A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer
about
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controlsLong Non-coding RNA ANRIL and Polycomb in Human Cancers and Cardiovascular DiseaseGenetic polymorphisms in the 9p21 region associated with risk of multiple cancersCommon genetic variants in the 9p21 region and their associations with multiple tumoursExpression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk.Identification of mutated core cancer modules by integrating somatic mutation, copy number variation, and gene expression data.Second generation sequencing of the mesothelioma tumor genome.Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarctionIdentification of gene fusion transcripts by transcriptome sequencing in BRCA1-mutated breast cancers and cell linesAbsence of p16INK4a and truncation of ARF tumor suppressors in chickens.Chromosomal alterations during lymphatic and liver metastasis formation of colorectal cancerdCaP: detecting differential binding events in multiple conditions and proteinsTailoring treatment of nonsmall cell lung cancer by tissue type: role of pemetrexed.Integrated Genomics for Pinpointing Survival Loci within Arm-Level Somatic Copy Number Alterations.Comprehensive analysis of CDKN2A (p16INK4A/p14ARF) and CDKN2B genes in 53 melanoma index cases considered to be at heightened risk of melanomaHigh expression of CAI2, a 9p21-embedded long noncoding RNA, contributes to advanced-stage neuroblastoma.Role for the MOV10 RNA helicase in polycomb-mediated repression of the INK4a tumor suppressor.Mapping of deletion breakpoints at the CDKN2A locus in melanoma: detection of MTAP-ANRIL fusion transcripts.Observations of the genomic landscape beyond 1p19q deletions and EGFR amplification in glioma.Genetic imbalances with impact on survival in colorectal cancer patients.Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarction.
P2860
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P2860
A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer
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2000 nî lūn-bûn
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2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
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2000 թվականի նոյեմբերին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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A methylthioadenosine phosphor ...... s frequently deleted in cancer
@ast
A methylthioadenosine phosphor ...... s frequently deleted in cancer
@en
A methylthioadenosine phosphor ...... s frequently deleted in cancer
@nl
type
label
A methylthioadenosine phosphor ...... s frequently deleted in cancer
@ast
A methylthioadenosine phosphor ...... s frequently deleted in cancer
@en
A methylthioadenosine phosphor ...... s frequently deleted in cancer
@nl
prefLabel
A methylthioadenosine phosphor ...... s frequently deleted in cancer
@ast
A methylthioadenosine phosphor ...... s frequently deleted in cancer
@en
A methylthioadenosine phosphor ...... s frequently deleted in cancer
@nl
P2093
P2860
P356
P1433
P1476
A methylthioadenosine phosphor ...... s frequently deleted in cancer
@en
P2093
P2860
P2888
P304
P356
10.1038/SJ.ONC.1203942
P407
P577
2000-11-23T00:00:00Z
P5875
P6179
1034797593