Результаты поиска - Heather Etchevers

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  1. 1
    The hedgehog pathway and ocular developmental anomalies

    The hedgehog pathway and ocular developmental anomalies по Florencia Cavodeassi, Sophie Creuzet, Heather Etchevers

    Опубликовано 2018
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  2. 2
    The diverse neural crest: from embryology to human pathology

    The diverse neural crest: from embryology to human pathology по Heather Etchevers, Élisabeth Dupin, Nicole M. Le Douarin

    Опубликовано 2019
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  3. 3
    Human neural tube defects: Developmental biology, epidemiology, and genetics

    Human neural tube defects: Developmental biology, epidemiology, and genetics по Eric Detrait, Timothy M. George, Heather Etchevers, John R. Gilbert, Michel Vekemans, Marcy C. Speer

    Опубликовано 2005
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  4. 4
    ISL1 Directly Regulates FGF10 Transcription during Human Cardiac Outflow Formation

    ISL1 Directly Regulates FGF10 Transcription during Human Cardiac Outflow Formation по Christelle Golzio, Emmanuelle Havis, Philippe Daubas, Grégory Nuel, Candice Babarit, Arnold Münnich, Michel Vekemans, Stéphane Zaffran, Stanislas Lyonnet, Heather Etchevers

    Опубликовано 2012
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    Artigo
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  5. 5
    Human neural crest cells display molecular and phenotypic hallmarks of stem cells

    Human neural crest cells display molecular and phenotypic hallmarks of stem cells по Sophie Thomas, Marie Thomas, Patrick Wincker, Candice Babarit, Pu‐Ting Xu, Marcy C. Speer, Arnold Münnich, Stanislas Lyonnet, Michel Vekemans, Heather Etchevers

    Опубликовано 2008
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    Artigo
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  6. 6
    Matthew-Wood Syndrome Is Caused by Truncating Mutations in the Retinol-Binding Protein Receptor Gene STRA6

    Matthew-Wood Syndrome Is Caused by Truncating Mutations in the Retinol-Binding Protein Receptor Gene STRA6 по Christelle Golzio, Jelena Martinovic-Bouriel, Sophie Thomas, Soumaya Mougou-Zrelli, Bettina Grattagliano‐Bessières, Maryse Bonnière, S. Delahaye, Arnold Munnich, Férechté Encha-Razavi, Stanislas Lyonnet, Michel Vekemans, Tania Attié‐Bitach, Heather Etchevers

    Опубликовано 2007
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    Artigo
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  7. 7
    Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

    Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome по Jeanne Amiel, Béatrice Laudier, Tania Attié‐Bitach, Ha Trang, Loïc de Pontual, Blanca Gener, Delphine Trochet, Heather Etchevers, Pierre F. Ray, Michel Simonneau, Michel Vekemans, Arnold Münnich, Claude Gaultier, Stanislas Lyonnet

    Опубликовано 2003
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    Artigo
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  8. 8
    Phenotypic spectrum of<i>STRA6</i>mutations: from Matthew-Wood syndrome to non-lethal anophthalmia

    Phenotypic spectrum of<i>STRA6</i>mutations: from Matthew-Wood syndrome to non-lethal anophthalmia по Nicolas Chassaing, Christelle Golzio, Sylvie Odent, Léopoldine Lequeux, Adeline Vigouroux, Jelena Martinovic-Bouriel, Francesco Danilo Tiziano, L. Masini, F. Piro, G Maragliano, Anne‐Lise Delezoide, Tania Attié‐Bitach, Sylvie Manouvrier‐Hanu, Heather Etchevers, Patrick Calvas

    Опубликовано 2009
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    Artigo
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  9. 9
    Multi-modal refinement of the human heart atlas during the first gestational trimester

    Multi-modal refinement of the human heart atlas during the first gestational trimester по Christopher De Bono, Yichi Xu, Samina Kausar, Marine Herbane, Camille Humbert, Sevda Rafatov, Chantal Missirian, Mathias Moreno, Weiyang Shi, Yorick Gitton, Alberto Lombardini, Ivo Vanzetta, Séverine Mazaud‐Guittot, Alain Chédotal, Anaı̈s Baudot, Stéphane Zaffran, Heather Etchevers

    Опубликовано 2025
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    Artigo
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  10. 10
    Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations

    Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations по Sarah Boissel, Orit Reish, Karine Proulx, Hiroko Kawagoe-Takaki, Barbara Sedgwick, Giles S.H. Yeo, Stephen Eyre, Christelle Golzio, Florence Molinari, Noman Kadhom, Heather Etchevers, Vladimı́r Saudek, I. Sadaf Farooqi, Philippe Froguel, Tomas Lindahl, Stephen O’Rahilly, Arnold Münnich, Laurence Colleaux

    Опубликовано 2009
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    Artigo
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  11. 11
    Targeted resequencing identifies <i>PTCH1</i> as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network

    Targeted resequencing identifies <i>PTCH1</i> as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network по Nicolas Chassaing, Erica E. Davis, Kelly McKnight, Adrienne R. Niederriter, Alexandre Causse, Véronique David, Annaïck Desmaison, Sophie Lamarre, Catherine Vincent‐Delorme, Laurent Pasquier, Christine Coubes, Didier Lacombe, Massimiliano Rossi, Jean‐Louis Dufier, Hélène Dollfus, Josseline Kaplan, Nicholas Katsanis, Heather Etchevers, Stanislas Faguer, Patrick Calvas

    Опубликовано 2016
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    Artigo
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  12. 12
    Mutational, functional, and expression studies of the<i>TCF4</i>gene in Pitt-Hopkins syndrome

