VPS35 mutations in Parkinson disease (Q35103751)

6 August 2017

VPS35 mutations in Parkinson disease (English)

1 reference

6 August 2017

1 reference

Andreas Puschmann

14

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Elizabeth Conibear

Elizabeth Conibear

16

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Ruey-Meei Wu

Ruey-Meei Wu

29

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Wyeth Wasserman

Wyeth W Wasserman

17

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Matthew J. Farrer

Matthew J Farrer

33

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Ryan J Uitti

30

Ryan J Uitti

1 reference

6 August 2017

31

Zbigniew K Wszolek

1 reference

6 August 2017

3

Owen A Ross

1 reference

6 August 2017

Carles Vilariño-Güell

1

Carles Vilariño-Güell

1 reference

6 August 2017

23

Anna Krygowska-Wajs

1 reference

6 August 2017

5

Jennifer M Kachergus

1 reference

Alexandra I Soto-Ortolaza

6 August 2017

7

Alexandra I Soto-Ortolaza

1 reference

6 August 2017

4

Justus C Dachsel

1 reference

6 August 2017

12

Heather L Melrose

1 reference

6 August 2017

11

Bahareh Behrouz

1 reference

6 August 2017

13

Emna Hentati

1 reference

6 August 2017

24

Tim Lynch

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6 August 2017

26

Alex Rajput

1 reference

6 August 2017

9

Greggory J Wilhoite

1 reference

6 August 2017

10

Justin A Bacon

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6 August 2017

19

Pierre R Burkhard

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6 August 2017

20

Ruth Djaldetti

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6 August 2017

21

Joseph Ghika

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6 August 2017

22

Faycal Hentati

1 reference

6 August 2017

25

Eldad Melamed

1 reference

6 August 2017

28

Alessandra Solida

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6 August 2017

Christian Wider

2

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6 August 2017

Sarah J Lincoln

6

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Stephanie A Cobb

8

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Daniel M Evans

15

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Jan O Aasly

18

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Ali H Rajput

27

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6 August 2017

François Vingerhoets

32

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6 August 2017

language of work or name

English

0 references

publication date

1 July 2011

1 reference

American Journal of Human Genetics

6 August 2017

1 reference

6 August 2017

89

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6 August 2017

162-167

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6 August 2017

1

1 reference

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

6 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

A comparative study of Lrrk2 function in primary neuronal cultures

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Alpha-synuclein promotes SNARE-complex assembly in vivo and in vitro

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Vps35 mediates vesicle transport between the mitochondria and peroxisomes

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

The retromer component SNX6 interacts with dynactin p150(Glued) and mediates endosome-to-TGN transport

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Targeted capture and massively parallel sequencing of 12 human exomes

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Membrane recruitment of the cargo-selective retromer subcomplex is catalysed by the small GTPase Rab7 and inhibited by the Rab-GAP TBC1D5

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

DCTN1 mutations in Perry syndrome

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Genetic variation of Omi/HtrA2 and Parkinson's disease

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Retromer deficiency observed in Alzheimer's disease causes hippocampal dysfunction, neurodegeneration, and Abeta accumulation

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Autosomal dominant dopa-responsive parkinsonism in a multigenerational Swiss family

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Functional architecture of the retromer cargo-recognition complex

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Complex segregation analysis of Parkinson's disease: The Mayo Clinic Family Study

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Genetics of Parkinson disease: paradigm shifts and future prospects.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Model-guided microarray implicates the retromer complex in Alzheimer's disease

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

High-resolution whole-genome association study of Parkinson disease.

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Role of the mammalian retromer in sorting of the cation-independent mannose 6-phosphate receptor

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Diagnostic criteria for Parkinson disease

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

Parkinson's disease. Second of two parts

9 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3135796

10.1016/J.AJHG.2011.06.001

9 July 2018

Identifiers

DOI

1 reference

6 August 2017

1 reference

6 August 2017

1 reference