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MATN1 encodes a member of von Willebrand factor A domain containing protein family.
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Human Monoclonal MATN1 Primary Antibody für ICC, ELISA - ABIN969278
Chamberlin, Ubagai, Mudd, Levy, Chou: Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene. in American journal of human genetics 1997
Show all 2 Pubmed References
Human Polyclonal MATN1 Primary Antibody für IF (p), IHC (p) - ABIN676178
Park, Woo, Lee: Ionically cross-linkable hyaluronate-based hydrogels for injectable cell delivery. in Journal of controlled release : official journal of the Controlled Release Society 2014
Human Polyclonal MATN1 Primary Antibody für IHC, IHC (p) - ABIN4332838
Bell, Piróg, Fresquet, Thornton, Boot-Handford, Briggs: Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation. in Arthritis and rheumatism 2012
The results show that matrilin-1 is indispensible for zebrafish cartilage formation and plays a role in the early collagen II-dependent developmental events.
Matrilin-1 is an inhibitor of neovascularization
this meta-analysis found an overall significant association of rs1149048 polymorphism with risk of AIS (zeige AR Antikörper), especially in Asian population.
The A allele of single nucleotide polymorphism rs1065755 in the MATN1 gene is associated with adolescent idiopathic scoliosis.
we concluded that MATN1 SNP is not associated with either adolescent idiopathic scoliosis predisposition or curve severity in Japanese.
There is an association between matrilin-1 levels and curve progression in adolescent idiopathic scoliosis.
Genotype GG of matrilin-1 gene is indicative of less bracing effectiveness in adolescent idiopathic scoliosis.
Matrilin-1 A-domains have a role in cartilage ECM (zeige MMRN1 Antikörper) assembly
Genotyping results showed Matrilin-1 polymorphism haplotype TGC (zeige TGM2 Antikörper) (ht4; 158T, 7987G, and 8572C alleles) had pronounced risk effect for mandibular prognathism compared with controls.
The tagSNP rs1149048 polymorphism in the MATN1 promoter region is associated with both susceptibility and disease severity in adolescent idiopathic scoliosis.
the tagSNP rs1149048 polymorphism in the MATN1 promoter region was associated with both susceptibility and disease progression in adolescent idiopathic scoliosis .
Results provide evidence that Matn1 plays a protective role in cartilage degeneration under altered mechanical environment.
Secretion of matrilin 3 (zeige MATN3 Antikörper) V194D mutant protein is not dependent on hetero-oligomerization with matrilin 1.
Expression of matrilin-1 during maturation of mouse skeletal tissues
The chondrocytes of the presumptive articular surface therefore appear to arise directly from a subpopulation of early chondrocytes that do not activate matrilin-1 expression rather than by redifferentiation from the flattened cells of the interzone.
Matrilin-1 and matrilin-3 (zeige MATN3 Antikörper) modulate collagen fibrillogenesis in cartilage and show that biochemical compensation might exist between matrilins, evidenced by Matn3 (zeige MATN3 Antikörper) deficiency.
Data show that the cartilage matrix protein subdomain of type VII (zeige TH Antikörper) collagen is pathogenic for epidermolysis bullosa acquisita.
Transgenic mice expressing mutant (D469Delta) cartilage oligomeric matrix protein (zeige COMP Antikörper) showed a slight gender specific growth retardation and both, tibial growth plate and sternum abnormalities.
This gene encodes a member of von Willebrand factor A domain containing protein family. This family of proteins are thought to be involved in the formation of filamentous networks in the extracellular matrices of various tissues. Mutations of this gene have been associated with variety of inherited chondrodysplasias.
matrilin 1, cartilage matrix protein
, matrilin 1
, cartilage matrix protein
, cartilage matrix protein-like
, matrilin 1, cartilage matrix protein 1