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The Prion Disease Database: a comprehensive transcriptome resource for systems biology research in prion diseases

Prion diseases reflect conformational conversion of benign isoforms of prion protein (PrP(C)) to malignant PrP(Sc) isoforms. Networks perturbed by PrP(Sc) accumulation and their ties to pathological events are poorly understood. Time-course transcriptomic and phenotypic data in animal models are cri...

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Autores principales: Gehlenborg, Nils, Hwang, Daehee, Lee, Inyoul Y., Yoo, Hyuntae, Baxter, David, Petritis, Brianne, Pitstick, Rose, Marzolf, Bruz, DeArmond, Stephen J., Carlson, George A., Hood, Leroy
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2790306/
https://www.ncbi.nlm.nih.gov/pubmed/20157484
http://dx.doi.org/10.1093/database/bap011
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author Gehlenborg, Nils
Hwang, Daehee
Lee, Inyoul Y.
Yoo, Hyuntae
Baxter, David
Petritis, Brianne
Pitstick, Rose
Marzolf, Bruz
DeArmond, Stephen J.
Carlson, George A.
Hood, Leroy
author_facet Gehlenborg, Nils
Hwang, Daehee
Lee, Inyoul Y.
Yoo, Hyuntae
Baxter, David
Petritis, Brianne
Pitstick, Rose
Marzolf, Bruz
DeArmond, Stephen J.
Carlson, George A.
Hood, Leroy
author_sort Gehlenborg, Nils
collection PubMed
description Prion diseases reflect conformational conversion of benign isoforms of prion protein (PrP(C)) to malignant PrP(Sc) isoforms. Networks perturbed by PrP(Sc) accumulation and their ties to pathological events are poorly understood. Time-course transcriptomic and phenotypic data in animal models are critical for understanding prion-perturbed networks in systems biology studies. Here, we present the Prion Disease Database (PDDB), the most comprehensive data resource on mouse prion diseases to date. The PDDB contains: (i) time-course mRNA measurements spanning the interval from prion inoculation through appearance of clinical signs in eight mouse strain-prion strain combinations and (ii) histoblots showing temporal PrP(Sc) accumulation patterns in brains from each mouse–prion combination. To facilitate prion research, the PDDB also provides a suite of analytical tools for reconstructing dynamic networks via integration of temporal mRNA and interaction data and for analyzing these networks to generate hypotheses. Database URL: http://prion.systemsbiology.net
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spelling pubmed-27903062009-12-08 The Prion Disease Database: a comprehensive transcriptome resource for systems biology research in prion diseases Gehlenborg, Nils Hwang, Daehee Lee, Inyoul Y. Yoo, Hyuntae Baxter, David Petritis, Brianne Pitstick, Rose Marzolf, Bruz DeArmond, Stephen J. Carlson, George A. Hood, Leroy Database (Oxford) Original Article Prion diseases reflect conformational conversion of benign isoforms of prion protein (PrP(C)) to malignant PrP(Sc) isoforms. Networks perturbed by PrP(Sc) accumulation and their ties to pathological events are poorly understood. Time-course transcriptomic and phenotypic data in animal models are critical for understanding prion-perturbed networks in systems biology studies. Here, we present the Prion Disease Database (PDDB), the most comprehensive data resource on mouse prion diseases to date. The PDDB contains: (i) time-course mRNA measurements spanning the interval from prion inoculation through appearance of clinical signs in eight mouse strain-prion strain combinations and (ii) histoblots showing temporal PrP(Sc) accumulation patterns in brains from each mouse–prion combination. To facilitate prion research, the PDDB also provides a suite of analytical tools for reconstructing dynamic networks via integration of temporal mRNA and interaction data and for analyzing these networks to generate hypotheses. Database URL: http://prion.systemsbiology.net Oxford University Press 2009 2009-09-17 /pmc/articles/PMC2790306/ /pubmed/20157484 http://dx.doi.org/10.1093/database/bap011 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5/uk/ This is Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Gehlenborg, Nils
Hwang, Daehee
Lee, Inyoul Y.
Yoo, Hyuntae
Baxter, David
Petritis, Brianne
Pitstick, Rose
Marzolf, Bruz
DeArmond, Stephen J.
Carlson, George A.
Hood, Leroy
The Prion Disease Database: a comprehensive transcriptome resource for systems biology research in prion diseases
title The Prion Disease Database: a comprehensive transcriptome resource for systems biology research in prion diseases
title_full The Prion Disease Database: a comprehensive transcriptome resource for systems biology research in prion diseases
title_fullStr The Prion Disease Database: a comprehensive transcriptome resource for systems biology research in prion diseases
title_full_unstemmed The Prion Disease Database: a comprehensive transcriptome resource for systems biology research in prion diseases
title_short The Prion Disease Database: a comprehensive transcriptome resource for systems biology research in prion diseases
title_sort prion disease database: a comprehensive transcriptome resource for systems biology research in prion diseases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2790306/
https://www.ncbi.nlm.nih.gov/pubmed/20157484
http://dx.doi.org/10.1093/database/bap011
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