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Matías Morín

Showing results (1-10 of 23) with videos related to

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FEMS Microbiology Letters|May 30, 2012
Expression of Alt a 1 allergen from Alternaria alternata in the yeast Yarrowia lipolyticaMatías Morín, Juan A Asturias, Angel Domínguez
Comparative Biochemistry and Physiology. Part D, Genomics & Proteomics|May 21, 2010
Proteome profile changes during mouse testis developmentMaría Paz, Matías Morín, Jesús Del Mazo
Journal of Mass Spectrometry : JMS|October 26, 2007
Proteomic analysis reveals metabolic changes during yeast to hypha transition in Yarrowia lipolyticaMatías Morín, Lucía Monteoliva, María Insenser, et al.
Human Genetics|January 19, 2022
Genetic etiology of non-syndromic hearing loss in EuropeIgnacio Del Castillo, Matías Morín, María Domínguez-Ruiz, et al.
Genes|April 3, 2021
A Novel Truncating Mutation in HOMER2 Causes Nonsyndromic Progressive DFNA68 Hearing Loss in a Spanish FamilyMaría Lachgar, Matías Morín, Manuela Villamar, et al.
Disease Models & Mechanisms|May 11, 2023
Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variantsMaría Lachgar-Ruiz, Matías Morín, Elisa Martelletti, et al.
Molecular Therapy. Nucleic Acids|July 10, 2019
Selective miRNA Modulation Fails to Activate HIV Replication in In Vitro Latency ModelsMaría Rosa López-Huertas, Matías Morín, Nadia Madrid-Elena, et al.
Frontiers in Genome Editing|May 15, 2023
Specific correction of pyruvate kinase deficiency-causing point mutations by CRISPR/Cas9 and single-stranded oligodeoxynucleotidesSara Fañanas-Baquero, Matías Morín, Sergio Fernández, et al.
Genes|July 25, 2019
Three New Mutations and Mild, Asymmetrical Phenotype in the Highly Distinctive LAMM Syndrome: A Report of Eight Further CasesAmina Al Yassin, Felice D'Arco, Matías Morín, et al.
Human Molecular Genetics|December 24, 2013
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membraneP Kevin Legan, Richard J Goodyear, Matías Morín, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
FEMS Microbiology Letters|May 30, 2012
Expression of Alt a 1 allergen from Alternaria alternata in the yeast Yarrowia lipolyticaMatías Morín, Juan A Asturias, Angel Domínguez
Comparative Biochemistry and Physiology. Part D, Genomics & Proteomics|May 21, 2010
Proteome profile changes during mouse testis developmentMaría Paz, Matías Morín, Jesús Del Mazo
Journal of Mass Spectrometry : JMS|October 26, 2007
Proteomic analysis reveals metabolic changes during yeast to hypha transition in Yarrowia lipolyticaMatías Morín, Lucía Monteoliva, María Insenser, et al.
Human Genetics|January 19, 2022
Genetic etiology of non-syndromic hearing loss in EuropeIgnacio Del Castillo, Matías Morín, María Domínguez-Ruiz, et al.
Genes|April 3, 2021
A Novel Truncating Mutation in HOMER2 Causes Nonsyndromic Progressive DFNA68 Hearing Loss in a Spanish FamilyMaría Lachgar, Matías Morín, Manuela Villamar, et al.
Disease Models & Mechanisms|May 11, 2023
Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variantsMaría Lachgar-Ruiz, Matías Morín, Elisa Martelletti, et al.
Molecular Therapy. Nucleic Acids|July 10, 2019
Selective miRNA Modulation Fails to Activate HIV Replication in In Vitro Latency ModelsMaría Rosa López-Huertas, Matías Morín, Nadia Madrid-Elena, et al.
Frontiers in Genome Editing|May 15, 2023
Specific correction of pyruvate kinase deficiency-causing point mutations by CRISPR/Cas9 and single-stranded oligodeoxynucleotidesSara Fañanas-Baquero, Matías Morín, Sergio Fernández, et al.
Genes|July 25, 2019
Three New Mutations and Mild, Asymmetrical Phenotype in the Highly Distinctive LAMM Syndrome: A Report of Eight Further CasesAmina Al Yassin, Felice D'Arco, Matías Morín, et al.
Human Molecular Genetics|December 24, 2013
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membraneP Kevin Legan, Richard J Goodyear, Matías Morín, et al.
Pageof 3