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Nicolas Lebrun

Showing results (21-30 of 44) with videos related to

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Human Molecular Genetics|November 2, 2013
Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdownYoann Saillour, Loïc Broix, Elodie Bruel-Jungerman, et al.
BMJ Open|June 26, 2024
Assessing biomarkers of remission in female patients with anorexia nervosa (REMANO): a protocol for a prospective cohort study with a nested case-control study using clinical, neurocognitive, biological, genetic, epigenetic and neuroimaging markers in a French specialised inpatient unitPhilibert Duriez, Virginie Tolle, Nicolas Ramoz, et al.
Neuroendocrinology|March 28, 2021
Effect of Growth Hormone Secretagogue Receptor Deletion on Growth, Pulsatile Growth Hormone Secretion, and Meal Pattern in Male and Female MiceAlexandra Labarthe, Philippe Zizzari, Oriane Fiquet, et al.
Translational Psychiatry|October 17, 2025
Unraveling the brain expression of bdnf in a mouse model of anorexia nervosaJingxian Cao, Nicolas Lebrun, Shiou-Ping Chen, et al.
European Journal of Human Genetics : EJHG|December 6, 2017
Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndromeNicolas Lebrun, Irina Giurgea, Alice Goldenberg, et al.
Frontiers in Endocrinology|November 1, 2021
Ghrelin Gene Deletion Alters Pulsatile Growth Hormone Secretion in Adult Female MiceRim Hassouna, Gimena Fernandez, Nicolas Lebrun, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2012
Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasisGinevra Zanni, Tito Calì, Vera M Kalscheuer, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|February 5, 2005
A survey of the Th2R and Th3R allelic variants in the circumsporozoite protein gene of P. falciparum parasites from western ThailandChutima Kumkhaek, Kooruethai Phra-ek, Pratap Singhasivanon, et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
Brain : a Journal of Neurology|May 27, 2014
The wide spectrum of tubulinopathies: what are the key features for the diagnosis?Nadia Bahi-Buisson, Karine Poirier, Franck Fourniol, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|November 2, 2013
Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdownYoann Saillour, Loïc Broix, Elodie Bruel-Jungerman, et al.
BMJ Open|June 26, 2024
Assessing biomarkers of remission in female patients with anorexia nervosa (REMANO): a protocol for a prospective cohort study with a nested case-control study using clinical, neurocognitive, biological, genetic, epigenetic and neuroimaging markers in a French specialised inpatient unitPhilibert Duriez, Virginie Tolle, Nicolas Ramoz, et al.
Neuroendocrinology|March 28, 2021
Effect of Growth Hormone Secretagogue Receptor Deletion on Growth, Pulsatile Growth Hormone Secretion, and Meal Pattern in Male and Female MiceAlexandra Labarthe, Philippe Zizzari, Oriane Fiquet, et al.
Translational Psychiatry|October 17, 2025
Unraveling the brain expression of bdnf in a mouse model of anorexia nervosaJingxian Cao, Nicolas Lebrun, Shiou-Ping Chen, et al.
European Journal of Human Genetics : EJHG|December 6, 2017
Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndromeNicolas Lebrun, Irina Giurgea, Alice Goldenberg, et al.
Frontiers in Endocrinology|November 1, 2021
Ghrelin Gene Deletion Alters Pulsatile Growth Hormone Secretion in Adult Female MiceRim Hassouna, Gimena Fernandez, Nicolas Lebrun, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 23, 2012
Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasisGinevra Zanni, Tito Calì, Vera M Kalscheuer, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|February 5, 2005
A survey of the Th2R and Th3R allelic variants in the circumsporozoite protein gene of P. falciparum parasites from western ThailandChutima Kumkhaek, Kooruethai Phra-ek, Pratap Singhasivanon, et al.
Neurogenetics|September 28, 2013
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyriaStéphanie Valence, Karine Poirier, Nicolas Lebrun, et al.
Brain : a Journal of Neurology|May 27, 2014
The wide spectrum of tubulinopathies: what are the key features for the diagnosis?Nadia Bahi-Buisson, Karine Poirier, Franck Fourniol, et al.
Pageof 5