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Iñigo Marcos-Alcalde

Showing results (1-10 of 20) with videos related to

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Bioinformatics (Oxford, England)|August 17, 2019
MEPSAnd: minimum energy path surface analysis over n-dimensional surfacesIñigo Marcos-Alcalde, Eduardo López-Viñas, Paulino Gómez-Puertas
Bioinformatics (Oxford, England)|August 2, 2015
MEPSA: minimum energy pathway analysis for energy landscapesIñigo Marcos-Alcalde, Javier Setoain, Jesús I Mendieta-Moreno, et al.
Biochemistry|January 17, 2013
Simulation of catalytic water activation in mitochondrial F1-ATPase using a hybrid quantum mechanics/molecular mechanics approach: an alternative role for β-Glu 188Fernando Martín-García, Jesús I Mendieta-Moreno, Iñigo Marcos-Alcalde, et al.
Neurology. Genetics|September 10, 2021
Dysfunctional Homozygous VRK1-D263G Variant Impairs the Assembly of Cajal Bodies and DNA Damage Response in Hereditary Spastic ParaplegiaPatricia Morejon-Garcia, Boris Keren, Iñigo Marcos-Alcalde, et al.
Advances in Protein Chemistry and Structural Biology|September 30, 2015
A Practical Quantum Mechanics Molecular Mechanics Method for the Dynamical Study of Reactions in BiomoleculesJesús I Mendieta-Moreno, Iñigo Marcos-Alcalde, Daniel G Trabada, et al.
Epilepsia|March 2, 2026
Mutation type-specific transcriptomic signatures and readthrough therapy rescue in SMC1A-related developmental and epileptic encephalopathyMaddalena Di Nardo, Francesca Sardina, Maria M Pallotta, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 30, 2024
Pathogenic effects of Leu200Pro and Arg387His VRK1 protein variants on phosphorylation targets and H4K16 acetylation in distal hereditary motor neuropathyAurora Campos-Díaz, Patricia Morejón-García, Eva Monte-Serrano, et al.
International Journal of Molecular Sciences|March 31, 2018
Human Mitochondrial HMG-CoA Synthase Deficiency: Role of Enzyme Dimerization Surface and Characterization of Three New PatientsBeatriz Puisac, Iñigo Marcos-Alcalde, María Hernández-Marcos, et al.
Genes|October 29, 2025
<i>ROGDI</i>-Related Disorder Resulting from Disruption of Complex Interactive Neuro-Dental Developmental Networks: A Review and Description of the First Missense VariantSopio Gverdtsiteli, Trine Bjørg Hammer, Xenia Hermann, et al.
Annals of Clinical and Translational Neurology|May 5, 2020
VRK1 (Y213H) homozygous mutant impairs Cajal bodies in a hereditary case of distal motor neuropathyAna T Marcos, Elena Martín-Doncel, Patricia Morejón-García, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|August 17, 2019
MEPSAnd: minimum energy path surface analysis over n-dimensional surfacesIñigo Marcos-Alcalde, Eduardo López-Viñas, Paulino Gómez-Puertas
Bioinformatics (Oxford, England)|August 2, 2015
MEPSA: minimum energy pathway analysis for energy landscapesIñigo Marcos-Alcalde, Javier Setoain, Jesús I Mendieta-Moreno, et al.
Biochemistry|January 17, 2013
Simulation of catalytic water activation in mitochondrial F1-ATPase using a hybrid quantum mechanics/molecular mechanics approach: an alternative role for β-Glu 188Fernando Martín-García, Jesús I Mendieta-Moreno, Iñigo Marcos-Alcalde, et al.
Neurology. Genetics|September 10, 2021
Dysfunctional Homozygous VRK1-D263G Variant Impairs the Assembly of Cajal Bodies and DNA Damage Response in Hereditary Spastic ParaplegiaPatricia Morejon-Garcia, Boris Keren, Iñigo Marcos-Alcalde, et al.
Advances in Protein Chemistry and Structural Biology|September 30, 2015
A Practical Quantum Mechanics Molecular Mechanics Method for the Dynamical Study of Reactions in BiomoleculesJesús I Mendieta-Moreno, Iñigo Marcos-Alcalde, Daniel G Trabada, et al.
Epilepsia|March 2, 2026
Mutation type-specific transcriptomic signatures and readthrough therapy rescue in SMC1A-related developmental and epileptic encephalopathyMaddalena Di Nardo, Francesca Sardina, Maria M Pallotta, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 30, 2024
Pathogenic effects of Leu200Pro and Arg387His VRK1 protein variants on phosphorylation targets and H4K16 acetylation in distal hereditary motor neuropathyAurora Campos-Díaz, Patricia Morejón-García, Eva Monte-Serrano, et al.
International Journal of Molecular Sciences|March 31, 2018
Human Mitochondrial HMG-CoA Synthase Deficiency: Role of Enzyme Dimerization Surface and Characterization of Three New PatientsBeatriz Puisac, Iñigo Marcos-Alcalde, María Hernández-Marcos, et al.
Genes|October 29, 2025
<i>ROGDI</i>-Related Disorder Resulting from Disruption of Complex Interactive Neuro-Dental Developmental Networks: A Review and Description of the First Missense VariantSopio Gverdtsiteli, Trine Bjørg Hammer, Xenia Hermann, et al.
Annals of Clinical and Translational Neurology|May 5, 2020
VRK1 (Y213H) homozygous mutant impairs Cajal bodies in a hereditary case of distal motor neuropathyAna T Marcos, Elena Martín-Doncel, Patricia Morejón-García, et al.
Pageof 2