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Cancer Chromosomes

Rohlfs EM, Puget N, Graham ML et al. An Alu-mediated 7.1 kb deletion of BRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10. Genes Chromosomes Cancer 2000 28[3] 300—307. [Pg.34]

Gress TM et al. Identification of genes with specific expression in pancreatic cancer by cDNA representational difference analysis. Genes Chromosom Cancer 1997 17 1-7. [Pg.115]

Kazmierczak, B., B. Thode, S. Bartnitzke, J. Bullerdiek, and W. Schloot. 1992. Pleomorphic adenoma cells vary in their susceptibility to SV40 transformation depending on the initial karyotype. Genes Chromosomes Cancer 5(1) 35-9. [Pg.639]

Masutani M, Nakagama H, Sugimura T (2003) Poly(ADP-ribose) and carcinogenesis. Genes Chromosomes Cancer 38 339—348... [Pg.67]

Carapeti M, Aguiar RC, Goldman JM, Cross NC (1998) A novel fusion between MOZ and the nuclear receptor coactivator TIF2 in acute myeloid leukemia. Blood 91 3127—3133 Chaffanet M, Gressin L, Preudhomme C, Soenen-Comu V, Bimbaum D, Pebusque MJ (2000) MOZ is fused to p300 in an acute monocytic leukemia with t(8 22). Genes Chromosomes. Cancer 28 138—144... [Pg.254]

Imamura T, Kakam N, Hibi S, Morimoto A, Eukushima Y, ljuin 1, Hada S, Kitabayashi 1, Abe T, Imashuku S (2003) Rearrangement of the MOZ gene in pediatric therapy-related myelodysplastic syndrome with a novel chromosomal translocation t(2 8)(p23 pll). Genes Chromosomes. Cancer 36 413 19... [Pg.256]

Rozman M, Camos M, Colomer D, Villamor N, Esteve J, Costa D, Carrio A, Aymerich M, Aguilar JL, Domingo A, Sole F, Gomis F, Florensa L, Montserrat E, Campo E (2004) Type I MOZICBP (MYST31CREBBP) is the most common chimeric transcript in acute myeloid leukemia with t(8 16)(pll pl3) translocation. Genes Chromosomes. Cancer 40 140-145 Rubinstein JH, Taybi H (1963) Broad thumbs and toes and facial abnormalities. Am J Dis Child 105 588-608... [Pg.260]

Tillinghast GW, Partee J, Albert P, Kelley JM, Burtow KH, Kelly K (2003) Analysis of genetic stabiUty at the EP300 and CREBBP loci in a panel of cancer cell Unes. Genes Chromosomes. Cancer 37 121—131 Timmermann S, Lehrrnann H, Polesskaya A, Harel-Bellan A (2001) Histone acetylation and disease. [Pg.261]

Boschman, G. A., Buys, C. H., van der Veen, A. Y Rens, W., Osinga, J., Slater, R. M and Aten, J. A. (1993) Identification of a tumor marker chromosome by flow sorting, DNA amplification in vitro, and in situ hybridization of the amplified product. Genes Chromosom. Cancer 6, 10-16. [Pg.279]

Stordal B, Peters G, Davey R. Similar ehromosomal changes in cisplatin- and oxaliplatin-resistant sublines of the H69 SCLC eell line are not associated with platinum resistance. Genes Chromosomes Cancer 2006 45 1094-1105. [Pg.87]

Tomlinson IP, Lambros MB, Roylanee RR. Loss of heterozygosity analysis practically and conceptually flawed Genes Chromosomes Cancer 2002 34 349-353. [Pg.100]

Masi, T. et al. 2005. Nitrosamine 4-(methylnitrosamino) -1 - (3-pyridyl) -1-butanone-induced pulmonary adenocarcinomas in Syrian golden hamsters contain beta-2-adrenergic receptor single-nucleotide polymorphisms. Genes Chromosomes Cancer, 44 (2), 212-217. [Pg.73]

A2. Achuthan, R., Bell, S. M., Leek, J. P., Roberts, P., Horgan, K., Markham, A. F., Selby, P. J., and MacLennan, K. A., Novel translocation of the BCL10 gene in a case of mucosa associated lymphoid tissue lymphoma. Genes Chromosomes Cancer 29, 347-349 (2000). [Pg.329]

