Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2000-12-4
pubmed:abstractText
Infant leukemia below the age of 12 months is a rare disease that exhibits a high frequency of 11q23 rearrangements. We assessed the presence of polymorphisms in several metabolic genes in 23 families of infants diagnosed with leukemia under 12 months of age in Italy. When polymorphism frequencies were calculated within families, frequencies of GST gene deletions were significantly higher than expected only among the parents of infants without the 11q23 rearrangement. These data suggest that the deletion of GST genes in parents may affect the risk of infant leukemia through a pathway independent of the MLL gene.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0145-2126
pubmed:author
pubmed:issnType
Print
pubmed:volume
24
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
971-4
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:11086181-Chromosome Mapping, pubmed-meshheading:11086181-Chromosomes, Human, Pair 11, pubmed-meshheading:11086181-Cytochrome P-450 CYP1A1, pubmed-meshheading:11086181-Cytochrome P-450 CYP2E1, pubmed-meshheading:11086181-DNA-Binding Proteins, pubmed-meshheading:11086181-Female, pubmed-meshheading:11086181-Gene Deletion, pubmed-meshheading:11086181-Gene Rearrangement, pubmed-meshheading:11086181-Genetic Predisposition to Disease, pubmed-meshheading:11086181-Genomic Imprinting, pubmed-meshheading:11086181-Glutathione Transferase, pubmed-meshheading:11086181-Humans, pubmed-meshheading:11086181-Infant, pubmed-meshheading:11086181-Isoenzymes, pubmed-meshheading:11086181-Italy, pubmed-meshheading:11086181-Leukemia, Myeloid, Acute, pubmed-meshheading:11086181-Male, pubmed-meshheading:11086181-Myeloid-Lymphoid Leukemia Protein, pubmed-meshheading:11086181-Precursor Cell Lymphoblastic Leukemia-Lymphoma, pubmed-meshheading:11086181-Proto-Oncogenes, pubmed-meshheading:11086181-Transcription Factors
pubmed:year
2000
pubmed:articleTitle
Deletion of parental GST genes as a possible susceptibility factor in the etiology of infant leukemia.
pubmed:affiliation
UMDNJ-Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't, Multicenter Study