rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
5
|
pubmed:dateCreated |
2008-11-27
|
pubmed:abstractText |
The Kindler syndrome (KS) protein kindlin-1 is a member of a protein complex that links cortical actin to integrins on the surface of basal keratinocytes. Loss of kindlin-1 leads to abnormalities of cell adhesion and motility, and to skin blistering and progressive poikiloderma as clinical symptoms.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
1365-2133
|
pubmed:author |
|
pubmed:issnType |
Electronic
|
pubmed:volume |
159
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1192-6
|
pubmed:meshHeading |
pubmed-meshheading:18652585-Adult,
pubmed-meshheading:18652585-Cell Adhesion,
pubmed-meshheading:18652585-Exons,
pubmed-meshheading:18652585-Frameshift Mutation,
pubmed-meshheading:18652585-Humans,
pubmed-meshheading:18652585-Immunoblotting,
pubmed-meshheading:18652585-Immunohistochemistry,
pubmed-meshheading:18652585-Keratinocytes,
pubmed-meshheading:18652585-Male,
pubmed-meshheading:18652585-Membrane Proteins,
pubmed-meshheading:18652585-Neoplasm Proteins,
pubmed-meshheading:18652585-Polymerase Chain Reaction,
pubmed-meshheading:18652585-Skin Diseases, Genetic
|
pubmed:year |
2008
|
pubmed:articleTitle |
C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytes.
|
pubmed:affiliation |
Department of Dermatology, University Medical Center Freiburg, Hauptstr. 7, 79104 Freiburg, Germany.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|