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Matías Morín

Showing results (11-20 of 23) with videos related to

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Current Protocols in Mouse Biology|March 12, 2020
Simple Protocol for Generating and Genotyping Genome-Edited Mice With CRISPR-Cas9 ReagentsAlmudena Fernández, Matías Morín, Diego Muñoz-Santos, et al.
Nature Genetics|April 14, 2009
Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing lossAngeles Mencía, Silvia Modamio-Høybjør, Nick Redshaw, et al.
Human Molecular Genetics|May 30, 2009
In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairmentMatías Morín, Keith E Bryan, Fernando Mayo-Merino, et al.
Genes|July 27, 2024
Novel Cases of Non-Syndromic Hearing Impairment Caused by Pathogenic Variants in Genes Encoding Mitochondrial Aminoacyl-tRNA SynthetasesMaría Domínguez-Ruiz, Margarita Olarte, Esther Onecha, et al.
International Journal of Molecular Sciences|April 23, 2022
CRISPR/Cas9-Mediated Allele-Specific Disruption of a Dominant <i>COL6A1</i> Pathogenic Variant Improves Collagen VI Network in Patient FibroblastsArístides López-Márquez, Matías Morín, Sergio Fernández-Peñalver, et al.
Frontiers in Immunology|October 13, 2022
Selective miRNA inhibition in CD8<sup>+</sup> cytotoxic T lymphocytes enhances HIV-1 specific cytotoxic responsesNadia Madrid-Elena, Sergio Serrano-Villar, Carolina Gutiérrez, et al.
Frontiers in Genetics|November 3, 2018
Parental Mosaicism in <i>PAX6</i> Causes Intra-Familial Variability: Implications for Genetic Counseling of Congenital Aniridia and MicrophthalmiaMaría Tarilonte, Matías Morín, Patricia Ramos, et al.
Biomedicines|November 25, 2023
Novel Pathogenic Variants in the Gene Encoding Stereocilin (<i>STRC</i>) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean SubjectsMaría Domínguez-Ruiz, Laura Ruiz-Palmero, Paula I Buonfiglio, et al.
Human Gene Therapy|May 28, 2025
Safe and Efficacious Permanent Removal of Large COL7A1 Exons for Gene Reframing as a Reliable Therapeutic Strategy for Recessive Dystrophic Epidermolysis BullosaSergio López-Manzaneda, Ángeles Mencía, José Bonafont, et al.
EMBO Molecular Medicine|September 11, 2023
Cingulin regulates hair cell cuticular plate morphology and is required for hearing in human and mouseGuang-Jie Zhu, Yuhang Huang, Linqing Zhang, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Current Protocols in Mouse Biology|March 12, 2020
Simple Protocol for Generating and Genotyping Genome-Edited Mice With CRISPR-Cas9 ReagentsAlmudena Fernández, Matías Morín, Diego Muñoz-Santos, et al.
Nature Genetics|April 14, 2009
Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing lossAngeles Mencía, Silvia Modamio-Høybjør, Nick Redshaw, et al.
Human Molecular Genetics|May 30, 2009
In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairmentMatías Morín, Keith E Bryan, Fernando Mayo-Merino, et al.
Genes|July 27, 2024
Novel Cases of Non-Syndromic Hearing Impairment Caused by Pathogenic Variants in Genes Encoding Mitochondrial Aminoacyl-tRNA SynthetasesMaría Domínguez-Ruiz, Margarita Olarte, Esther Onecha, et al.
International Journal of Molecular Sciences|April 23, 2022
CRISPR/Cas9-Mediated Allele-Specific Disruption of a Dominant <i>COL6A1</i> Pathogenic Variant Improves Collagen VI Network in Patient FibroblastsArístides López-Márquez, Matías Morín, Sergio Fernández-Peñalver, et al.
Frontiers in Immunology|October 13, 2022
Selective miRNA inhibition in CD8<sup>+</sup> cytotoxic T lymphocytes enhances HIV-1 specific cytotoxic responsesNadia Madrid-Elena, Sergio Serrano-Villar, Carolina Gutiérrez, et al.
Frontiers in Genetics|November 3, 2018
Parental Mosaicism in <i>PAX6</i> Causes Intra-Familial Variability: Implications for Genetic Counseling of Congenital Aniridia and MicrophthalmiaMaría Tarilonte, Matías Morín, Patricia Ramos, et al.
Biomedicines|November 25, 2023
Novel Pathogenic Variants in the Gene Encoding Stereocilin (<i>STRC</i>) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean SubjectsMaría Domínguez-Ruiz, Laura Ruiz-Palmero, Paula I Buonfiglio, et al.
Human Gene Therapy|May 28, 2025
Safe and Efficacious Permanent Removal of Large COL7A1 Exons for Gene Reframing as a Reliable Therapeutic Strategy for Recessive Dystrophic Epidermolysis BullosaSergio López-Manzaneda, Ángeles Mencía, José Bonafont, et al.
EMBO Molecular Medicine|September 11, 2023
Cingulin regulates hair cell cuticular plate morphology and is required for hearing in human and mouseGuang-Jie Zhu, Yuhang Huang, Linqing Zhang, et al.
Pageof 3