Linked Life Data

21545772

Source:http://linkedlifedata.com/resource/pubmed/id/21545772

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2011-5-6
pubmed:abstractText
The underlying molecular mechanism leading to the OPMD causing mutation in the PABPN1 gene has not been elucidated so far. Two models are under consideration: the first model is the polymerase slippage mechanism. The second model is unequal crossing over. The aim of the present study is to correlate clinical, fine structural, and molecular genetic data.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0722-5091
pubmed:author
pubmed:issnType
Print
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
94-103
pubmed:meshHeading
pubmed-meshheading:21545772-Aged, pubmed-meshheading:21545772-Aged, 80 and over, pubmed-meshheading:21545772-Female, pubmed-meshheading:21545772-Gene Expression Regulation, pubmed-meshheading:21545772-Humans, pubmed-meshheading:21545772-Intranuclear Inclusion Bodies, pubmed-meshheading:21545772-Male, pubmed-meshheading:21545772-Microscopy, Electron, Transmission, pubmed-meshheading:21545772-Middle Aged, pubmed-meshheading:21545772-Muscle, Skeletal, pubmed-meshheading:21545772-Muscle Weakness, pubmed-meshheading:21545772-Muscular Dystrophy, Oculopharyngeal, pubmed-meshheading:21545772-Mutation, pubmed-meshheading:21545772-Poly(A)-Binding Protein II, pubmed-meshheading:21545772-RNA, Messenger, pubmed-meshheading:21545772-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:21545772-Trinucleotide Repeat Expansion
pubmed:articleTitle
Oculopharyngeal muscle dystrophy: fine structure and mRNA expression levels of PABPN1.
pubmed:affiliation
Department of Neuropathology, University Hospital, RWTH Aachen, Germany. jmschroder@ukaachen.de
pubmed:publicationType
Journal Article