(Q25255429)

6 July 2017

Exclusion of PINK1 as candidate gene for the late-onset form of Parkinson's disease in two European populations (English)

1 reference

6 July 2017

1 reference

Joerg T Epplen

6

0 references

Anna Melissa Schlitter

1

object named as

Anna Melissa Schlitter

1 reference

6 July 2017

Martin Kurz

2

1 reference

6 July 2017

Jan P Larsen

3

1 reference

6 July 2017

Dirk Woitalla

4

1 reference

6 July 2017

Thomas Mueller

5

1 reference

6 July 2017

Gabriele Dekomien

7

1 reference

6 July 2017

language of work or name

English

0 references

publication date

14 December 2005

1 reference

Journal of Negative Results in BioMedicine

6 July 2017

1 reference

6 July 2017

4

1 reference

6 July 2017

1

0 references

page(s)

10

1 reference

https://scigraph.springernature.com/pub.10.1186/1477-5751-4-10

6 July 2017

0 references

cites work

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

BRCA1 1675delA and 1135insA account for one third of Norwegian familial breast-ovarian cancer and are associated with later disease onset than less frequent mutations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

A common LRRK2 mutation in idiopathic Parkinson's disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

Parkinson's disease: mechanisms and models

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonism

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

Mitochondria and dopamine: new insights into recessive parkinsonism

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

Mitochondria, oxidative damage, and inflammation in Parkinson's disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

The epidemiology of Parkinson's disease in the county of Rogaland, Norway

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

Clinical diagnosis of Parkinson's disease. Proposal of diagnostic subgroups classified at different levels of confidence.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

Genetic association study of PINK1 coding polymorphisms in Parkinson's disease.

28 September 2017

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-4-10

Parkin mutations and susceptibility alleles in late-onset Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-4-10

Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-4-10

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1325256

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

28 November 2018

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-4-10

Familial Parkinson's disease: a community-based study

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16354302

12 December 2020

inferred from PubMed ID database lookup

Polymerase chain reaction—single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16354302

12 December 2020

inferred from PubMed ID database lookup

Mitochondria, Oxidative Damage, and Inflammation in Parkinson's Disease

1 reference

https://api.crossref.org/works/10.1186%2F1477-5751-4-10

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1186/1477-5751-4-10

1 reference

Dimensions Publication ID

6 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1477-5751-4-10

release_3e6xec2m2feoboqaft3mhkxd5u

9 September 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/3e6xec2m2feoboqaft3mhkxd5u

24 November 2022

mapped directly with Wikidata item

PMCID

1325256

1 reference

6 July 2017

1 reference