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Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research

Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1330881855

Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research

About this item

Full title

Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research

Author / Creator

Wray, Selina , Self, Matthew , Lewis, Patrick A. , Taanman, Jan-Willem , Ryan, Natalie S. , Mahoney, Colin J. , Liang, Yuying , Devine, Michael J. , Sheerin, Una-Marie , Houlden, Henry , Morris, Huw R. , Healy, Daniel , Marti-Masso, Jose-Felix , Preza, Elisavet , Barker, Suzanne , Sutherland, Margaret , Corriveau, Roderick A. , D'Andrea, Michael , Schapira, Anthony H. V. , Uitti, Ryan J. , Guttman, Mark , Opala, Grzegorz , Jasinska-Myga, Barbara , Puschmann, Andreas , Nilsson, Christer , Espay, Alberto J. , Slawek, Jaroslaw , Gutmann, Ludwig , Boeve, Bradley F. , Boylan, Kevin , Stoessl, A. Jon , Ross, Owen A. , Maragakis, Nicholas J. , Van Gerpen, Jay , Gerstenhaber, Melissa , Gwinn, Katrina , Dawson, Ted M. , Isacson, Ole , Marder, Karen S. , Clark, Lorraine N. , Przedborski, Serge E. , Finkbeiner, Steven , Rothstein, Jeffrey D. , Wszolek, Zbigniew K. , Rossor, Martin N. , Hardy, John , NINDS Huntington's Disease iPSC Consortium , NINDS Parkinson's Disease iPSC Consortium , NINDS ALS iPSC Consortium , Faculty of Medicine , Medicinska fakulteten , Strategiska forskningsområden (SFO) , Institutionen för kliniska vetenskaper, Lund , Strategic research areas (SRA) , Lunds universitet , Department of Clinical Sciences, Lund , Sektion IV , Profilområden och andra starka forskningsmiljöer , Lund University , Section IV , Psychiatry (Lund) , MultiPark: Multidisciplinary research focused on Parkinson´s disease , Psykiatri, Lund and Profile areas and other strong research environments

Publisher

United States: Public Library of Science

Journal title

PloS one, 2012-08, Vol.7 (8), p.e43099

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Our understanding of the molecular mechanisms of many neurological disorders has been greatly enhanced by the discovery of mutations in genes linked to familial forms of these diseases. These have facilitated the generation of cell and animal models that can be used to understand the underlying molecular pathology. Recently, there has been a surge...

Alternative Titles

Full title

Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1330881855

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1330881855

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0043099

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