Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: SLC41A1[original query] |
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Genetic variability at the PARK16 locus. European journal of human genetics : EJHG 2010 Dec 18 (12): 1356-9. Tucci Arianna, Nalls Mike A, Houlden Henry, Revesz Tamas, Singleton Andrew B, Wood Nicholas W, Hardy John, Paisán-Ruiz Co |
Genetic variants in the RAB7L1 and SLC41A1 genes of the PARK16 locus in Chinese Parkinson's disease patients. The International journal of neuroscience 2011 Nov 121 (11): 632-6. Yan Yaping, Tian Jun, Mo Xiaoyun, Zhao Guohua, Yin Xinzhen, Pu Jiali, Zhang Baoro |
P268S in NOD2 associates with susceptibility to Parkinson's disease in Chinese population. Behavioral and brain functions : BBF 2013 9 (1): 19. Ma Qilin, An Xingkai, Li Zhiming, Zhang Huanjing, Huang Wenqing, Cai Liangliang, Hu Peng, Lin Qing, Tzeng Chi-Me |
Variant R244H in Na+/Mg2+ exchanger SLC41A1 in Taiwanese Parkinson's disease is associated with loss of Mg2+ efflux function. Parkinsonism & related disorders 2014 Jun 20 (6): 600-3. Lin Chih-Hsin, Wu Yih-Ru, Chen Wan-Ling, Wang Hao-Chun, Lee Chi-Mei, Lee-Chen Guey-Jen, Chen Chiung-M |
Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Aug . Wang Ling, Cheng Lan, Li Nan-Nan, Yu Wen-Juan, Sun Xiao-Yi, Peng Ro |
Fine mapping and resequencing of the PARK16 locus in Parkinson's disease. Journal of human genetics 2015 Jul 60 (7): 357-62. Pihlstrøm Lasse, Rengmark Aina, Bjørnarå Kari Anne, Dizdar Nil, Fardell Camilla, Forsgren Lars, Holmberg Björn, Larsen Jan Petter, Linder Jan, Nissbrandt Hans, Tysnes Ole-Bjørn, Dietrichs Espen, Toft Mathi |
Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population. Genetic testing and molecular biomarkers 2016 Sep . Madadi Faranak, Shekari Khaniani Mahmoud, Esmaili Shandiz Ehsan, Ayromlou Hormoz, Najmi Safa, Emamalizadeh Babak, Taghavi Shaghayegh, Jamshidi Javad, Tafakhori Abbas, Shahidi Gholam-Ali, Darvish Hosse |
Associations of rs823128, rs1572931, and rs823156 polymorphisms with reduced Parkinson's disease risks. Neuroreport 2017 Jul . Bai Ye, Dong Lihong, Huang Xinghua, Zheng Shuanglin, Qiu Ping, Lan Fengh |
SNPs rs11240569, rs708727, and rs823156 in SLC41A1 Do Not Discriminate Between Slovak Patients with Idiopathic Parkinson's Disease and Healthy Controls: Statistics and Machine-Learning Evidence. International journal of molecular sciences 2019 9 20 (19): . Cibulka Michal, Brodnanova Maria, Grendar Marian, Grofik Milan, Kurca Egon, Pilchova Ivana, Osina Oto, Tatarkova Zuzana, Dobrota Dusan, Kolisek Mart |
Cyclin M2 (CNNM2) knockout mice show mild hypomagnesaemia and developmental defects. Scientific reports 2021 4 11 (1): 8217. Franken Gijs A C, Seker Murat, Bos Caro, Siemons Laura A H, van der Eerden Bram C J, Christ Annabel, Hoenderop Joost G J, Bindels René J M, Müller Dominik, Breiderhoff Tilman, de Baaij Jeroen H |
Mutation analysis of seven SLC family transporters for early-onset Parkinson's disease in Chinese population. Neurobiology of aging 2021 Mar . Li ChunYu, Ou RuWei, Chen YongPing, Gu XiaoJing, Wei QianQian, Cao Bei, Zhang LingYu, Hou YanBing, Liu KunCheng, Chen XuePing, Song Wei, Zhao Bi, Wu Ying, Shang HuiFa |
Alzheimer's Disease-Associated SNP rs708727 in SLC41A1 May Increase Risk for Parkinson's Disease: Report from Enlarged Slovak Study. International journal of molecular sciences 2022 2 23 (3): . Cibulka Michal, Brodnanova Maria, Grendar Marian, Necpal Jan, Benetin Jan, Han Vladimir, Kurca Egon, Nosal Vladimir, Skorvanek Matej, Vesely Branislav, Stanclova Andrea, Lasabova Zora, Pös Zuzana, Szemes Tomas, Stuchlik Stanislav, Grofik Milan, Kolisek Mart |
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- Page last updated:Apr 22, 2024
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