Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development
about
Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhereDistribution and isolation of four laminin variants; tissue restricted distribution of heterotrimers assembled from five different subunitsMLC1 is associated with the dystrophin-glycoprotein complex at astrocytic endfeetMerosin, a tissue-specific basement membrane protein, is a laminin-like proteinPrimary structure of the human laminin A chain. Limited expression in human tissuesHuman laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissuesThe laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoformDiseased muscles that lack dystrophin or laminin-alpha2 have altered compositions and proliferation of mononuclear cell populationsLaminin isoforms in endothelial and perivascular basement membranesDystroglycan is a binding protein of laminin and merosin in peripheral nerveMild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chainIntegrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophyStructure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophyChondroitinase C Selectively Degrades Chondroitin Sulfate Glycosaminoglycans that Inhibit Axonal Growth within the Endoneurium of Peripheral NerveDistribution and function of laminins in the neuromuscular system of developing, adult, and mutant miceExpression and in vitro function of beta 1-integrin laminin receptors in the developing avian ciliary ganglion.A biologically active sequence of the laminin alpha2 large globular 1 domain promotes cell adhesion through syndecan-1 by inducing phosphorylation and membrane localization of protein kinase Cdelta.Improving Reproducibility of Phenotypic Assessments in the DyW Mouse Model of Laminin-α2 Related Congenital Muscular Dystrophy.Amelioration of laminin-alpha2-deficient congenital muscular dystrophy by somatic gene transfer of miniagrin.Laminins: structure and genetic regulation.Laminins and human disease.Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2.Defining the interaction of the Treponema pallidum adhesin Tp0751 with laminin.Basement membrane proteins: structure, assembly, and cellular interactions.Distinct and overlapping ligand specificities of the alpha 3A beta 1 and alpha 6A beta 1 integrins: recognition of laminin isoforms.Laminin-5 in the progression of carcinomas.The laminin family.Targeting Schwann cells by nonlytic arenaviral infection selectively inhibits myelinationDefective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse.Expression of laminins and their integrin receptors in different conditions of synovial membrane and synovial membrane-like interface tissue.Distribution patterns of extracellular matrix components and adhesion receptors are intricately modulated during first trimester cytotrophoblast differentiation along the invasive pathway, in vivo.Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology.Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle.Intestinal epithelial restitution. Involvement of specific laminin isoforms and integrin laminin receptors in wound closure of a transformed model epithelium.Altered expression of laminins in Crohn's disease small intestinal mucosaIncreased steady-state levels of mRNA coding for extracellular matrix components in kidneys of NZB/W F1 mice.Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.The spatial organization of Descemet's membrane-associated type IV collagen in the avian cornea.Partial laminin alpha2 chain restoration in alpha2 chain-deficient dy/dy mouse by primary muscle cell culture transplantation
P2860
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P2860
Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development
description
1988 nî lūn-bûn
@nan
1988 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի մարտին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Merosin, a protein specific fo ...... n nerve and muscle development
@ast
Merosin, a protein specific fo ...... n nerve and muscle development
@en
Merosin, a protein specific fo ...... nerve and muscle development.
@nl
type
label
Merosin, a protein specific fo ...... n nerve and muscle development
@ast
Merosin, a protein specific fo ...... n nerve and muscle development
@en
Merosin, a protein specific fo ...... nerve and muscle development.
@nl
prefLabel
Merosin, a protein specific fo ...... n nerve and muscle development
@ast
Merosin, a protein specific fo ...... n nerve and muscle development
@en
Merosin, a protein specific fo ...... nerve and muscle development.
@nl
P2860
P356
P1476
Merosin, a protein specific fo ...... n nerve and muscle development
@en
P2093
P2860
P304
P356
10.1073/PNAS.85.5.1544
P407
P577
1988-03-01T00:00:00Z