(Q34577165)

3 August 2017

Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism (English)

1 reference

3 August 2017

1 reference

parkinsonian syndrome

1 reference

9

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Suzanne Lesage

series ordinal

1

object named as

Suzanne Lesage

1 reference

3 August 2017

8

Alexandra Dürr

1 reference

3 August 2017

3

Ebba Lohmann

1 reference

3 August 2017

6

Sabine Janin

1 reference

3 August 2017

4

Lucette Lacomblez

1 reference

3 August 2017

5

Helio Teive

1 reference

3 August 2017

Periquet Magali

2

1 reference

PubMed ID

17068781

3 August 2017

Pierre-Yves Cousin

series ordinal

7

1 reference

PubMed ID

17068781

3 August 2017

French Parkinson Disease Genetics Study Group

series ordinal

10

1 reference

3 August 2017

1 January 2007

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3 August 2017

1 reference

3 August 2017

28

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3 August 2017

1

1 reference

3 August 2017

27-32

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New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism

3 August 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

The genomic structure and promoter region of the human parkin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Genetics of Parkinson's disease: LRRK2 on the rise

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Genetic analysis of parkin co-regulated gene (PACRG) in patients with early-onset parkinsonism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Genetics of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Parkin-deficient mice exhibit nigrostriatal deficits but not loss of dopaminergic neurons

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Distribution, type, and origin of Parkin mutations: review and case studies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

A Product of the Human Gene Adjacent to parkin Is a Component of Lewy Bodies and Suppresses Pael Receptor-induced Cell Death

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Parkin gene inactivation alters behaviour and dopamine neurotransmission in the mouse

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Accumulation of the authentic parkin substrate aminoacyl-tRNA synthetase cofactor, p38/JTV-1, leads to catecholaminergic cell death.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

It's a double knock-out! The quaking mouse is a spontaneous deletion of parkin and parkin co-regulated gene (PACRG).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

How much phenotypic variation can be attributed to parkin genotype?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

The neurological mutant quaking(viable) is Parkin deficient.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Deletion of the Parkin coregulated gene causes male sterility in the quaking(viable) mouse mutant

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Association between early-onset Parkinson's disease and mutations in the parkin gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Single-nucleotide polymorphisms in the promoter region of the PARKIN gene and Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Association study of Parkin gene polymorphisms with idiopathic Parkinson disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Parkin-deficient mice are not a robust model of parkinsonism

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Proteomic analysis of parkin knockout mice: alterations in energy metabolism, protein handling and synaptic function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

MUTANT MICE (QUAKING AND JIMPY) WITH DEFICIENT MYELINATION IN THE CENTRAL NERVOUS SYSTEM

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Essential tremor-the most common movement disorder in older people.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Identification and characterization of the human parkin gene promoter

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Complex relationship between Parkin mutations and Parkinson disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Functional association of the parkin gene promoter with idiopathic Parkinson's disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Identification of a novel gene linked to parkin via a bi-directional promoter

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

N-myc regulates parkin expression

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20436

7 January 2021

Identifiers

DOI

10.1002/HUMU.20436

1 reference

3 August 2017

1 reference

PubMed ID

17068781