Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5197
pubmed:dateCreated
1995-2-16
pubmed:abstractText
Lamellar ichthyosis is a severe congenital skin disorder characterized by generalized large scales and variable redness. Affected individuals in three families exhibited drastically reduced keratinocyte transglutaminase (TGK) activity. In two of these families, expression of TGK transcripts was diminished or abnormal and no TGK protein was detected. Homozygous or compound heterozygous mutations of the TGK gene were identified in all families. These data suggest that defects in TGK cause lamellar ichthyosis and that intact cross-linkage of cornified cell envelopes is required for epidermal tissue homeostasis.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0036-8075
pubmed:author
pubmed:issnType
Print
pubmed:day
27
pubmed:volume
267
pubmed:geneSymbol
TGK
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
525-8
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:7824952-Base Sequence, pubmed-meshheading:7824952-Cell Membrane, pubmed-meshheading:7824952-Cells, Cultured, pubmed-meshheading:7824952-Codon, pubmed-meshheading:7824952-Female, pubmed-meshheading:7824952-Gene Deletion, pubmed-meshheading:7824952-Genetic Linkage, pubmed-meshheading:7824952-Heterozygote, pubmed-meshheading:7824952-Homozygote, pubmed-meshheading:7824952-Humans, pubmed-meshheading:7824952-Ichthyosis, Lamellar, pubmed-meshheading:7824952-Introns, pubmed-meshheading:7824952-Keratinocytes, pubmed-meshheading:7824952-Male, pubmed-meshheading:7824952-Membrane Proteins, pubmed-meshheading:7824952-Molecular Sequence Data, pubmed-meshheading:7824952-Mutation, pubmed-meshheading:7824952-Pedigree, pubmed-meshheading:7824952-Point Mutation, pubmed-meshheading:7824952-Protein Precursors, pubmed-meshheading:7824952-Transglutaminases
pubmed:year
1995
pubmed:articleTitle
Mutations of keratinocyte transglutaminase in lamellar ichthyosis.
pubmed:affiliation
Department of Dermatology, Centre Hospitalier Universitaire Vandois (CHUV), Hôpital de Beaumont, Lausanne, Switzerland.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't