Visualizar Tese - Instituto de Biociências - Unesp

Visualizar Tese - Instituto de Biociências - Unesp Visualizar Tese - Instituto de Biociências - Unesp

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Cirilo, PDRREFERÊNCIAS221Martinez-Mir A, Glaser B, Chuang GS et al. Germline Fumarate Hydratase Mutations in Families withMultiple Cutaneous and Uterine Leiomyomata. J Invest Dermatol, 741-744, 2003.McCarroll SA, Kuruvilla FG, Korn JM et al. Integrated detection and population-genetic analysis ofSNPs and copy number variation. Nat Genet, 40, 1166-1174, 2008.Meadows KL, Andrews DM, Xu Z et al. Genome-wide analysis of loss of heterozygosity and copynumber amplification in uterine leiomyomas using the 100K single nucleotidepolymorphism array. Exp Mol Pathol, Epub ahead of print, 2011.Melchor L, Saucedo-Cuevas LP, Muñoz-Repeto I et al. Comprehensive characterization of the DNAamplification at 13q34 in human breast cancer reveals TFDP1 and CUL4A as likely candidatetarget genes. Breast Cancer Res, 11, R86, 2009.Meloni AM, Surti U, Sandberg AA. Deletion of chromosome 13 in leiomyomas of the uterus. CancerGenet Cytogenet, 53, 199-203, 1991.Mertens HJ, Heineman MJ, Theunissen PH et al. Androgen, estrogen and progesterone receptorexpression in the human uterus during the menstrual cycle. Eur J Obstet Gynecol ReprodBiol, 98, 58-65, 2001.Mesquita FS, Dyer SN, Heinrich DA et al. Reactive oxygen species mediate mitogenic growth factorsignaling pathways in human leiomyoma smooth muscle cells. Biol Reprod, 82, 341-351,2010.Meza-Zepeda LA, Kresse SH, Barragan-Polania AH et al. Array comparative genomic hybridizationreveals distinct DNA copy number differences between gastrointestinal stromal tumors andleiomyosarcomas. Cancer Res, 66, 8984-8993, 2006.Micci F, Teixeira MR, Haugom L et al. Genomic aberrations in carcinomas of the uterine corpus.Genes Chrom Cancer, 40, 229-246, 2004.Middlebrook BS, Eldin K, Li X et al. Smad1-Smad5 ovarian conditional knockout mice develop adisease profile similar to the juvenile form of human granulosa cell tumors. Endocrinology,150, 5208-5217, 2009.Mills RE, Walter K, Stewart C et al. Mapping copy number variation by population-scale genomesequencing. Nature, 470, 59-65, 2011.Minelli L, Romagnolo C, Giambanco L et al. Uterine leiomyoma metastasis as a first sign of breastcancer. J Am Assoc Gynecol Laparosc, 5, 213-215, 1998.Misao R, Nakanishi Y, Fujimoto J et al. Expression of sex hormone-binding globulin mRNA in uterineleiomyoma, myometrium and endometrium of human subjects. Gynecol Endocrinol, 9, 317-323, 1995.Mitelman Database of Chromosome Aberrations and Gene Fusions in Cancer (2011). Mitelman F,Johansson B and Mertens F (Eds.), http://cgap.nci.nih.gov/Chromosomes/Mitelman.Mitelman F, Johansson B, Mertens F. The impact of translocations and gene fusions on cancercausation Nature Rev Cancer, 7, 233-245, 2007.

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Cirilo, PDRREFERÊNCIAS221Martinez-Mir A, Glaser B, Chuang GS et al. Germline Fumarate Hydratase Mutations in Families withMultiple Cutaneous and Uterine Leiomyomata. J Invest Dermatol, 741-744, 2003.McCarroll SA, Kuruvilla FG, Korn JM et al. Integrated <strong>de</strong>tection and population-genetic analysis ofSNPs and copy number variation. Nat Genet, 40, 1166-1174, 2008.Meadows KL, Andrews DM, Xu Z et al. Genome-wi<strong>de</strong> analysis of loss of heterozygosity and copynumber amplification in uterine leiomyomas using the 100K single nucleoti<strong>de</strong>polymorphism array. Exp Mol Pathol, Epub ahead of print, 2011.Melchor L, Saucedo-Cuevas LP, Muñoz-Repeto I et al. Comprehensive characterization of the DNAamplification at 13q34 in human breast cancer reveals TFDP1 and CUL4A as likely candidatetarget genes. Breast Cancer Res, 11, R86, 2009.Meloni AM, Surti U, Sandberg AA. Deletion of chromosome 13 in leiomyomas of the uterus. CancerGenet Cytogenet, 53, 199-203, 1991.Mertens HJ, Heineman MJ, Theunissen PH et al. Androgen, estrogen and progesterone receptorexpression in the human uterus during the menstrual cycle. Eur J Obstet Gynecol ReprodBiol, 98, 58-65, 2001.Mesquita FS, Dyer SN, Heinrich DA et al. Reactive oxygen species mediate mitogenic growth factorsignaling pathways in human leiomyoma smooth muscle cells. Biol Reprod, 82, 341-351,2010.Meza-Zepeda LA, Kresse SH, Barragan-Polania AH et al. Array comparative genomic hybridizationreveals distinct DNA copy number differences between gastrointestinal stromal tumors andleiomyosarcomas. Cancer Res, 66, 8984-8993, 2006.Micci F, Teixeira MR, Haugom L et al. Genomic aberrations in carcinomas of the uterine corpus.Genes Chrom Cancer, 40, 229-246, 2004.Middlebrook BS, Eldin K, Li X et al. Smad1-Smad5 ovarian conditional knockout mice <strong>de</strong>velop adisease profile similar to the juvenile form of human granulosa cell tumors. Endocrinology,150, 5208-5217, 2009.Mills RE, Walter K, Stewart C et al. Mapping copy number variation by population-scale genomesequencing. Nature, 470, 59-65, 2011.Minelli L, Romagnolo C, Giambanco L et al. Uterine leiomyoma metastasis as a first sign of breastcancer. J Am Assoc Gynecol Laparosc, 5, 213-215, 1998.Misao R, Nakanishi Y, Fujimoto J et al. Expression of sex hormone-binding globulin mRNA in uterineleiomyoma, myometrium and endometrium of human subjects. Gynecol Endocrinol, 9, 317-323, 1995.Mitelman Database of Chromosome Aberrations and Gene Fusions in Cancer (2011). Mitelman F,Johansson B and Mertens F (Eds.), http://cgap.nci.nih.gov/Chromosomes/Mitelman.Mitelman F, Johansson B, Mertens F. The impact of translocations and gene fusions on cancercausation Nature Rev Cancer, 7, 233-245, 2007.

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