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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
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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 |
format | Text |
id | pubmed-2790306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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