Works matching IS 10452257 AND DT 2000 AND VI 27 AND IP 3
Results: 15
PRK, a cell cycle gene localized to 8p21, is downregulated in head and neck cancer.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 332, doi. 10.1002/(SICI)1098-2264(200003)27:3<332::AID-GCC15>3.0.CO;2-K
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Non-random involvement of chromosome 13 in patients with persistent or relapsed disease after bone-marrow transplantation for chronic myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 278, doi. 10.1002/(SICI)1098-2264(200003)27:3<278::AID-GCC8>3.0.CO;2-H
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Modification in the inherent mode of allelic replication in lymphocytes of patients suffering from renal cell carcinoma: A novel genetic alteration associated with malignancy.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 270, doi. 10.1002/(SICI)1098-2264(200003)27:3<270::AID-GCC7>3.0.CO;2-7
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Two regions of homozygous deletion clusters at chromosome band 9p21 in human lung cancer.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 308, doi. 10.1002/(SICI)1098-2264(200003)27:3<308::AID-GCC12>3.0.CO;2-W
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Genomic FHIT analysis in RER<sup>+</sup> and RER<sup>−</sup> adenocarcinomas of the pancreas.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 239, doi. 10.1002/(SICI)1098-2264(200003)27:3<239::AID-GCC3>3.0.CO;2-X
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Novel gene fusion of COX6C at 8q22-23 to HMGIC at 12q15 in a uterine leiomyoma.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 303, doi. 10.1002/(SICI)1098-2264(200003)27:3<303::AID-GCC11>3.0.CO;2-3
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Identification of breakpoint cluster regions at 1p36.3 and 3q21 in hematologic malignancies with t(1;3)(p36;q21).
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 229, doi. 10.1002/(SICI)1098-2264(200003)27:3<229::AID-GCC2>3.0.CO;2-0
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MLL-CBP fusion transcript in a therapy-related acute myeloid leukemia with the t(11;16)(q23;p13) which developed in an acute lymphoblastic leukemia patient with Fanconi anemia.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 264, doi. 10.1002/(SICI)1098-2264(200003)27:3<264::AID-GCC6>3.0.CO;2-#
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A sporadic breast tumor with a somatically acquired complex genomic rearrangement in BRCA1.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 295, doi. 10.1002/(SICI)1098-2264(200003)27:3<295::AID-GCC10>3.0.CO;2-F
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Recurrent allelic deletions of chromosome arms 15q and 16q in human small cell lung carcinomas.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 323, doi. 10.1002/(SICI)1098-2264(200003)27:3<323::AID-GCC14>3.0.CO;2-P
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Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 217, doi. 10.1002/(SICI)1098-2264(200003)27:3<217::AID-GCC1>3.0.CO;2-A
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Genetic and phenotypic changes associated with the acquisition of tumorigenicity in human bladder cancer.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 252, doi. 10.1002/(SICI)1098-2264(200003)27:3<252::AID-GCC5>3.0.CO;2-9
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t(11;14)-positive mantle cell lymphomas exhibit complex karyotypes and share similarities with B-cell chronic lymphocytic leukemia.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 285, doi. 10.1002/(SICI)1098-2264(200003)27:3<285::AID-GCC9>3.0.CO;2-M
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Molecular analysis of the candidate tumor suppressor gene ING1 in human head and neck tumors with 13q deletions.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 319, doi. 10.1002/(SICI)1098-2264(200003)27:3<319::AID-GCC13>3.0.CO;2-P
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Allelotyping of anaplastic thyroid carcinoma: Frequent allelic losses on 1q, 9p, 11, 17, 19p, and 22q.
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- Genes, Chromosomes & Cancer, 2000, v. 27, n. 3, p. 244, doi. 10.1002/(SICI)1098-2264(200003)27:3<244::AID-GCC4>3.0.CO;2-7
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