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Christo Goridis

Showing results (11-20 of 27) with videos related to

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Molecular and Cellular Biology|May 5, 2005
Generation and characterization of Rgs4 mutant miceNicolas Grillet, Alexandre Pattyn, Candice Contet, et al.
Development (Cambridge, England)|November 25, 2003
Phox2b controls the development of peripheral chemoreceptors and afferent visceral pathwaysStéphane Dauger, Alexandre Pattyn, Frédéric Lofaso, et al.
Respiratory Physiology & Neurobiology|August 29, 2009
PHOX2B in respiratory control: lessons from congenital central hypoventilation syndrome and its mouse modelsJeanne Amiel, Véronique Dubreuil, Nélina Ramanantsoa, et al.
Nature Neuroscience|May 11, 2004
Ascl1/Mash1 is required for the development of central serotonergic neuronsAlexandre Pattyn, Nicolas Simplicio, J Hikke van Doorninck, et al.
Neural Development|June 21, 2008
Identification of Phox2b-regulated genes by expression profiling of cranial motoneuron precursorsPatrick Pla, Marie-Rose Hirsch, Stéphane Le Crom, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
Epibranchial ganglia orchestrate the development of the cranial neurogenic crestEva Coppola, Murielle Rallu, Juliette Richard, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 17, 2008
A human mutation in Phox2b causes lack of CO2 chemosensitivity, fatal central apnea, and specific loss of parafacial neuronsVéronique Dubreuil, Nélina Ramanantsoa, Delphine Trochet, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 2006
Precraniate origin of cranial motoneuronsHéloïse D Dufour, Zoubida Chettouh, Carole Deyts, et al.
Development (Cambridge, England)|August 4, 2004
Integration of anteroposterior and dorsoventral regulation of Phox2b transcription in cranial motoneuron progenitors by homeodomain proteinsOmar Abdel Samad, Marc J Geisen, Giuliana Caronia, et al.
Human Mutation|April 15, 2008
Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse)Delphine Trochet, Loïc de Pontual, Maria Helena Estêvao, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Molecular and Cellular Biology|May 5, 2005
Generation and characterization of Rgs4 mutant miceNicolas Grillet, Alexandre Pattyn, Candice Contet, et al.
Development (Cambridge, England)|November 25, 2003
Phox2b controls the development of peripheral chemoreceptors and afferent visceral pathwaysStéphane Dauger, Alexandre Pattyn, Frédéric Lofaso, et al.
Respiratory Physiology & Neurobiology|August 29, 2009
PHOX2B in respiratory control: lessons from congenital central hypoventilation syndrome and its mouse modelsJeanne Amiel, Véronique Dubreuil, Nélina Ramanantsoa, et al.
Nature Neuroscience|May 11, 2004
Ascl1/Mash1 is required for the development of central serotonergic neuronsAlexandre Pattyn, Nicolas Simplicio, J Hikke van Doorninck, et al.
Neural Development|June 21, 2008
Identification of Phox2b-regulated genes by expression profiling of cranial motoneuron precursorsPatrick Pla, Marie-Rose Hirsch, Stéphane Le Crom, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
Epibranchial ganglia orchestrate the development of the cranial neurogenic crestEva Coppola, Murielle Rallu, Juliette Richard, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 17, 2008
A human mutation in Phox2b causes lack of CO2 chemosensitivity, fatal central apnea, and specific loss of parafacial neuronsVéronique Dubreuil, Nélina Ramanantsoa, Delphine Trochet, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 2006
Precraniate origin of cranial motoneuronsHéloïse D Dufour, Zoubida Chettouh, Carole Deyts, et al.
Development (Cambridge, England)|August 4, 2004
Integration of anteroposterior and dorsoventral regulation of Phox2b transcription in cranial motoneuron progenitors by homeodomain proteinsOmar Abdel Samad, Marc J Geisen, Giuliana Caronia, et al.
Human Mutation|April 15, 2008
Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse)Delphine Trochet, Loïc de Pontual, Maria Helena Estêvao, et al.
Pageof 3