Type I transglutaminase accumulation in the endoplasmic reticulum may be an underlying cause of autosomal recessive congenital ichthyosis

Journal of Biological Chemistry

Volumn 285, Issue 41, 2010, Pages 31634-31646

  Jiang, Haibing ^a   Jans, Ralph ^b   Xu, Wen ^a   Rorke, Ellen A ^a   Lin, Chen Yong ^a   Chen, Ya Wen ^a   Fang, Shengyun ^a   Zhong, Yongwang ^a   Eckert, Richard L ^a  

^a UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE   (United States)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AGGRESOME; AGGRESOMES; CHEMICAL CHAPERONE; ENDOPLASMIC RETICULUM; ENDOPLASMIC RETICULUM MEMBRANES; KERATINOCYTES; MISFOLDING; PATHOGENIC MECHANISMS; PLASMA MEMBRANES; PROTEIN MISFOLDING; SKIN DISEASE; TRANSGLUTAMINASES; UBIQUITINYLATION; UNDERLYING CAUSE;

CELL MEMBRANES;

CHAPERONE; MEMBRANE PROTEIN; PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE; PROTEIN GLUTAMINE GAMMA GLUTAMYLTRANSFERASE 1; UNCLASSIFIED DRUG; TRANSGLUTAMINASE 1;

AGGRESOME; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CELL MEMBRANE; CONTROLLED STUDY; DISEASE ASSOCIATION; ENDOPLASMIC RETICULUM; GENE MUTATION; HUMAN; HUMAN CELL; ICHTHYOSIS; KERATINOCYTE; PATHOGENESIS; POINT MUTATION; PRIORITY JOURNAL; PROTEIN FOLDING; PROTEIN PROCESSING; PROTEIN STRUCTURE; PROTEIN TRANSPORT; UBIQUITINATION; CELL CULTURE; ENZYMOLOGY; GENETIC DISORDER; GENETICS; MALE; METABOLISM;

CELL MEMBRANE; CELLS, CULTURED; ENDOPLASMIC RETICULUM; GENETIC DISEASES, INBORN; HUMANS; ICHTHYOSIS; KERATINOCYTES; MALE; POINT MUTATION; PROTEIN FOLDING; PROTEIN TRANSPORT; TRANSGLUTAMINASES; UBIQUITINATION;

EID: 77957783963     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.128645     Document Type: Article

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