HuGE Literature Finder
Records 1-30
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Functional monoamine oxidase B gene intron 13 polymorphism predicts putaminal dopamine turnover in de novo Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2018 Sep . Löhle Matthias, Mangone Graziella, Wolz Martin, Beuthien-Baumann Bettina, Oehme Liane, van den Hoff Jörg, Kotzerke Jörg, Reichmann Heinz, Corvol Jean-Christophe, Storch Alexand |
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MAO-B and COMT Genetic Variations Associated With Levodopa Treatment Response in Patients With Parkinson's Disease.
Journal of clinical pharmacology 2018 Mar . Sampaio Tiago Furtado, Dos Santos Erinaldo Ubirajara Damasceno, de Lima Gessica Dayane Cordeiro, Dos Anjos Rute Salgues Gueiros, da Silva Ronaldo Celerino, Asano Amdore Guescel C, Asano Nadja Maria Jorge, Crovella Sergio, de Souza Paulo Roberto Eleutér |
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Dopamine D2 receptor gene variants and response to rasagiline in early Parkinson's disease: a pharmacogenetic study.
Brain : a journal of neurology 2016 May . Masellis Mario, Collinson Shannon, Freeman Natalie, Tampakeras Maria, Levy Joseph, Tchelet Amir, Eyal Eli, Berkovich Elijahu, Eliaz Rom E, Abler Victor, Grossman Iris, Fitzer-Attas Cheryl, Tiwari Arun, Hayden Michael R, Kennedy James L, Lang Anthony E, Knight Jo, |
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Association between monoamine oxidase B A644G polymorphism and Parkinson's disease risk: a meta-analysis in the Chinese population.
Genetics and molecular research : GMR 2016 15 (2): . Liu J J, Wang W, Meng M, Liang C S, Zhang J |
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Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson's disease.
Brain : a journal of neurology 2015 May 138 (Pt 5): 1271-83. Moreau Caroline, Meguig Sayah, Corvol Jean-Christophe, Labreuche Julien, Vasseur Francis, Duhamel Alain, Delval Arnaud, Bardyn Thomas, Devedjian Jean-Christophe, Rouaix Nathalie, Petyt Gregory, Brefel-Courbon Christine, Ory-Magne Fabienne, Guehl Dominique, Eusebio Alexandre, Fraix Valérie, Saulnier Pierre-Jean, Lagha-Boukbiza Ouhaid, Durif Frank, Faighel Mirela, Giordana Caroline, Drapier Sophie, Maltête David, Tranchant Christine, Houeto Jean-Luc, Debû Bettina, Azulay Jean-Philippe, Tison François, Destée Alain, Vidailhet Marie, Rascol Olivier, Dujardin Kathy, Defebvre Luc, Bordet Régis, Sablonnière Bernard, Devos David, |
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[Polymorphisms of catechol-O-methyltransferase and monoamine oxidase B genes among Chinese patients with Parkinson's disease].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Feb 32 (1): 1-5. Hao Hongying, Shao Ming, An Jing, Chen Chushuang, Feng Xiuli, Xie Shu, Gu Zhuqin, Chen Bi |
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Association of Catechol-O-Methyltransferase and monoamine oxidase B gene polymorphisms with motor complications in parkinson's disease in a Chinese population.
Parkinsonism & related disorders 2014 Oct 20 (10): 1041-5. Hao Hongying, Shao Ming, An Jing, Chen Chushuang, Feng Xiuli, Xie Shu, Gu Zhuqin, Chan Piu, |
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Functional polymorphisms of the MAO gene with Parkinson disease susceptibility: a meta-analysis.
Journal of the neurological sciences 2014 Oct 345 (1-2): 97-105. Sun Yong-Xin, Wang Xiao-Hong, Xu Ai-Hua, Zhao Jiu-H |
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Impact of COMT H108L, MAOB int 13 A>G and DRD2 haplotype on the susceptibility to Parkinson's disease in South Indian subjects.
