Search Results - "Medical genetics"

Hereditary Hemochromatosis <it>(HFE) </it>genotypes in heart failure: Relation to etiology and prognosis by Torp-Pedersen Christian, Jespersgaard Cathrine, Hedley Paula, Hassager Christian, Gustafsson Finn, Pecini Redi, Møller Daniel V, Christiansen Michael, Køber Lars V

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Association of ABO polymorphisms and pancreatic Cancer/ Cardiocerebrovascular disease: a meta-analysis by Yanxia Li, Luyang Liu, Yubei Huang, Hong Zheng, Lian Li

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Influence of leukotriene gene polymorphisms on chronic rhinosinusitis by Duval Melanie, Cabaluna Myrna, Hudson Thomas J, Bossé Yohan, Al-Shemari Hasan, Lemire Mathieu, Vallee-Smedja Sophie, Frenkiel Saul, Desrosiers Martin

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The (FTO) gene polymorphism is associated with metabolic syndrome risk in Egyptian females: a case- control study by Mina S. Khella, Nadia M. Hamdy, Ashraf I. Amin, Hala O. El-Mesallamy

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MicroRNA-19b-3p promotes cell proliferation and osteogenic differentiation of BMSCs by interacting with lncRNA H19 by Gan Xiaoling, Liu Shuaibin, Liang Kailu

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<it>IL6 and CRP </it>haplotypes are associated with COPD risk and systemic inflammation: a case-control study by Passos Valéria, Kotz Daniel, Houwing-Duistermaat Jeanine J, Spruit Martijn A, Dentener Mieke A, Yanbaeva Dilyara G, Wouters Emiel FM

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The occurrence of germline <it>BRCA1 </it>and <it>BRCA2 </it>sequence alterations in Slovenian population by Hočevar Marko, De Grève Jacques, Teugels Erik, Žgajnar Janez, Krajc Mateja, Stegel Vida, Novaković Srdjan

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Exploring multilocus associations of inflammation genes and colorectal cancer risk using hapConstructor by Abo Ryan, Herrick Jennifer S, Wolff Roger K, Curtin Karen, Slattery Martha L

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The phenomena of balanced effect between α-globin gene and of β-globin gene by Liangying Zhong, Xin Gan, Lingling Xu, Chujia Liang, Yingjun Xie, Wenbin Lin, Peisong Chen, Min Liu

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Failure to replicate an association of SNPs in the oxidized LDL receptor gene (<it>OLR1</it>) with CAD by Risch Neil, Myers Richard, Li Jun, Iribarren Carlos, Hlatky Mark, Go Alan, Grove Megan L, Fortmann Stephen P, Boerwinkle Eric, Assimes Themistocles L, Knowles Joshua W, Sidney Stephen, Southwick Audrey, Volcik Kelly A, Quertermous Thomas

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Methylenetetrahydrofolate Reductase Polymorphisms and Risk of Acute Lymphoblastic Leukemia-Evidence from an updated meta-analysis including 35 studies by Wang Haigang, Wang Jiali, Zhao Lixia, Liu Xinchun, Mi Wenjie

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A case report of Chinese brothers with inherited <it>MECP2-</it>containing duplication: autism and intellectual disability, but not seizures or respiratory infections by Xu Xiu, Xu Qiong, Zhang Ying, Zhang Xiaodi, Cheng Tianlin, Wu Bingbing, Ding Yanhua, Lu Ping, Zheng Jingjing, Zhang Min, Qiu Zilong, Yu Xiang

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Weighted correlation network and differential expression analyses identify candidate genes associated with BRAF gene in melanoma by Bin Zhao, Yanqiu You, Zheng Wan, Yunhan Ma, Yani Huo, Hongyi Liu, Yuanyuan Zhou, Wei Quan, Weibin Chen, Xiaohong Zhang, Fujun Li, Yilin Zhao

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IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance by Murphy Rinki, Ibáñez Lourdes, Hattersley Andrew, Tost Jörg

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Effects of common haplotypes of the ileal sodium dependent bile acid transporter gene on the development of sporadic and familial colorectal cancer: A case control study by Friedrichs Nicolaus, Plassmann Dominik, Schulte-Witte Hildegard, Becker Ursula, Keppeler Hildegard, Lamberti Christoph, Jungck Matthias, Grünhage Frank, Buettner Reinhard, Aretz Stefan, Sauerbruch Tilman, Lammert Frank

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Resequencing <it>PNMT </it>in European hypertensive and normotensive individuals: no common susceptibilily variants for hypertension and purifying selection on intron 1 by Viigimaa Margus, Ots Mai, Kozich Viktor, Juhanson Peeter, Kepp Katrin, Laan Maris

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Mutant POLQ and POLZ/REV3L DNA polymerases may contribute to the favorable survival of patients with tumors with POLE mutations outside the exonuclease domain by Fangjin Huang, Hisashi Tanaka, Beatrice S. Knudsen, Joanne K. Rutgers

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Autism genetic database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites by Talebizadeh Zohreh, Matuszek Gregory

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Effects of interacting networks of cardiovascular risk genes on the risk of type 2 diabetes mellitus (the CODAM study) by Feskens Edith JM, Schiffers Paul MH, Kallen Carla JH, Zhang Jian, van Greevenbroek Marleen MJ, de Bruin Tjerk WA

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Non-replication study of a genome-wide association study for hypertension and blood pressure in African Americans by Kidambi Srividya, Ghosh Soumitra, Kotchen Jane M, Grim Clarence E, Krishnaswami Shanthi, Kaldunski Mary L, Cowley Allen W, Patel Shailendra B, Kotchen Theodore A

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