about
Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genesbmp1 and mini fin are functionally redundant in regulating formation of the zebrafish dorsoventral axisCharacterization of a novel gene product (mammalian tolloid-like) with high sequence similarity to mammalian tolloid/bone morphogenetic protein-1ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-beta bioavailability regulationOrder of intron removal influences multiple splice outcomes, including a two-exon skip, in a COL5A1 acceptor-site mutation that results in abnormal pro-alpha1(V) N-propeptides and Ehlers-Danlos syndrome type IBiosynthetic processing of the pro-alpha 1(V)2pro-alpha 2(V) collagen heterotrimer by bone morphogenetic protein-1 and furin-like proprotein convertasesA missense mutation in type VII collagen in two affected siblings with recessive dystrophic epidermolysis bullosaStructural organization and genetic localization of the human bone morphogenetic protein 1/mammalian tolloid geneBMP-1/Tolloid-like metalloproteases process endorepellin, the angiostatic C-terminal fragment of perlecanSecreted Frizzled-related protein 2 is a procollagen C proteinase enhancer with a role in fibrosis associated with myocardial infarctionCleavage and oligomerization of gliomedin, a transmembrane collagen required for node of ranvier formationBone morphogenetic protein 1 processes prolactin to a 17-kDa antiangiogenic factor.Induced ablation of Bmp1 and Tll1 produces osteogenesis imperfecta in mice.Characterization of the six zebrafish clade B fibrillar procollagen genes, with evidence for evolutionarily conserved alternative splicing within the pro-alpha1(V) C-propeptide.Post-translational proteolytic processing of procollagen C-terminal proteinase enhancer releases a metalloproteinase inhibitor.Low resolution structure determination shows procollagen C-proteinase enhancer to be an elongated multidomain glycoprotein.Procollagen C proteinase enhancer 1 genes are important determinants of the mechanical properties and geometry of bone and the ultrastructure of connective tissues.Biosynthetic processing of the Pro-alpha1(V)Pro-alpha2(V)Pro-alpha3(V) procollagen heterotrimer.Complete structural organization of the human alpha 1 (V) collagen gene (COL5A1): divergence from the conserved organization of other characterized fibrillar collagen genes.Interleukin-17-dependent autoimmunity to collagen type V in atherosclerosisStructural organization and expression patterns of the human and mouse genes for the type I procollagen COOH-terminal proteinase enhancer protein.Developmental roles of the BMP1/TLD metalloproteinases.α3(V) collagen is critical for glucose homeostasis in mice due to effects in pancreatic islets and peripheral tissuesInhibition of bone morphogenetic protein 1 by native and altered forms of alpha2-macroglobulin.Use of Bmp1/Tll1 doubly homozygous null mice and proteomics to identify and validate in vivo substrates of bone morphogenetic protein 1/tolloid-like metalloproteinasesMetalloproteinases in Drosophila to humans that are central players in developmental processes.ECM roles in the function of metabolic tissues.Homozygosity and Heterozygosity for Null Col5a2 Alleles Produce Embryonic Lethality and a Novel Classic Ehlers-Danlos Syndrome-Related PhenotypeAttenuated BMP1 function compromises osteogenesis, leading to bone fragility in humans and zebrafish.BMP1 controls TGFbeta1 activation via cleavage of latent TGFbeta-binding proteinComprehensive mass spectrometric mapping of the hydroxylated amino acid residues of the α1(V) collagen chain.Th-17, monokines, collagen type V, and primary graft dysfunction in lung transplantation.Mucosal Administration of Collagen V Ameliorates the Atherosclerotic Plaque Burden by Inducing Interleukin 35-dependent Tolerance.The bone morphogenetic protein 1/Tolloid-like metalloproteinasesSimian virus 40 large T antigen isoelectric focuses as multiple species with varying phosphate content.Expression of alpha 2 type I collagen in W8 cells increases cell adhesion and decreases colony formation in soft agar.Differential requirement for P2X7R function in IL-17 dependent vs. IL-17 independent cellular immune responses.TIMP-3 inhibits the procollagen N-proteinase ADAMTS-2.A translocation interrupts the COL5A1 gene in a patient with Ehlers-Danlos syndrome and hypomelanosis of Ito.COL5A1: fine genetic mapping and exclusion as candidate gene in families with nail-patella syndrome, tuberous sclerosis 1, hereditary hemorrhagic telangiectasia, and Ehlers-Danlos Syndrome type II
P50
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P50
description
hulumtues
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researcher
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wetenschapper
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հետազոտող
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name
Daniel S Greenspan
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Daniel S Greenspan
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Daniel S Greenspan
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Daniel S. Greenspan
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دانييل إس. جرينسبان
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type
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Daniel S Greenspan
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Daniel S Greenspan
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Daniel S Greenspan
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Daniel S. Greenspan
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دانييل إس. جرينسبان
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prefLabel
Daniel S Greenspan
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Daniel S Greenspan
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Daniel S Greenspan
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Daniel S. Greenspan
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دانييل إس. جرينسبان
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P106
P1153
7102791607
P21
P31
P496
0000-0001-8096-7446