Zobrazeno 1 - 10
of 79
pro vyhledávání: '"D'Hulst, Gommaar"'
Autor:
D'Hulst, Gommaar, Hodžić, Deni, Leuenberger, Rahel, Arnet, Janik, Westerhuis, Elena, Roth, Ralf, Schmidt-Trucksäss, Arno, Knaier, Raphael, Wagner, Jonathan
Publikováno v:
International Journal of Sports Physiology & Performance; Aug2024, Vol. 19 Issue 8, p780-791, 12p
Publikováno v:
In Molecular Metabolism December 2022 66
Autor:
Zhang, Jing, Muri, Jonathan, Fitzgerald, Gillian, Gorski, Tatiane, Gianni-Barrera, Roberto, Masschelein, Evi, D’Hulst, Gommaar, Gilardoni, Paola, Turiel, Guillermo, Fan, Zheng, Wang, TongTong, Planque, Mélanie, Carmeliet, Peter, Pellerin, Luc, Wolfrum, Christian, Fendt, Sarah-Maria, Banfi, Andrea, Stockmann, Christian, Soro-Arnáiz, Inés, Kopf, Manfred, De Bock, Katrien
Publikováno v:
In Cell Metabolism 2 June 2020 31(6):1136-1153
Autor:
Masschelein, Evi1 (AUTHOR), D'Hulst, Gommaar1 (AUTHOR), Zvick, Joel2 (AUTHOR), Hinte, Laura3 (AUTHOR), Soro-Arnaiz, Inés1 (AUTHOR), Gorski, Tatiane1 (AUTHOR), von Meyenn, Ferdinand3 (AUTHOR), Bar-Nur, Ori2 (AUTHOR), De Bock, Katrien1 (AUTHOR) katrien-debock@ethz.ch
Publikováno v:
Skeletal Muscle. 7/9/2020, Vol. 10 Issue 1, p1-15. 15p.
Autor:
Scheuren, Ariane C., D'Hulst, Gommaar, Kuhn, Gisela A., Masschelein, Evi, Wehrle, Esther, De Bock, Katrien, Müller, Ralph
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 11, Iss 4, Pp 1121-1140 (2020)
Background Frailty is a geriatric syndrome characterized by increased susceptibility to adverse health outcomes. One major determinant thereof is the gradual weakening of the musculoskeletal system and the associated osteosarcopenia. To improve our u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d67250d1c5daa6e17d76d0d2b2acab69
https://doaj.org/article/a99a8a388d83469c8da426eb0e6d217a
https://doaj.org/article/a99a8a388d83469c8da426eb0e6d217a
Autor:
Domenig, Seraina A, Bundschuh, Nicola, Lenardič, Ajda, Ghosh, Adhideb, Kim, Inseon, Qabrati, Xhem, D'Hulst, Gommaar, Bar-Nur, Ori
Publikováno v:
Stem Cell Reports, 17 (2)
Genetic mutations in dystrophin manifest in Duchenne muscular dystrophy (DMD), the most commonly inherited muscle disease. Here, we report on reprogramming of fibroblasts from two DMD mouse models into induced myogenic progenitor cells (iMPCs) by Myo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f1dded117dae104a4064e438efa1894
Publikováno v:
Neuroendocrinology; 2022, Vol. 112 Issue 7, p673-701, 29p
Autor:
Scheuren, Ariane, D'Hulst, Gommaar, Kuhn, Gisela, Masschelein, Evi, Wehrle, Esther, De Bock, Katrien, Müller, Ralph
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, 11 (4)
Background Frailty is a geriatric syndrome characterized by increased susceptibility to adverse health outcomes. One major determinant thereof is the gradual weakening of the musculoskeletal system and the associated osteosarcopenia. To improve our u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______150::88c1ef21c2805e37273317919af79a1a
https://hdl.handle.net/20.500.11850/424113
https://hdl.handle.net/20.500.11850/424113
Akademický článek
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Autor:
Masschelein, Evi, D’Hulst, Gommaar, Zvick, Joel, Hinte, Laura, Soro-Arnaiz, Inés, Tatiane Gorski, Meyenn, Ferdinand Von, Bar-Nur, Ori, Bock, Katrien De
Additional file 7: Table S1. Phenotypic characterization and muscle weights normalized to tibia length. Statistics: one-way ANOVA test with Tukey correction for multiple comparisons (*p < 0.05 VResRun vs. Control). Values represent mean ± SEM. n = 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d7e2a5171c1e2936e8ad133c1b48518