Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ophélie Nicolle"'
Autor:
Aurélien Bidaud-Meynard, Anne Bourdais, Ophélie Nicolle, Maela Duclos, Jad Saleh, Frank M. Ruemmele, Henner F. Farin, Delphine Delacour, Despina Moshous, Grégoire Michaux
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 17, Iss 6, Pp 1072-1075 (2024)
Externí odkaz:
https://doaj.org/article/17e3bd79c7ab45dea4123ebff58c2eeb
Autor:
Mohammed H. Mosa, Ophélie Nicolle, Sophia Maschalidi, Fernando E. Sepulveda, Aurelien Bidaud-Meynard, Constantin Menche, Birgitta E. Michels, Grégoire Michaux, Geneviève de Saint Basile, Henner F. Farin
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 6, Iss 4, Pp 477-493.e1 (2018)
Background & Aims: Microvillus inclusion disease (MVID) is a congenital intestinal malabsorption disorder caused by defective apical vesicular transport. Existing cellular models do not fully recapitulate this heterogeneous pathology. The aim of this
Externí odkaz:
https://doaj.org/article/ef293e491f7240379703b18ddd4ab05a
Maintenance of the polarity of the epithelial cells facing the lumen of the small intestine is crucial to ensure the vectorial absorption of nutrients as well as the integrity of the apical brush border and the intestinal barrier. Polarized vesicular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aaa3026926bc7c712c46068057817f49
https://doi.org/10.1101/2023.05.12.540539
https://doi.org/10.1101/2023.05.12.540539
The master kinase PAR-4/LKB1 appears as a major regulator of intestinal physiology. It is in particular mutated in the Peutz-Jeghers syndrome, an inherited disorder in which patients develop benign intestine polyps. Moreover, ectopic activation of PA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5afffda220e882f9922c076f0a431f88
https://hal.science/hal-03859203
https://hal.science/hal-03859203
Autor:
Aurélien Bidaud-Meynard, Ophélie Nicolle, Anne Bourdais, Maela Duclos, Jad Saleh, Frank Ruemmele, Henner F Farin, Delphine Delacour, Despina Moshous, Grégoire Michaux
Publikováno v:
BioRxiv
BioRxiv, 2022, ⟨10.1101/2022.11.04.515188⟩
BioRxiv, 2022, ⟨10.1101/2022.11.04.515188⟩
SummaryIntestinal microvillus atrophy is a major cause of enteropathies such as idiopathic or congenital diarrhea that are often associated with severe morbidity. It can be caused by genetic disorders, inflammatory diseases, toxins or pathogens. In p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4952918ea8e1b8d5ba0b90922c9baeac
https://hal.science/hal-03854108/document
https://hal.science/hal-03854108/document
Autor:
Grégoire Michaux, Anne Pacquelet, Camille N. Plancke, François Robin, Aurélien Bidaud-Meynard, Flora Demouchy, Ophélie Nicolle, Shashi Kumar Suman
Publikováno v:
Development (Cambridge, England)
Development (Cambridge, England), Company of Biologists, 2021, ⟨10.1242/dev.200029⟩
Development
Development (Cambridge, England), 2021, 148 (23), ⟨10.1242/dev.200029⟩
Development (Cambridge, England), Company of Biologists, 2021, ⟨10.1242/dev.200029⟩
Development
Development (Cambridge, England), 2021, 148 (23), ⟨10.1242/dev.200029⟩
The intestinal brush border is made of an array of microvilli that increases the membrane surface area for nutrient processing, absorption, and host defence. Studies on mammalian cultured epithelial cells uncovered some of the molecular players and p
Autor:
João J, Ramalho, Jorian J, Sepers, Ophélie, Nicolle, Ruben, Schmidt, Janine, Cravo, Grégoire, Michaux, Mike, Boxem
Publikováno v:
Development (Cambridge, England). 147(14)
ERM proteins are conserved regulators of cortical membrane specialization that function as membrane-actin linkers and molecular hubs. The activity of ERM proteins requires a conformational switch from an inactive cytoplasmic form into an active membr
ERM proteins are conserved regulators of cortical membrane specialization, that function as membrane–actin linkers and molecular hubs. Activity of ERM proteins requires a conformational switch from an inactive cytoplasmic form into an active membra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1315eb4e91046974d32ac9d7442e97b7
Publikováno v:
Development (Cambridge, England)
Development (Cambridge, England), 2019, 146 (11), pp.174508. ⟨10.1242/dev.174508⟩
Development (Cambridge, England), Company of Biologists, 2019, 146 (11), pp.174508. ⟨10.1242/dev.174508⟩
Development
Development (Cambridge, England), 2019, 146 (11), pp.174508. ⟨10.1242/dev.174508⟩
Development (Cambridge, England), Company of Biologists, 2019, 146 (11), pp.174508. ⟨10.1242/dev.174508⟩
Development
Intestine function relies on the strong polarity of intestinal epithelial cells and the array of microvilli forming a brush border at their luminal pole. Combining a genetic RNA interference (RNAi) screen with in vivo super-resolution imaging in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc01b2866852ccac21766c7295300ad
https://univ-rennes.hal.science/hal-02153480/document
https://univ-rennes.hal.science/hal-02153480/document
Autor:
André Le Bivic, Ophélie Nicolle, Marion Rabant, Dominique Massey-Harroche, Nicole Brousse, Olivier Goulet, Grégoire Michaux, Frank M. Ruemmele
Publikováno v:
Biology of the Cell. 108:19-28
BACKGROUND INFORMATION: . Microvillus inclusion disease (MVID) is a genetic disorder affecting intestinal absorption. It is caused by mutations in MYO5B or syntaxin 3 (STX3) affecting apical membrane trafficking. Morphologically MVID is characterised