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Identifying genes that regulate bone remodeling as potential therapeutic targets
Bone remodeling, a coupled process involving bone resorption and formation, is initiated by mechanical signals and is controlled by local and systemic factors that regulate osteoblast and osteoclast differentiation and function. An excess of resorption over formation leads to the bone loss and incre...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213103/ https://www.ncbi.nlm.nih.gov/pubmed/15781576 http://dx.doi.org/10.1084/jem.20050354 |
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author | Krane, Stephen M. |
author_facet | Krane, Stephen M. |
author_sort | Krane, Stephen M. |
collection | PubMed |
description | Bone remodeling, a coupled process involving bone resorption and formation, is initiated by mechanical signals and is controlled by local and systemic factors that regulate osteoblast and osteoclast differentiation and function. An excess of resorption over formation leads to the bone loss and increased propensity to fracture that is characteristic of osteoporosis. A newly described inhibitor of osteoblast differentiation, Ciz, interferes with bone morphogenic protein signaling. As a consequence, Ciz-deficient mice develop increased bone mass. |
format | Text |
id | pubmed-2213103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22131032008-03-11 Identifying genes that regulate bone remodeling as potential therapeutic targets Krane, Stephen M. J Exp Med Commentary Bone remodeling, a coupled process involving bone resorption and formation, is initiated by mechanical signals and is controlled by local and systemic factors that regulate osteoblast and osteoclast differentiation and function. An excess of resorption over formation leads to the bone loss and increased propensity to fracture that is characteristic of osteoporosis. A newly described inhibitor of osteoblast differentiation, Ciz, interferes with bone morphogenic protein signaling. As a consequence, Ciz-deficient mice develop increased bone mass. The Rockefeller University Press 2005-03-21 /pmc/articles/PMC2213103/ /pubmed/15781576 http://dx.doi.org/10.1084/jem.20050354 Text en Copyright © 2005, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Commentary Krane, Stephen M. Identifying genes that regulate bone remodeling as potential therapeutic targets |
title | Identifying genes that regulate bone remodeling as potential therapeutic targets |
title_full | Identifying genes that regulate bone remodeling as potential therapeutic targets |
title_fullStr | Identifying genes that regulate bone remodeling as potential therapeutic targets |
title_full_unstemmed | Identifying genes that regulate bone remodeling as potential therapeutic targets |
title_short | Identifying genes that regulate bone remodeling as potential therapeutic targets |
title_sort | identifying genes that regulate bone remodeling as potential therapeutic targets |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2213103/ https://www.ncbi.nlm.nih.gov/pubmed/15781576 http://dx.doi.org/10.1084/jem.20050354 |
work_keys_str_mv | AT kranestephenm identifyinggenesthatregulateboneremodelingaspotentialtherapeutictargets |