Wu MS, Lee CW, Shun CT, Wang HP, Lee WJ, Chang MC, Sheu JC, Lin JT. Distinct clinicopathologic and genetic profiles in sporadic gastric cancer with different mutator phenotypes. Genes Chromosomes Cancer 2000 27 403-411. [Pg.488]

Solinas-Toldo S, Lampel S, Stilgenbauer S, Nickolenko J, Benner A, Dohner H, Cremer T, Lichter P. Matrix-based comparative genomic hybridization biochips to screen for genomic imbalances. Genes Chromosomes Cancer 1997 20(4) 399-407. [Pg.636]

Clarke LA, Veiga I, Isidro G, Jordtm P, Ramos JS et al (2000) Pathological exon skipping in an HNPCC proband with MLHl splice acceptor site mutation. Genes Chromosomes Cancer 29 367-370... [Pg.412]

Cheng JQ, Lee W-C, Klein MA, et al. 1999a. Frequent mutations of NF2 and allelic loss from chromosome band 22ql2 in malignant mesothelioma Evidence for a two-hit mechanism of NF2 inactivation. Genes Chromosomes Cancer 24 238-242. [Pg.244]

Flejter WL, Li FP, Antman KH, et al. 1989. Recurring loss involving chromosomes 1, 3, and 22 in malignant mesothelioma Possible sites of tumor suppressor genes. Genes Chromosomes Cancer 1 148-154. [Pg.266]

Lu YY, Jhanwar SC, Cheng JQ, et al. 1994b. Deletion mapping of the short arm of chromosome 3 in human malignant mesothelioma. Genes Chromosomes Cancer 9 76-80. [Pg.296]

Weaver ZA, McCormack SJ, Liyanage M et al. A recurring pattern of chromosomal aberrations in mammary gland tumors of MMTV-c-myc transgenic mice. Genes Chromosomes Cancer 1999 25 251-60. [Pg.461]

Sun, P. C., El-Mofty, S. K., Haughey, B. H. and Scholnick, S. B. (1995). Allelic loss in squamous cell carcinomas of the larynx discordance between primary and metastatic tumors. Genes Chromosomes Cancer 14, 145-148. [Pg.335]

Wasenius, V. M., Jekunen, A., Monni, O., Joensuu, H., Aebi, S., Howell, S. B. and Knuutila, S. (1997) Comparative genomic hybridization analysis of chromosomal changes occurring during development of acquired resistance to cisplatin in human ovarian carcinoma cells. Genes Chromosomes Cancer 18, 286-291. [Pg.233]

Motokura T, Arnold A. PRADl/cycLm D1 protooncogene genomic organization, 5 DNA sequence, and sequence of a tumor-specific rearrangement breakpoint. Genes Chromosomes Cancer 1993 7 89-95. [Pg.1480]

Abrams, E.S., S.E. Murdaugh and L.S. Lerman. Comprehensive screening of the human KRAS2 gene for sequence variants. Genes Chromosomes Cancer 6 73-85, 1993. [Pg.280]

Hoglund, M., Frigyesi, A., Sail, T., Gisselsson, D., and Mitelman, F (2005). Statistical behavior of complex cancer karyotypes. Genes Chromosomes Cancer 42(4), 327-341. [Pg.160]

Stenman G, Kindblom LG, Angervall L. Reciprocal translocation t(12 22)(ql3]3) in clear-cell sarcoma of tendons and aponeuroses. Genes Chromosomes Cancer. 1992 4 122-127. [Pg.134]

Pierotti MA, Borgarzone I, Borello MG, et al. Cytogenetics and molecular genetics of carcinomas arising from thyroid epithelial folliculat cells. Genes Chromosomes Cancer. 1996 16 1-14. [Pg.333]


See other pages where Cancer Chromosomes is mentioned: [Pg.633]    [Pg.42]    [Pg.258]    [Pg.259]    [Pg.259]    [Pg.260]    [Pg.261]    [Pg.315]    [Pg.315]    [Pg.315]    [Pg.750]    [Pg.177]    [Pg.177]    [Pg.290]    [Pg.290]    [Pg.85]    [Pg.100]    [Pg.296]    [Pg.109]    [Pg.195]    [Pg.304]    [Pg.290]   
See also in sourсe #XX -- [ Pg.221 , Pg.225 , Pg.226 , Pg.227 ]




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Cancer Philadelphia chromosome

Cancer chromosomal translocations

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