rdf:type |
|
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0017263,
umls-concept:C0023467,
umls-concept:C0030705,
umls-concept:C0079419,
umls-concept:C0185117,
umls-concept:C0443199,
umls-concept:C1333205,
umls-concept:C1413247,
umls-concept:C1417862,
umls-concept:C1425102,
umls-concept:C1517813,
umls-concept:C1705535,
umls-concept:C2911684
|
pubmed:issue |
12
|
pubmed:dateCreated |
2008-11-21
|
pubmed:abstractText |
mRNA expression levels of certain genes have shown predictive value for the outcome of cytarabine-treated AML-patients. We hypothesized that genetic variants play a role in the regulation of the transcription of these genes. We studied leukoblasts from 82 patients with acute myeloid leukemia and observed various extent and frequency of differential allelic expression in the CDA, DCK, NT5C2, NT5C3, and TP53 genes. Our attempts to identify the causative regulatory single nucleotide polymorphisms by a bioinformatics approach did not succeed. However, our results indicate that genetic variations are at least in part responsible for the differences in overall expression levels of these genes.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/5'-Nucleotidase,
http://linkedlifedata.com/resource/pubmed/chemical/Cytarabine,
http://linkedlifedata.com/resource/pubmed/chemical/Cytidine Deaminase,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxycytidine Kinase,
http://linkedlifedata.com/resource/pubmed/chemical/Equilibrative Nucleoside...,
http://linkedlifedata.com/resource/pubmed/chemical/Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/NT5C2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/NT5C3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/SLC29A1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/TP53 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Protein p53
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
1521-009X
|
pubmed:author |
|
pubmed:issnType |
Electronic
|
pubmed:volume |
36
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
2419-23
|
pubmed:meshHeading |
pubmed-meshheading:18775979-5'-Nucleotidase,
pubmed-meshheading:18775979-Alleles,
pubmed-meshheading:18775979-Cytarabine,
pubmed-meshheading:18775979-Cytidine Deaminase,
pubmed-meshheading:18775979-Deoxycytidine Kinase,
pubmed-meshheading:18775979-Equilibrative Nucleoside Transporter 1,
pubmed-meshheading:18775979-Gene Expression,
pubmed-meshheading:18775979-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:18775979-Glycoproteins,
pubmed-meshheading:18775979-Heterozygote,
pubmed-meshheading:18775979-Homozygote,
pubmed-meshheading:18775979-Humans,
pubmed-meshheading:18775979-Leukemia, Myeloid, Acute,
pubmed-meshheading:18775979-Polymorphism, Single Nucleotide,
pubmed-meshheading:18775979-Tumor Suppressor Protein p53
|
pubmed:year |
2008
|
pubmed:articleTitle |
Differential allelic expression in leukoblast from patients with acute myeloid leukemia suggests genetic regulation of CDA, DCK, NT5C2, NT5C3, and TP53.
|
pubmed:affiliation |
Laboratoire de Cytologie Analytique, INSERM U590, Faculté de Médecine Rockefeller, 8, Avenue Rockefeller, 69008 Lyon, France. jordheim@yahoo.com
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|