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rdf:type |
|
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lifeskim:mentions |
umls-concept:C0013018,
umls-concept:C0015576,
umls-concept:C0079153,
umls-concept:C0170518,
umls-concept:C0205314,
umls-concept:C0324403,
umls-concept:C0332281,
umls-concept:C0547040,
umls-concept:C0679622,
umls-concept:C1280551,
umls-concept:C1416714,
umls-concept:C1519478
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pubmed:issue |
1
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|
pubmed:dateCreated |
2005-7-20
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|
pubmed:abstractText |
Epidermolytic hyperkeratosis in humans is caused by dominant-negative mutations in suprabasal epidermal keratins 1 and 10. However, spontaneous keratin mutations have not been confirmed in a species other than human.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0007-0963
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
153
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
51-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:16029326-Animals,
pubmed-meshheading:16029326-Dog Diseases,
pubmed-meshheading:16029326-Dogs,
pubmed-meshheading:16029326-Female,
pubmed-meshheading:16029326-Gene Expression,
pubmed-meshheading:16029326-Genes, Recessive,
pubmed-meshheading:16029326-Hyperkeratosis, Epidermolytic,
pubmed-meshheading:16029326-Keratin-10,
pubmed-meshheading:16029326-Keratins,
pubmed-meshheading:16029326-Male,
pubmed-meshheading:16029326-Pedigree,
pubmed-meshheading:16029326-Point Mutation,
pubmed-meshheading:16029326-RNA Splice Sites,
pubmed-meshheading:16029326-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:16029326-Skin
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pubmed:year |
2005
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pubmed:articleTitle |
Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs.
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pubmed:affiliation |
Comparative Dermatology Laboratory, Texas A&M University, College Station, TX, USA. credillekm@lilly.com
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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