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Conclusions MEIS1 variants were associated with an increased risk of RLS in migraine patients. It is possible that an imbalance in iron homeostasis and the dopaminergic system may represent a link between RLS incidence and migraines.
We speculate that ACTR2 and MEIS1 might respectively play a role in the pathogenesis of the observed deafness and cardiomyopathy...the patient carrying a 2p14p15 deletion including OTX1 had normal kidneys and genitalia, thus confirming that OTX1 haploinsufficiency is not invariably associated with genitourinary defects.
results reveal that MEIS1, through induction of SYTL1, promotes leukemogenesis and supports leukemic cell homing and engraftment, facilitating interactions between leukemic cells and bone marrow stroma.
Meis1 regulates expression and activation of Syk (show SYK ELISA Kits) in Hoxa9 (show HOXA9 ELISA Kits)-driven leukemia.
Here we present the result of a 4-stage genome-wide association study composed of 5,953 adolescent idiopathic scoliosis patients and 8,137 controls. Overall, we identified three novel susceptible loci including rs7593846 at 2p14 near MEIS1 , rs7633294 at 3p14.1 near MAGI1 (show MAGI1 ELISA Kits) and rs9810566 at 3q26.2 near TNIK (show TNIK ELISA Kits)
Results show that Meis1 may have a positive feedback with Msi1 (show MSI1 ELISA Kits) during the esophageal squamous cell carcinoma progression.
Meis1 functions as an important regulator during the progression of acute myeloid leukemia (show BCL11A ELISA Kits).
MEIS1 drivesMalignant peripheral nerve sheath tumors cell growth via the transcription factor ID1 (show ID1 ELISA Kits), thereby suppressing expression of the cell cycle inhibitor p27 (show PAK2 ELISA Kits)(Kip (show CIB1 ELISA Kits)) and maintaining cell survival.
it was observed that ER stimulated gene expression by interacting with MEIS1 and FOXP3 (show FOXP3 ELISA Kits), and ER inhibited gene expression by interacting with THRB (show THRB ELISA Kits) and GRHL1 (show GRHL1 ELISA Kits).
this is the first report on the MEIS1 gene in esophageal squamous cell carcinoma
Hth+Tsh-induced tissue overgrowth requires the BMP2 (show BMP2 ELISA Kits) Dpp (show TGFb ELISA Kits) and the abnormal hyperactivation of its pathway. Rather than using autocrine Dpp (show TGFb ELISA Kits) expression, Hth+Tsh cells increase their avidity for Dpp (show TGFb ELISA Kits), produced locally, by upregulating extracellular matrix components.
the satellite repeats get transcribed in wild type embryos and that this transcription depends on the presence of Hth, which binds to them as well as to the ribosomal DNA region.
The retinal determination gene Dachshund restricts cell proliferation by limiting the activity of the Homothorax-Yorkie (show YAP1 ELISA Kits) complex
Hth functions together with its co-factor Extradenticle to repress the R8-specific factor Senseless in dorsal rim (show RBBP8 ELISA Kits) area R8 cells, allowing expression of an ultraviolet-sensitive R7 Rhodopsin (show RHO ELISA Kits).
Functional dissection of the splice variants of the Drosophila gene homothorax (hth
Data indicate that loss of Lethal giant larvae (Lgl) tumor suppressor in the wing primordium induced epithelial neoplasia in its Homothorax (Hth)-expressing proximal domain.
cooperative binding sites for En, with the homeodomain-containing Hox (show MSH2 ELISA Kits) cofactors Extradenticle (Exd) and Homothorax (Hth) was localized, within two CRMs that drive similar expression patterns
Hox (show MSH2 ELISA Kits) genes and homothorax are required for motoneuron survival.
In the flight muscles, exd and hth are genetically upstream of another muscle identity gene, salm, and are direct transcriptional regulators of the signature flight muscle structural gene, Actin88F.
Loss of Ct and Hth in the antenna disc resulted in ectopic eye development in the antenna.
Data indicate that MiR (show MYLIP ELISA Kits)-144 regulates primitive hematopoiesis through repression of meis1 during embryogenesis.
