Human Genome Epidemiology Literature Finder

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Records 1 - 6 (of 6 Records)

Query Trace: Disease and SLC2A3[original query]
Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntington's disease. Human molecular genetics 2014 Jun 23 (12): 3129-37. Vittori Angelica, Breda Carlo, Repici Mariaelena, Orth Michael, Roos Raymund A C, Outeiro Tiago F, Giorgini Flaviano, Hollox Edward J, Similar articles in PubMed
Major Contribution of Genomic Copy Number Variation in Syndromic Congenital Heart Disease: The Use of MLPA as the First Genetic Test. Molecular syndromology 2017 9 8 (5): 227-235. Monteiro Rejane A C, de Freitas Mariana L, Vianna Gabrielle S, de Oliveira Valdirene T, Pietra Rafaella X, Ferreira Luana C A, Rocha Patrícia P O, da S Gonçalves Michele, da C César Giovana, de S Lima Joziele, Medeiros Paula F V, Mazzeu Juliana F, Jehee Fernanda Similar articles in PubMed
mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas. Yonsei medical journal 2018 Aug 59 (6): 746-753. Suh Sunghwan, Kim Yun Hak, Goh Tae Sik, Jeong Dae Cheon, Lee Chi Seung, Jang Jeon Yeob, Cha Wonjae, Han Myoung Eun, Kim Seong Jang, Kim In Joo, Pak Kyoungju Similar articles in PubMed
Influence of genetic copy number variants of the human GLUT3 glucose transporter gene SLC2A3 on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication study. Molecular genetics and metabolism reports 2019 4 19 100470. Simpfendorfer Kim R, Li Wentian, Shih Andrew, Wen Hongxiu, Kothari Harini P, Einsidler Edward A, Wuster Arthur, Hunkapiller Julie, Behrens Timothy W, Graham Robert R, Townsend Michael J, Behar Doron M, Hu Rui, Greenspan Elliott, Gregersen Peter Similar articles in PubMed
SLC2A3 rs12842 polymorphism and risk for Alzheimer's disease. Neurological research 2020 Jul 1-9. Arseniou Stylianos, Siokas Vasileios, Aloizou Athina-Maria, Stamati Polyxeni, Mentis Alexios-Fotios A, Tsouris Zisis, Dastamani Metaxia, Peristeri Eleni, Valotassiou Varvara, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi Similar articles in PubMed
SLC2A3 variants in familial and sporadic congenital heart diseases in a Chinese Yunnan population. Journal of clinical laboratory analysis 2022 4 36 (6): e24456. Ma Lijing, Xu Jiaxin, Tang Qisheng, Cao Yu, Kong Ruize, Li Kunlin, Liu Jie, Jiang Liho Similar articles in PubMed