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The mutation m.13513G>A impairs cardiac function, favoring a neuroectoderm commitment, in a mutant‐load dependent way

Journal of cellular physiology, 2019-11, Vol.234 (11), p.19511-19522

2019

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Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology

International journal of molecular sciences, 2022-11, Vol.23 (22), p.13964

2022

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iPSCs: A powerful tool for skeletal muscle tissue engineering

Journal of cellular and molecular medicine, 2019-06, Vol.23 (6), p.3784-3794

2019

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The thyroid hormone receptor β induces DNA damage and premature senescence

The Journal of cell biology, 2014-01, Vol.204 (1), p.129-146

2014

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Reprogramming for Cardiac Regeneration-Strategies for Innovation

Journal of cellular physiology, 2016-09, Vol.231 (9), p.1849-1851

2016

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IPSCs, a Promising Tool to Restore Muscle Atrophy

Journal of cellular physiology, 2016-02, Vol.231 (2), p.259-260

2016

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Glutamyl-tRNAGln amidotransferase is essential for mammalian mitochondrial translation in vivo

Biochemical journal, 2014-05, Vol.460 (1), p.91-101

2014

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The pathogenicity scoring system for mitochondrial tRNA mutations revisited

Molecular genetics & genomic medicine, 2014-03, Vol.2 (2), p.107-114

2014

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Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861CT in the OPA1 Gene

International journal of molecular sciences, 2024-07, Vol.25 (13)

2024

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Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene

International journal of molecular sciences, 2024-06, Vol.25 (13), p.7240

2024

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Enhanced tumorigenicity by mitochondrial DNA mild mutations

Oncotarget, 2015-05, Vol.6 (15), p.13628-13643

2015

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iPSCs-based anti-aging therapies: Recent discoveries and future challenges

Ageing research reviews, 2016-05, Vol.27, p.37-41

2016

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Generation and characterization of human USH2A retinal disease model

Acta ophthalmologica (Oxford, England), 2022-12, Vol.100 (S275), p.n/a

2022

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Estudio Transversal Comparativo de la Relación Maxilo-Mandibular de McNamara Aplicadas a Sujetos Mexicanos

International journal of morphology, 2016-06, Vol.34 (2), p.454-459

2016

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Mitochondrial DNA depletion and POLG mutations in a patient with sensory ataxia, dysarthria and ophthalmoplegia

Medicina clínica, 2010-10, Vol.135 (10), p.452-455

2010

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Expression of Tuftelin in Human Dental Germs/Expresion de Tuftelina en Germenes Dentales Humanos

International journal of morphology, 2017-03, Vol.35 (1), p.293

2017

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iPSC s: A powerful tool for skeletal muscle tissue engineering

Journal of cellular and molecular medicine, 2019-06, Vol.23 (6), p.3784-3794

2019

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Transversal Comparative Study of McNamara Maxillofacial Mandibular Ratio Applied in Mexican Subjects/Estudio Transversal Comparativo de la Relacion Maxilo-Mandibular de McNamara Aplicadas a Sujetos Mexicanos

International journal of morphology, 2016-06, Vol.34 (2), p.454

2016

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Correction: Enhanced tumorigenicity by mitochondrial DNA mild mutations

Oncotarget, 2020-03, Vol.11 (11), p.1006-1006

2020

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The thyroid hormone receptor [Beta] induces DNA damage and premature senescence

The Journal of cell biology, 2014-01, Vol.204 (1), p.129

2014

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Expresión de Tuftelina en Gérmenes Dentales Humanos

International journal of morphology, 2017-03, Vol.35 (1), p.293-298

2017

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Perfil, expectativas y grado de satisfacción de los visitantes del estero El Salado en Puerto Vallarta, JAL

Revista caribeña de ciencias sociales, 2019 (7)

2019

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Expresión de Tuftelina en Gérmenes Dentales Humanos

International journal of morphology, 2017-03, Vol.35 (1), p.293-298

2017

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The mutation m.13513G>A impairs cardiac function, favoring a neuroectoderm commitment, in a mutant‐load dependent way

Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology

iPSCs: A powerful tool for skeletal muscle tissue engineering

The thyroid hormone receptor β induces DNA damage and premature senescence

Reprogramming for Cardiac Regeneration-Strategies for Innovation

IPSCs, a Promising Tool to Restore Muscle Atrophy

Glutamyl-tRNAGln amidotransferase is essential for mammalian mitochondrial translation in vivo

The pathogenicity scoring system for mitochondrial tRNA mutations revisited

Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861CT in the OPA1 Gene

Creation of an Isogenic Human iPSC-Based RGC Model of Dominant Optic Atrophy Harboring the Pathogenic Variant c.1861C>T (p.Gln621Ter) in the OPA1 Gene

Enhanced tumorigenicity by mitochondrial DNA mild mutations

iPSCs-based anti-aging therapies: Recent discoveries and future challenges

Generation and characterization of human USH2A retinal disease model

OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes

Estudio Transversal Comparativo de la Relación Maxilo-Mandibular de McNamara Aplicadas a Sujetos Mexicanos

Mitochondrial DNA depletion and POLG mutations in a patient with sensory ataxia, dysarthria and ophthalmoplegia

Expression of Tuftelin in Human Dental Germs/Expresion de Tuftelina en Germenes Dentales Humanos

iPSC s: A powerful tool for skeletal muscle tissue engineering

Transversal Comparative Study of McNamara Maxillofacial Mandibular Ratio Applied in Mexican Subjects/Estudio Transversal Comparativo de la Relacion Maxilo-Mandibular de McNamara Aplicadas a Sujetos Mexicanos

Correction: Enhanced tumorigenicity by mitochondrial DNA mild mutations

The thyroid hormone receptor [Beta] induces DNA damage and premature senescence

OPAI mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Commentary

Expresión de Tuftelina en Gérmenes Dentales Humanos

Perfil, expectativas y grado de satisfacción de los visitantes del estero El Salado en Puerto Vallarta, JAL

Expresión de Tuftelina en Gérmenes Dentales Humanos

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