Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain - Test2 - elhamkhani - TriplyDB

Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain

Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain

http://www.wikidata.org/entity/Q33649391

about

Is inhibition of kinase activity the only therapeutic strategy for LRRK2-associated Parkinson's disease?Identification of a Japanese family with LRRK2 p.R1441G-related Parkinson's disease Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.Reevaluation of phosphorylation sites in the Parkinson disease-associated leucine-rich repeat kinase 2 LRRK2 in Parkinson's disease: genetic and clinical studies from patients.Neurogenetic disorders in the Basque population.Leucine-Rich Repeat Kinase (LRRK2) Genetics and Parkinson's Disease.Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing.The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot LARGE-PD: Examining the genetics of Parkinson's disease in Latin America.Human R1441C LRRK2 regulates the synaptic vesicle proteome and phosphoproteome in a Drosophila model of Parkinson's disease.

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P2860

Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain

http://www.wikidata.org/entity/Q33649391

description

2009 nî lūn-bûn

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2009 թուականի Մարտին հրատարակուած գիտական յօդուած

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2009 թվականի մարտին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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Hao Deng

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Jon Infante

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Juan J Zarranz

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Karen L Edwards

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P2860

The mitochondrial lineage U8a reveals a Paleolithic settlement in the Basque country

Parkinson's disease: clinical features and diagnosis

Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism.

The mutation rate in the human mtDNA control region

Parkinson's disease

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

A common LRRK2 mutation in idiopathic Parkinson's disease

Cross-cultural estimation of the human generation interval for use in genetics-based population divergence studies

Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation

Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.

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