Rafael Garesse

Instituto de Investigaciones Biomédicas Sols-Morreale — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

35h-index4.0kcitations141works0.02yr avg
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Research Topics

Mitochondrial Function and Pathology(84), ATP Synthase and ATPases Research(34), Metabolism and Genetic Disorders(30), RNA modifications and cancer(18), RNA and protein synthesis mechanisms(9)

Publications141 total

Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology
International Journal of Molecular Sciences·2022· 8 citedOpen Access
Mitochondrial DNA from osteoarthritic patients drives functional impairment of mitochondrial activity: a study on transmitochondrial cybrids
Cytotherapy·2021· 9 cited
Mitochondrial DNA: Defects, Maintenance Genes and Depletion
2021· 1 cited
Mitochondrial Dysfunction and Calcium Dysregulation in Leigh Syndrome Induced Pluripotent Stem Cell Derived Neurons
International Journal of Molecular Sciences·2020· 35 citedOpen Access
Células iPSCs: Una aproximación prometedora para el estudio y posible tratamiento de las enfermedades raras
Biblos-e Archivo (Universidad Autónoma de Madrid)·2020Open Access
Correction: Enhanced tumorigenicity by mitochondrial DNA mild mutations
Oncotarget·2020· 1 citedOpen Access
La revista índice, el instituto nacional de estadística y la universidad
Indice: Revista de Estadística y Sociedad·2020
C6orf203 controls OXPHOS function through modulation of mitochondrial protein biosynthesis
2019· 1 citedOpen Access
The mutation m.13513G>A impairs cardiac function, favoring a neuroectoderm commitment, in a mutant‐load dependent way
Journal of Cellular Physiology·2019· 19 cited
Derivation of an aged mouse induced pluripotent stem cell line, IISHDOi005-A
Stem Cell Research·2019· 1 citedOpen Access
Pathogenic variants in glutamyl-tRNAGln amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorder
Nature Communications·2018· 53 citedOpen Access
Establishment of a human iPSC line, IISHDOi004-A, from a patient with Usher syndrome associated with the mutation c.2276G>T; p.Cys759Phe in the USH2A gene
Stem Cell Research·2018· 4 citedOpen Access
NDUFS2 Mitochondrial Complex I deficiency induces adipose tissue degeneration via IIS in a Drosophila melanogaster model.
IBJ Plus·2018Open Access
Generation of a human iPSC line, IISHDOi002-A, with a 46, XY/47, XYY mosaicism and belonging to an African mitochondrial haplogroup
Stem Cell Research·2018· 2 citedOpen Access
Artemia Molecular Genetics
2018· 2 cited
ROBERTO MARCO, un universitario ejemplar con espíritu multidisciplinar: "Oda biográfica de un universitario ejemplar". "Algunos pensamientos y recuerdos en memoria de Roberto Marco". "Gracias, Roberto"
Encuentros multidisciplinares·2018
Roberto Marco: Un universitario ejemplar con espíritu multidisciplinar
LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)·2018Open Access
Evolución en la UAM de la investigación, de las infraestructuras científicas y de la innovación
Dialnet (Universidad de la Rioja)·2018
El Parque Científico de Madrid
Dialnet (Universidad de la Rioja)·2018
Establishment of a human DOA 'plus' iPSC line, IISHDOi003-A, with the mutation in the OPA1 gene: c.1635C > A; p.Ser545Arg
Stem Cell Research·2017· 8 citedOpen Access
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Frequent Co-authors

Miguel Ángel Fernández‐Moreno(15), Laurie S. Kaguni(14), Belén Bornstein(12), M. Esther Gallardo(10), Joaquı́n Arenas(10), Miguel A. Martı́n(9), Yolanda Campos(8), Manuel Calleja(7), Roberto Di Marco(6), Rosana Hernández‐Sierra(6), Yuichi Matsushima(5), Carmen G. Vallejo(4), Cristina Ugalde(4), José Ramón Valverde(4), Cristina Adán(4), Emiliano González‐Vioque(4), Paula Clemente(4), Pilar de la Peña(3), Beatriz Batuecas(3), Filippo M. Santorelli(3)