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Toulouse

Showing results (251-260 of 283) with videos related to

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Journal of Clinical Medicine|December 23, 2023
Frailty in Older Patients with Transthyretin Cardiac AmyloidosisStéphanie Cazalbou, Louise Naccache, Sandrine Sourdet, et al.
Physical Review Letters|January 15, 2016
Driving Spin Excitations by Hydrostatic Pressure in BiFeO(3)J Buhot, C Toulouse, Y Gallais, et al.
Nature Communications|January 22, 2022
Emerging spin-phonon coupling through cross-talk of two magnetic sublatticesMads C Weber, Mael Guennou, Donald M Evans, et al.
American Journal of Medical Genetics|December 3, 1999
Analysis of 14 CAG repeat-containing genes in schizophreniaR Joober, C Benkelfat, A Toulouse, et al.
American Journal of Medical Genetics|April 17, 1999
Lack of association between the hSKCa3 channel gene CAG polymorphism and schizophreniaR Joober, C Benkelfat, K Brisebois, et al.
The Journal of Clinical Investigation|June 4, 2008
Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type IIMasoud Shekarabi, Nathalie Girard, Jean-Baptiste Rivière, et al.
Physical Chemistry Chemical Physics : PCCP|June 27, 2024
Flux and fluence effects on the vacuum-UV photodesorption and photoprocessing of CO<sub>2</sub> icesAntoine B Hacquard, Daniela Torres-DÍaz, Romain Basalgète, et al.
Nature Communications|May 27, 2018
Fossilized skin reveals coevolution with feathers and metabolism in feathered dinosaurs and early birdsMaria E McNamara, Fucheng Zhang, Stuart L Kearns, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 26, 2021
SCN1A-related epilepsy with recessive inheritance: Two further familiesRaffaella Moretti, Lionel Arnaud, Delphine Bouteiller, et al.
Neurobiology of Disease|March 10, 2005
Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in micePatrick Dion, Vijayalakshmi Shanmugam, Claudia Gaspar, et al.
Pageof 29

Showing results (251-260 of 283) with videos related to

Sort By:
Pageof 29
Journal of Clinical Medicine|December 23, 2023
Frailty in Older Patients with Transthyretin Cardiac AmyloidosisStéphanie Cazalbou, Louise Naccache, Sandrine Sourdet, et al.
Physical Review Letters|January 15, 2016
Driving Spin Excitations by Hydrostatic Pressure in BiFeO(3)J Buhot, C Toulouse, Y Gallais, et al.
Nature Communications|January 22, 2022
Emerging spin-phonon coupling through cross-talk of two magnetic sublatticesMads C Weber, Mael Guennou, Donald M Evans, et al.
American Journal of Medical Genetics|December 3, 1999
Analysis of 14 CAG repeat-containing genes in schizophreniaR Joober, C Benkelfat, A Toulouse, et al.
American Journal of Medical Genetics|April 17, 1999
Lack of association between the hSKCa3 channel gene CAG polymorphism and schizophreniaR Joober, C Benkelfat, K Brisebois, et al.
The Journal of Clinical Investigation|June 4, 2008
Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type IIMasoud Shekarabi, Nathalie Girard, Jean-Baptiste Rivière, et al.
Physical Chemistry Chemical Physics : PCCP|June 27, 2024
Flux and fluence effects on the vacuum-UV photodesorption and photoprocessing of CO<sub>2</sub> icesAntoine B Hacquard, Daniela Torres-DÍaz, Romain Basalgète, et al.
Nature Communications|May 27, 2018
Fossilized skin reveals coevolution with feathers and metabolism in feathered dinosaurs and early birdsMaria E McNamara, Fucheng Zhang, Stuart L Kearns, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 26, 2021
SCN1A-related epilepsy with recessive inheritance: Two further familiesRaffaella Moretti, Lionel Arnaud, Delphine Bouteiller, et al.
Neurobiology of Disease|March 10, 2005
Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in micePatrick Dion, Vijayalakshmi Shanmugam, Claudia Gaspar, et al.
Pageof 29