Works matching IS 10452257 AND DT 1998 AND VI 23 AND IP 1
Results: 13
Increased levels of a chromosome 21-encoded tumour invasion and metastasis factor (TIAM1) mRNA in bone marrow of down syndrome children during the acute phase of AML(M7).
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 61, doi. 10.1002/(SICI)1098-2264(199809)23:1<61::AID-GCC9>3.0.CO;2-4
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Isolation of a novel TP53 target gene from a colon cancer cell line carrying a highly regulated wild-type TP53 expression system.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 1, doi. 10.1002/(SICI)1098-2264(199809)23:1<1::AID-GCC1>3.0.CO;2-Y
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Frequent rearrangements of chromosomes 1, 7, and 8 in primary liver cancer.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 26, doi. 10.1002/(SICI)1098-2264(199809)23:1<26::AID-GCC5>3.0.CO;2-8
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Chromosome abnormalities in squamous cell carcinoma of the urethra.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 72, doi. 10.1002/(SICI)1098-2264(199809)23:1<72::AID-GCC11>3.0.CO;2-G
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A common region of allelic loss on chromosome region 3p25.3-26.3 in nasopharyngeal carcinoma.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 21, doi. 10.1002/(SICI)1098-2264(199809)23:1<21::AID-GCC4>3.0.CO;2-8
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Recurrent integration of papillomavirus DNA within the human 12q14-15 uterine breakpoint region in genital carcinomas.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 55, doi. 10.1002/(SICI)1098-2264(199809)23:1<55::AID-GCC8>3.0.CO;2-5
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Molecular analysis of 1p36 breakpoints in two Merkel cell carcinomas.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 67, doi. 10.1002/(SICI)1098-2264(199809)23:1<67::AID-GCC10>3.0.CO;2-B
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Cytogenetic and molecular characterization of random chromosomal rearrangements activating the drug resistance gene, MDR1/P-glycoprotein, in drug-selected cell lines and patients with drug refractory ALL.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 44, doi. 10.1002/(SICI)1098-2264(199809)23:1<44::AID-GCC7>3.0.CO;2-6
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Chromosome banding analysis of gynecomastias and breast carcinomas in men.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 16, doi. 10.1002/(SICI)1098-2264(199809)23:1<16::AID-GCC3>3.0.CO;2-9
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Der(16)t(1;16) is a secondary chromosome aberration in at least eighteen different types of human cancer.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 78, doi. 10.1002/(SICI)1098-2264(199809)23:1<78::AID-GCC13>3.0.CO;2-A
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Deregulated expression of the TAL1 gene by t(1;5)(p32;q31) in patient with T-cell acute lymphoblastic leukemia.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 36, doi. 10.1002/(SICI)1098-2264(199809)23:1<36::AID-GCC6>3.0.CO;2-7
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Rearrangement between the MYH11 gene at 16p13 and D12S158 at 12p13 in a case of acute myeloid leukemia M1 (AML-M1).
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 10, doi. 10.1002/(SICI)1098-2264(199809)23:1<10::AID-GCC2>3.0.CO;2-9
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Identification of a 100-kb region of common allelic loss on chromosome bands 10q25-q26 in human endometrial cancer.
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- Genes, Chromosomes & Cancer, 1998, v. 23, n. 1, p. 74, doi. 10.1002/(SICI)1098-2264(199809)23:1<74::AID-GCC12>3.0.CO;2-E
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