Works matching IS 10452257 AND DT 2008 AND VI 47 AND IP 2
Results: 9
Cutaneous T-cell lymphoma-associated lung cancers show chromosomal aberrations differing from primary lung cancer.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 107, doi. 10.1002/gcc.20513
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- Article
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: A nordic series of 24 cases and review of the literature.
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- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 149, doi. 10.1002/gcc.20517
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- Article
Arylamine N-acetyltransferase 1 expression in breast cancer cell lines: A potential marker in estrogen receptor-positive tumors.
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- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 118, doi. 10.1002/gcc.20512
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- Article
Recurrent deletions at 6q in early age of onset non-HNPCC- and non-FAP-associated intestinal carcinomas. Evidence for a novel cancer susceptibility locus at 6q14-q22.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 159, doi. 10.1002/gcc.20516
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- Article
Mutational inactivation of TGFBR2 in microsatellite unstable colon cancer arises from the cooperation of genomic instability and the clonal outgrowth of transforming growth factor β resistant cells.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 95, doi. 10.1002/gcc.20511
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- Publication type:
- Article
Polymorphisms in nonhomologous end-joining genes associated with breast cancer risk and chromosomal radiosensitivity.
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- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 137, doi. 10.1002/gcc.20515
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- Article
Disabled-1 is a large common fragile site gene, inactivated in multiple cancers.
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- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 165, doi. 10.1002/gcc.20519
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- Article
Amplification of PRKCI, located in 3q26, is associated with lymph node metastasis in esophageal squamous cell carcinoma.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 127, doi. 10.1002/gcc.20514
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- Publication type:
- Article
Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas.
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- Genes, Chromosomes & Cancer, 2008, v. 47, n. 2, p. 175, doi. 10.1002/gcc.20518
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- Article