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Lorea Blázquez

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

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Advances in Experimental Medicine and Biology|March 12, 2015
U1 interference (U1i) for antiviral approachesLorea Blázquez, Puri Fortes
ACS Nano|November 16, 2023
Engineering U1-Based Tetracycline-Inducible Riboswitches to Control Gene Expression in MammalsEric Rovira, Beatriz Moreno, Nerea Razquin, et al.
Scientific Reports|February 4, 2026
3D heterotypic models of glioblastoma reveal the impact of microglia on cellular organization and the production of a distinct secretomeClara García-Sáez, Josune Alonso-Marañón, Mikel García-Puga, et al.
Human Mutation|July 19, 2013
In vitro correction of a pseudoexon-generating deep intronic mutation in LGMD2A by antisense oligonucleotides and modified small nuclear RNAsLorea Blázquez, Ana Aiastui, Maria Goicoechea, et al.
Muscle & Nerve|October 19, 2011
Does the severity of the LGMD2A phenotype in compound heterozygotes depend on the combination of mutations?Amets Sáenz, Yasuko Ono, Hiroyuki Sorimachi, et al.
Nature Communications|July 24, 2023
ORC1 binds to cis-transcribed RNAs for efficient activation of replication originsAina Maria Mas, Enrique Goñi, Igor Ruiz de Los Mozos, et al.
Annals of Clinical and Translational Neurology|October 7, 2025
SNUPN-Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein InsightsNuria Muelas, Pablo Iruzubieta, Alberto Damborenea, et al.
Brain : a Journal of Neurology|February 17, 2024
Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like featuresPablo Iruzubieta, Alberto Damborenea, Mihaela Ioghen, et al.
Acta Neuropathologica|September 16, 2024
Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosisMónica Zufiría, Oihane Pikatza-Menoio, Maddi Garciandia-Arcelus, et al.
Molecular Therapy. Nucleic Acids|February 24, 2025
Advanced delivery systems for gene editing: A comprehensive review from the GenE-HumDi COST Action Working GroupAlessia Cavazza, Francisco J Molina-Estévez, Álvaro Plaza Reyes, et al.
Pageof 1

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

Sort By:
Pageof 1
Advances in Experimental Medicine and Biology|March 12, 2015
U1 interference (U1i) for antiviral approachesLorea Blázquez, Puri Fortes
ACS Nano|November 16, 2023
Engineering U1-Based Tetracycline-Inducible Riboswitches to Control Gene Expression in MammalsEric Rovira, Beatriz Moreno, Nerea Razquin, et al.
Scientific Reports|February 4, 2026
3D heterotypic models of glioblastoma reveal the impact of microglia on cellular organization and the production of a distinct secretomeClara García-Sáez, Josune Alonso-Marañón, Mikel García-Puga, et al.
Human Mutation|July 19, 2013
In vitro correction of a pseudoexon-generating deep intronic mutation in LGMD2A by antisense oligonucleotides and modified small nuclear RNAsLorea Blázquez, Ana Aiastui, Maria Goicoechea, et al.
Muscle & Nerve|October 19, 2011
Does the severity of the LGMD2A phenotype in compound heterozygotes depend on the combination of mutations?Amets Sáenz, Yasuko Ono, Hiroyuki Sorimachi, et al.
Nature Communications|July 24, 2023
ORC1 binds to cis-transcribed RNAs for efficient activation of replication originsAina Maria Mas, Enrique Goñi, Igor Ruiz de Los Mozos, et al.
Annals of Clinical and Translational Neurology|October 7, 2025
SNUPN-Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein InsightsNuria Muelas, Pablo Iruzubieta, Alberto Damborenea, et al.
Brain : a Journal of Neurology|February 17, 2024
Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like featuresPablo Iruzubieta, Alberto Damborenea, Mihaela Ioghen, et al.
Acta Neuropathologica|September 16, 2024
Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosisMónica Zufiría, Oihane Pikatza-Menoio, Maddi Garciandia-Arcelus, et al.
Molecular Therapy. Nucleic Acids|February 24, 2025
Advanced delivery systems for gene editing: A comprehensive review from the GenE-HumDi COST Action Working GroupAlessia Cavazza, Francisco J Molina-Estévez, Álvaro Plaza Reyes, et al.
Pageof 1