Search Results - "Medical genetics"

Role of TGF-β1 haplotypes in the occurrence of myocardial infarction in young Italian patients by Frea Simone, Guarrera Simonetta, Carturan Sonia, Bergerone Serena, Franco Erica, Palumbo Luigi, Crobu Francesca, Trevi Gianpaolo, Piazza Alberto, Matullo Giuseppe

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Genetic polymorphisms located in genes related to immune and inflammatory processes are associated with end-stage renal disease: a preliminary study by Jimenez-Sousa Ma, López Elisabeth, Fernandez-Rodríguez Amanda, Tamayo Eduardo, Fernández-Navarro Pablo, Segura-Roda Laura, Heredia María, Gómez-Herreras José I, Bustamante Jesús, García-Gómez Juan, Bermejo-Martin Jesús F, Resino Salvador

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Prediction of lung cancer risk in a Chinese population using a multifactorial genetic model by Li Huan, Yang Lixin, Zhao Xueying, Wang Jiucun, Qian Ji, Chen Hongyan, Fan Weiwei, Liu Hongcheng, Jin Li, Wang Weimin, Lu Daru

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Association between CYP19 gene SNP rs2414096 Polymorphism and polycystic ovary syndrome in Chinese women by Yi Long, Ke Lu, Sun Hai-Xiang, Liang Feng-Jing, Wu Xiao-Ke, Cao Yun-Xia, Ge Hui-Juan, Sun Jing, Jin Jia-Li, Wu Zhi-Wei, Wang Yong

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Association of IL-18 polymorphisms with rheumatoid arthritis and systemic lupus erythematosus in Asian populations: a meta-analysis by Chen Shuilian, Jiang Feng, Ren Jiangping, Liu Jiajing, Meng Wei

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Evaluation of nine candidate genes in patients with normal tension glaucoma: a case control study by Reinthal Eva, Pasutto Francesca, Müller-Myhsok Bertram, Gramer Eugen, Wolf Christiane, Wissinger Bernd, Weisschuh Nicole

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The morality of assisted reproduction and genetic manipulation A moralidade da reprodução assistida e da manipulação genética by Maurizio Mori

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Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome by Winkelmann Bernhard R, März Winfried, Kleber Marcus E, Quyyumi Arshed A, Waddy Salina P, Eapen Danny J, Patel Riyaz S, Patel Yesha, Hazen Stanley L, Allayee Hooman, Jones Philip, Cresci Sharon, Morgan Thomas M, House John A, Boehm Bernhard O, Krumholz Harlan M, Spertus John A

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Eight previously unidentified mutations found in the <it>OA1 </it>ocular albinism gene by Dufier Jean-Louis, Kaplan Josseline, Mezer Eedy, Said Edith, Lacombe Didier, Sutherland Joanne, Levin Alex V, Héon Elise, Bonneau Dominique, Munier Francis L, Schorderet Daniel F, Dollfus Hélène, Marchant Dominique, Jaliffa Carolina, Vêtu Christelle, Roche Olivier, Mayeur Hélène, Marsac Cécile, Menasche Maurice, Abitbol Marc

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Identification of ATP2C1 mutations in the patients of Hailey-Hailey disease by Xiaoli Li, Dingwei Zhang, Jiahui Ding, Li Li, Zhenghui Wang

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IL23R in the Swedish, Finnish, Hungarian and Italian populations: association with IBD and psoriasis, and linkage to celiac disease by Vatta Serena, Not Tarcisio, Paavola-Sakki Paulina, Halme Leena, Turunen Ulla, Färkkilä Martti, Széles György, Pocsai Zsuzsa, Ádány Róza, Kaukinen Katri, Kurppa Kalle, Korponay-Szabo Ilma R, Ziberna Fabiana, Lappalainen Maarit, Suomela Sari, Kainu Kati, Dukes Emma, Koskinen Lotta LE, Einarsdottir Elisabet, Ventura Alessandro, Löfberg Robert, Torkvist Leif, Bresso Francesca, Halfvarson Jonas, Mäki Markku, Kontula Kimmo, Saarialho-Kere Ulpu, Kere Juha, D'Amato Mauro, Saavalainen Päivi

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Identification of a rare 17p13.3 duplication including the <it>BHLHA9</it> and <it>YWHAE</it> genes in a family with developmental delay and behavioural problems by Capra Valeria, Mirabelli-Badenier Marisol, Stagnaro Michela, Rossi Andrea, Tassano Elisa, Gimelli Stefania, Gimelli Giorgio

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Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease by Pfeiffer Ronald F, Rudolph Alice, Halter Cheryl A, Pauciulo Michael W, Kissell Diane K, Pankratz Nathan, Simon David K, Nichols William C, Foroud Tatiana

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EEG alpha phenotypes: linkage analyses and relation to alcohol dependence in an American Indian community study by Phillips Evelyn, Gizer Ian R, Ehlers Cindy L, Wilhelmsen Kirk C

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Single nucleotide polymorphisms at the <it>TRAF1/C5 </it>locus are associated with rheumatoid arthritis in a Han Chinese population by Ma Shi, Yang Minghui, Long Wubin, Luo Ruijun, Liu Jian, Lu Fang, Liu Jianping, Zhou Bin, Wu Lijun, Liu Xiaoqi, He Fei, Wu Fengxia, Zhang Dinging, Zhu Jing, Wu Xiaodan, Shi Yi, Wu Tong, Lin Ying, Yang Jiyun, Yuan Guohua, Yang Zhenglin

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The G-Protein β3 subunit 825 TT genotype is associated with epigastric pain syndrome-like dyspepsia by Hori Kazutoshi, Kim Yongmin, Tomita Toshihiko, Tanaka Junji, Sakurai Jun, Toyoshima Fumihiko, Yokoyama Tetsuji, Nakajima Shigemi, Oshima Tadayuki, Matsumoto Takayuki, Miwa Hiroto

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Role of TSP-1 as prognostic marker in various cancers: a systematic review and meta-analysis by Shengjie Sun, Huiyu Dong, Tao Yan, Junchen Li, Bianjiang Liu, Pengfei Shao, Jie Li, Chao Liang

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The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency by Tomlinson Ian PM, Launonen Virpi, Bayley Jean-Pierre

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Toll-like receptor gene polymorphisms are associated with susceptibility to graves' ophthalmopathy in Taiwan males by Liu Yu-Huei, Lin Hui-Ju, Chen Rong-Hsing, Liao Wen-Ling, Chen Wen-Chi, Tsai Yuhsin, Wan Lei, Tsai Fuu-Jen

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The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity by Sun Manna, Zhou Tianhong, Li Liyan, Cai Ren, Shang Xuan, Zhang Xinhua, Chen Wanqun, Xiong Fu, Xu Xiangmin

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