Mario
Torrado Oubiña
Universidade da Coruña
La Coruña, EspañaPublicaciones en colaboración con investigadores/as de Universidade da Coruña (42)
2022
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Identification of an elusive spliceogenic MYBPC3 variant in an otherwise genotype-negative hypertrophic cardiomyopathy pedigree
Scientific Reports, Vol. 12, Núm. 1
2021
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A cryptic splice-altering KCNQ1 variant in trans with R259L leading to Jervell and Lange-Nielsen syndrome
npj Genomic Medicine, Vol. 6, Núm. 1
2020
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A Pathogenic Galactosidase A Mutation Coexisting With an MYBPC3 Mutation in a Female Patient With Hypertrophic Cardiomyopathy
Canadian Journal of Cardiology, Vol. 36, Núm. 9, pp. 1554.e1-1554.e3
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Cryptic Splice-Altering Variants in MYBPC3 Are a Prevalent Cause of Hypertrophic Cardiomyopathy
Circulation: Genomic and Precision Medicine, Vol. 13, Núm. 3, pp. E002905
2018
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A Novel Heterozygous Intronic Mutation in the FBN1 Gene Contributes to FBN1 RNA Missplicing Events in the Marfan Syndrome
BioMed Research International, Vol. 2018
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Interplay between cardiac transcription factors and non-coding RNAs in predisposing to atrial fibrillation
Journal of Molecular Medicine, Vol. 96, Núm. 7, pp. 601-610
2016
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Myocardial transcription factors in diastolic dysfunction: clues for model systems and disease
Heart Failure Reviews, Vol. 21, Núm. 6, pp. 783-794
2015
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A MicroRNA-Transcription factor blueprint for early atrial arrhythmogenic remodeling
BioMed Research International, Vol. 2015
2014
2012
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In search of novel targets for heart disease: Myocardin and myocardin-related transcriptional cofactors
Biochemistry Research International
2011
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Targeted gene-silencing reveals the functional significance of myocardin signaling in the failing heart
PLoS ONE, Vol. 6, Núm. 10
2010
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Exon-skipping brain natriuretic peptide variant is overexpressed in failing myocardium and attenuates brain natriuretic peptide production in vitro
Experimental Biology and Medicine, Vol. 235, Núm. 8, pp. 941-951
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Identification of candidate genes potentially relevant to chamber-specific remodeling in postnatal ventricular myocardium
Journal of Biomedicine and Biotechnology, Vol. 2010
2009
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Detection of protein interactions based on GFP fragment complementation by fluorescence microscopy and spectrofluorometry
BioTechniques, Vol. 45, Núm. 5 SUPPL., pp. 65
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In vivo forced expression of myocardin in ventricular myocardium transiently impairs systolic performance in early neonatal pig heart
International Journal of Developmental Biology, Vol. 53, Núm. 8-10, pp. 1457-1467
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Intron retention generates ANKRD1 splice variants that are co-regulated with the main transcript in normal and failing myocardium
Gene, Vol. 440, Núm. 1-2, pp. 28-41
2008
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Detection of protein interactions based on GFP fragment complementation by fluorescence microscopy and spectrofluorometry
BioTechniques, Vol. 44, Núm. 1, pp. 70-74
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The enigmatic role of the ankyrin repeat domain 1 gene in heart development and disease
International Journal of Developmental Biology, Vol. 52, Núm. 7, pp. 811-821
2006
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Differential atrial versus ventricular ANKRD1 gene expression is oppositely regulated at diastolic heart failure
FEBS Letters, Vol. 580, Núm. 17, pp. 4182-4187
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The cardiac ankyrin repeat domain 1 protein: Do you know enough about its dimerization properties? [1]
Journal of Muscle Research and Cell Motility