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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2010-10-4
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pubmed:abstractText |
The aim of this study was to investigate the association of a 11 nucleotide deletion, the c.469+46_56del mutation, in the intron of the homeobox MSX1 gene and breast cancer occurrence and characteristics.
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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 |
Oct
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pubmed:issn |
1877-783X
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pubmed:author |
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pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
34
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
652-5
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pubmed:dateRevised |
2011-6-17
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pubmed:meshHeading |
pubmed-meshheading:20638926-Adult,
pubmed-meshheading:20638926-Aged,
pubmed-meshheading:20638926-Aged, 80 and over,
pubmed-meshheading:20638926-Base Sequence,
pubmed-meshheading:20638926-Breast Neoplasms,
pubmed-meshheading:20638926-Female,
pubmed-meshheading:20638926-Genetic Predisposition to Disease,
pubmed-meshheading:20638926-Humans,
pubmed-meshheading:20638926-MSX1 Transcription Factor,
pubmed-meshheading:20638926-Middle Aged,
pubmed-meshheading:20638926-Molecular Sequence Data,
pubmed-meshheading:20638926-Polymerase Chain Reaction,
pubmed-meshheading:20638926-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:20638926-Sequence Deletion
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pubmed:year |
2010
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pubmed:articleTitle |
The c.469+46_56del mutation in the homeobox MSX1 gene--a novel risk factor in breast cancer?
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pubmed:affiliation |
Department of Molecular Genetics, University of Lodz, Banacha 12/16, 90-237 Lodz, Poland.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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