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Juliette Nectoux

Showing results (1-10 of 67) with videos related to

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Molecular Diagnosis & Therapy|December 7, 2017
Current, Emerging, and Future Applications of Digital PCR in Non-Invasive Prenatal DiagnosisJuliette Nectoux
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 14, 2025
Genetic counseling, prenatal diagnosis and newborn screening in Duchenne muscular dystrophyFrance Leturcq, Camille Verebi, Juliette Nectoux
Journal of Molecular Neuroscience : MN|January 31, 2015
Differential Expression and Regulation of Brain-Derived Neurotrophic Factor (BDNF) mRNA Isoforms in Brain Cells from Mecp2(308/y) Mouse ModelAudrey Rousseaud, Chloé Delépine, Juliette Nectoux, et al.
Journal of Genetic Counseling|June 19, 2024
A retrospective cohort study and review of the literature about germline mosaicism in Duchenne/Becker muscular dystrophy prenatal counseling: How to estimate the recurrence risk in clinical settings?Camille Verebi, Victor Gravrand, Thierry Bienvenu, et al.
Neuromuscular Disorders : NMD|January 11, 2025
Chronic pain as a presenting feature of dysferlinopathyLucia Sanchez-Casado, Teresinha Evangelista, Juliette Nectoux, et al.
Journal of Human Genetics|December 3, 2010
An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brainYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
FEBS Letters|December 15, 2012
MeCP2 deficiency is associated with impaired microtubule stabilityChloé Delépine, Juliette Nectoux, Nadia Bahi-Buisson, et al.
European Journal of Human Genetics : EJHG|June 13, 2013
Mutations in the C-terminus of CDKL5: proceed with cautionBertrand Diebold, Chloé Delépine, Svetlana Gataullina, et al.
Psychoneuroendocrinology|December 8, 2023
The value of plasma cell-free DNA levels as biomarker in patients with eating disorders: A preliminary studyCamille Verebi, Juliette Nectoux, Philibert Duriez, et al.
Brain Research|September 28, 2021
HDAC inhibitor ameliorates behavioral deficits in Mecp2<sup>308/y</sup> mouse model of Rett syndromeNicolas Lebrun, Chloé Delépine, Mohamed Selloum, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Molecular Diagnosis & Therapy|December 7, 2017
Current, Emerging, and Future Applications of Digital PCR in Non-Invasive Prenatal DiagnosisJuliette Nectoux
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 14, 2025
Genetic counseling, prenatal diagnosis and newborn screening in Duchenne muscular dystrophyFrance Leturcq, Camille Verebi, Juliette Nectoux
Journal of Molecular Neuroscience : MN|January 31, 2015
Differential Expression and Regulation of Brain-Derived Neurotrophic Factor (BDNF) mRNA Isoforms in Brain Cells from Mecp2(308/y) Mouse ModelAudrey Rousseaud, Chloé Delépine, Juliette Nectoux, et al.
Journal of Genetic Counseling|June 19, 2024
A retrospective cohort study and review of the literature about germline mosaicism in Duchenne/Becker muscular dystrophy prenatal counseling: How to estimate the recurrence risk in clinical settings?Camille Verebi, Victor Gravrand, Thierry Bienvenu, et al.
Neuromuscular Disorders : NMD|January 11, 2025
Chronic pain as a presenting feature of dysferlinopathyLucia Sanchez-Casado, Teresinha Evangelista, Juliette Nectoux, et al.
Journal of Human Genetics|December 3, 2010
An isoform of the severe encephalopathy-related CDKL5 gene, including a novel exon with extremely high sequence conservation, is specifically expressed in brainYann Fichou, Juliette Nectoux, Nadia Bahi-Buisson, et al.
FEBS Letters|December 15, 2012
MeCP2 deficiency is associated with impaired microtubule stabilityChloé Delépine, Juliette Nectoux, Nadia Bahi-Buisson, et al.
European Journal of Human Genetics : EJHG|June 13, 2013
Mutations in the C-terminus of CDKL5: proceed with cautionBertrand Diebold, Chloé Delépine, Svetlana Gataullina, et al.
Psychoneuroendocrinology|December 8, 2023
The value of plasma cell-free DNA levels as biomarker in patients with eating disorders: A preliminary studyCamille Verebi, Juliette Nectoux, Philibert Duriez, et al.
Brain Research|September 28, 2021
HDAC inhibitor ameliorates behavioral deficits in Mecp2<sup>308/y</sup> mouse model of Rett syndromeNicolas Lebrun, Chloé Delépine, Mohamed Selloum, et al.
Pageof 7