HuGE Literature Finder
Records 1-16
|
Association of polymorphisms and reduced expression levels of the NR4A2 gene with Parkinson's disease in a Mexican population.
Journal of the neurological sciences 2017 Aug 379 58-63. Ruiz-Sánchez Elizabeth, Yescas Petra, Rodríguez-Violante Mayela, Martínez-Rodríguez Nancy, Díaz-López Jesica N, Ochoa Adriana, Valdes-Rojas Sergio S, Magos-Rodríguez Daniel, Rojas-Castañeda Julio C, Cervantes-Arriaga Amin, Canizales-Quinteros Samuel, Rojas Patric |
|
NR4A2 genetic variation and Parkinson's disease: evidence from a systematic review and meta-analysis.
Neuroscience letters 2017 Apr . Liu Hongmei, Liu Hongbo, Li Ting, Cui Jiayi, Fu Yingmei, Ren Juanjuan, Sun Xiujia, Jiang Ping, Yu Shunying, Li Chun |
|
Genetic analysis of NR4A2 gene in a large population of Han Chinese patients with Parkinson's disease.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2012 Jul . Liu H, Tao Q, Deng H, Ming M, Ding Y, Xu P, Chen S, Song Z, Le W |
|
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?
Movement disorders : official journal of the Movement Disorder Society 2009 Apr 24 (6): 833-8. Sutherland Greg T, Halliday Glenda M, Silburn Peter A, Mastaglia Frank L, Rowe Dominic B, Boyle Richard S, O'Sullivan John D, Ly Tina, Wilton Steve D, Mellick George |
|
[Association of the polymorphisms in NURR1 gene with Parkinson's disease].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2008 Dec 25 (6): 693-6. Wu Yan, Peng Rong, Chen Wenjun, Zhang Jinhong, Li Tao, Wang Yingcheng, Gou Yingru, Yuan Guang |
|
Nuclear receptor NR4A2 IVS6 +18insG and brain derived neurotrophic factor (BDNF) V66M polymorphisms and risk of Taiwanese Parkinson's disease.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Jun 144B (4): 458-62. Chen Chiung-Mei, Chen I-Cheng, Chang Kuo-Hsuan, Chen Yi-Chun, Lyu Rong-Kuo, Liu Yen-Tzu, Hu Fen-Ju, Chao Chih-Ying, Lee-Chen Guey-Jen, Wu Yih- |
|
NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach.
Movement disorders : official journal of the Movement Disorder Society 2006 Nov 21 (11): 1960-3. Healy Daniel G, Abou-Sleiman Patrick M, Ahmadi Kourosh R, Gandhi Sonia, Muqit Miratul M, Bhatia Kailash P, Quinn Niall P, Lees Andrew J, Holton Janice L, Revesz Tamas, Wood Nicholas |
|
Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2006 Jul 21 (7): 906-9. Grimes David A, Han Fabin, Panisset Michel, Racacho Lemuel, Xiao Fengxia, Zou Ruobing, Westaff Kelly, Bulman Dennis |
|
Nurr1 mutational screen in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2004 Dec 19 (12): 1503-5. Tan Eng-King, Chung Henry, Chandran Vandana R, Tan Chris, Shen Hui, Yew Kenneth, Pavanni Ratnagopal, Puvan Kathi-avelu, Wong Meng-Cheong, Teoh Mei-Lin, Yih Yuan, Zhao |
|
NR4A2 and schizophrenia: lack of association in a Portuguese/Brazilian study.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004 Jul 128B (1): 41-5. Ruano Dina, Macedo António, Dourado Ana, Soares Maria João, Valente José, Coelho Isabel, Santos Vítor, Azevedo Maria Helena, Goodman Ann, Hutz Mara Helena, Gama Clarissa, Lobato Maria Inês, Belmonte-de-Abreu Paulo, Palha Joana Almei |
|
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2004 Jun 19 (6): 649-55. Nichols William C, Uniacke Sean K, Pankratz Nathan, Reed Terry, Simon David K, Halter Cheryl, Rudolph Alice, Shults Clifford W, Conneally P Michael, Foroud Tatiana, |
|
Genetic analysis of Nurr1 haplotypes in Parkinson's disease.
Neuroscience letters 2003 Aug 347 (3): 139-42. Tan Eng-King, Chung Henry, Zhao Yi, Shen Hui, Chandran V R, Tan Chris, Teoh Mei-lin, Yih Yuan, Pavanni Ratnagopal, Wong Meng-Cheo |
|
NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003 Jul 120B (1): 51-7. Carmine Andrea, Buervenich Silvia, Galter Dagmar, Jönsson Erik G, Sedvall Göran C, Farde Lars, Gustavsson J Petter, Bergman Hans, Chowdari Kodavali V, Nimgaonkar Vishwajit L, Anvret Maria, Sydow Olof, Olson La |
|
A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease.
Archives of neurology 2003 May 60 (5): 722-5. Zheng Kangni, Heydari Bobak, Simon David |
|
Mutations in NR4A2 associated with familial Parkinson disease.
Nature genetics 2003 Jan 33 (1): 85-9. Le Wei-Dong, Xu Pingyi, Jankovic Joseph, Jiang Hong, Appel Stanley H, Smith Roy G, Vassilatis Demetrios |
|
Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson's disease.
Neurology 2002 Mar 58 (6): 881-4. Xu P-Y, Liang R, Jankovic J, Hunter C, Zeng Y-X, Ashizawa T, Lai D, Le W |
- Page last reviewed:Jul 30, 2019
- Page last updated:Jan 23, 2020
- Content source: