Хайлтын үр дүнгүүд - Nadège Bondurand

  • 20-н 1 - 20 үр дүнгүүдийг харуулж байна
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  1. 1
    Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10

    Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10 -н Nadège Bondurand

    Хэвлэсэн 2001
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    Artigo
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  2. 2
    Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome

    Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome -н Nadège Bondurand

    Хэвлэсэн 2000
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    Artigo
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  3. 3
    The role of SOX10 during enteric nervous system development

    The role of SOX10 during enteric nervous system development -н Nadège Bondurand, MH Sham

    Хэвлэсэн 2013
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  4. 4
    Mouse models of Hirschsprung disease and other developmental disorders of the enteric nervous system: Old and new players

    Mouse models of Hirschsprung disease and other developmental disorders of the enteric nervous system: Old and new players -н Nadège Bondurand, E. Michelle Southard‐Smith

    Хэвлэсэн 2016
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  5. 5
    News from the endothelin-3/EDNRB signaling pathway: Role during enteric nervous system development and involvement in neural crest-associated disorders

    News from the endothelin-3/EDNRB signaling pathway: Role during enteric nervous system development and involvement in neural crest-associated disorders -н Nadège Bondurand, Sylvie Dufour, Véronique Pingault

    Хэвлэсэн 2018
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  6. 6
    SOX10: 20 years of phenotypic plurality and current understanding of its developmental function

    SOX10: 20 years of phenotypic plurality and current understanding of its developmental function -н Véronique Pingault, Lisa Zerad, William Bertani‐Torres, Nadège Bondurand

    Хэвлэсэн 2021
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  7. 7
    Functional Analysis of Sox10 Mutations Found in Human Waardenburg-Hirschsprung Patients

    Functional Analysis of Sox10 Mutations Found in Human Waardenburg-Hirschsprung Patients -н Kirsten Kuhlbrodt, Claudia Schmidt, Elisabeth Sock, Véronique Pingault, Nadège Bondurand, Michel Goossens, Michael Wegner

    Хэвлэсэн 1998
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    Artigo
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  8. 8
    Identification and functional analysis of<i>SOX10</i>missense mutations in different subtypes of waardenburg syndrome

    Identification and functional analysis of<i>SOX10</i>missense mutations in different subtypes of waardenburg syndrome -н Asma Chaoui, Yuli Watanabe, Renaud Touraine, Viviane Baral, Michel Goossens, Véronique Pingault, Nadège Bondurand

    Хэвлэсэн 2011
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    Artigo
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  9. 9
    Review and update of mutations causing Waardenburg syndrome

    Review and update of mutations causing Waardenburg syndrome -н Véronique Pingault, D. Ente, Florence Dastot‐Le Moal, Michel Goossens, Sandrine Marlin, Nadège Bondurand

    Хэвлэсэн 2010
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  10. 10
    Mutation of the Sry-related <i>Sox10</i> gene in <i>Dominant megacolon</i> , a mouse model for human Hirschsprung disease

    Mutation of the Sry-related <i>Sox10</i> gene in <i>Dominant megacolon</i> , a mouse model for human Hirschsprung disease -н Beate Herbarth, Véronique Pingault, Nadège Bondurand, Kirsten Kuhlbrodt, Irm Hermans‐Borgmeyer, Aldamaria Puliti, N Lemort, M. Goossens, Michael Wegner

    Хэвлэсэн 1998
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    Artigo
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  11. 11
    Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease

    Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease -н V. Cacheux, Florence Dastot‐Le Moal, H Kääriäinen, Nadège Bondurand, Risto Rintala, Brigitte Boissier, Megan J. Wilson, David Mowat, M. Goossens

    Хэвлэсэн 2001
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    Artigo
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  12. 12
    Expression of the <i>SOX10</i> gene during human development

    Expression of the <i>SOX10</i> gene during human development -н Nadège Bondurand, Alexandra Kobetz, Véronique Pingault, N Lemort, Férechté Encha‐Razavi, G Couly, Derk E. Goerich, Michael Wegner, Marc Abitbol, Michel Goossens

    Хэвлэсэн 1998
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    Artigo
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  13. 13
    A Molecular Analysis of the Yemenite Deaf-Blind Hypopigmentation Syndrome: SOX10 Dysfunction Causes Different Neurocristopathies

    A Molecular Analysis of the Yemenite Deaf-Blind Hypopigmentation Syndrome: SOX10 Dysfunction Causes Different Neurocristopathies -н Nadège Bondurand, Kirsten Kuhlbrodt, Véronique Pingault, Janna Enderich, M. Sajus, Niels Tommerup, Mette Warburg, Raoul C. M. Hennekam, Andrew Read, Michael Wegner, Michel Goossens

    Хэвлэсэн 1999
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    Artigo
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  14. 14
    How Tissue Mechanical Properties Affect Enteric Neural Crest Cell Migration