Indian journal of biochemistry & biophysics 2013 Oct 50 (5): 436-41. Kumudini Nadella, Umai Addepally, Devi Yalavarthy Prameela, Naushad Shaik Mohammad, Mridula Rukmini, Borgohain Rupam, Kutala Vijay Kum |
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Association of monoamine oxidase B and catechol-O-methyltransferase polymorphisms with sporadic Parkinson's disease in an Iranian population.
Folia neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences 2012 50 (4): 382-9. Torkaman-Boutorabi Anahita, Ali Shahidi Gholam, Choopani Samira, Reza Zarrindast Mohamm |
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The catechol-O-methyltransferase and monoamine oxidase B polymorphisms and levodopa therapy in the Iranian patients with sporadic Parkinson's disease.
Acta neurobiologiae experimentalis 2012 72 (3): 272-82. Torkaman-Boutorabi Anahita, Shahidi Gholam Ali, Choopani Samira, Rezvani Mohammad, Pourkosary Kosar, Golkar Majid, Zarrindast Mohammad-Re |
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Genetic polymorphisms involved in dopaminergic neurotransmission and risk for Parkinson's disease in a Japanese population.
BMC neurology 2011 11 (1): 89. Kiyohara Chikako, Miyake Yoshihiro, Koyanagi Midori, Fujimoto Takahiro, Shirasawa Senji, Tanaka Keiko, Fukushima Wakaba, Sasaki Satoshi, Tsuboi Yoshio, Yamada Tatsuo, Oeda Tomoko, Shimada Hiroyuki, Kawamura Nobutoshi, Sakae Nobutaka, Fukuyama Hidenao, Hirota Yoshio, Nagai Masaki, |
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Smoking, genes encoding dopamine pathway and risk for Parkinson's disease.
Neuroscience letters 2010 Sep 482 (1): 31-4. Gu Zhuqin, Feng Xiuli, Dong Xiumin, Chan P |
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A case-control study of Parkinson's disease and tobacco use: gene-tobacco interactions.
Movement disorders : official journal of the Movement Disorder Society 2010 May 25 (7): 912-9. De Palma Giuseppe, Dick Finlay D, Calzetti Stefano, Scott Neil W, Prescott Gordon J, Osborne Aileen, Haites Neva, Mozzoni Paola, Negrotti Anna, Scaglioni Augusto, Mutti Antonio, |
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Polymorphism in environment responsive genes and association with Parkinson disease.
Molecular and cellular biochemistry 2008 May 312 (1-2): 131-8. Singh Madhu, Khan Anwar J, Shah Parag P, Shukla Rakesh, Khanna V K, Parmar Devend |
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Gene-gene interaction between FGF20 and MAOB in Parkinson disease.
Annals of human genetics 2008 Mar 72 (Pt 2): 157-62. Gao X, Scott W K, Wang G, Mayhew G, Li Y J, Vance J M, Martin E |
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Gene-environment interactions in parkinsonism and Parkinson's disease: the Geoparkinson study.
Occupational and environmental medicine 2007 Oct 64 (10): 673-80. Dick F D, De Palma G, Ahmadi A, Osborne A, Scott N W, Prescott G J, Bennett J, Semple S, Dick S, Mozzoni P, Haites N, Wettinger S Bezzina, Mutti A, Otelea M, Seaton A, Soderkvist P, Felice A, |
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Family-based case-control study of MAOA and MAOB polymorphisms in Parkinson disease.
Movement disorders : official journal of the Movement Disorder Society 2006 Dec 21 (12): 2175-80. Kang Sun J, Scott William K, Li Yi-Ju, Hauser Michael A, van der Walt Joelle M, Fujiwara Kenichiro, Mayhew Gregory M, West Sandra G, Vance Jeffery M, Martin Eden |
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Family-based case-control study of cigarette smoking and Parkinson disease.
Neurology 2005 Feb 64 (3): 442-7. Scott W K, Zhang F, Stajich J M, Scott B L, Stacy M A, Vance J |
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Catechol-O-methyltransferase and monoamine oxidase B genes and susceptibility to sporadic Parkinson's disease in a Polish population.
