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MSX1 encodes a member of the muscle segment homeobox gene family. Additionally we are shipping MSX1 Proteins (18) and MSX1 Kits (4) and many more products for this protein.
Showing 10 out of 92 products:
Human Polyclonal MSX1 Primary Antibody for DB, EIA - ABIN493137
Davidson: The function and evolution of Msx genes: pointers and paradoxes. in Trends in genetics : TIG 1995
Show all 4 references for ABIN493137
Human Monoclonal MSX1 Primary Antibody for ELISA, WB - ABIN969296
Li, Cui, Fang, Mei: [A novel mutation of MSX1 gene in a Chinese pedigree with oligodontia]. in Zhonghua kou qiang yi xue za zhi = Zhonghua kouqiang yixue zazhi = Chinese journal of stomatology 2008
Show all 2 references for ABIN969296
Dog (Canine) Polyclonal MSX1 Primary Antibody for WB - ABIN2779956
Lee, Andersen, Cabernard, Manning, Tran, Lanskey, Bashirullah, Doe: Drosophila Aurora-A kinase inhibits neuroblast self-renewal by regulating aPKC/Numb cortical polarity and spindle orientation. in Genes & development 2006
Show all 2 references for ABIN2779956
Dog (Canine) Polyclonal MSX1 Primary Antibody for IHC, WB - ABIN2777275
Djoussé, Knowlton, Hayden, Almqvist, Brinkman, Ross, Margolis, Rosenblatt, Durr, Dode, Morrison, Novelletto, Frontali, Trent, McCusker, Gómez-Tortosa, Mayo Cabrero, Jones, Zanko, Nance, Abramson, Suchowersky, Paulsen, Harrison, Yang, Cupples, Mysore, Guse: Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. in Neurogenetics 2004
Show all 2 references for ABIN2777275
Human Polyclonal MSX1 Primary Antibody for IF (cc), IF (p) - ABIN1385926
Mu, Wu, Zhu, Li, Tang, Yao, Yang, Peng, Li, Hua: The function of Msx1 gene in promoting meiosis of dairy goat male germline stem cells (mGSCs). in Cell biochemistry and function 2013
Human Polyclonal MSX1 Primary Antibody for IHC, ELISA - ABIN185250
Blin-Wakkach, Lezot, Ghoul-Mazgar, Hotton, Monteiro, Teillaud, Pibouin, Orestes-Cardoso, Papagerakis, Macdougall, Robert, Berdal: Endogenous Msx1 antisense transcript: in vivo and in vitro evidences, structure, and potential involvement in skeleton development in mammals. in Proceedings of the National Academy of Sciences of the United States of America 2001
Cow (Bovine) Polyclonal MSX1 Primary Antibody for EIA, IHC (p) - ABIN374442
Villafranca, Lázaro, Salinas, Garcés: Stimulated Brillouin scattering gain profile characterization by interaction between two narrow-linewidth optical sources. in Optics express 2009
The SNPs rs3821949 and rs12532 in the MSX1 gene were associated with congenital heart diseases in Chinese Han populations.
The sequence dependence of local conformation of DNA enables MSX1 glutamine50>lysine to make hydrogen bond with its target nucleotide(s) of DNA.
a Japanese family with nonsyndromic tooth agenesis caused by a novel nucleotide substitution in the intronic region between exons 1 and 2 of the MSX1 gene, is reported.
TBP (show TBP Antibodies) attenuates Msx1-mediated glycoprotein hormone alpha (show CGA Antibodies) transcriptional repression.
From a genetically diverse etiology MSX 1 799 G >T gene variant may be a good screening marker for NSCL (show NHLH1 Antibodies)/P in Raichur patients
Results were suggestive of a positive association between MSX1 rs11726039 and non-syndromic cleft lip with or without cleft palate in the South Indian population.
The present study provides no evidence that MSX1 polymorphisms (rs3775261, rs1042484, rs12532, rs6446693, rs4464513 and rs1907998) play a major role in non-syndromic cleft lip and/or palate
Methylation changes were enriched in MSX1, CCND2 (show CCND2 Antibodies), and DAXX (show DAXX Antibodies) at specific loci within the hippocampus of patients with schizophrenia and bipolar disorder.
A comprehensive meta-analysis of 4 case-control studies was conducted to explore the association between polymorphisms of Msh homeobox 1 (MSX1) and transforming growth factor-beta1 (TGF-beta1 (show TGFB1 Antibodies)) genes and hypodontia.
a non-stop (show USP22 Antibodies) mutation in MSX1 is responsible for oligodontia
Msx1 may play a role in repressing gene expression in the fetal and postnatal periods.
Data show that the spatiotemporal expression of claudin-1 (show CLDN1 Antibodies) is dysregulated in homeobox (show PRRX1 Antibodies) (Msx) genes Msx1d/d/Msx2d/d uteri.
MSX1 linked the arterial shear stimulus to arteriogenic remodeling by activating the endothelial but not medial layer to a proinflammatory state because EC but not smooth muscle cell
Msx1 and Msx2 are direct transcriptional targets of Lhx2 (show LHX2 Antibodies).
Msx1 appears to act as a modeling factor for membranous bone.
analysis of a BMP signaling pathway that regulates the expression of the odontogenic gene Msx1 and determines the fate of dental mesenchyme during early tooth development
Msx1 supports vascular mineralization by directing the osteogenic programming of aortic progenitors in diabetic arteriosclerosis.
Msx1 and Msx2 proteins activate Atoh1 (show ATOH1 Antibodies) transcription by specifically interacting with several homeodomain binding sites in the Atoh1 (show ATOH1 Antibodies) 3' enhancer.
Study concludes that MSX1 may promote proliferation and prevent the differentiation of dental mesenchymal cells by the inhibition of Bmp2 (show BMP2 Antibodies) and Bmp4 (show BMP4 Antibodies) expression.
Msx1 interacts with Lhx6 (show LHX6 Antibodies) and Sna (show SNAI1 Antibodies) in vivo. A network of transcription factors operates during early tooth morphogenesis.
Msx1 functions as a negative regulator early in pituitary development by repressing the gonadotrope-specific alphaGSU (show CGA Antibodies) and GnRHR (show GNRHR Antibodies) genes.
Suppression of MSX1 affects oocyte maturation, embryo cleavage rate, and expression of numerous genes suggesting important role for MSX1 in embryo development.
This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia.
, homeobox protein Hox-7
, homeobox protein MSX-1
, msh homeo box 1
, msh homeobox 1-like protein
, msh homeobox homolog 1
, homeo box, msh-like 1
, homeobox, msh-like 1
, muscle-segment homeobox
, msh homeo box homolog 1
, Hbox 7
, homeobox protein GHOX-7