(Q54562638)

English

Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis.

scientific article published on 12 January 2007

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scholarly article

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis. (English)

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

Parkinson's disease

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based on heuristic

inferred from title

Angelo Antonini

9

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Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

Stefano Goldwurm

10

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

object named as

Inke R König

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Hartwig R. Siebner

14

object named as

Hartwig Siebner

1 reference

Europe PubMed Central

1 June 2018

Alexander Münchau

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Alexander Münchau

1 reference

Europe PubMed Central

1 June 2018

11

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Suzanne Lesage

1 reference

Europe PubMed Central

1 June 2018

Nicola Vanacore

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Nicola Vanacore

1 reference

Europe PubMed Central

1 June 2018

Christine Klein

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Christine Klein

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Europe PubMed Central

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8

object named as

Giuseppe Meco

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Europe PubMed Central

1 June 2018

Vincenzo Bonifati

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object named as

Vincenzo Bonifati

1 reference

Europe PubMed Central

1 June 2018

17

object named as

Ben A Oostra

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

author name string

Anne Grünewald

1

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Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

Guido J Breedveld

2

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

Katja Lohmann-Hedrich

3

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

Christan F Rohé

4

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

Johann Hagenah

6

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

Alexandra Dürr

12

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Europe PubMed Central

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http://europepmc.org/abstract/MED/17219214

Ferdinand Binkofski

13

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Europe PubMed Central

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http://europepmc.org/abstract/MED/17219214

Alexis Brice

16

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

publication date

12 January 2007

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

8

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1 June 2018

http://europepmc.org/abstract/MED/17219214

2

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1 June 2018

http://europepmc.org/abstract/MED/17219214

103-109

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1 June 2018

http://europepmc.org/abstract/MED/17219214

https://scigraph.springernature.com/pub.10.1007/s10048-006-0072-y

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Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PINK1 mutations are associated with sporadic early-onset parkinsonism

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of Parkinson disease: Implications for neurological care

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A heterozygous effect for PINK1 mutations in Parkinson's disease?

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical Spectrum of Homozygous and Heterozygous PINK1 Mutations in a Large German Family With Parkinson Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous and heterozygous PINK1 mutations: Considerations for diagnosis and care of Parkinson's disease patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonsense-mediated decay approaches the clinic

1 reference

https://pubmed.ncbi.nlm.nih.gov/17219214

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-006-0072-Y

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

1 reference

Europe PubMed Central

1 June 2018

http://europepmc.org/abstract/MED/17219214

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