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A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

opublikowano w: American Journal of Human Genetics

data publikacji: 2011-07-15

język: język angielski

główny temat: choroba Parkinsona, late-onset Parkinson disease

Cites articles 37

Data

Tytuł

Autorzy

2011-02-19

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

Vincent Plagnol, Alexis Brice, Kári Stefánsson, Claudia Schulte, Maria Martinez, Nicholas W. Wood, Suzanne Lesage, Thomas Gasse, John Anthony Hardy, Peter Heutink, Andrew Singleton, Manu Sharma, Dena G. Hernandez, Michele T M Hu, Daan Velseboer, Daniela Berg, Una-Marie Sheerin
2010-04

A method and server for predicting damaging missense mutations

Peer Bork, Leonid Peshkin
2010-07-08

Vps35 mediates vesicle transport between the mitochondria and peroxisomes
2009-12

Genome-wide association study reveals genetic risk underlying Parkinson's disease

Christian Gieger, Thomas Illig, Henry Houlden, Sampath Arepalli, Peter Lichtner, Daniela Berg, Rejko Krüger, Günther Deuschl, Katrina Gwinn, Delia Lorenz, Michael Steffens, Sonja Scholz, Claudia Schulte, Jose Bras, Honglei Chen, Yikyung Park, Michael S. Okun, Alison Goate, Stephen Chanock, Thomas Gasse, Kelly D Foote, Christine Klein, John Anthony Hardy, Hubert H Fernandez, Mark R Cookson, Joel S Perlmutter, Xuemei Huang, Andrew Singleton, Coro Paisán-Ruíz, Arthur Schatzkin, Olaf Riess, Bryan Traynor, Manu Sharma, Dena G. Hernandez, Stefan Schreiber, Javier Simón Sánchez, J Raphael Gibbs, Michael Marmot, Albert R Hollenbeck
2009-10-01

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease

Cyrus P Zabetian, Jose Bras, Elvira Valeria De Marco, Matthew J. Farrer, Ziv Gan-Or, Anthony Lang, Ikuko Mizuta, Giuseppe Nicoletti, Catarina R. Oliveira, Ruth Ottman, Avi Orr-Urtreger, Lygia Veiga Pereira, Aldo Quattrone, Claudia Schulte, Yihong Zhao, Ignacio F Mata, Anat Mirelman, Daniela Berg, Karen S. Marder, Alexis Brice, Andrew Singleton
2009-12

Improved prediction of protein side-chain conformations with SCWRL4

Roland Dunbrack
2009-12

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
2008-03

GROMACS 4: Algorithms for Highly Efficient, Load-Balanced, and Scalable Molecular Simulation

David van der Spoel, Erik Lindahl
2008-11-12

VPS10P-domain receptors - regulators of neuronal viability and function

Thomas E Willnow, Anders Nykjaer
2007-10-25

Functional architecture of the retromer cargo-recognition complex
2007-02

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

Ekaterina Rogaeva, Peter Henry St George-Hyslop, Gerold Schmitt-Ulms, Olav M. Andersen, Rivka Inzelberg, Thomas E Willnow, Clinton Baldwin, Joseph H. Lee, Kathryn L. Lunetta, Sandro Sorbi, Lindsay A. Farrer, Dennis W. Dickson, Robert C. Green, Richard Mayeux, Toshitaka Kawarai, Ronald C. Petersen, L. Adrienne Cupples, Neill R Graff-Radford, Amalia Bruni, Innocenzo Rainero, Lorenzo Pinessi, Yosuke Wakutani, Christopher Bohm, Taiichi Katayama, Nobuto Shibata, Ranjan Duara, Fanggeng Zou, Robert P Friedland, You-Qiang Song, Steven G. Younkin
2007-12-01

Drosophila Vps35 function is necessary for normal endocytic trafficking and actin cytoskeleton organisation

Cahir J O'Kane, Viktor Korolchuk, Carolina Gómez-Llorente
2007-05-25

SNAP: predict effect of non-synonymous polymorphisms on function

Yana Bromberg, Burkhard Rost
2006-11-13

Interchangeable but essential functions of SNX1 and SNX2 in the association of retromer with endosomes and the trafficking of mannose 6-phosphate receptors

Juan S. Bonifacino
2006-09-15

The human Vps29 retromer component is a metallo-phosphoesterase for a cation-independent mannose 6-phosphate receptor substrate peptide
2006-08-01

Retrograde transport from endosomes to the trans-Golgi network

Juan S. Bonifacino
2005-01-29

A common LRRK2 mutation in idiopathic Parkinson's disease

Andrew Lees, Kailash Phatechand Bhatia, Niall P Quinn, Vincenzo Bonifati, Andrew Singleton, D.G. Healy, Janice Holton
2005-08-01

KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes

Christian Gieger, Thomas Illig
2005-01-01

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

Alessio Di Fonzo, Stefano Goldwurm, Nicola Vanacore, Cristina Sampaio, Giuseppe Meco, Vincenzo Bonifati, Ben A Oostra
2005-01-01

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

Nathan Pankratz, Tatiana Foroud, Dena G. Hernandez, Andrew Singleton, Cheryl A. Halter, Alice Rudolph, Clifford W. Shults, Terry Reed
2005-01

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

Alessio Di Fonzo, Stefano Goldwurm, Joaquim Ferreira, Fabrizio Stocchi, Nicola Vanacore, Cristina Sampaio, Giuseppe Meco, Vincenzo Bonifati, Ben A Oostra, Leonor Correia Guedes, Christan F Rohé, Guido J Breedveld, Egberto Reis Barbosa, Fabrizio Edito
2004-05-21

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

Bruno Dallapiccola, Enza Maria Valente, William P. Gilks, Anna Rita Bentivoglio, Robert J. Harvey, Alberto Albanese, Pietro Cortelli, Nicholas W. Wood, Viviana Caputo, Robert L. Nussbaum, D.G. Healy
2004-11-18

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

Thomas Meitinger, Bertram Müller-Myhsok, Alexander Zimprich, Friedrich Asmus, Peter Lichtner, Jon Stoessl, Matthew J. Farrer, Dennis W. Dickson, Thomas Gasse, Ryan J Uitti, Zbigniew Wszołek, Donald Brian Calne, Saskia Biskup, Tim M Strom, Mary M Hulihan, Jennifer M Kachergus
2004-11-18

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

Andrew Lees, José Félix Martí Massó, Andrew Singleton, Coro Paisán-Ruíz, Nicholas W. Wood
2004-11-01

Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews
2004-08-01

SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodies

Ian G. McKeith, Christopher Morris, Dena G. Hernandez, Aideen M McInerney-Leo
2003-01-10

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

Cornelia M. van Duijn, Alexis Brice, Ferdinando Squitieri, John Van Swieten, Nicola Vanacore, Peter Heutink, Giuseppe Meco, Vincenzo Bonifati, Ben A Oostra, Marieke Cornelia Johanna Dekker, Patrizia Rizzu, Onno Schaap, Guido J Breedveld
2003-12-01

A point-charge force field for molecular mechanics simulations of proteins based on condensed-phase quantum mechanical calculations

Chun Wu, Ray Luo, Junmei Wang
2002-01

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Stacey S. Cherny
2002-09-01

Human non-synonymous SNPs: server and survey

Peer Bork
2000-05-22

A five-site model for liquid water and the reproduction of the density anomaly by rigid, nonpolarizable potential functions

William L. Jorgensen, Michael W. Mahoney
1998-04-09

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

Artykuł - wd:Q24633417

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