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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2011-7-19
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pubmed:abstractText |
Mutations of the gene encoding isocitrate dehydrogenase (IDH) have been shown in a significant proportion of diffuse gliomas. These mutations are specific to gliomas and their utility for diagnosis and prognostication of these tumors is being proclaimed. The present study was conducted with the aim of assessing frequency of IDH1 mutations in gliomas, their correlation with other molecular alterations along with a comprehensive review of available literature.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1096-0945
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pubmed:author |
pubmed-author:BilaV NVN,
pubmed-author:ChosdolKunzangK,
pubmed-author:JhaPankajP,
pubmed-author:JhaPreranaP,
pubmed-author:KaleShashank SharadSS,
pubmed-author:MahapatraAshok KumarAK,
pubmed-author:SarkarChitraC,
pubmed-author:SharmaMehar ChandMC,
pubmed-author:SharmaVikasV,
pubmed-author:SinghGeetikaG,
pubmed-author:SuriAshishA,
pubmed-author:SuriVaishaliV
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pubmed:copyrightInfo |
Copyright © 2011 Elsevier Inc. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
91
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
385-93
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pubmed:meshHeading |
pubmed-meshheading:21569770-Adolescent,
pubmed-meshheading:21569770-Adult,
pubmed-meshheading:21569770-Age Factors,
pubmed-meshheading:21569770-Brain Neoplasms,
pubmed-meshheading:21569770-Child,
pubmed-meshheading:21569770-Child, Preschool,
pubmed-meshheading:21569770-Chromosome Deletion,
pubmed-meshheading:21569770-Chromosomes, Human, Pair 1,
pubmed-meshheading:21569770-Chromosomes, Human, Pair 19,
pubmed-meshheading:21569770-DNA, Neoplasm,
pubmed-meshheading:21569770-DNA Mutational Analysis,
pubmed-meshheading:21569770-Female,
pubmed-meshheading:21569770-Glioma,
pubmed-meshheading:21569770-Hospitals, Teaching,
pubmed-meshheading:21569770-Humans,
pubmed-meshheading:21569770-In Situ Hybridization, Fluorescence,
pubmed-meshheading:21569770-Infant,
pubmed-meshheading:21569770-Isocitrate Dehydrogenase,
pubmed-meshheading:21569770-Loss of Heterozygosity,
pubmed-meshheading:21569770-Male,
pubmed-meshheading:21569770-Middle Aged,
pubmed-meshheading:21569770-Mutation,
pubmed-meshheading:21569770-Neoplasm Staging,
pubmed-meshheading:21569770-Tumor Suppressor Protein p53,
pubmed-meshheading:21569770-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
IDH1 mutations in gliomas: first series from a tertiary care centre in India with comprehensive review of literature.
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pubmed:affiliation |
Department of Pathology, All India Institute of Medical Sciences, Delhi, India.
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pubmed:publicationType |
Journal Article,
Review
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