Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: SLC29A3[original query] |
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Mutations in the SLC29A3 gene are not a common cause of isolated autoantibody negative type 1 diabetes. JOP : Journal of the pancreas 2009 10 (4): 457-8. Edghill Emma L, Hameed Shihab, Verge Charles F, Rubio-Cabezas Oscar, Argente Jesús, Sumnik Zdenek, Dusatkova Petra, Cliffe Simon T, Hennekam Raoul C M, Buckley Michael F, Hussain Khalid, Ellard Sian, Attersley Andrew |
Contribution of adenosine related genes to the risk of depression with disturbed sleep. Journal of affective disorders 2010 Oct 126 (1-2): 134-9. Gass Natalia, Ollila Hanna M, Utge Siddheshwar, Partonen Timo, Kronholm Erkki, Pirkola Sami, Suhonen Johanna, Silander Kaisa, Porkka-Heiskanen Tarja, Paunio Tii |
Genomic polymorphisms of SLC29A3 associated with overall survival in advanced non-small-cell lung cancer treated with gemcitabine. Medical oncology (Northwood, London, England) 2014 Apr 31 (4): 865. Chen Xiaoxia, Zhang Ling, Ren Shengxiang, Li Xuefei, Zhou Fei, Li Wei, Gao Guanghui, He Yayi, Zhou Caic |
Genome-Wide Analysis of Protein-Coding Variants in Leprosy. The Journal of investigative dermatology 2017 Aug . Liu Hong, Wang Zhenzhen, Li Yi, Yu Gongqi, Fu Xi'an, Wang Chuan, Liu Wenting, Yu Yongxiang, Bao Fangfang, Irwanto Astrid, Liu Jian, Chu Tongsheng, Andiappan Anand Kumar, Maurer-Stroh Sebastian, Limviphuvadh Vachiranee, Wang Honglei, Mi Zihao, Sun Yonghu, Sun Lele, Wang Ling, Wang Chaolong, You Jiabao, Li Jinghui, Foo Jia Nee, Liany Herty, Meah Wee Yang, Niu Guiye, Yue Zhenhua, Zhao Qing, Wang Na, Yu Meiwen, Yu Wenjun, Cheng Xiujun, Khor Chiea Chuen, Sim Kar Seng, Aung Tin, Wang Ningli, Wang Deyun, Shi Li, Ning Yong, Zheng Zhongyi, Yang Rongde, Li Jinlan, Yang Jun, Yan Liangbin, Shen Jianping, Zhang Guocheng, Chen Shumin, Liu Jianjun, Zhang Fur |
Discovering novel SNPs that are correlated with patient outcome in a Singaporean cancer patient cohort treated with gemcitabine-based chemotherapy. BMC cancer 2018 May 18 (1): 555. Limviphuvadh Vachiranee, Tan Chee Seng, Konishi Fumikazu, Jenjaroenpun Piroon, Xiang Joy Shengnan, Kremenska Yuliya, Mu Yar Soe, Syn Nicholas, Lee Soo Chin, Soo Ross A, Eisenhaber Frank, Maurer-Stroh Sebastian, Yong Wei Pe |
Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of <5 years in the Iranian population. Diabetic medicine : a journal of the British Diabetic Association 2019 7 36 (12): 1694-1702. Yaghootkar H, Abbasi F, Ghaemi N, Rabbani A, Wakeling M N, Eshraghi P, Enayati S, Vakili S, Heidari S, Patel K, Sayarifard F, Borhan-Dayani S, McDonald T J, Ellard S, Hattersley A T, Amoli M M, Vakili R, Colclough |
A novel 3' untranslated region mutation in the SLC29A3 gene associated with pigmentary hypertrichosis and non-autoimmune insulin-dependent diabetes mellitus syndrome. Pediatric diabetes 2019 3 20 (4): 474-481. Riachi Melissa, Bas Firdevs, Darendeliler Feyza, Hussain Khal |
The third case of TNFRSF11A-associated dysosteosclerosis with a mutation producing elongating proteins. Journal of human genetics 2020 10 66 (4): 371-377. Xue Jing-Yi, Wang Zheng, Smithson Sarah F, Burren Christine P, Matsumoto Naomichi, Nishimura Gen, Ikegawa Shiro, Guo Lo |
Single-Nucleotide Polymorphisms Related to Leprosy Risk and Clinical Phenotypes Among Chinese Population. Pharmacogenomics and personalized medicine 2021 14 813-821. Long Si-Yu, Wang Le, Jiang Hai-Qin, Shi Ying, Zhang Wen-Yue, Xiong Jing-Shu, Sun Pei-Wen, Chen Yan-Qing, Mei You-Ming, Pan Chun, Ge Gai, Wang Zhen-Zhen, Wu Zi-Wei, Yu Mei-Wen, Wang Hong-She |
Identification of Shared and Asian-Specific Loci for Systemic Lupus Erythematosus and Evidence for Roles of Type III Interferon Signaling and Lysosomal Function in the Disease: A Multi-Ancestral Genome-Wide Association Study.
Arthritis & rheumatology (Hoboken, N.J.) 2021 Nov . Wang Yong-Fei, Wei Wei, Tangtanatakul Pattarin, Zheng Lichuan, Lei Yao, Lin Zhiming, Qian Chengmin, Qin Xiao, Hou Fei, Zhang Xinyu, Shao Li, Satproedprai Nusara, Mahasirimongkol Surakameth, Pisitkun Prapaporn, Song Qin, Lau Yu Lung, Zhang Yan, Hirankarn Nattiya, Yang Wanli |
Phenotypic intrafamilial variability including H syndrome and Rosai-Dorfman disease associated with the same c.1088G?>?A mutation in the SLC29A3 gene. Human genomics 2021 10 15 (1): 63. Chouk Hamza, Ben Rejeb Mohamed, Boussofara Lobna, Elmabrouk Ha?fa, Ghariani Najet, Sriha Badreddine, Saad Ali, H'Mida Dorra, Denguezli Moham |
Genome-wide association study of leprosy in Malawi and Mali.
PLoS pathogens 2022 9 18 (9): e1010312. Gilchrist James J, Auckland Kathryn, Parks Tom, Mentzer Alexander J, Goldblatt Lily, Naranbhai Vivek, Band Gavin, Rockett Kirk A, Toure Ousmane B, Konate Salimata, Sissoko Sibiri, Djimdé Abdoulaye A, Thera Mahamadou A, Doumbo Ogobara K, Sow Samba, Floyd Sian, Pönnighaus Jörg M, Warndorff David K, Crampin Amelia C, Fine Paul E M, Fairfax Benjamin P, Hill Adrian V |
Loss-of-function of ENT3 drives histiocytosis and inflammation through TLR-MAPK signaling. Blood 2023 9 . Ruth Shiloh, Ruth Lubin, Odeya David, Ifat Geron, Elimelech Okon, Idit Hazan, Marketa Zaliova, Gil Amarilyo, Yehudit Birger, Yael Borovitz, Dafna Brik, Arnon Broides, Sarit Cohen-Kedar, Liora Harel, Eyal Kristal, Daria Kozlova, Galina Ling, Mika Shapira Rootman, Noa Shefer Averbuch, Shiri Spielman, Jan Trka, Shai Izraeli, Simon Yona, Sarah Elitz |
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- Page last updated:Apr 22, 2024
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