(Q51678671)

English

LRRK2 P755L variant in sporadic Parkinson's disease.

scientific article published on 16 October 2008

LRRK2 P755L variant in sporadic Parkinson’s disease

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scholarly article

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

LRRK2 P755L variant in sporadic Parkinson's disease. (English)

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

Parkinson's disease

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based on heuristic

inferred from title

Manabu Funayama

4

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

Nobutaka Hattori

12

object named as

Nobutaka Hattori

1 reference

Europe PubMed Central

9 April 2018

Yoshikuni Mizuno

10

object named as

Yoshikuni Mizuno

1 reference

Europe PubMed Central

9 April 2018

Hiroyuki Tomiyama

1

object named as

Hiroyuki Tomiyama

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

7

object named as

Miho Murata

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

Shin-Ichiro Kubo

9

object named as

Shin-Ichiro Kubo

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

5

object named as

Hiroyo Yoshino

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

author name string

Ikuko Mizuta

2

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

Yuanzhe Li

3

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

Lin Li

6

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

Mitsutoshi Yamamoto

8

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

Tatsushi Toda

11

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

publication date

16 October 2008

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

Journal of Human Genetics

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Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

53

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Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

1012-1015

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Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

11-12

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

https://scigraph.springernature.com/pub.10.1007/s10038-008-0336-5

0 references

A common LRRK2 mutation in idiopathic Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lrrk2 pathogenic substitutions in Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenicity of LRRK2 P755L variant in Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kinase activity of mutant LRRK2 mediates neuronal toxicity

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinicogenetic study of mutations inLRRK2 exon 41 in Parkinson's disease patients from 18 countries

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of LRRK2 P755L variant in Caucasian patients with Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel P755L mutation in LRRK2 gene associated with Parkinson's disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18923807

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-008-0336-5

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

1 reference

Europe PubMed Central

9 April 2018

http://europepmc.org/abstract/MED/18923807

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