Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nicholas P. Legendre"'
Autor:
Masakazu Yamamoto, Nicholas P. Legendre, Arpita A. Biswas, Alexander Lawton, Shoko Yamamoto, Shahragim Tajbakhsh, Gabrielle Kardon, David J. Goldhamer
Publikováno v:
Stem Cell Reports, Vol 10, Iss 3, Pp 956-969 (2018)
Summary: MyoD and Myf5 are fundamental regulators of skeletal muscle lineage determination in the embryo, and their expression is induced in satellite cells following muscle injury. MyoD and Myf5 are also expressed by satellite cell precursors develo
Externí odkaz:
https://doaj.org/article/9b4548a4ca7e458ca4e98e0ced50c621
Autor:
John B. Lees-Shepard, Masakazu Yamamoto, Arpita A. Biswas, Sean J. Stoessel, Sarah-Anne E. Nicholas, Cathy A. Cogswell, Parvathi M. Devarakonda, Michael J. Schneider, Samantha M. Cummins, Nicholas P. Legendre, Shoko Yamamoto, Vesa Kaartinen, Jeffrey W. Hunter, David J. Goldhamer
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-14 (2018)
Fibrodysplasia ossificans progressiva is a severe disorder characterized by heterotopic ossification, and is caused by mutations in ACVR1. Here, the authors show that expression of mutant ACVR1 in fibro/adipogenic progenitors recapitulates disease pr
Externí odkaz:
https://doaj.org/article/cce620ded4304ad1a71c991a24918aac
Autor:
Shoko Yamamoto, Shahragim Tajbakhsh, Arpita A. Biswas, Alexander Lawton, David J. Goldhamer, Gabrielle Kardon, Masakazu Yamamoto, Nicholas P. Legendre
Publikováno v:
Stem Cell Reports
Stem Cell Reports, Vol 10, Iss 3, Pp 956-969 (2018)
Stem Cell Reports, Vol 10, Iss 3, Pp 956-969 (2018)
Summary MyoD and Myf5 are fundamental regulators of skeletal muscle lineage determination in the embryo, and their expression is induced in satellite cells following muscle injury. MyoD and Myf5 are also expressed by satellite cell precursors develop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5980b88c72e5698567987ccce8f296c
http://europepmc.org/articles/PMC5918368
http://europepmc.org/articles/PMC5918368
Autor:
Jeffrey W. Hunter, Nicholas P. Legendre, David J. Goldhamer, Sarah Anne E. Nicholas, Masakazu Yamamoto, Michael J Schneider, Arpita A. Biswas, Samantha M. Cummins, Sean J. Stoessel, John B Lees-Shepard, Shoko Yamamoto, Cathy A. Cogswell, Vesa Kaartinen, Parvathi M. Devarakonda
Publikováno v:
Nature Communications
Nature Communications, Vol 9, Iss 1, Pp 1-14 (2018)
Nature Communications, Vol 9, Iss 1, Pp 1-14 (2018)
Fibrodysplasia ossificans progressiva (FOP) is a rare autosomal-dominant disorder characterized by progressive and profoundly disabling heterotopic ossification (HO). Here we show that fibro/adipogenic progenitors (FAPs) are a major cell-of-origin of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7492bcdb795aaa02d1efcd6ee5a91e12
http://europepmc.org/articles/PMC5797136
http://europepmc.org/articles/PMC5797136