Highly distinct genetic programs for peripheral nervous system formation in chordates
Chowdhury, Rafath, Roure, Agnès, le Pétillon, Yann, Mayeur, Hélène, Daric, Vladimir, Darras, Sébastien
Published in BMC biology (27.06.2022)
Published in BMC biology (27.06.2022)
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Evolutionary origin of vertebrate OCT4/POU5 functions in supporting pluripotency
Sukparangsi, Woranop, Morganti, Elena, Lowndes, Molly, Mayeur, Hélène, Weisser, Melanie, Hammachi, Fella, Peradziryi, Hanna, Roske, Fabian, Hölzenspies, Jurriaan, Livigni, Alessandra, Godard, Benoit Gilbert, Sugahara, Fumiaki, Kuratani, Shigeru, Montoya, Guillermo, Frankenberg, Stephen R, Mazan, Sylvie, Brickman, Joshua M
Published in Nature communications (21.09.2022)
Published in Nature communications (21.09.2022)
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Journal Article
Diversification of habenular organization and asymmetries in teleosts: Insights from the Atlantic salmon and European eel
Michel, Léo, Palma, Karina, Cerda, Mauricio, Lagadec, Ronan, Mayeur, Hélène, Fuentès, Michaël, Besseau, Laurence, Martin, Patrick, Magnanou, Elodie, Blader, Patrick, Concha, Miguel L., Mazan, Sylvie
Published in Frontiers in cell and developmental biology (03.11.2022)
Published in Frontiers in cell and developmental biology (03.11.2022)
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Journal Article
Loss of Active Neurogenesis in the Adult Shark Retina
Hernández-Núñez, Ismael, Robledo, Diego, Mayeur, Hélène, Mazan, Sylvie, Sánchez, Laura, Adrio, Fátima, Barreiro-Iglesias, Antón, Candal, Eva
Published in Frontiers in cell and developmental biology (11.02.2021)
Published in Frontiers in cell and developmental biology (11.02.2021)
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Journal Article
When Bigger Is Better: 3D RNA Profiling of the Developing Head in the Catshark Scyliorhinus canicula
Mayeur, Hélène, Lanoizelet, Maxence, Quillien, Aurélie, Menuet, Arnaud, Michel, Léo, Martin, Kyle John, Dejean, Sébastien, Blader, Patrick, Mazan, Sylvie, Lagadec, Ronan
Published in Frontiers in cell and developmental biology (22.10.2021)
Published in Frontiers in cell and developmental biology (22.10.2021)
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Journal Article
Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome
Schorderet, Daniel F., Nichini, Olivia, Boisset, Gaëlle, Polok, Bozena, Tiab, Leila, Mayeur, Hélène, Raji, Bahija, de la Houssaye, Gauillaume, Abitbol, Marc M., Munier, Francis L.
Published in American journal of human genetics (01.05.2008)
Published in American journal of human genetics (01.05.2008)
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Journal Article
Prosomeric organization of the hypothalamus in an elasmobranch, the catshark Scyliorhinus canicula
Santos-Durán, Gabriel N, Menuet, Arnaud, Lagadec, Ronan, Mayeur, Hélène, Ferreiro-Galve, Susana, Mazan, Sylvie, Rodríguez-Moldes, Isabel, Candal, Eva
Published in Frontiers in neuroanatomy (08.04.2015)
Published in Frontiers in neuroanatomy (08.04.2015)
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Journal Article
The ancestral role of nodal signalling in breaking L/R symmetry in the vertebrate forebrain
Lagadec, Ronan, Laguerre, Laurent, Menuet, Arnaud, Amara, Anis, Rocancourt, Claire, Péricard, Pierre, Godard, Benoît G, Celina Rodicio, Maria, Rodriguez-Moldes, Isabel, Mayeur, Hélène, Rougemont, Quentin, Mazan, Sylvie, Boutet, Agnès
Published in Nature communications (30.03.2015)
Published in Nature communications (30.03.2015)
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Journal Article
Neurogenetic asymmetries in the catshark developing habenulae: mechanistic and evolutionary implications
Lagadec, Ronan, Lanoizelet, Maxence, Sánchez-Farías, Nuria, Hérard, Fanny, Menuet, Arnaud, Mayeur, Hélène, Billoud, Bernard, Rodriguez-Moldes, Isabel, Candal, Eva, Mazan, Sylvie
Published in Scientific reports (15.03.2018)
Published in Scientific reports (15.03.2018)
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Journal Article
Eight previously unidentified mutations found in the OA1 ocular albinism gene
Mayeur, Hélène, Roche, Olivier, Vêtu, Christelle, Jaliffa, Carolina, Marchant, Dominique, Dollfus, Hélène, Bonneau, Dominique, Munier, Francis L, Schorderet, Daniel F, Levin, Alex V, Héon, Elise, Sutherland, Joanne, Lacombe, Didier, Said, Edith, Mezer, Eedy, Kaplan, Josseline, Dufier, Jean-Louis, Marsac, Cécile, Menasche, Maurice, Abitbol, Marc
Published in BMC medical genetics (28.04.2006)
Published in BMC medical genetics (28.04.2006)
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Journal Article
Mutation in the Human Homeobox Gene NKX5-3Causes an Oculo-Auricular Syndrome
Schorderet, Daniel F, Nichini, Olivia, Boisset, Gaëlle, Polok, Bozena, Tiab, Leila, Mayeur, Hélène, Raji, Bahija, Houssaye, Gauillaume de la, Abitbol, Marc M, Munier, Francis L
Published in American journal of human genetics (09.05.2008)
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Published in American journal of human genetics (09.05.2008)
Journal Article
Eight previously unidentified mutations found in the OA1ocular albinism gene
Mayeur, Hélène, Roche, Olivier, Vêtu, Christelle, Jaliffa, Carolina, Marchant, Dominique, Dollfus, Hélène, Bonneau, Dominique, Munier, Francis L, Schorderet, Daniel F, Levin, Alex V, Héon, Elise, Sutherland, Joanne, Lacombe, Didier, Said, Edith, Mezer, Eedy, Kaplan, Josseline, Dufier, Jean-Louis, Marsac, Cécile, Menasche, Maurice, Abitbol, Marc
Published in BMC medical genetics (28.04.2006)
Published in BMC medical genetics (28.04.2006)
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Journal Article
Evolutionary Origin of Vertebrate OCT4/POU5 Functions in Supporting Pluripotency
Sukparangsi, Woranop, Morganti, Elena, Lowndes, Molly, Mayeur, Hélène, Weisser, Melanie, Fella Hammachi, Peradziryi, Hanna, Roske, Fabian, Hölzenspies, Jurriaan, Livigni, Alessandra, Benoit Gilbert Godard, Sugahara, Fumiaki, Kuratani, Shigeru, Montoya, Guillermo, Frankenberg, Stephen R, Mazan, Sylvie, Brickman, Joshua M
Published in bioRxiv (13.04.2022)
Published in bioRxiv (13.04.2022)
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