Zobrazeno 1 - 5 of 5 pro vyhledávání: '"Olinda Alegria"'
1
Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome
Autor: Omar Akil, Didier Dulon, Samantha Papal, Vincent Michel, Paul Avan, Alice Emptoz, Aziz El-Amraoui, Olinda Alegria-Prévot, Sedigheh Delmaghani, Pranav Patni, Lawrence R. Lustig, Christine Petit, Alain Aghaie, Abdelaziz Tlili, Elise Pepermans, Yohan Bouleau, Saaid Safieddine, Margot Tertrais, Matteo Cortese, Philippe F.Y. Vincent
Publikováno v: Journal of Clinical Investigation
Journal of Clinical Investigation, 2018, 128 (8), pp.3382-3401. ⟨10.1172/JCI94351⟩
Journal of Clinical Investigation, American Society for Clinical Investigation, 2018, 128 (8), pp.3382-3401. 〈10.1172/JCi94351〉
Journal of Clinical Investigation, American Society for Clinical Investigation, 2018, 128 (8), pp.3382-3401. ⟨10.1172/JCI94351⟩
The journal of clinical investigation
Clarin-1, a tetraspan-like membrane protein defective in Usher syndrome type IIIA (USH3A), is essential for hair bundle morphogenesis in auditory hair cells. We report a new synaptic role for clarin-1 in mouse auditory hair cells elucidated by charac
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::442a4774c92de44a660e270a911cd4e4
https://hal-pasteur.archives-ouvertes.fr/pasteur-01858480/file/Dulon_ElAmraoui_2017.pdf
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2
Injury-Induced Senescence Enables In Vivo Reprogramming in Skeletal Muscle
Autor: Han Li, Patricia Flamant, Shahragim Tajbakhsh, Olinda Alegria, Coralie Cazin, Sabela Búa Aguín, Hiroshi Sakai, Laurence Fiette, Rana Salam, Isabelle Roux, Aurélie Chiche, Mathieu von Joest
Publikováno v: Cell Stem Cell
Cell Stem Cell, 2017, 20 (3), pp.407-414.e4. ⟨10.1016/j.stem.2016.11.020⟩
International audience; In vivo reprogramming is a promising approach for tissue regeneration in response to injury. Several examples of in vivo reprogramming have been reported in a variety of lineages, but some including skeletal muscle have so far
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168f481f8de21d31f9186f7169288f08
https://pubmed.ncbi.nlm.nih.gov/28257706
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3
Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia
Autor: Dominique Weil, Sébastien Chardenoux, Paul Avan, Vincent Michel, Nicolas Michalski, Olinda Alegria-Prévot, Marcio Do Cruzeiro, Isabelle Perfettini, Guy P. Richardson, Richard J. Goodyear, Isabelle Foucher, Elisa Caberlotto, Jean-Pierre Hardelin, Amel Bahloul, Christine Petit, Elise Pepermans
Publikováno v: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, 2011, 108 (14), pp.5825-30. ⟨10.1073/pnas.1017114108⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2011, 108 (14), pp.5825-30. ⟨10.1073/pnas.1017114108⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2011, 108 (14), pp.5825-30. 〈10.1073/pnas.1017114108〉
The mechanotransducer channels of auditory hair cells are gated by tip-links, oblique filaments that interconnect the stereocilia of the hair bundle. Tip-links stretch from the tips of stereocilia in the short and middle rows to the sides of neighbor
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::febdb8d77e9fd42c618b02efa7a96e0a
https://hal-pasteur.archives-ouvertes.fr/pasteur-01472844/file/PNAS-2011-Caberlotto-5825-30.pdf
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4
Abnormal urethra formation in mouse models of Split-hand/split-foot malformation type 1 and type 4
Autor: Giovanni Levi, Olinda Alegria, Kentaro Suzuki, Alea A. Mills, Gen Yamada, Takeshi Kurita, Masataka Ito, Ottavia Barbieri, Maxence Vieux-Rochas, Ryuma Haraguchi, Tsutomu Ogata, Naomi Nakagata
Publikováno v: European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2008, 16 (1), pp.36-44. ⟨10.1038/sj.ejhg.5201925⟩
European Journal of Human Genetics, Nature Publishing Group, 2007, epub ahead of print. ⟨10.1038/sj.ejhg.5201925⟩
Urogenital birth defects are one of the common phenotypes observed in hereditary human disorders. In particular, limb malformations are often associated with urogenital developmental abnormalities, as the case for Hand-foot-genital syndrome displayin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afd38a2f9533c40f64b33ecdcae91790
https://hal.archives-ouvertes.fr/hal-02135949
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5
Transfection of multiple pulmonary cell types following intravenous injection of PEI-DNA in normal and CFTR mutant mice
Autor: Giovanni Levi, Fariel Dif, Barbara A. Demeneix, Chakib Djediat, Olinda Alegria
Publikováno v: The Journal of Gene Medicine
The Journal of Gene Medicine, Wiley, 2006, 8 (1), pp.82-9. ⟨10.1002/jgm.831⟩
HAL
The Journal of Gene Medicine, Wiley, 2006, 8(1), pp.82-89
BACKGROUND: The polycationic vector polyethylenimine (PEI) has been shown to be a powerful agent for transfecting the mouse lung after injection of plasmid-based polyplexes through the tail vein. These findings raise therapeutic prospects for a numbe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f23f9314eeb6554a9e65937b9578b8b
https://pubmed.ncbi.nlm.nih.gov/16142827
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Plný text Recenzováno Digitální knihovna AV ČR
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