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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1989-5-23
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pubmed:abstractText |
We herein propose that specific chromosomal aberrations associated with specific neoplasms are not necessarily inherited as a constitutional trait. High-risk individuals may have a tendency to undergo specific somatic mutations or chromosomal rearrangements at a relatively low frequency in all tissues as mosaicism. This may potentiate the development of specific somatic cancers. Our hypothesis may be applicable to both hereditary and sporadic types of neoplasms.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0250-7005
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
17-9
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2539769-Aged,
pubmed-meshheading:2539769-Carcinoma, Renal Cell,
pubmed-meshheading:2539769-Disease Susceptibility,
pubmed-meshheading:2539769-Humans,
pubmed-meshheading:2539769-Kidney Neoplasms,
pubmed-meshheading:2539769-Male,
pubmed-meshheading:2539769-Mosaicism,
pubmed-meshheading:2539769-Neoplasms,
pubmed-meshheading:2539769-Wilms Tumor
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pubmed:articleTitle |
Genetic susceptibility, somatic mosaicisms and predisposition to human cancer.
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pubmed:affiliation |
Department of Cell Biology, University of Texas M.D. Anderson Cancer Center, Houston 77030.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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