    Mutational, functional, and expression studies of the<i>TCF4</i>gene in Pitt-Hopkins syndrome по Loïc de Pontual, Yves Mathieu, Christelle Golzio, Marlène Rio, Valérie Malan, Nathalie Boddaert, Christine Soufflet, Capucine Pïcard, Anne Durandy, Angus Dobbie, Delphine Héron, Bertrand Isidor, Jacques Motté, Ruth Newburry-Ecob, Laurent Pasquier, Marc Tardieu, G��raldine Viot, Francis Jaubert, Arnold Münnich, Laurence Colleaux, Michel Vekemans, Heather Etchevers, Stanislas Lyonnet, Jeanne Amiel

    Опубликовано 2009
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  13. 13
    Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development

    Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development по Damien Sanlaville, Heather Etchevers, Marie Gonzalès, Jéléna Martinovic, Mathieu Clément‐Ziza, Anne‐Lise Delezoide, M. C. Aubry, Anna Pelet, Sophie Chemouny, Corinne Cruaud, Sophie Audollent, Chantal Esculpavit, Géraldine Goudefroye, Catherine Ozilou, C. Fredouille, Nicole Joyé, N. Morichon-Delvallez, Yves Dumez, Jean Weissenbach, Arnold Münnich, Jeanne Amiel, Férechté Encha‐Razavi, Stanislas Lyonnet, Michel Vekemans, Tania Attié‐Bitach

    Опубликовано 2005
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    Artigo
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  14. 14
    Macrophage-Derived IL1β and TNFα Regulate Arginine Metabolism in Neuroblastoma

    Macrophage-Derived IL1β and TNFα Regulate Arginine Metabolism in Neuroblastoma по Livingstone Fultang, Laura D. Gamble, Luciana Gneo, Andrea M. Berry, Sharon A. Egan, Fenna De Bie, Orli Yogev, Georgina L. Eden, Sarah Booth, Samantha Brownhill, Ashley Vardon, Carmel McConville, Paul N. Cheng, Murray D. Norris, Heather Etchevers, Jayne Murray, David S. Ziegler, Louis Chesler, Ronny Schmidt, Susan A. Burchill, Michelle Haber, Carmela De Santo, Francis Mussai

    Опубликовано 2018
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    Artigo
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  15. 15
    Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome

    Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome по Houda Karmous‐Benailly, Jéléna Martinovic, Marie‐Claire Gubler, Yoann Sirot, Laure Clech, Catherine Ozilou, Joëlle Augé, Nora Brahimi, Heather Etchevers, Eric Detrait, Chantal Esculpavit, Sophie Audollent, Géraldine Goudefroye, Marie Gonzalès, Julia Tantau, Philippe Loget, Madeleine Joubert, Dominique Gaillard, Corinne Jeanne‐Pasquier, Anne‐Lise Delezoide, Marie-Odile Peter, Ghislaine Plessis, Brigitte Simon‐Bouy, Hélène Dollfus, Martine Le Merrer, Arnold Münnich, Férechté Encha‐Razavi, Michel Vekemans, Tania Attié‐Bitach

    Опубликовано 2005
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  16. 16
    Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries

    Heterogeneity of neuroblastoma cell identity defined by transcriptional circuitries по Valentina Boeva, Caroline Louis‐Brennetot, Agathe Peltier, Simon Durand, Cécile Pierre‐Eugène, Virginie Raynal, Heather Etchevers, Sophie Thomas, Alban Lermine, Estelle Daudigeos‐Dubus, Birgit Geoerger, Martin F. Orth, Thomas G. P. Grünewald, Elise Diaz, Bertrand Ducos, Didier Surdez, Ángel M. Carcaboso, И В Медведева, Thomas Deller, Valérie Combaret, Eve Lapouble, Gaëlle Pierron, Sandrine Grossetête-Lalami, Sylvain Baulande, Gudrun Schleiermacher, Emmanuel Barillot, Hermann Rohrer, Olivier Delattre, Isabelle Janoueix‐Lerosey

    Опубликовано 2017
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  17. 17
    A roadmap for the Human Developmental Cell Atlas

    A roadmap for the Human Developmental Cell Atlas по Muzlifah Haniffa, Deanne Taylor, Sten Linnarsson, Bruce J. Aronow, Gary D. Bader, Roger A. Barker, Pablo G. Cámara, J. Gray Camp, Alain Chédotal, Andrew J. Copp, Heather Etchevers, Paolo Giacobini, Berthold Göttgens, Guoji Guo, Ania Hupalowska, Kylie R. James, Emily Kirby, Arnold R. Kriegstein, Joakim Lundeberg, John C. Marioni, Kerstin B. Meyer, Kathy K. Niakan, Mats Nilsson, Bayanne Olabi, Dana Pe’er, Aviv Regev, Jennifer Rood, Orit Rozenblatt–Rosen, Rahul Satija, Sarah A. Teichmann, Barbara Treutlein, Roser Vento‐Tormo, Simone Webb, Pascal Barbry, Omer Ali Bayraktar, Sam Behjati, Andreas Bosio, Bruno Canque, Frédéric Chalmel, Yorick Gitton, Deborah J. Henderson, Anne Jørgensen, Steven Lisgo, Jinyue Liu, Emma Lundberg, Jean‐Léon Maître, Séverine Mazaud‐Guittot, Elizabeth Robertson, Antoine D. Rolland, Raphaël Scharfmann, Michèle Souyri, Erik Sundström, Stéphane Zaffran, Matthias Zilbauer

    Опубликовано 2021
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