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Homeodomain proteins, such as MIXL1, are transcription factors that regulate cell fate during development (Hart et al., 2005 [PubMed 15982639]).[supplied by OMIM, Mar 2008].. 再加上，我们可以发MIXL1 蛋白 (4) 和 和数多这个蛋白质的别的产品。
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Findings support the existence of a novel MIXL1-c REL (显示 NFkBP65 抗体) mediated survival axis in AML (显示 RUNX1 抗体) that can be targeted by BMPR1 (显示 BMPR1A 抗体) inhibitors. (MIXL1- human gene, Mixl1- mouse ortholog, MIXL1- protein).
results demonstrate that Mixl1 and Flk1 (显示 KDR 抗体) play roles...during dimethyl sulfoxide-induced mesodermal specification in P19 (显示 CDKN2D 抗体) cells.
Brachyury (显示 TBX1 抗体) and related Tbx proteins interact with the Mixl1 homeodomain protein and negatively regulate Mixl1 transcriptional activity
These results demonstrate for a functional role for TGF-beta (显示 TGFB1 抗体) ligands in regulation of mammalian Mixl1, identify FoxH1 (显示 FOXH1 抗体) as an essential co-activator, and implicate Nodal as the embryonic regulator of Mixl1 in mesendoderm morphogenesis.
MIXL1 protein is differentially expressed in non-Hodgkin lymphoma and Hodgkin lymphoma; findings suggest that MIXL1 overexpression may play a role in driving proliferatin or blocking differentiation in lymphoma oncogenesis
Targeted insertion in human embryonic stem cells of sequences encoding green fluorescent protein (GFP) into the locus of MIXL1, a gene transiently expressed in the primitive streak during embryogenesis.
In this study, we demonstrated that forced expression of Mix-like protein 1 (encoded by Mixl1) can be used to guide contribution of mouse embryonic stem cells to endodermal organs after blastocyst injection.
Embryonic localization of Mixl1 shows its co-localized with the early hematopoietic marker, Runx1 (显示 RUNX1 抗体), in the allantois and visceral yolk sac (显示 ADCY10 抗体) blood islands.
At later stages, in contrast with wild-type embryos, E7.5-8.0, Mixl1 knockout (KO) KO/KO (显示 KRT8 抗体) embryos lacked morphologically recognizable midline structures such as the node and notochord.
These data support the hypothesis that Mixl1 directly regulates Pdgfralpha and Flk1 (显示 KDR 抗体) gene expression.
results strongly suggest that Gsc (显示 GSC 抗体) is a direct target gene of Mixl1 during embryogenesis.
required for the morphogenesis of axial mesoderm, the heart and the gut (显示 GUSB 抗体) during embryogenesis
Mixl1 is required for efficient haematopoiesis and BMP4 (显示 BMP4 抗体)-induced ventral mesoderm patterning in differentiating ES cells
all mice reconstituted with Mixl1-transduced bone marrow developed fatal, transplantable acute myeloid leukemia (显示 BCL11A 抗体) with a mean latency period of 200 days
As goosecoid (显示 GSC 抗体) is itself induced in a Foxh1 (显示 FOXH1 抗体)-dependent manner, we propose that Foxh1 (显示 FOXH1 抗体) initiates positive and negative transcriptional circuits to refine cell fate decisions during gastrulation
Homeodomain proteins, such as MIXL1, are transcription factors that regulate cell fate during development (Hart et al., 2005
Mix1 homeobox-like 1 (Xenopus laevis)
, Mix-like homeobox protein 1
, MIX1 homeobox-like protein 1
, homeobox protein MIXL1
, homeodomain protein MIX
, mix.1 homeobox-like protein
, CMIX homeobox
, Mix1 homeobox-like 1