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Michel Koenig

Showing results (81-90 of 126) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 1, 2016
Dynamic X-ray diffraction observation of shocked solid iron up to 170 GPaAdrien Denoeud, Norimasa Ozaki, Alessandra Benuzzi-Mounaix, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolismTorunn Fiskerstrand, Dorra H'mida-Ben Brahim, Stefan Johansson, et al.
International Journal of Molecular Sciences|December 17, 2024
Congenital Titinopathies Linked to Mutations in <i>TTN</i> Metatranscript-Only ExonsAurélien Perrin, Rocio Garcia-Uzquiano, Tanya Stojkovic, et al.
Annals of Neurology|March 24, 2005
Distinguishing the four genetic causes of Jouberts syndrome-related disordersEnza Maria Valente, Sarah E Marsh, Marco Castori, et al.
Physical Review. E|October 16, 2021
Laser astrophysics experiment on the amplification of magnetic fields by shock-induced interfacial instabilitiesTakayoshi Sano, Shohei Tamatani, Kazuki Matsuo, et al.
The Journal of Chemical Physics|July 26, 2006
Laser-driven shock experiments on precompressed water: Implications for "icy" giant planetsKanani K M Lee, L Robin Benedetti, Raymond Jeanloz, et al.
Neurology|August 15, 2014
The pleiotropic movement disorders phenotype of adult ataxia-telangiectasiaAurélie Méneret, Yara Ahmar-Beaugendre, Guillaume Rieunier, et al.
Brain : a Journal of Neurology|December 27, 2013
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardationMartial Mallaret, Matthis Synofzik, Jaeho Lee, et al.
The Journal of Molecular Diagnostics : JMD|May 17, 2022
Long-Reads Sequencing Strategy to Localize Variants in TTN Repeated DomainsAurélien Perrin, Charles Van Goethem, Corinne Thèze, et al.
Brain : a Journal of Neurology|July 27, 2022
RFC1 nonsense and frameshift variants cause CANVAS: clues for an unsolved pathophysiologyMehdi Benkirane, Dylan Da Cunha, Cecilia Marelli, et al.
Pageof 13

Showing results (81-90 of 126) with videos related to

Sort By:
Pageof 13
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2016
Dynamic X-ray diffraction observation of shocked solid iron up to 170 GPaAdrien Denoeud, Norimasa Ozaki, Alessandra Benuzzi-Mounaix, et al.
American Journal of Human Genetics|August 28, 2010
Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolismTorunn Fiskerstrand, Dorra H'mida-Ben Brahim, Stefan Johansson, et al.
International Journal of Molecular Sciences|December 17, 2024
Congenital Titinopathies Linked to Mutations in <i>TTN</i> Metatranscript-Only ExonsAurélien Perrin, Rocio Garcia-Uzquiano, Tanya Stojkovic, et al.
Annals of Neurology|March 24, 2005
Distinguishing the four genetic causes of Jouberts syndrome-related disordersEnza Maria Valente, Sarah E Marsh, Marco Castori, et al.
Physical Review. E|October 16, 2021
Laser astrophysics experiment on the amplification of magnetic fields by shock-induced interfacial instabilitiesTakayoshi Sano, Shohei Tamatani, Kazuki Matsuo, et al.
The Journal of Chemical Physics|July 26, 2006
Laser-driven shock experiments on precompressed water: Implications for "icy" giant planetsKanani K M Lee, L Robin Benedetti, Raymond Jeanloz, et al.
Neurology|August 15, 2014
The pleiotropic movement disorders phenotype of adult ataxia-telangiectasiaAurélie Méneret, Yara Ahmar-Beaugendre, Guillaume Rieunier, et al.
Brain : a Journal of Neurology|December 27, 2013
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardationMartial Mallaret, Matthis Synofzik, Jaeho Lee, et al.
The Journal of Molecular Diagnostics : JMD|May 17, 2022
Long-Reads Sequencing Strategy to Localize Variants in TTN Repeated DomainsAurélien Perrin, Charles Van Goethem, Corinne Thèze, et al.
Brain : a Journal of Neurology|July 27, 2022
RFC1 nonsense and frameshift variants cause CANVAS: clues for an unsolved pathophysiologyMehdi Benkirane, Dylan Da Cunha, Cecilia Marelli, et al.
Pageof 13