Parkinson's Disease in Saudi Patients: A Genetic Study

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Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approach Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families Evidence for prehistoric origins of the G2019S mutation in the North African Berber population.

P2860

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P2860

Parkinson's Disease in Saudi Patients: A Genetic Study

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http://www.wikidata.org/entity/Q35746162

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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name

Parkinson's Disease in Saudi Patients: A Genetic Study

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Parkinson's Disease in Saudi Patients: A Genetic Study

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Parkinson's Disease in Saudi Patients: A Genetic Study

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Parkinson's Disease in Saudi Patients: A Genetic Study

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Parkinson's Disease in Saudi Patients: A Genetic Study

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Parkinson's Disease in Saudi Patients: A Genetic Study

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P1476

Parkinson's Disease in Saudi Patients: A Genetic Study

@en

P2093

Abeer E Mustafa

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Amna I Magrashi

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Asma I Tahir

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Bashayer A Alsaffar

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Bashayer R Al-Mubarak

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Basma S AlAbdulaziz

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Dania S Khalil

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Eman A Alyemni

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Hussam Abou Al-Shaar

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Maha I AlTurki

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P2860

I-TASSER server for protein 3D structure prediction

Parkinson's Disease: Genetics and Pathogenesis

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

Parkin suppresses unfolded protein stress-induced cell death through its E3 ubiquitin-protein ligase activity

Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1

Structure of the C-terminal RING finger from a RING-IBR-RING/TRIAD motif reveals a novel zinc-binding domain distinct from a RING

I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure.

Genetics of Parkinson's disease

Structure of the Parkin in-between-ring domain provides insights for E3-ligase dysfunction in autosomal recessive Parkinson's disease

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e0135950

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scholarly article

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10.1371/JOURNAL.PONE.0135950

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English

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Nada Al Tassan

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Parkinson's disease

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Parkinson's Disease in Saudi Patients: A Genetic Study

about

P2860

P2860

Parkinson's Disease in Saudi Patients: A Genetic Study

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P921

P932