Rafael Garesse
Madrid, MD 28029, Spain
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 38 publications
Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology.
Journal: International journal of molecular sciences
Published: October 04, 2022
Mitochondrial Dysfunction and Calcium Dysregulation in Leigh Syndrome Induced Pluripotent Stem Cell Derived Neurons.
Journal: International journal of molecular sciences
Published: April 11, 2020
Correction: Enhanced tumorigenicity by mitochondrial DNA mild mutations.
Journal: Oncotarget
Published: March 28, 2020
Mitochondrial DNA from osteoarthritic patients drives functional impairment of mitochondrial activity: a study on transmitochondrial cybrids.
Journal: Cytotherapy
Published: August 21, 2019
Derivation of an aged mouse induced pluripotent stem cell line, IISHDOi005-A.
Journal: Stem cell research
Published: October 05, 2018
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.
Journal: Stem cell research
Published: May 13, 2018
The mutation m.13513G>A impairs cardiac function, favoring a neuroectoderm commitment, in a mutant-load dependent way.
Journal: Journal of cellular physiology
Published: May 03, 2018
Generation of a human iPSC line, IISHDOi002-A, with a 46, XY/47, XYY mosaicism and belonging to an African mitochondrial haplogroup.
Journal: Stem cell research
Published: November 07, 2017
Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle disease.
Journal: Stem cell research
Published: July 18, 2017
Human COA3 Is an Oligomeric Highly Flexible Protein in Solution.
Journal: Biochemistry
Published: October 30, 2016
Last Updated: 09/26/2026