Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 52 Records) |
Query Trace: SLC2A1[original query] |
---|
Paroxysmal Dyskinesia in Children: from Genes to the Clinic. Journal of clinical neurology (Seoul, Korea) 2018 Jul . Kim Soo Yeon, Lee Jin Sook, Kim Woo Joong, Kim Hyuna, Choi Sun Ah, Lim Byung Chan, Kim Ki Joong, Chae Jong H |
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 |
Molecular Genetic Characterization of Patients With Focal Epilepsy Using a Customized Targeted Resequencing Gene Panel. Frontiers in neurology 2018 7 9 515. Tsai Meng-Han, Chan Chung-Kin, Chang Ying-Chao, Lin Chih-Hsiang, Liou Chia-Wei, Chang Wen-Neng, Ng Ching-Ching, Lim Kheng-Seang, Hwang Daw-Ya |
Development of a rapid functional assay that predicts GLUT1 disease severity. Neurology. Genetics 2018 12 4 (6): e297. Zaman Sasha M, Mullen Saul A, Petrovski Slavé, Maljevic Snezana, Gazina Elena V, Phillips A Marie, Jones Gabriel Davis, Hildebrand Michael S, Damiano John, Auvin Stéphane, Lerche Holger, Weber Yvonne G, Berkovic Samuel F, Scheffer Ingrid E, Reid Christopher A, Petrou Stev |
Investigation of SLC2A1 gene variants in genetic generalized epilepsy patients with eyelid myoclonia. Epileptic disorders : international epilepsy journal with videotape 2018 Oct 20 (5): 396-400. Alt?okka-Uzun Güne?, Özdemir Özkan, U?ur-??eri Sibel, Bebek Nerses, Gürses Candan, Özbek U?ur, Baykan Bet |
The contribution of genetic variants of SLC2A1 gene in T2DM and T2DM-nephropathy: association study and meta-analysis. Renal failure 2018 Nov 40 (1): 561-576. Stefanidis I, Tziastoudi M, Tsironi E E, Dardiotis E, Tachmitzi S V, Fotiadou A, Pissas G, Kytoudis K, Sounidaki M, Ampatzis G, Mertens P R, Liakopoulos V, Eleftheriadis T, Hadjigeorgiou G M, Santos M, Zintzaras |
Cross-disease analysis identified novel common genes for both lung adenocarcinoma and lung squamous cell carcinoma. Oncology letters 2019 9 18 (4): 3463-3470. Zhang Guanghui, Wang Weijie, Huang Weiyang, Xie Xiaoli, Liang Zhigang, Cao Hongb |
Dissecting the phenotypic and genetic spectrum of early childhood-onset generalized epilepsies. Seizure 2019 8 71 222-228. Kim Soo Yeon, Jang Se Song, Kim Jong-Il, Kim Hunmin, Hwang Hee, Choi Ji Eun, Chae Jong-Hee, Kim Ki Joong, Lim Byung Ch |
Associations between the HaeIII Single Nucleotide Polymorphism in the SLC2A1 Gene and Diabetic Nephropathy in Korean Patients with Type 2 Diabetes Mellitus. Journal of Korean medical science 2019 Jun 34 (24): e171. Lee Dong Hwa, Won Gun Woo, Lee Yong Hee, Ku Eu Jeong, Oh Tae Keun, Jeon Hyun Jeo |
Molecular Characterisation of Canine Osteosarcoma in High Risk Breeds. Cancers 2020 8 12 (9): . Simpson Siobhan, Dunning Mark, de Brot Simone, Alibhai Aziza, Bailey Clara, Woodcock Corinne L, Mestas Madeline, Akhtar Shareen, Jeyapalan Jennie N, Lothion-Roy Jennifer, Emes Richard D, Allegrucci Cinzia, Rizvanov Albert A, Mongan Nigel P, Rutland Catrin |
Thrombotic, inflammatory, and HIF-regulated genes and thrombosis risk in polycythemia vera and essential thrombocythemia. Blood advances 2020 3 4 (6): 1115-1130. Gangaraju Radhika, Song Jihyun, Kim Soo Jin, Tashi Tsewang, Reeves Brandi N, Sundar Krishna M, Thiagarajan Perumal, Prchal Josef |
Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants. Cells 2020 10 9 (11): . Sutherland Heidi G, Maksemous Neven, Albury Cassie L, Ibrahim Omar, Smith Robert A, Lea Rod A, Haupt Larisa M, Jenkins Bronwyn, Tsang Benjamin, Griffiths Lyn |
The genetic map of diabetic nephropathy: evidence from a systematic review and meta-analysis of genetic association studies. Clinical kidney journal 2020 10 13 (5): 768-781. Tziastoudi Maria, Stefanidis Ioannis, Zintzaras Eli |
Polymorphism in the HaeIII single nucleotide polymorphism of the SLC2A1 gene and cardiovascular disease in the early type 2 diabetes mellitus. Diabetes & vascular disease research 0 18 (5): 14791641211041225. Lee Dong-Hwa, Won Gun Woo, Lee Yong Hee, Shin Jong Sung, Ku Eu Jeong, Oh Tae Keun, Jeon Hyun Jeo |
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 |
SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population. Human genetics 2021 11 141 (1): 81-99. Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous |
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 |
Diabetic kidney disease: Are the reported associations with single-nucleotide polymorphisms disease-specific? World journal of diabetes 2021 Oct 12 (10): 1765-1777. Saracyn Marek, Kisiel Bart?omiej, Franaszczyk Maria, Brodowska-Kania Dorota, ?mudzki Wawrzyniec, Ma?ecki Robert, Niemczyk Longin, Dyrla Przemys?aw, Kami?ski Grzegorz, P?oski Rafa?, Niemczyk Stanis? |
Impact of germline polymorphisms in genes regulating glucose uptake on positron emission tomography findings and outcome in diffuse large B-cell lymphoma: results from the PETAL trial. Journal of cancer research and clinical oncology 2021 Oct . Broecker-Preuss Martina, Becher-Boveleth Nina, Müller Stefan P, Hüttmann Andreas, Hanoun Christine, Grafe Hong, Richter Julia, Klapper Wolfram, Rekowski Jan, Bockisch Andreas, Dührsen Ulri |
The Association Between Genetic Polymorphisms of Transporter Genes and Prognosis of Platinum-Based Chemotherapy in Lung Cancer Patients. Pharmacogenomics and personalized medicine 2022 15 817-825. He Jia, Wang Zhan, Zou Ting, Wang Ying, Li Xiang-Ping, Chen Ju |
Predicting Differences in Treatment Response and Survival Time of Lung Adenocarcinoma Patients Based on a Prognostic Risk Model of Glycolysis-Related Genes. Frontiers in genetics 2022 6 13 828543. Zhao Rongchang, Ding Dan, Ding Yan, Han Rongbo, Wang Xiujuan, Zhu Chunro |
Genetic Variants of Glycogen Metabolism Genes Were Associated With Liver PDFF Without Increasing NAFLD Risk. Frontiers in genetics 2022 4 13 830445. Yang Liu, Sun Zewen, Li Jiuling, Pan Xingchen, Wen Jianping, Yang Jianli, Wang Qing, Chen Pe |
Genetic Modulation of the GLUT1 Transporter Expression-Potential Relevance in Complex Diseases. Biology 2022 11 11 (11): . Kulin Anna, Kucsma Nóra, Bohár Balázs, Literáti-Nagy Botond, Korányi László, Cserepes Judit, Somogyi Anikó, Sarkadi Balázs, Szabó Edit, Várady Györ |
Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique. Balkan medical journal 2022 11 40 (1): 13-20. Atl? Engin, Gürkan Hakan, Güldiken Babürhan, Eker Damla, Yalç?ntepe Sinem, Demir Selma, Atl? Emine ?kb |
Polymorphisms in glucose homeostasis genes are associated with cardiovascular and renal parameters in patients with diabetic nephropathy. Annals of medicine 2022 10 54 (1): 3039-3051. Mota-Zamorano Sonia, González Luz M, Robles Nicolás R, Valdivielso José M, Arévalo-Lorido José C, López-Gómez Juan, Gervasini Guiller |
Multi-omics analyses based on genes associated with oxidative stress and phospholipid metabolism revealed the intrinsic molecular characteristics of pancreatic cancer. Scientific reports 2023 8 13 (1): 13564. Hongdong Wang, Hui Guo, Jiaao Sun, Yuefeng Wa |
Genetic analysis of dystonia-related genes in Parkinson's disease. Frontiers in aging neuroscience 2023 6 15 1207114. Yige Wang, Yuwen Zhao, Hongxu Pan, Qian Zeng, Xiaoxia Zhou, Yaqin Xiang, Zhou Zhou, Qian Xu, Qiying Sun, Jieqiong Tan, Xinxiang Yan, Jinchen Li, Jifeng Guo, Beisha Tang, Qiao Yu, Zhenhua L |
Whole-Genome Sequencing Among Kazakhstani Children with Early-Onset Epilepsy Revealed New Gene Variants and Phenotypic Variability. Molecular neurobiology 2023 4 . Mirgul Bayanova, Aidos K Bolatov, Assiya Bazenova, Lyazzat Nazarova, Alissa Nauryzbayeva, Naanlep Matthew Tanko, Saule Rakhimova, Nazerke Satvaldina, Diana Samakyzy, Ulan Kozhamkulov, Ulykbek Kairov, Ainur Akilzhanova, Dos Sarbass |
Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders. The Journal of molecular diagnostics : JMD 2023 4 . Se Hee Kim, Soon Sung Kwon, Mi Ri Park, Hyeon Ah Lee, Ji Hun Kim, JiHoon Cha, Sangwoo Kim, Seung Tae Baek, Se Hoon Kim, Joon Soo Lee, Heung Dong Kim, Jong Rak Choi, Seung-Tae Lee, Hoon-Chul Ka |
Associations Between Single Nucleotide Polymorphisms of Hypoxia-Related Genes and Capsule Formation in Hepatocellular Carcinoma. Journal of hepatocellular carcinoma 2023 10 10 1785-1797. Shanshan Chen, Youjia Duan, Yongchao Zhang, Long Cheng, Liang Cai, Xiaopu Hou, Wei |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: