。
Showing 10 out of 89 products:
Human Monoclonal FOXD3 Primary Antibody for ELISA, WB - ABIN966161
Hromas, Moore, Johnston, Socha, Klemsz: Drosophila forkhead homologues are expressed in a lineage-restricted manner in human hematopoietic cells. in Blood 1993
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Human Monoclonal FOXD3 Primary Antibody for ELISA, WB - ABIN969152
Saleem, Banerjee-Basu, Berry, Baxevanis, Walter: Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1. in American journal of human genetics 2001
Human Monoclonal FOXD3 Primary Antibody for IHC, ELISA - ABIN969153
Gregory, Barlow, McLay, Kaul, Swarbreck, Dunham, Scott, Howe, Woodfine, Spencer, Jones, Gillson, Searle, Zhou, Kokocinski, McDonald, Evans, Phillips, Atkinson, Cooper, Jones, Hall, Andrews, Lloyd et al.: The DNA sequence and biological annotation of human chromosome 1. ... in Nature 2006
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Foxd3 rescues the prdm1a (显示 PRDM1 抗体) loss-of-function neural crest phenotype.
These results reveal dynamic and differential regulation of FoxD3 in distinct neural crest subpopulations, suggesting that heterogeneity is encrypted at the regulatory level
analysis of how a FoxD3 gene trap line reveals neural crest precursor movement and a role for FoxD3 in their specification
tfap2a (显示 TFAP2A 抗体) and foxd3 are expressed during gastrulation prior to neural crest induction in distinct, complementary, domains; tfap2a (显示 TFAP2A 抗体) is expressed in the ventral non-neural ectoderm and foxd3 in the dorsal mesendoderm and ectoderm
analysis of a Foxd3/mitfa (显示 MITF 抗体) transcriptional switch that governs whether a bi-potent pigment precursor will attain either an iridophore or a melanophore fate
foxd3 is an essential Nodal-dependent regulator of zebrafish mesoderm development.
Decrement of function of foxd3 and/or sox10, two genes important for the development and specification of neural crest, resulted in a reduction and/or loss of GnRH cells of the midbrain, as well as a reduction in the number of terminal nerve GnRH cells.
zebrafish Foxd3 is necessary for the differentiation of a subset of neural crest cell fates, perhaps in precursors of particular neural crest lineages.
Foxd3, a well-known regulator in neural crest development, is also involved in myf5 (显示 MYF5 抗体) regulation
Foxd3 selectively specifies premigratory neural crest cells for a neuronal, glial or cartilage fate by inducing the expression of lineage-associated transcription factors in these cells and regulating their subsequent migration.
On the basis of these data, FOXD3 is a potent repressor of DCLK1 (显示 DCLK1 抗体)-S expression in normal cells; loss of FOXD3 in hCCCs/hCRCs allows upregulation of DCLK1 (显示 DCLK1 抗体)-S, imparting a potent invasive potential to the cells
FOXD3 knockdown resulted in enhanced ATC (显示 SRPK1 抗体) proliferation, invasion and migration and diminished cellular apoptosis. Further, we showed that FOXD3 regulated expression of E-cadherin (显示 CDH1 抗体) by modulating MAPK (显示 MAPK1 抗体)/EKR signaling pathway that promotes EMT (显示 ITK 抗体) and metastasis during thyroid carcinogenesis.
Results show that FOXD3 expression was reduced in colon cancer cells. Its knockdown dramatically increased the proliferation of tumor cells, enhanced cell invasiveness and inhibited cell apoptosis. The study indicates that FOXD3 may play a protective role in human colon formation by regulating EGFR (显示 EGFR 抗体)/Ras/Raf (显示 RAF1 抗体)/MEK (显示 MAP2K1 抗体)/ERK (显示 EPHB2 抗体) signal pathway.
FOXO4 (显示 FOXO4 抗体) and FOXD3 were shown independently predictive of overall survival in gastric cancer
FOXD3/miR (显示 MLXIP 抗体)-214/MED19 (显示 MED19 抗体) axis is important for the regulation of growth, invasion and metastasis of colorectal cancer
total of 1799 differentially methylated regions were identified including SLC6A3, Rab40C, ZNF584, and FOXD3 whose significant methylation differences were confirmed in breast cancer patients through quantitative real-time polymerase chain reaction.Methylation of those aforementioned genes in white blood cells of our young patients may highlight their potential as early epimarkers
Results showed that silencing FoxD3 in lung cancer cell lines stimulated cell growth and inhibited cell apoptosis.
FOXD3 is sufficient but not necessary to drive PAX3 (显示 PAX3 抗体) expression in melanoma cells.
The present study finds that the aspirin-FOXD3-OLA1P2-STAT3 (显示 STAT3 抗体) axis exhibits exciting anticancer effects and provides new insights into the chemopreventive mechanisms underlying aspirin use
FOXD3 might serve as an independent prognostic biomarker and a potential therapeutic target for high-grade gliomas, which warrant further investigation.
FOXD3-AS1 (显示 ARSB 抗体) serves as a sponge or as a competing endogenous noncoding RNA for miR (显示 MLXIP 抗体)-150, restricting its capability to promote cell growth and thereby exaggerating hyperoxia-induced lung epithelial cell death
suggest that CHD7 (显示 CHD3 抗体), Oct3/4 (显示 POU5F1 抗体), Sox2 (显示 SOX2 抗体), and Nanog (显示 NANOG 抗体) directly induce FoxD3 expression when stimulated by BMP2 (显示 BMP2 抗体)/Wnt3a (显示 WNT3A 抗体) signaling, that FoxD3 promotes Sox10 (显示 SOX10 抗体) expression, and that histone H3K4 methylation play important roles in this process of neural crest-derived stem cell formation
this study shows that Foxd3 suppresses the production of IL-10 (显示 IL10 抗体)+ Breg cells by directly binding the IL-10 (显示 IL10 抗体) promoter
Foxd3 poises enhancers in pluripotent stem cells by recruiting multiple epigenetic enzymes that together simultaneously initiate and repress enhancer activity.
analysis of a cycle of activation and deactivation of Foxd3 required for exit from naive pluripotency and subsequent primordial germ cell specification
Foxd3 suppresses NFAT (显示 NFATC1 抗体)-mediated differentiation to maintain self-renewal of embryonic stem cells
In a xenograft tumor model, FOXD3 overexpression inhibits tumor growth and angiogenesis.
Data indicate that homeobox b5 (Hoxb5 (显示 HOXB5 抗体)) regulated the neural crest (NC)development by directly inducing Forkhead box D3 gene (Foxd3).
Foxd3 induced mutant ESCs (显示 NR2E3 抗体) precociously express genes required for mesoderm induction, but they are likely unable to differentiate into skeletal muscle.
Data indicate that growth factor receptor (显示 RYK 抗体) protein binding protein 2 (Grb2 (显示 GRB2 抗体)) is upregulated and regulated by Forkhead Box D3 (Foxd3), and pregulated Grb2 (显示 GRB2 抗体) interacts with huntingtin (Htt (显示 HTT 抗体)).
This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. Mutations in this gene cause autoimmune susceptibility 1.
fork head domain protein 6
, forkhead box protein D3
, mother superior
, forkhead box D3
, HNF3/FH transcription factor genesis
, HNF-3/forkhead homolog 2
, hepatocyte nuclear factor 3 forkhead homolog 2
, winged helix protein CWH-3
, winged-helix protein CWH-3