Chromosomes, Human, Pair 6
This graph shows the total number of publications written about "Chromosomes, Human, Pair 6" by people in the URMC Research Network by year, and whether "Chromosomes, Human, Pair 6" was a major or minor topic of these publication.
Below are the most recent publications written about "Chromosomes, Human, Pair 6" by people in Profiles.
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Wang HY, Huang LJ, Liu Z, Garcia R, Li S, Galliani CA. Erythroblastic sarcoma presenting as bilateral ovarian masses in an infant with pure erythroid leukemia. Hum Pathol. 2011 May; 42(5):749-58.
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Feldman AL, Dogan A, Smith DI, Law ME, Ansell SM, Johnson SH, Porcher JC, Ozsan N, Wieben ED, Eckloff BW, Vasmatzis G. Discovery of recurrent t(6;7)(p25.3;q32.3) translocations in ALK-negative anaplastic large cell lymphomas by massively parallel genomic sequencing. Blood. 2011 Jan 20; 117(3):915-9.
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Cycon KA, Rimsza LM, Murphy SP. Alterations in CIITA constitute a common mechanism accounting for downregulation of MHC class II expression in diffuse large B-cell lymphoma (DLBCL). Exp Hematol. 2009 Feb; 37(2):184-194.
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Slovak ML, Gundacker H, Bloomfield CD, Dewald G, Appelbaum FR, Larson RA, Tallman MS, Bennett JM, Stirewalt DL, Meshinchi S, Willman CL, Ravindranath Y, Alonzo TA, Carroll AJ, Raimondi SC, Heerema NA. A retrospective study of 69 patients with t(6;9)(p23;q34) AML emphasizes the need for a prospective, multicenter initiative for rare 'poor prognosis' myeloid malignancies. Leukemia. 2006 Jul; 20(7):1295-7.
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Denison SR, Callahan G, Becker NA, Phillips LA, Smith DI. Characterization of FRA6E and its potential role in autosomal recessive juvenile parkinsonism and ovarian cancer. Genes Chromosomes Cancer. 2003 Sep; 38(1):40-52.
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Wang N. Cytogenetics and molecular genetics of ovarian cancer. Am J Med Genet. 2002 Oct 30; 115(3):157-63.
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Iqbal MA, Akhtar M, Ulmer C, Al-Dayel F, Paterson MC. FISH analysis in chromophobe renal-cell carcinoma. Diagn Cytopathol. 2000 Jan; 22(1):3-6.
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O'Neill ME, Marietta J, Nishimura D, Wayne S, Van Camp G, Van Laer L, Negrini C, Wilcox ER, Chen A, Fukushima K, Ni L, Sheffield VC, Smith RJ. A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6. Hum Mol Genet. 1996 Jun; 5(6):853-6.
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Weitkamp LR, Moss AJ, Lewis RA, Hall WJ, MacCluer JW, Schwartz PJ, Locati EH, Tzivoni D, Vincent GM, Robinson JL, et al. Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype. Am J Hum Genet. 1994 Dec; 55(6):1230-41.
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Phatak PD, Cappuccio JD. Management of hereditary hemochromatosis. Blood Rev. 1994 Dec; 8(4):193-8.
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