P268S in NOD2 associates with susceptibility to Parkinson’s disease in Chinese population
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Zhiming Li | Q. Lin | C. Tzeng | Qilin Ma | X. An | Wenqing Huang | Liang-liang Cai | Huan-jing Zhang | Peng Hu | Qing Lin
[1] Zhiming Li,et al. P268S in NOD2 associates with susceptibility to Parkinson’s disease in Chinese population , 2013, Behavioral and Brain Functions.
[2] Xiaoming Yang,et al. Confirmation of three inflammatory bowel disease susceptibility loci in a Chinese cohort , 2012, International Journal of Colorectal Disease.
[3] M. Nalls,et al. Genetic variability at the PARK16 locus , 2010, European Journal of Human Genetics.
[4] Yih-Ru Wu,et al. Genetic analysis of Parkin in early onset Parkinson's disease (PD): Novel intron 9 g > a single nucleotide polymorphism and risk of Taiwanese PD , 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[5] 羅 芳宜,et al. Alteration of PAFAH1B1 in Human Lung Cancer and Its Roles in Tumor Progression and Poor Survival , 2010 .
[6] E. Hirsch,et al. Neuroinflammation in Parkinson's disease: a target for neuroprotection? , 2009, The Lancet Neurology.
[7] A. Fleig,et al. SLC41A1 Is a Novel Mammalian Mg2+ Carrier* , 2008, Journal of Biological Chemistry.
[8] J. Burgunder,et al. LRRK2 Gly2385Arg variant is a risk factor of Parkinson’s disease among Han‐Chinese from mainland China , 2008, European journal of neurology.
[9] A. Lang,et al. Deciphering the role of heterozygous mutations in genes associated with parkinsonism , 2007, The Lancet Neurology.
[10] F. Mastaglia,et al. Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's Disease , 2007, Movement disorders : official journal of the Movement Disorder Society.
[11] G. Opala,et al. CARD15 variants in patients with sporadic Parkinson's disease , 2007, Neuroscience Research.
[12] N. Hattori,et al. Leucine-Rich Repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population , 2007, Neuroreport.
[13] N. Quinn,et al. A heterozygous effect for PINK1 mutations in Parkinson's disease? , 2006, Annals of neurology.
[14] T. Joh,et al. Microglia, major player in the brain inflammation: their roles in the pathogenesis of Parkinson's disease , 2006, Experimental & Molecular Medicine.
[15] T. Gillis,et al. Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study. , 2006, Archives of neurology.
[16] Matthew J. Farrer,et al. LRRK2 in Parkinson's disease: protein domains and functional insights , 2006, Trends in Neurosciences.
[17] C. Klein. Implications of genetics on the diagnosis and care of patients with Parkinson disease. , 2006, Archives of neurology.
[18] N. Hattori,et al. Diverse Effects of Pathogenic Mutations of Parkin That Catalyze Multiple Monoubiquitylation in Vitro* , 2006, Journal of Biological Chemistry.
[19] M. Farrer,et al. The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients , 2005, Neuroscience Letters.
[20] J. Si,et al. [NOD2/CARD15 gene polymorphisms and susceptibility to Crohn's disease in Chinese Han population]. , 2005, Zhonghua nei ke za zhi.
[21] Zhenxin Zhang,et al. Parkinson's disease in China: prevalence in Beijing, Xian, and Shanghai , 2005, The Lancet.
[22] E. Eriksson,et al. Interaction of polymorphisms in the genes encoding interleukin‐6 and estrogen receptor beta on the susceptibility to Parkinson's disease , 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[23] P. Mcgeer,et al. Inflammation and neurodegeneration in Parkinson's disease. , 2004, Parkinsonism & related disorders.
[24] P. Lockhart,et al. Parkin genetics: one model for Parkinson's disease. , 2004, Human molecular genetics.
[25] J. Hoenicka,et al. The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementia , 2004, Annals of neurology.
[26] T. Dawson,et al. Molecular Pathways of Neurodegeneration in Parkinson's Disease , 2003, Science.
[27] W. Dauer,et al. Parkinson's Disease Mechanisms and Models , 2003, Neuron.
[28] D. Jewell,et al. NOD2/CARD15 gene polymorphisms and Crohn's disease in the Chinese population , 2003, Alimentary pharmacology & therapeutics.
[29] S. Fahn. Description of Parkinson's Disease as a Clinical Syndrome , 2003, Annals of the New York Academy of Sciences.
[30] J. Hugot,et al. Gene–environment interaction modulated by allelic heterogeneity in inflammatory diseases , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[31] S. Foster,et al. Host Recognition of Bacterial Muramyl Dipeptide Mediated through NOD2 , 2003, The Journal of Biological Chemistry.
[32] Judy H. Cho,et al. Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan. , 2003, Gastroenterology.
[33] K. Huse,et al. Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations , 2003, European Journal of Human Genetics.
[34] Yusuke Nakamura,et al. Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease , 2002, Journal of Human Genetics.
[35] Tony Wyss-Coray,et al. Inflammation in Neurodegenerative Disease—A Double-Edged Sword , 2002, Neuron.
[36] L. Bradbury,et al. Role of NOD2 variants in spondylarthritis. , 2002, Arthritis and rheumatism.
[37] K. Marder,et al. Evaluation of 50 probands with early-onset Parkinson’s disease for Parkin mutations , 2002, Neurology.
[38] C. Kaltschmidt,et al. Stimulus-dependent activation of NF-κB specifies apoptosis or neuroprotection in cerebellar granule cells , 2002, NeuroMolecular Medicine.
[39] Judy H. Cho,et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease , 2001, Nature.
[40] S. Yamaoka,et al. Nod2, a Nod1/Apaf-1 Family Member That Is Restricted to Monocytes and Activates NF-κB* , 2001, The Journal of Biological Chemistry.
[41] Shinsei Minoshima,et al. Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase , 2000, Nature Genetics.
[42] Bonifati,et al. Association between early-onset Parkinson's disease and mutations in the parkin gene. , 2000, The New England journal of medicine.
[43] J. Woo,et al. The α-Synuclein Gene and Parkinson Disease in a Chinese Population , 2000 .
[44] J. Woo,et al. The alpha-synuclein gene and Parkinson disease in a Chinese population. , 2000, Archives of neurology.
[45] R. Krüger,et al. Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. , 1998, Nature genetics.
[46] Y Agid,et al. Nuclear translocation of NF-kappaB is increased in dopaminergic neurons of patients with parkinson disease. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[47] Robert L. Nussbaum,et al. Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease , 1997 .
[48] S E Ide,et al. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. , 1997, Science.
[49] L. Forno,et al. Neuropathology of Parkinson's Disease , 1996, Journal of neuropathology and experimental neurology.
[50] J. Hughes,et al. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. , 1992, Journal of neurology, neurosurgery, and psychiatry.
[51] T. Nagatsu. [Biochemistry of Parkinson's disease]. , 1988, Seikagaku. The Journal of Japanese Biochemical Society.