Mutation of human keratin 18 in association with cryptogenic cirrhosis
about
Identification of Mrj, a DnaJ/Hsp40 family protein, as a keratin 8/18 filament regulatory proteinKeratin attenuates tumor necrosis factor-induced cytotoxicity through association with TRADDKeratin 20 helps maintain intermediate filament organization in intestinal epitheliaPhosphorylation of human keratin 8 in vivo at conserved head domain serine 23 and at epidermal growth factor-stimulated tail domain serine 431Phosphorylation of human keratin 18 serine 33 regulates binding to 14-3-3 proteinsToward unraveling the complexity of simple epithelial keratins in human diseaseGenetic disorders of palm skin and nailHeat shock protein 70 expression, keratin phosphorylation and Mallory body formation in hepatocytes from griseofulvin-intoxicated miceCytokeratin 8 protects from hepatotoxicity, and its ratio to cytokeratin 18 determines the ability of hepatocytes to form Mallory bodiesHuman keratin diseases: the increasing spectrum of disease and subtlety of the phenotype-genotype correlation.Increased levels of keratin 16 alter epithelialization potential of mouse skin keratinocytes in vivo and ex vivo.Pairwise assembly determines the intrinsic potential for self-organization and mechanical properties of keratin filamentsKeratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies.Mutation analysis of human cytokeratin 8 gene in malignant rhabdoid tumor: a possible association with intracytoplasmic inclusion body formation.Keratins: guardians of the liver.Keratin expression in human tissues and neoplasms.Keratins in health and cancer: more than mere epithelial cell markersBile acid-induced Mallory body formation in drug-primed mouse liver.Simple epithelium keratins are required for maintenance of hepatocyte integrity.The keratin cytoskeleton in liver diseases.Incidental medical information in whole-exome sequencing.A disease- and phosphorylation-related nonmechanical function for keratin 8.Functional differences between keratins of stratified and simple epithelia.Mutation of a major keratin phosphorylation site predisposes to hepatotoxic injury in transgenic mice"IF-pathies": a broad spectrum of intermediate filament-associated diseases.Cryptogenic chronic hepatitis and its changing guise in adults.Defining Molecular Phenotypes of Mesenchymal and hematopoietic Stem Cells derived from Peripheral blood of Acute Lymphocytic Leukemia patients for regenerative stem cell therapy.Keratins modulate c-Flip/extracellular signal-regulated kinase 1 and 2 antiapoptotic signaling in simple epithelial cells.Establishment and molecular characterization of mesenchymal stem cell lines derived from human visceral & subcutaneous adipose tissues.Hepatocyte cytokeratins are hyperphosphorylated at multiple sites in human alcoholic hepatitis and in a mallory body mouse model.Lessons from keratin 18 knockout mice: formation of novel keratin filaments, secondary loss of keratin 7 and accumulation of liver-specific keratin 8-positive aggregates.Expression of regeneration-associated cytoskeletal proteins reveals differences and similarities between regenerating organs.Epidermolytic palmoplantar keratoderma due to a novel type of keratin mutation, a 3-bp insertion in the keratin 9 helix termination motifNovel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1
P2860
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P2860
Mutation of human keratin 18 in association with cryptogenic cirrhosis
description
1997 nî lūn-bûn
@nan
1997 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
name
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@ast
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@en
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@nl
type
label
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@ast
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@en
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@nl
prefLabel
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@ast
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@en
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@nl
P2093
P2860
P356
P1476
Mutation of human keratin 18 in association with cryptogenic cirrhosis
@en
P2093
P2860
P356
10.1172/JCI119127
P407
P577
1997-01-01T00:00:00Z