    How Tissue Mechanical Properties Affect Enteric Neural Crest Cell Migration -н Nicolas R. Chevalier, Elodie Gazquez, Laurent Bidault, Thomas Guilbert, Carine Vias, E. Vian, Yuli Watanabe, Laurent Muller, Stéphane Germain, Nadège Bondurand, Sylvie Dufour, V. Fleury

    Хэвлэсэн 2016
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    Artigo
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  15. 15
    ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development

    ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development -н Nadjet Gacem, Anthula Kavo, Lisa Zerad, Laurence Richard, Stéphane Mathis, Raj P. Kapur, Mélanie Parisot, Jeanne Amiel, Sylvie Dufour, Pierre de la Grange, Véronique Pingault, J.M. Vallat, Nadège Bondurand

    Хэвлэсэн 2020
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    Artigo
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  16. 16
    An ADAR1 dsRBD3-PKR kinase domain interaction on dsRNA inhibits PKR activation

    An ADAR1 dsRBD3-PKR kinase domain interaction on dsRNA inhibits PKR activation -н Ketty Sinigaglia, Anna Cherian, Qiupei Du, Valentina Lacovich, Dragana Vukić, Janka Melicherová, Pavla Linhartová, Lisa Zerad, Stanislav Stejskal, Radek Malı́k, Jan Procházka, Nadège Bondurand, Radislav Sedláček, Mary A. O’Connell, Liam P. Keegan

    Хэвлэсэн 2024
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    Artigo
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  17. 17
    Deletions at the SOX10 Gene Locus Cause Waardenburg Syndrome Types 2 and 4

    Deletions at the SOX10 Gene Locus Cause Waardenburg Syndrome Types 2 and 4 -н Nadège Bondurand, Florence Dastot‐Le Moal, Laure Stanchina, Nathalie Collot, Viviane Baral, Sandrine Marlin, Tania Attié‐Bitach, Irina Giurgea, Laurent Skopinski, William Reardon, Annick Toutain, Pierre Sarda, Echaieb Anis, Marilyn Lackmy-Port-Lis, Renaud Touraine, Jeanne Amiel, Michel Goossens, Véronique Pingault

    Хэвлэсэн 2007
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  18. 18
    Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness

    Loss-of-Function Mutations in SOX10 Cause Kallmann Syndrome with Deafness -н Véronique Pingault, Virginie Bodereau, Viviane Baral, Séverine Marcos, Yuli Watanabe, Asma Chaoui, Corinne Fouveaut, Chrystel Leroy, O. Vérier‐Mine, Christine Francannet, Delphine Dupin‐Deguine, F. Archambeaud, François-Joseph Kurtz, Jacques Young, Jérôme Bertherat, Sandrine Marlin, Michel Goossens, Jean‐Pierre Hardelin, Catherine Dodé, Nadège Bondurand

    Хэвлэсэн 2013
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    Artigo
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  19. 19
    White paper on guidelines concerning enteric nervous system stem cell therapy for enteric neuropathies

    White paper on guidelines concerning enteric nervous system stem cell therapy for enteric neuropathies -н Alan J. Burns, Allan M. Goldstein, Donald F. Newgreen, Lincon A. Stamp, Karl‐Herbert Schäfer, Marco Metzger, Ryo Hotta, Heather M. Young, Peter W. Andrews, Nikhil Thapar, Jaime Belkind‐Gerson, Nadège Bondurand, Joel C. Bornstein, Wood Yee Chan, Kathryn S.E. Cheah, Michael D. Gershon, Robert O. Heuckeroth, Robert M.W. Hofstra, Lothar Just, Raj P. Kapur, Sebastian K. King, Conor J. McCann, Nándor Nagy, Esw Ngan, Florian Obermayr, Vassilis Pachnis, Pankaj J. Pasricha, MH Sham, Paul Kwong Hang Tam, Pieter Vanden Berghe

    Хэвлэсэн 2016
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  20. 20
    Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans

    Dysregulation of the NRG1/ERBB pathway causes a developmental disorder with gastrointestinal dysmotility in humans -н Thuy-Linh Le, Louise Galmiche, J Levý, Pim Suwannarat, Debby M.E.I. Hellebrekers, Khomgrit Morarach, Franck Boismoreau, Tom E. J. Theunissen, Mathilde Lefebvre, Anna Pelet, Jéléna Martinovic, A. Gélot, Fabien Guimiot, Amanda Calleroz, Cyril Gitiaux, Marie Hully, Olivier Goulet, Christophe Chardot, Séverine Drunat, Yline Capri, Christine Bôle‐Feysot, Patrick Nitschké, Sandra Whalen, L. Mouthon, Holly E. Babcock, Robert M.W. Hofstra, Irenaeus F.M. de Coo, Anne‐Claude Tabet, Thierry Jo Molina, Boris Keren, Alice Brooks, Hubert J.M. Smeets, Ulrika Marklund, Christopher T. Gordon, Stanislas Lyonnet, Jeanne Amiel, Nadège Bondurand

    Хэвлэсэн 2021
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    Artigo
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