SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population - Wikidata - wikimedia - TriplyDB

SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population

SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population

http://www.wikidata.org/entity/Q35859538

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α-Synuclein genetic variants predict faster motor symptom progression in idiopathic Parkinson disease Glia and alpha-synuclein in neurodegeneration: A complex interaction Exploring the Effects of Genetic Variants on Clinical Profiles of Parkinson's Disease Assessed by the Unified Parkinson's Disease Rating Scale and the Hoehn-Yahr Stage Variants in SNCA Gene Are Associated with Parkinson's Disease Risk and Cognitive Symptoms in a Brazilian Sample.Evaluation of the role of SNCA variants in survival without neurological disease A powerful yeast model to investigate the synergistic interaction of α-synuclein and tau in neurodegeneration.Cognitive impairment and dementia in Parkinson's disease: clinical features, diagnosis, and management.Premotor biomarkers for Parkinson's disease - a promising direction of research.Analysis of LRRK2, SNCA, and ITGA8 Gene Variants with Sporadic Parkinson's Disease Susceptibility in Chinese Han Population.Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.Characterization of saliva microbiota's functional feature based on metagenomic sequencing The impact of mitochondrial DNA and nuclear genes related to mitochondrial functioning on the risk of Parkinson's disease.Genetic Variants in SNCA and the Risk of Sporadic Parkinson's Disease and Clinical Outcomes: A Review Interactions Between α-Synuclein and Tau Protein: Implications to Neurodegenerative Disorders.Identifying the Association Between Alzheimer's Disease and Parkinson's Disease Using Genome-Wide Association Studies and Protein-Protein Interaction Network.Meta-analysis of the association between variants in MAPT and neurodegenerative diseases.SNCA Gene, but Not MAPT, Influences Onset Age of Parkinson's Disease in Chinese and Australians.Mutations in PRKN and SNCA Genes Important for the Progress of Parkinson's Disease.SNCA rs356219 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.Interaction between SNCA, LRRK2 and GAK increases susceptibility to Parkinson's disease in a Chinese population.The Length of SNCA Rep1 Microsatellite May Influence Cognitive Evolution in Parkinson's Disease.A Comprehensive Analysis of the Association Between Polymorphisms and the Risk of Parkinson's Disease

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P2860

SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population

http://www.wikidata.org/entity/Q35859538

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2011 nî lūn-bûn

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2011年論文

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SNCA and MAPT genes: Independe ...... ease in the Italian population

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SNCA and MAPT genes: Independe ...... ease in the Italian population

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SNCA and MAPT genes: Independe ...... ease in the Italian population

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SNCA and MAPT genes: Independe ...... ease in the Italian population

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SNCA and MAPT genes: Independe ...... ease in the Italian population

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P356

J.PARKRELDIS.2011.10.014

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Parkinsonism and Related Disorders

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SNCA and MAPT genes: Independe ...... ease in the Italian population

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Francesca Sironi

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Giulia Soldà

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Ilaria Guella

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Luca Trotta

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Margherita Canesi

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Rosanna Asselta

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Silvana Tesei

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Stefano Duga

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Stefano Goldwurm

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P2860

Parkinson's disease: from monogenic forms to genetic susceptibility factors

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

Genome-wide association study reveals genetic risk underlying Parkinson's disease

The SNPlex genotyping system: a flexible and scalable platform for SNP genotyping

Gene-environment interactions: key to unraveling the mystery of Parkinson's disease

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

Statistical methods in cancer research. Volume II--The design and analysis of cohort studies

Parkinson's disease

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10.1016/J.PARKRELDIS.2011.10.014

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3

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2011-11-21T00:00:00Z

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51818985

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22104010

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Parkinson's disease

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3314966

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