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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1987-7-8
|
pubmed:abstractText |
Recurrent chromosomal abnormalities in retinoblastomas involve numbers 13, 1, and 6, as well as homogeneously staining regions (HSR) and double minutes (DMS). Evidence suggesting that chromosome 13 contains a gene responsible for tumorigenesis has already been presented. We postulate that the genetic changes resulting from abnormalities of chromosomes 1 and 6 and the HSR/DMS provide a selective growth advantage to cells in which they occur. Support for this hypothesis, as it relates to the HSR/DMS and oncogene amplification, is discussed.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0167-6784
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
8
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
3-10
|
pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:3295640-Chromosome Aberrations,
pubmed-meshheading:3295640-Chromosome Deletion,
pubmed-meshheading:3295640-Chromosome Disorders,
pubmed-meshheading:3295640-Chromosomes, Human, Pair 1,
pubmed-meshheading:3295640-Chromosomes, Human, Pair 13,
pubmed-meshheading:3295640-Chromosomes, Human, Pair 6,
pubmed-meshheading:3295640-Eye Neoplasms,
pubmed-meshheading:3295640-Humans,
pubmed-meshheading:3295640-Oncogenes,
pubmed-meshheading:3295640-Retinoblastoma
|
pubmed:year |
1987
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pubmed:articleTitle |
Retinoblastoma, chromosome abnormalities and oncogene expression.
|
pubmed:publicationType |
Journal Article,
Review
|