European neurology 2005 53 (2): 68-73. Bia?ecka Monika, Dro?dzik Marek, Honczarenko Krystyna, Gawro?ska-Szklarz Barbara, Stankiewicz Jan, Dabrowska Ewa, Kubisiak Maciej, K?odowska-Duda Gabriela, Opala Grzego |
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The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease.
Acta neurologica Scandinavica 2004 Oct 110 (4): 260-6. Bia?ecka M, Dro?dzik M, K?odowska-Duda G, Honczarenko K, Gawro?ska-Szklarz B, Opala G, Stankiewicz |
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Association of variations in monoamine oxidases A and B with Parkinson's disease subgroups.
Genomics 2004 Mar 83 (3): 454-60. Parsian A, Racette B, Zhang Z H, Rundle M, Perlmutter J |
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DNA sequence analysis of monoamine oxidase B gene coding and promoter regions in Parkinson's disease cases and unrelated controls.
Movement disorders : official journal of the Movement Disorder Society 2004 Jan 19 (1): 76-83. Costa-Mallen Paola, Afsharinejad Zahra, Kelada Samir N, Costa Lucio G, Franklin Gary M, Swanson Phillip D, Longstreth W T, Viernes Hannah-Malia A, Farin Federico M, Smith-Weller Terri, Checkoway Harv |
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Lack of effect of polymorphisms in dopamine metabolism related genes on imaging of TRODAT-1 in striatum of asymptomatic volunteers and patients with Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2003 Jul 18 (7): 804-12. Lynch David R, Mozley P David, Sokol Set, Maas Nicole M C, Balcer Laura J, Siderowf Andrew |
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Monoamine oxidase B polymorphism, cigarette smoking and risk of Parkinson's disease: a study in an Asian population.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003 Jul 120B (1): 58-62. Tan E K, Chai A, Lum S Y, Shen H, Tan C, Teoh M L, Yih Y, Wong M C, Zhao |
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Genetic and environmental risk factors and their interactions for Parkinson's disease in a Chinese population.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2003 May 10 (3): 313-5. Chan D K Y, Mellick G D, Hung W T, Woo |
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Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2002 Nov 17 (6): 1305-11. Goudreau John L, Maraganore Demetrius M, Farrer Matthew J, Lesnick Timothy G, Singleton Andrew B, Bower James H, Hardy John A, Rocca Walter |
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Gender difference in the interaction of smoking and monoamine oxidase B intron 13 genotype in Parkinson's disease.
Neurotoxicology 2002 Oct 23 (4-5): 515-9. Kelada Samir N, Costa-Mallen Paola, Costa Lucio G, Smith-Weller Terry, Franklin Gary M, Swanson Phillip D, Longstreth W T, Checkoway Harv |
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MAOB intron 13 and COMT codon 158 polymorphisms, cigarette smoking, and the risk of PD.
Neurology 2002 May 58 (9): 1381-7. Hernán M A, Checkoway H, O'Brien R, Costa-Mallen P, De Vivo I, Colditz G A, Hunter D J, Kelsey K T, Ascherio |
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[Polymorphism of MAO-B gene and NAD(P)H: quinone oxidoreductase gene in Parkinson's disease]
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2001 Apr 18 (2): 122-4. Shao M, Liu Z, Tao E, Chen B |
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The COMT L allele modifies the association between MAOB polymorphism and PD in Taiwanese.
Neurology 2001 Feb 56 (3): 375-82. Wu R M, Cheng C W, Chen K H, Lu S L, Shan D E, Ho Y F, Chern H |
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The relationship between monoamine oxidase B (MAOB) A644G polymorphism and Parkinson disease risk: a meta-analysis.
Annals of Saudi medicine 0 34 (1): 12-7. Liu Ying, Wang Zhiyun, Zhang Bens |
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- Page last updated:Aug 05, 2020
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