Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2009-7-27
pubmed:abstractText
A single nucleotide polymorphism in the 3'-untranslated region of the progranulin gene (GRN; 3'UTR+78C>T; rs5848) was reported to alter the risk for frontotemporal lobar degeneration with ubiquitin-positive inclusions (FTLD-U). rs5848 is located within a micro-RNA binding site and affects the expression of GRN.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1468-1331
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
909-11
pubmed:meshHeading
pubmed-meshheading:19473366-Adult, pubmed-meshheading:19473366-Aged, pubmed-meshheading:19473366-Aged, 80 and over, pubmed-meshheading:19473366-European Continental Ancestry Group, pubmed-meshheading:19473366-Female, pubmed-meshheading:19473366-Gene Frequency, pubmed-meshheading:19473366-Genetic Predisposition to Disease, pubmed-meshheading:19473366-Genotype, pubmed-meshheading:19473366-Humans, pubmed-meshheading:19473366-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:19473366-Male, pubmed-meshheading:19473366-Middle Aged, pubmed-meshheading:19473366-Parkinson Disease, pubmed-meshheading:19473366-Poland, pubmed-meshheading:19473366-Polymorphism, Single Nucleotide, pubmed-meshheading:19473366-Risk Factors, pubmed-meshheading:19473366-United States, pubmed-meshheading:19473366-Young Adult
pubmed:year
2009
pubmed:articleTitle
GRN 3'UTR+78 C>T is not associated with risk for Parkinson's disease.
pubmed:affiliation
Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA. jasinskamyga.barbara@mayo.edu
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural