Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2007-8-6
pubmed:abstractText
The aim of this study was to determine the potential synchronous contribution of alterations in TGF-betaRII, BAX, IGFIIR, caspase-5, hMSH3 and hMSH6 genes to the development and clinical outcome of bladder cancer, in relation to p53 mutations, microsatellite status and hMLH1/hMSH2 expression.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/CASP5 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Caspases, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Neoplasm, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/G-T mismatch-binding protein, http://linkedlifedata.com/resource/pubmed/chemical/MSH3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Receptor, IGF Type 2, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Transforming Growth..., http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Protein p53, http://linkedlifedata.com/resource/pubmed/chemical/bcl-2-Associated X Protein, http://linkedlifedata.com/resource/pubmed/chemical/transforming growth factor-beta...
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0031-3025
pubmed:author
pubmed:issnType
Print
pubmed:volume
39
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
425-32
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:17676485-Adult, pubmed-meshheading:17676485-Aged, pubmed-meshheading:17676485-Aged, 80 and over, pubmed-meshheading:17676485-Caspases, pubmed-meshheading:17676485-DNA, Neoplasm, pubmed-meshheading:17676485-DNA-Binding Proteins, pubmed-meshheading:17676485-Female, pubmed-meshheading:17676485-Gene Expression Regulation, Neoplastic, pubmed-meshheading:17676485-Humans, pubmed-meshheading:17676485-Male, pubmed-meshheading:17676485-Microsatellite Instability, pubmed-meshheading:17676485-Middle Aged, pubmed-meshheading:17676485-Multivariate Analysis, pubmed-meshheading:17676485-Mutation, pubmed-meshheading:17676485-Neoplasm Invasiveness, pubmed-meshheading:17676485-Protein-Serine-Threonine Kinases, pubmed-meshheading:17676485-Receptor, IGF Type 2, pubmed-meshheading:17676485-Receptors, Transforming Growth Factor beta, pubmed-meshheading:17676485-Survival Analysis, pubmed-meshheading:17676485-Tumor Suppressor Protein p53, pubmed-meshheading:17676485-Urinary Bladder Neoplasms, pubmed-meshheading:17676485-Urothelium, pubmed-meshheading:17676485-bcl-2-Associated X Protein
pubmed:year
2007
pubmed:articleTitle
TGF-betaRII, BAX, IGFIIR, caspase-5, hMSH3 and hMSH6 alterations are not associated with microsatellite instability or p53 mutations in invasive urothelial carcinoma of the urinary bladder.
pubmed:affiliation
Department of Pathology, Medical School, National and Kapodistrian University of Athens, Greece. asaetta@med.uoa.gr
pubmed:publicationType
Journal Article