Molecular processes of chromosome 9p21 deletions in human cancers.
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Molecular profiling uncovers a p53-associated role for microRNA-31 in inhibiting the proliferation of serous ovarian carcinomas and other cancersMeta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian womenEvaluation of somatic copy number estimation tools for whole-exome sequencing data.Two mature products of MIR-491 coordinate to suppress key cancer hallmarks in glioblastoma.Amplified and homozygously deleted genes in glioblastoma: impact on gene expression levelsExpression of p16 gene and Rb protein in gastric carcinoma and their clinicopathological significanceOptimizing PCR assays for DNA-based cancer diagnosticsMolecular footprints of human lung cancer progression.A novel approach for determining cancer genomic breakpoints in the presence of normal DNAMicrohomology-mediated end joining in fission yeast is repressed by pku70 and relies on genes involved in homologous recombination.Rad1, rad10 and rad52 mutations reduce the increase of microhomology length during radiation-induced microhomology-mediated illegitimate recombination in saccharomyces cerevisiae.Molecular structure of double-minute chromosomes bearing amplified copies of the epidermal growth factor receptor gene in gliomas.Different molecular mechanisms causing 9p21 deletions in acute lymphoblastic leukemia of childhood.Amplification and thrifty single-molecule sequencing of recurrent somatic structural variations.Translating next generation sequencing to practice: opportunities and necessary steps.Copy number variation in archival melanoma biopsies versus benign melanocytic lesions.MicroRNA-31 modulates tumour sensitivity to radiation in oesophageal adenocarcinoma.Genomic profiling of malignant pleural mesothelioma with array-based comparative genomic hybridization shows frequent non-random chromosomal alteration regions including JUN amplification on 1p32.Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes.Transflip mutations produce deletions in pancreatic cancer.Mapping of deletion breakpoints at the CDKN2A locus in melanoma: detection of MTAP-ANRIL fusion transcripts.L1 retrotransposons in human cancersParp-1 deficiency causes an increase of deletion mutations and insertions/rearrangements in vivo after treatment with an alkylating agent.
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Molecular processes of chromosome 9p21 deletions in human cancers.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
@zh
2003年學術文章
@zh-hant
name
Molecular processes of chromosome 9p21 deletions in human cancers.
@en
Molecular processes of chromosome 9p21 deletions in human cancers.
@nl
type
label
Molecular processes of chromosome 9p21 deletions in human cancers.
@en
Molecular processes of chromosome 9p21 deletions in human cancers.
@nl
prefLabel
Molecular processes of chromosome 9p21 deletions in human cancers.
@en
Molecular processes of chromosome 9p21 deletions in human cancers.
@nl
P2093
P2860
P356
P1433
P1476
Molecular processes of chromosome 9p21 deletions in human cancers.
@en
P2093
Hiroyuki Kuwano
John D Minna
Jun Yokota
Shigeru Sasaki
Takashi Kohno
Yoshitaka Sekido
Yukiko Kitagawa
P2860
P2888
P304
P356
10.1038/SJ.ONC.1206589
P407
P577
2003-06-01T00:00:00Z