The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence. (Q40223841)

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20 December 2019

title

The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence (English)

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20 December 2019

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3

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20 December 2019

Alessio Di Fonzo

5

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20 December 2019

Prasanna R. Kolatkar

14

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20 December 2019

author name string

E K Tan

1

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20 December 2019

Y Zhao

2

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20 December 2019

M G Tan

4

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20 December 2019

L Sun

6

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20 December 2019

S Fook-Chong

7

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20 December 2019

S Tang

8

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20 December 2019

E Chua

9

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20 December 2019

Y Yuen

10

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20 December 2019

L Tan

11

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20 December 2019

R Pavanni

12

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20 December 2019

M C Wong

13

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20 December 2019

C S Lu

15

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20 December 2019

V Bonifati

16

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20 December 2019

J J Liu

17

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20 December 2019

publication date

30 September 2006

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20 December 2019

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20 December 2019

volume

120

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20 December 2019

issue

6

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20 December 2019

page(s)

857-863

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https://scigraph.springernature.com/pub.10.1007/s00439-006-0268-0

20 December 2019

exact match

0 references

cites work

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease

1 reference

Crossref

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Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

21 January 2018

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12 December 2020

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

1 reference

12 December 2020

Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease

1 reference

12 December 2020

Testing association between LRRK2 and Parkinson's disease and investigating linkage disequilibrium

1 reference

12 December 2020

LRRK2 in Parkinson's disease: protein domains and functional insights

1 reference

12 December 2020

Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease

1 reference

12 December 2020

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan

1 reference

12 December 2020

A common LRRK2 mutation in idiopathic Parkinson's disease

1 reference

12 December 2020

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

1 reference

12 December 2020

Common variants of LRRK2 are not associated with sporadic Parkinson's disease

1 reference

12 December 2020

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

1 reference

12 December 2020

Lrrk2 pathogenic substitutions in Parkinson's disease

1 reference

12 December 2020

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

1 reference

12 December 2020

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

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12 December 2020

LRRK2 gene in Parkinson disease: Mutation analysis and case control association study

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12 December 2020

Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease

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12 December 2020

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

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12 December 2020

Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity

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12 December 2020

Posttranslational myristoylation of caspase-activated p21-activated protein kinase 2 (PAK2) potentiates late apoptotic events

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12 December 2020

Analysis of LRRK2 functional domains in nondominant Parkinson disease.

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12 December 2020

Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association

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12 December 2020

The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease

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12 December 2020

Posttranslational N-myristoylation is required for the anti-apoptotic activity of human tGelsolin, the C-terminal caspase cleavage product of human gelsolin.

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12 December 2020

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.

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12 December 2020

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

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12 December 2020

Expanding insights of mitochondrial dysfunction in Parkinson's disease.

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12 December 2020

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

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12 December 2020

The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity

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12 December 2020

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

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12 December 2020

Posttranslational N-myristoylation of BID as a molecular switch for targeting mitochondria and apoptosis

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12 December 2020

The PROSITE database.

1 reference

12 December 2020