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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 104 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 EIA, WB - ABIN1108305
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 ABIN1108305
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
Human Monoclonal MSX1 Primary Antibody for ELISA, WB - ABIN969296
Mizokami, Egashira, Takekoshi, Itoh, Itoh, Osamura, Matsumae: Expression of MSX1 in human normal pituitaries and pituitary adenomas. in Endocrine pathology 2009
Show all 2 references for ABIN969296
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
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
Human Polyclonal MSX1 Primary Antibody for IHC (p), IHC - ABIN268531
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
Human Polyclonal MSX1 Primary Antibody for FACS, IF (cc) - 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
The results of this study suggest an association between CL/P susceptibility and SNP1 (show SNRNP70 Antibodies), located near the MSX1 gene, in the Mexican population.
Our study showed that TGFA (show TGFA Antibodies)/TGFB3 (show TGFB3 Antibodies)/MSX1 gene polymorphisms were associated with congenital NSHI. The distribution of genotype frequencies and allele frequencies of TGFA (show TGFA Antibodies) rs3771494, TGFB3 (show TGFB3 Antibodies) rs3917201 and rs2268626, and MSX1 rs3821949 and rs62636562 were significantly different between the case and the control groups
MSX1 was able to inhibit the Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signaling pathway, and that the ability to regulate the Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signaling pathway is critical for MSX1 to suppress glioblastoma cell migration and invasion.
mutations in MSX1 gene might play an important role in hypodontia cases involving pre-molars and is a risk factor for this ethnic population mainly of Arabs and is first report linking these mutations with tooth agenesis.
identification and characterization of a novel intronic mutation in the MSX1 gene in a large Chinese pedigree, adding to the small repertoire of MSX1 mutations associated with autosomal dominant tooth agenesis.
study reports 2 novel MSX1 mutations (c.739C>T; p.Pro247Ser and c.607G>A; p.Ala203Thr) in 2 Thai families; one is associated with preaxial polydactyly of the left hand, bilateral cleft lip and palate, hypodontia, microdontia and dens invaginatus; the other is associated with unilateral cleft lip and palate, microdontia and hypodontia
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.
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