Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: SLC2A3[original query] |
---|
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.
Molecular psychiatry 2011 Jan 16 (1): 97-107. Roeske D, Ludwig K U, Neuhoff N, Becker J, Bartling J, Bruder J, Brockschmidt F F, Warnke A, Remschmidt H, Hoffmann P, Müller-Myhsok B, Nöthen M M, Schulte-Körne |
Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree. Molecular psychiatry 2011 May 16 (5): 491-503. Lesch K-P, Selch S, Renner T J, Jacob C, Nguyen T T, Hahn T, Romanos M, Walitza S, Shoichet S, Dempfle A, Heine M, Boreatti-Hümmer A, Romanos J, Gross-Lesch S, Zerlaut H, Wultsch T, Heinzel S, Fassnacht M, Fallgatter A, Allolio B, Schäfer H, Warnke A, Reif A, Ropers H-H, Ullmann |
No Mutation in the SLC2A3 Gene in Cohorts of GLUT1 Deficiency Syndrome-Like Patients Negative for SLC2A1 and in Patients with AHC Negative for ATP1A3. JIMD reports 2014 12 115-20. Bizec C Le, Nicole S, Panagiotakaki E, Seta N, Vuillaumier-Barrot |
Copy number variation at chromosome 5q21.2 is associated with intraocular pressure. Investigative ophthalmology & visual science 2013 May 54 (5): 3607-12. Nag Abhishek, Venturini Cristina, Hysi Pirro G, Arno Matthew, Aldecoa-Otalora Astarloa Estibaliz, Macgregor Stuart, Hewitt Alex W, Young Terri L, Mitchell Paul, Viswanathan Ananth C, Mackey David A, Hammond Christopher |
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, |
Genetic dyslexia risk variant is related to neural connectivity patterns underlying phonological awareness in children. NeuroImage 2015 Sep 118 414-21. Skeide Michael A, Kirsten Holger, Kraft Indra, Schaadt Gesa, Müller Bent, Neef Nicole, Brauer Jens, Wilcke Arndt, Emmrich Frank, Boltze Johannes, Friederici Angela |
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome. American journal of human genetics 2015 May 96 (5): 753-64. Mlynarski Elisabeth E, Sheridan Molly B, Xie Michael, Guo Tingwei, Racedo Silvia E, McDonald-McGinn Donna M, Gai Xiaowu, Chow Eva W C, Vorstman Jacob, Swillen Ann, Devriendt Koen, Breckpot Jeroen, Digilio Maria Cristina, Marino Bruno, Dallapiccola Bruno, Philip Nicole, Simon Tony J, Roberts Amy E, Piotrowicz Ma?gorzata, Bearden Carrie E, Eliez Stephan, Gothelf Doron, Coleman Karlene, Kates Wendy R, Devoto Marcella, Zackai Elaine, Heine-Suñer Damian, Shaikh Tamim H, Bassett Anne S, Goldmuntz Elizabeth, Morrow Bernice E, Emanuel Beverly S, |
Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry. American journal of medical genetics. Part A 2016 Sep . Prakash Siddharth K, Bondy Carolyn A, Maslen Cheryl L, Silberbach Michael, Lin Angela E, Perrone Laura, Limongelli Giuseppe, Michelena Hector I, Bossone Eduardo, Citro Rodolfo, , Lemaire Scott A, Body Simon C, Milewicz Dianna |
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 |
SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder. Journal of child psychology and psychiatry, and allied disciplines 2017 Feb . Merker Sören, Reif Andreas, Ziegler Georg C, Weber Heike, Mayer Ute, Ehlis Ann-Christine, Conzelmann Annette, Johansson Stefan, Müller-Reible Clemens, Nanda Indrajit, Haaf Thomas, Ullmann Reinhard, Romanos Marcel, Fallgatter Andreas J, Pauli Paul, Strekalova Tatyana, Jansch Charline, Vasquez Alejandro Arias, Haavik Jan, Ribasés Marta, Ramos-Quiroga Josep Antoni, Buitelaar Jan K, Franke Barbara, Lesch Klaus-Pet |
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 |
Dyslexia associated functional variants in Europeans are not associated with dyslexia in Chinese. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2019 Jul . Liu Lingfei, Gu Huaiting, Hou Fang, Xie Xinyan, Li Xin, Zhu Bing, Zhang Jiajia, Wei Wen-Hua, Song Ranr |
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 |
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 |
F-FDG PET/CT metabolic parameters correlate with EIF2S2 expression status in colorectal cancer. Journal of Cancer 2021 9 12 (19): 5838-5847. Yang Jian-Wei, Yuan Ling-Ling, Gao Yan, Liu Xu-Sheng, Wang Yu-Jiao, Zhou Lu-Meng, Kui Xue-Yan, Li Xiao-Hui, Ke Chang-Bin, Pei Zhi-J |
Effects of functional variants of vitamin C transporter genes on apolipoprotein E E4-associated risk of cognitive decline: The Nakajima study. PloS one 2021 16 (11): e0259663. Hayashi Koji, Noguchi-Shinohara Moeko, Sato Takehiro, Hosomichi Kazuyoshi, Kannon Takayuki, Abe Chiemi, Domoto Chiaki, Yuki-Nozaki Sohshi, Mori Ayaka, Horimoto Mai, Yokogawa Masami, Sakai Kenji, Iwasa Kazuo, Komai Kiyonobu, Ishimiya Mai, Nakamura Hiroyuki, Ishida Natsuko, Suga Yukio, Ishizaki Junko, Ishigami Akihito, Tajima Atsushi, Yamada Masahi |
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 |
Novel Immune-Related Ferroptosis Signature in Esophageal Cancer: An Informatics Exploration of Biological Processes Related to the TMEM161B-AS1/hsa-miR-27a-3p/GCH1 Regulatory Network. Frontiers in genetics 2022 3 13 829384. Lu Min, Li Jiaqi, Fan Xin, Xie Fei, Fan Jie, Xiong Yuanpi |
Single-cell transcriptome analysis reveals the clinical implications of myeloid-derived suppressor cells in head and neck squamous cell carcinoma. Pathology oncology research : POR 2023 7 29 1611210. Wenru Jiang, Kangyao Hu, Xiaofei Liu, Jili Gao, Liping Z |
Metabolic heterogeneity in early-stage lung adenocarcinoma revealed by RNA-seq and scRNA-seq. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2023 1 . Zhang Yang, Shi Jiang, Luo Junfang, Liu Cong, Zhu Li |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: