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Dominique Bonneau

Showing results (51-60 of 253) with videos related to

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Experimental Neurology|October 27, 2019
Oxidative stress contributes differentially to the pathophysiology of Charcot-Marie-Tooth disease type 2KJulien Cassereau, Arnaud Chevrollier, Philippe Codron, et al.
The British Journal of Dermatology|May 5, 2023
Gain-of-function variants in the KDF1 gene cause hidradenitis suppurativa associated with ectodermal dysplasia by stabilizing IκB kinase αAlban Ziegler, Frédéric Ebstein, Hanan Shamseldin, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 13, 2019
Prenatal diagnosis of Desbuquois dysplasia type 1 by whole exome sequencing before the occurrence of specific ultrasound signsClara Houdayer, Alban Ziegler, Françoise Boussion, et al.
Acta Neuropathologica Communications|April 5, 2024
Letter to the editor on: prophylactic nicotinamide treatment protects from rotenone-induced neurodegeneration by increasing mitochondrial content and volumeCinzia Bocca, Judith Kouassi-Nzoughet, Juan Manuel Chao de la Barca, et al.
Medecine Sciences : M/S|October 9, 2010
[From yeast to neurodegenerative diseases: ten years of exploration of mitochondrial dynamic disorders]Guy Lenaers, Patrizia Amati-Bonneau, Cécile Delettre, et al.
Human Mutation|February 1, 2011
Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutationsPauline Krug, Vincent Morinière, Sandrine Marlin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2004
Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation familyBruno Mortemousque, Patrizia Amati-Bonneau, François Couture, et al.
Neurocase|November 28, 2019
Specific cognitive theory of mind and behavioral dysfunctions in early manifest Huntington disease: a case reportMarie Caillaud, Mickael Laisney, Alexandre Bejanin, et al.
Pharmacology, Biochemistry, and Behavior|January 28, 2006
Modafinil-induced modulation of working memory and plasma corticosterone in chronically-stressed miceChristophe Piérard, Pierrette Liscia, Magalie Valleau, et al.
European Journal of Endocrinology|April 5, 2024
Heterozygous gain of function variant in GUCY1A2 may cause autonomous ovarian hyperfunctionTheresa Wittrien, Alban Ziegler, Anne Rühle, et al.
Pageof 26

Showing results (51-60 of 253) with videos related to

Sort By:
Pageof 26
Experimental Neurology|October 27, 2019
Oxidative stress contributes differentially to the pathophysiology of Charcot-Marie-Tooth disease type 2KJulien Cassereau, Arnaud Chevrollier, Philippe Codron, et al.
The British Journal of Dermatology|May 5, 2023
Gain-of-function variants in the KDF1 gene cause hidradenitis suppurativa associated with ectodermal dysplasia by stabilizing IκB kinase αAlban Ziegler, Frédéric Ebstein, Hanan Shamseldin, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 13, 2019
Prenatal diagnosis of Desbuquois dysplasia type 1 by whole exome sequencing before the occurrence of specific ultrasound signsClara Houdayer, Alban Ziegler, Françoise Boussion, et al.
Acta Neuropathologica Communications|April 5, 2024
Letter to the editor on: prophylactic nicotinamide treatment protects from rotenone-induced neurodegeneration by increasing mitochondrial content and volumeCinzia Bocca, Judith Kouassi-Nzoughet, Juan Manuel Chao de la Barca, et al.
Medecine Sciences : M/S|October 9, 2010
[From yeast to neurodegenerative diseases: ten years of exploration of mitochondrial dynamic disorders]Guy Lenaers, Patrizia Amati-Bonneau, Cécile Delettre, et al.
Human Mutation|February 1, 2011
Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutationsPauline Krug, Vincent Morinière, Sandrine Marlin, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2004
Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation familyBruno Mortemousque, Patrizia Amati-Bonneau, François Couture, et al.
Neurocase|November 28, 2019
Specific cognitive theory of mind and behavioral dysfunctions in early manifest Huntington disease: a case reportMarie Caillaud, Mickael Laisney, Alexandre Bejanin, et al.
Pharmacology, Biochemistry, and Behavior|January 28, 2006
Modafinil-induced modulation of working memory and plasma corticosterone in chronically-stressed miceChristophe Piérard, Pierrette Liscia, Magalie Valleau, et al.
European Journal of Endocrinology|April 5, 2024
Heterozygous gain of function variant in GUCY1A2 may cause autonomous ovarian hyperfunctionTheresa Wittrien, Alban Ziegler, Anne Rühle, et al.
Pageof 26