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Making choices—how stochastic decisions determine disease progression
In this issue of Genes & Development, Ginart and colleagues (pp. 567–578) study a mouse model for Russell-Silver syndrome (RSS) and show that similar cells within one individual can display distinct gene expression patterns because of epigenetic marks that are established stochastically during e...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782042/ https://www.ncbi.nlm.nih.gov/pubmed/26944674 http://dx.doi.org/10.1101/gad.278952.116 |
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author | Park, Ki-Sun Pfeifer, Karl |
author_facet | Park, Ki-Sun Pfeifer, Karl |
author_sort | Park, Ki-Sun |
collection | PubMed |
description | In this issue of Genes & Development, Ginart and colleagues (pp. 567–578) study a mouse model for Russell-Silver syndrome (RSS) and show that similar cells within one individual can display distinct gene expression patterns because of epigenetic marks that are established stochastically during early development. Their results provide an excellent explanation for phenotypes seen in RSS and other imprinting disorders and especially help us understand how patients with similar or even identical genetic mutations can display distinct disease profiles. |
format | Online Article Text |
id | pubmed-4782042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47820422016-09-01 Making choices—how stochastic decisions determine disease progression Park, Ki-Sun Pfeifer, Karl Genes Dev Outlook In this issue of Genes & Development, Ginart and colleagues (pp. 567–578) study a mouse model for Russell-Silver syndrome (RSS) and show that similar cells within one individual can display distinct gene expression patterns because of epigenetic marks that are established stochastically during early development. Their results provide an excellent explanation for phenotypes seen in RSS and other imprinting disorders and especially help us understand how patients with similar or even identical genetic mutations can display distinct disease profiles. Cold Spring Harbor Laboratory Press 2016-03-01 /pmc/articles/PMC4782042/ /pubmed/26944674 http://dx.doi.org/10.1101/gad.278952.116 Text en Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Outlook Park, Ki-Sun Pfeifer, Karl Making choices—how stochastic decisions determine disease progression |
title | Making choices—how stochastic decisions determine disease progression |
title_full | Making choices—how stochastic decisions determine disease progression |
title_fullStr | Making choices—how stochastic decisions determine disease progression |
title_full_unstemmed | Making choices—how stochastic decisions determine disease progression |
title_short | Making choices—how stochastic decisions determine disease progression |
title_sort | making choices—how stochastic decisions determine disease progression |
topic | Outlook |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782042/ https://www.ncbi.nlm.nih.gov/pubmed/26944674 http://dx.doi.org/10.1101/gad.278952.116 |
work_keys_str_mv | AT parkkisun makingchoiceshowstochasticdecisionsdeterminediseaseprogression AT pfeiferkarl makingchoiceshowstochasticdecisionsdeterminediseaseprogression |