A group of type I keratin genes on human chromosome 17: characterization and expression
about
Characterization of a 190-kilobase pair domain of human type I hair keratin genesKeratin 16 and keratin 17 mutations cause pachyonychia congenitaIsolation and characterization of ERBB3, a third member of the ERBB/epidermal growth factor receptor family: evidence for overexpression in a subset of human mammary tumorsThe genetic basis of Weber-Cockayne epidermolysis bullosa simplexIsolation, sequence, and expression of a human keratin K5 gene: transcriptional regulation of keratins and insights into pairwise controlOnset of re-epithelialization after skin injury correlates with a reorganization of keratin filaments in wound edge keratinocytes: defining a potential role for keratin 16Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skinIdentification of protein IT of the intestinal cytoskeleton as a novel type I cytokeratin with unusual properties and expression patternsS100A11, S100A10, annexin I, desmosomal proteins, small proline-rich proteins, plasminogen activator inhibitor-2, and involucrin are components of the cornified envelope of cultured human epidermal keratinocytesMutation of a type II keratin gene (K6a) in pachyonychia congenitacDNA cloning, expression, and assembly characteristics of mouse keratin 16.Linkage of epidermolysis bullosa simplex to keratin gene loci.Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevus.Identification of the genetic locus for keratosis palmaris et plantaris on chromosome 17 near the RARA and keratin type I genes.Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex.A mutation (Met-->Arg) in the type I keratin (K14) gene responsible for autosomal dominant epidermolysis bullosa simplex.Human keratin diseases: hereditary fragility of specific epithelial tissues.Allele frequencies and segregation of human polymorphic keratins K4 and K5Host regulatory network response to infection with highly pathogenic H5N1 avian influenza virus.Comparative map for mice and humans.Transcriptome and ultrastructural changes in dystrophic Epidermolysis bullosa resemble skin aging.Use of monospecific antisera and cRNA probes to localize the major changes in keratin expression during normal and abnormal epidermal differentiationThe use of retinoic acid to probe the relation between hyperproliferation-associated keratins and cell proliferation in normal and malignant epidermal cells.Epidermal differentiation: the bare essentialsThe amino acid sequence of component 7c, a type II intermediate-filament protein from wool.The basal keratin network of stratified squamous epithelia: defining K15 function in the absence of K14.TGF-beta and retinoic acid: regulators of growth and modifiers of differentiation in human epidermal cells.A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats.Keratin: a journey of three decades.Keith R. Porter Lecture, 1996. Of mice and men: genetic disorders of the cytoskeleton.Enhancer elements directing cell-type-specific expression of cytokeratin genes and changes of the epithelial cytoskeleton by transfections of hybrid cytokeratin genes.Overexpression of human keratin 16 produces a distinct skin phenotype in transgenic mouse skin.Microsequencing of proteins recorded in human two-dimensional gel protein databases.The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71.Molecular, cellular and histological changes in skin from a larval to an adult phenotype during bony fish metamorphosis.Defining the complex epithelia that comprise the canine claw with molecular markers of differentiation.Tissue selective expression of conditionally-regulated ROCK by gene targeting to a defined locus.Activation of the silent human cytokeratin 17 pseudogene-promoter region by cryptic enhancer elements of the cytokeratin 17 gene.Reorganization of the interchromosomal network during keratinocyte differentiation.
P2860
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P2860
A group of type I keratin genes on human chromosome 17: characterization and expression
description
1988 nî lūn-bûn
@nan
1988 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի փետրվարին 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
A group of type I keratin genes on human chromosome 17: characterization and expression
@ast
A group of type I keratin genes on human chromosome 17: characterization and expression
@en
A group of type I keratin genes on human chromosome 17: characterization and expression
@en-gb
A group of type I keratin genes on human chromosome 17: characterization and expression
@nl
type
label
A group of type I keratin genes on human chromosome 17: characterization and expression
@ast
A group of type I keratin genes on human chromosome 17: characterization and expression
@en
A group of type I keratin genes on human chromosome 17: characterization and expression
@en-gb
A group of type I keratin genes on human chromosome 17: characterization and expression
@nl
prefLabel
A group of type I keratin genes on human chromosome 17: characterization and expression
@ast
A group of type I keratin genes on human chromosome 17: characterization and expression
@en
A group of type I keratin genes on human chromosome 17: characterization and expression
@en-gb
A group of type I keratin genes on human chromosome 17: characterization and expression
@nl
P2093
P2860
P921
P356
P1476
A group of type I keratin genes on human chromosome 17: characterization and expression
@en
P2093
A RayChaudhury
M M Le Beau
M Rosenberg
P2860
P304
P356
10.1128/MCB.8.2.722
P407
P577
1988-02-01T00:00:00Z