LRRK2 P755L variant in sporadic Parkinson's disease. (Q51678671)

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scientific article published on 16 October 2008

LRRK2 P755L variant in sporadic Parkinson’s disease

Language	Label	Description	Also known as
English	LRRK2 P755L variant in sporadic Parkinson's disease.	scientific article published on 16 October 2008	LRRK2 P755L variant in sporadic Parkinson’s disease

Statements

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

11-12

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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

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

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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

ResearchGate publication ID

0 references

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