(Q46724331)

English

Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China

scientific article published on 30 April 2013

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

Parkinson's disease

1 reference

based on heuristic

inferred from title

author name string

Jiangping Cai

1

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

Yi Lin

2

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

Wanjin Chen

3

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

Qifang Lin

4

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

Bin Cai

5

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

Ning Wang

6

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

Weihong Zheng

7

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

publication date

30 April 2013

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

Neurological Sciences

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

34

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

11

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

2001-2006

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

LRRK2 and Parkinson disease

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Parkin protects against LRRK2 G2019S mutant-induced dopaminergic neurodegeneration in Drosophila.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Intramolecular activation mechanism of the Dictyostelium LRRK2 homolog Roco protein GbpC.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Confirmation of LRRK2 S1647T variant as a risk factor for Parkinson's disease in southern China

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

LRRK2 R1398H polymorphism is associated with decreased risk of Parkinson's disease in a Han Chinese population.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Association of Parkinson's disease with six single nucleotide polymorphisms located in four PARK genes in the northern Han Chinese population.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Lrrk2 R1628P in non-Chinese Asian races

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Is the G2019S LRRK2 mutation common in all southern European populations?

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Genetic structure of the Han Chinese population revealed by genome-wide SNP variation

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10072-013-1436-3

21 January 2018

LRRK2 R1628P increases risk of Parkinson's disease: replication evidence

1 reference

https://pubmed.ncbi.nlm.nih.gov/23624603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians

1 reference

https://pubmed.ncbi.nlm.nih.gov/23624603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/23624603

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10072-013-1436-3

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

release_7xkuqno4xvd2dk6v357tufy3qm

1 reference

https://api.fatcat.wiki/v0/release/7xkuqno4xvd2dk6v357tufy3qm

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/23624603

ResearchGate publication ID

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