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MATN1 encodes a member of von Willebrand factor A domain containing protein family. Zusätzlich bieten wir Ihnen Matrilin 1, Cartilage Matrix Protein Antikörper (78) und Matrilin 1, Cartilage Matrix Protein Proteine (3) und viele weitere Produktgruppen zu diesem Protein an.
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The results show that matrilin-1 is indispensible for zebrafish cartilage formation and plays a role in the early collagen II-dependent developmental events.
Data suggest that matrilins 1 and 3 dose-dependently mediate weak cell attachment without promoting focal adhesion formation.
polymorphisms associated with mandibular retrognathism
Matrilin-1 is an inhibitor of neovascularization
this meta-analysis found an overall significant association of rs1149048 polymorphism with risk of AIS, especially in Asian population.
no significant difference in single nucleotide polymorphism between adolescent idiopathic scoliosis cases and controls
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 assembly
Genotyping results showed Matrilin-1 polymorphism haplotype TGC (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.
Pseudoachondroplasia is associated with mutations in the cartilage oligomatrix protein gene.
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 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 modulate collagen fibrillogenesis in cartilage and show that biochemical compensation might exist between matrilins, evidenced by Matn3 deficiency.
Data show that the cartilage matrix protein subdomain of type VII collagen is pathogenic for epidermolysis bullosa acquisita.
Transgenic mice expressing mutant (D469Delta) cartilage oligomeric matrix protein 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