Works matching IS 10452257 AND DT 2002 AND VI 34 AND IP 1
Results: 16
Double minute chromosomes in acute myeloid leukemia and myelodysplastic syndrome: Identification of new amplification regions by fluorescence in situ hybridization and spectral karyotyping.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 42, doi. 10.1002/gcc.10038
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Genomic organization and expression of the rearranged REL proto-oncogene in the human B-cell lymphoma cell line RC-K8.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 129, doi. 10.1002/gcc.10051
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APC/CTNNB1 (β-catenin) pathway alterations in human prostate cancers.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 9, doi. 10.1002/gcc.10037
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- Article
Comprehensive mutational analysis of the VHL gene in sporadic renal cell carcinoma: Relationship to clinicopathological parameters.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 58, doi. 10.1002/gcc.10054
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Late-appearing MLL rearrangement arising as a secondary change in adult acute myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 126, doi. 10.1002/gcc.10011
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Gains of 12q are the most frequent genomic imbalances in adult fibrosarcoma and are correlated with a poor outcome.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 69, doi. 10.1002/gcc.10036
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Molecular genetic analysis of chromosome 9 candidate tumor-suppressor loci in bladder cancer cell lines.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 86, doi. 10.1002/gcc.10050
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Mapping of nasopharyngeal carcinoma tumor-suppressive activity to a 1.8-megabase region of chromosome band 11q13.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 97, doi. 10.1002/gcc.10048
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Comprehensive karyotyping of the HT-29 colon adenocarcinoma cell line.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 1, doi. 10.1002/gcc.10003
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- Article
Sequencing of intron 3 of HMGA2 uncovers the existence of a novel exon.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 17, doi. 10.1002/gcc.10018
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Mutations of the AML1 gene in acute myeloid leukemia of FAB types M0 and M7.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 24, doi. 10.1002/gcc.10031
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Aberrations of the hSNF5/INI1 gene are restricted to malignant rhabdoid tumors or atypical teratoid/rhabdoid tumors in pediatric solid tumors.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 33, doi. 10.1002/gcc.10052
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Combined comparative genomic hybridization and genomic microarray for detection of gene amplifications in pulmonary artery intimal sarcomas and adrenocortical tumors.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 48, doi. 10.1002/gcc.10035
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Genetic analysis of mediastinal nonseminomatous germ cell tumors in children and adolescents.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 115, doi. 10.1002/gcc.10053
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Identification of amplified and expressed genes in breast cancer by comparative hybridization onto microarrays of randomly selected cDNA clones.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 104, doi. 10.1002/gcc.10039
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- Article
The position of pulmonary carcinoids within the spectrum of neuroendocrine tumors of the lung and other tissues.
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- Genes, Chromosomes & Cancer, 2002, v. 34, n. 1, p. 78, doi. 10.1002/gcc.10049
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- Article