Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Virginie, Hauser"'
Autor:
Laurine Miscopein Saler, Virginie Hauser, Mathieu Bartoletti, Charlotte Mallart, Marianne Malartre, Laura Lebrun, Anne-Marie Pret, Laurent Théodore, Fabienne Chalvet, Sophie Netter
Publikováno v:
PLoS Genetics, Vol 16, Iss 11, p e1009128 (2020)
Many studies have focused on the mechanisms of stem cell maintenance via their interaction with a particular niche or microenvironment in adult tissues, but how formation of a functional niche is initiated, including how stem cells within a niche are
Externí odkaz:
https://doaj.org/article/42d593a753d846378a56f4d500fe4604
Publikováno v:
Current Biology. 32:4225-4239.e7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d95270b07c3364497adb43935876d88
https://doi.org/10.1016/j.cub.2022.08.025
https://doi.org/10.1016/j.cub.2022.08.025
Autor:
Laurine, Miscopein Saler, Virginie, Hauser, Mathieu, Bartoletti, Charlotte, Mallart, Marianne, Malartre, Laura, Lebrun, Anne-Marie, Pret, Laurent, Théodore, Fabienne, Chalvet, Sophie, Netter
Publikováno v:
PLoS Genetics
PLoS Genetics, 2020, 16 (11), pp.e1009128. ⟨10.1371/journal.pgen.1009128⟩
PLoS Genetics, Public Library of Science, 2020, 16 (11), pp.e1009128. ⟨10.1371/journal.pgen.1009128⟩
PLoS Genetics, Vol 16, Iss 11, p e1009128 (2020)
PLoS Genetics, 2020, 16 (11), pp.e1009128. ⟨10.1371/journal.pgen.1009128⟩
PLoS Genetics, Public Library of Science, 2020, 16 (11), pp.e1009128. ⟨10.1371/journal.pgen.1009128⟩
PLoS Genetics, Vol 16, Iss 11, p e1009128 (2020)
Many studies have focused on the mechanisms of stem cell maintenance via their interaction with a particular niche or microenvironment in adult tissues, but how formation of a functional niche is initiated, including how stem cells within a niche are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::57752569e6764ac93f33591b15d56e17
https://hal.science/hal-03001980/file/file.pdf
https://hal.science/hal-03001980/file/file.pdf
Autor:
Mathieu Bartoletti, Sophie Netter, Laurent Théodore, Fabienne Chalvet, Laurine Miscopein Saler, Anne-Marie Pret, Virginie Hauser
Many studies have focused on the mechanisms of stem cell maintenanceviatheir interaction with a particular niche or microenvironment in adult tissues, but how formation of a functional niche is initiated, including how stem cells within a niche are e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c15354a31a326bd735a34fd964bb1e4
https://doi.org/10.1101/689323
https://doi.org/10.1101/689323
Autor:
Tom H. Stevens, Tobias Hermle, Laurie A. Graham, Virginie Hauser, Matias Simons, Maria Clara Guida, Margret Ryan
Publikováno v:
Molecular Biology of the Cell
ATP6AP2 (also known as the [pro]renin receptor) is a type I transmembrane protein that can be cleaved into two fragments in the Golgi apparatus. While in Drosophila ATP6AP2 functions in the planar cell polarity (PCP) pathway, recent human genetic stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c3a505a3e7dd365d8f6e186ba36da6f
https://pubmed.ncbi.nlm.nih.gov/29995586
https://pubmed.ncbi.nlm.nih.gov/29995586
Autor:
Maria Clara Guida, Dulce Quelhas, Stefanie Jäger, Ganna Panasyuk, Thorsten Marquardt, Sandrine Duvet, Erika Souche, Oliver Kretz, Virginie Hauser, Gert Matthijs, Magda Cannata Serio, Maria A. Rujano, Esther M. Maier, Thomas D. Bird, Julien H. Park, Michael Schwake, Wendy H. Raskind, Janine Reunert, Peter Freisinger, Romain Péanne, François Foulquier, Daisy Rymen, Paula Garcia, Matias Simons, Nevan J. Krogan, Yoshinao Wada, Susana Nobre
Publikováno v:
The Journal of experimental medicine, vol 214, iss 12
The Journal of Experimental Medicine
The Journal of Experimental Medicine, 2017, The Journal of Experimental Medicine, 214 (12), pp.3707-3729. ⟨10.1084/jem.20170453⟩
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
The Journal of Experimental Medicine
The Journal of Experimental Medicine, 2017, The Journal of Experimental Medicine, 214 (12), pp.3707-3729. ⟨10.1084/jem.20170453⟩
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Rujano et al. report mutations in ATP6AP2 leading to liver disease, immunodeficiency, and psychomotor impairment. ATP6AP2 deficiency impairs the assembly and function of the V-ATPase proton pump, causing defects in protein glycosylation and autophagy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d131232641f255ae6d991e44fe325123
https://hdl.handle.net/10400.16/2228
https://hdl.handle.net/10400.16/2228