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Molecular and Cellular Biology
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May 5, 2005
Generation and characterization of Rgs4 mutant mice
Nicolas Grillet, Alexandre Pattyn, Candice Contet, et al.
Development (Cambridge, England)
|
November 25, 2003
Phox2b controls the development of peripheral chemoreceptors and afferent visceral pathways
Stéphane 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 models
Jeanne Amiel, Véronique Dubreuil, Nélina Ramanantsoa, et al.
Nature Neuroscience
|
May 11, 2004
Ascl1/Mash1 is required for the development of central serotonergic neurons
Alexandre 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 precursors
Patrick 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 crest
Eva 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 neurons
Véronique 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 motoneurons
Héloïse 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 proteins
Omar 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.
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of 3
Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
Molecular and Cellular Biology
|
May 5, 2005
Generation and characterization of Rgs4 mutant mice
Nicolas Grillet, Alexandre Pattyn, Candice Contet, et al.
Development (Cambridge, England)
|
November 25, 2003
Phox2b controls the development of peripheral chemoreceptors and afferent visceral pathways
Stéphane 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 models
Jeanne Amiel, Véronique Dubreuil, Nélina Ramanantsoa, et al.
Nature Neuroscience
|
May 11, 2004
Ascl1/Mash1 is required for the development of central serotonergic neurons
Alexandre 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 precursors
Patrick 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 crest
Eva 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 neurons
Véronique 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 motoneurons
Héloïse 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 proteins
Omar 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.
Page
of 3