Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
about
Dominant dystrophic epidermolysis bullosa: identification of a Gly-->Ser substitution in the triple-helical domain of type VII collagenPremature termination codons on both alleles of the type VII collagen gene (COL7A1) in three brothers with recessive dystrophic epidermolysis bullosaLocalization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locusLaminin 5 binds the NC-1 domain of type VII collagenA new FACIT of the collagen family: COL21A1Interactions of the amino-terminal noncollagenous (NC1) domain of type VII collagen with extracellular matrix components. A potential role in epidermal-dermal adherence in human skinWARP is a new member of the von Willebrand factor A-domain superfamily of extracellular matrix proteinsAminoglycosides restore full-length type VII collagen by overcoming premature termination codons: therapeutic implications for dystrophic epidermolysis bullosa.Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus.Diagnostic dilemma of "sporadic" cases of dystrophic epidermolysis bullosa: a new dominant or mitis recessive mutation?Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities.Injection of recombinant human type VII collagen corrects the disease phenotype in a murine model of dystrophic epidermolysis bullosa.Epitope mapping of type VII collagen. Identification of discrete peptide sequences recognized by sera from patients with acquired epidermolysis bullosa.Laminins and human disease.Prevalence of collagen VII-specific autoantibodies in patients with autoimmune and inflammatory diseasesThe genetics of human skin disease.Human type VII collagen: genetic linkage of the gene (COL7A1) on chromosome 3 to dominant dystrophic epidermolysis bullosa.Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation.Molecular genetics of the cutaneous basement membrane zone. Perspectives on epidermolysis bullosa and other blistering skin diseases.Type VII collagen gene expression by cultured human cells and in fetal skin. Abundant mRNA and protein levels in epidermal keratinocytesGenetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils.Dystrophic epidermolysis bullosa.Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene.Recurrent nonsense mutations within the type VII collagen gene in patients with severe recessive dystrophic epidermolysis bullosa.The modular architecture of vertebrate collagens.Prenatal diagnosis for recessive dystrophic epidermolysis bullosa in 10 families by mutation and haplotype analysis in the type VII collagen gene (COL7A1)Basic fibroblast growth factor: a missing link between collagen VII, increased collagenase, and squamous cell carcinoma in recessive dystrophic epidermolysis bullosa.Transforming growth factor-beta stimulates collagen VII expression by cutaneous cells in vitroDetection of Type VII Collagen Autoantibodies Before the Onset of Bullous Systemic Lupus Erythematosus.Clinical presentation, pathogenesis, diagnosis, and treatment of epidermolysis bullosa acquisitaAutoimmunity against type VII collagen in inflammatory bowel diseaseType VII collagen: the anchoring fibril protein at fault in dystrophic epidermolysis bullosa.Epidermolysis bullosa acquisita.The recombinant expression of full-length type VII collagen and characterization of molecular mechanisms underlying dystrophic epidermolysis bullosa.Immune mechanism-targeted treatment of experimental epidermolysis bullosa acquisita.Deletion of the R78 G protein-coupled receptor gene from rat cytomegalovirus results in an attenuated, syncytium-inducing mutant strain.Characterization of molecular mechanisms underlying mutations in dystrophic epidermolysis bullosa using site-directed mutagenesis.Expression of integrins and basement membrane components by wound keratinocytes.Autoantibodies to type VII collagen mediate Fcgamma-dependent neutrophil activation and induce dermal-epidermal separation in cryosections of human skin.The carboxyl terminus of type VII collagen mediates antiparallel dimer formation and constitutes a new antigenic epitope for epidermolysis Bullosa acquisita autoantibodies.
P2860
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P2860
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
description
1991 nî lūn-bûn
@nan
1991 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@ast
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@en
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@nl
type
label
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@ast
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@en
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@nl
prefLabel
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@ast
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@en
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@nl
P2093
P2860
P356
P1476
Human type VII collagen: cDNA cloning and chromosomal mapping of the gene
@en
P2093
D T Woodley
J Ryynänen
M G Mattei
M G Parente
P2860
P304
P356
10.1073/PNAS.88.16.6931
P407
P577
1991-08-15T00:00:00Z