rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
3
|
pubmed:dateCreated |
2000-3-2
|
pubmed:abstractText |
A polymorphism in hMSH2 gene has been associated with an increased susceptibility to develop colorectal cancer (CRC). Here we show that it is a genetic risk factor for CRC in the Spanish population. However, its presence does not apparently affect hMSH2 function.
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pubmed:commentsCorrections |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0007-0920
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
82
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
535-7
|
pubmed:dateRevised |
2009-11-18
|
pubmed:meshHeading |
pubmed-meshheading:10682661-Adult,
pubmed-meshheading:10682661-Aged,
pubmed-meshheading:10682661-Aged, 80 and over,
pubmed-meshheading:10682661-Alternative Splicing,
pubmed-meshheading:10682661-Base Sequence,
pubmed-meshheading:10682661-Colorectal Neoplasms,
pubmed-meshheading:10682661-DNA Primers,
pubmed-meshheading:10682661-DNA-Binding Proteins,
pubmed-meshheading:10682661-Exons,
pubmed-meshheading:10682661-Humans,
pubmed-meshheading:10682661-Introns,
pubmed-meshheading:10682661-Middle Aged,
pubmed-meshheading:10682661-MutS Homolog 2 Protein,
pubmed-meshheading:10682661-Polymorphism, Genetic,
pubmed-meshheading:10682661-Proto-Oncogene Proteins
|
pubmed:year |
2000
|
pubmed:articleTitle |
Intron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancer.
|
pubmed:affiliation |
Laboratori d'Investigació Gastrointestinal, Institut de Recerca, Hospital de Sant Pau, Barcelona, Spain.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|