Loss of meis1 is associated with impaired hematopoiesis as well as vascular development.
This study demonistrated that Meis1 plays an important role in establishing the retinotectal map and organizing the visual system in zebrafish.
The Hox (show MSH2 ELISA Kits) cofactor Meis1 acts upstream of gata1 (show GATA1 ELISA Kits) to regulate primitive hematopoiesis.
Results implicate meis1 as a positive cell cycle regulator in early retinal cells, and provide evidence of an evolutionary conserved function for Hth/Meis genes in the maintenance of the proliferative, multipotent cell state during early eye development.
These results implicate that meis1 is a novel regulator involved in endothelial cell development, presumably affecting the vegf signaling pathway.
Data show that Irx7 and Irx1b are required for the proper formation and specification of rhombomeres 1 to 4, and that Irx7 functionally interacts with Meis1.1 to activate the expression of anterior hindbrain markers, such as krox20 (show EGR2 ELISA Kits).
Results show Meis1 Is expressed in normal and aberrant ducts, pancreatic intraepithelial neoplasia, and pancreatic ductal adenocarcinoma and that its expression increases cell migration in pancreatic cancer through transcriptional activation of Mcam (show MCAM ELISA Kits).
the Hoxa9 (show HOXA9 ELISA Kits)- and Meis1-associated upregulation of Flt3 (show FLT3 ELISA Kits) is a passive event with regard to leukemia development in mice and with limited relevance to the AML (show RUNX1 ELISA Kits) pathology.
We found that expression of Emx2 (show EMX2 ELISA Kits) and Lhx2 (show LHX2 ELISA Kits) initiated between neuronal progenitor and neuronal precursor stages. As far as the sensory neurons of the vomeronasal organ are concerned, Meis1 and Meis2 (show MEIS2 ELISA Kits) were only expressed in the apical layer, together with Gnai2 (show GNAI2 ELISA Kits), but not in the basal layer.
we show that simultaneous deletion of Meis1 and Meis2 (show MEIS2 ELISA Kits) in presumptive lens ectoderm results in arrested lens development in the pre-placodal stage, and neither lens placode nor lens is formed. We found that in the presumptive lens ectoderm of Meis1/Meis2 (show MEIS2 ELISA Kits) deficient embryos Pax6 (show PAX6 ELISA Kits) expression is absent
Meis1 is a major regulator of sympathetic target-field innervation and Meis1 deficient sympathetic neurons die by apoptosis from early embryonic stages to perinatal stages.
PCBP2 (show PCBP2 ELISA Kits) overexpression rescues the Meis1 effects of Akt (show AKT1 ELISA Kits)-mTOR (show FRAP1 ELISA Kits) pathway and hypertrophy of cardiomyocytes.
Data indicate roles of myeloid ecotropic viral integration site 1 protein (Meis1) in both megakaryopoiesis and erythropoiesis.
Tumorigenesis by Meis1 overexpression is accompanied by a change of DNA target-sequence specificity which allows binding to the AP-1 (show JUN ELISA Kits) element.
Sequential binding of MEIS1 and NKX2-5 (show NKX2-5 ELISA Kits) on the Popdc2 (show POPDC2 ELISA Kits) gene demonstrate a mechanism for spatiotemporal regulation of enhancers during cardiogenesis.
Pbx3 contributes to Hoxa9 (show HOXA9 ELISA Kits) leukemogenesis through stabilization of the Meis1 protein.
Homeobox genes, of which the most well-characterized category is represented by the HOX genes, play a crucial role in normal development. In addition, several homeoproteins are involved in neoplasia. This gene encodes a homeobox protein belonging to the TALE ('three amino acid loop extension') family of homeodomain-containing proteins.
Meis1, myeloid ecotropic viral integration site 1 homolog
, homeobox protein Meis1
, leukemogenic homolog protein
, XMeis1-2 protein
, Meis homeobox 1
, gene II
, homeobox protein Meis1-like
, myeloid ecotropic viral integration site 1
, myeloid ecotropic viral insertion site-1a protein