Below are the most recent publications written about "Chromosomes, Human, Pair 10" by people in Profiles.
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Hasbrook M, Yonekawa Y, Van Laere L, Shah AR, Capone A. Bilateral persistent fetal vasculature and a chromosome 10 mutation including COX15. Can J Ophthalmol. 2017 12; 52(6):e203-e205.
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Shi J, Sung H, Zhang B, Lu W, Choi JY, Xiang YB, Kim MK, Iwasaki M, Long J, Ji BT, Park SK, Zheng Y, Tsugane S, Yoo KY, Wang W, Noh DY, Han W, Kim SW, Lee MH, Lee JW, Lee JY, Shen CY, Matsuo K, Ahn SH, Gao YT, Shu XO, Cai Q, Kang D, Zheng W. New breast cancer risk variant discovered at 10q25 in East Asian women. Cancer Epidemiol Biomarkers Prev. 2013 Jul; 22(7):1297-303.
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Elco CP, Mari?o-Enr?quez A, Abraham JA, Dal Cin P, Hornick JL. Hybrid myxoinflammatory fibroblastic sarcoma/hemosiderotic fibrolipomatous tumor: report of a case providing further evidence for a pathogenetic link. Am J Surg Pathol. 2010 Nov; 34(11):1723-7.
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Hadley D, Orlin A, Brown G, Brucker AJ, Ho AC, Regillo CD, Donoso LA, Tian L, Kaderli B, Stambolian D. Analysis of six genetic risk factors highly associated with AMD in the region surrounding ARMS2 and HTRA1 on chromosome 10, region q26. Invest Ophthalmol Vis Sci. 2010 Apr; 51(4):2191-6.
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Annable K, Donnenfeld AE, Fischer RL, Knops J. Prenatal diagnosis of a jumping translocation. Prenat Diagn. 2008 Aug; 28(8):767-9.
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Fogt F, Selim AM, Xu GX, Prinz MK, Eagle RC, Budimlija ZM. Uveal melanocytomas: genetic comparison with uveal and dermal melanomas. Arch Ophthalmol. 2005 Mar; 123(3):377-80.
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Fujisawa H, Kurrer M, Reis RM, Yonekawa Y, Kleihues P, Ohgaki H. Acquisition of the glioblastoma phenotype during astrocytoma progression is associated with loss of heterozygosity on 10q25-qter. Am J Pathol. 1999 Aug; 155(2):387-94.
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Tohma Y, Gratas C, Biernat W, Peraud A, Fukuda M, Yonekawa Y, Kleihues P, Ohgaki H. PTEN (MMAC1) mutations are frequent in primary glioblastomas (de novo) but not in secondary glioblastomas. J Neuropathol Exp Neurol. 1998 Jul; 57(7):684-9.
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el-Rifai W, Sarlomo-Rikala M, Andersson LC, Miettinen M, Knuutila S. DNA copy number changes in gastrointestinal stromal tumors--a distinct genetic entity. Ann Chir Gynaecol. 1998; 87(4):287-90.
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Gatalica B, Pulkkinen L, Li K, Kuokkanen K, Ryyn?nen M, McGrath JA, Uitto J. Cloning of the human type XVII collagen gene (COL17A1), and detection of novel mutations in generalized atrophic benign epidermolysis bullosa. Am J Hum Genet. 1997 Feb; 60(2):352-65.