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Stem Cell Research|June 28, 2016
Generation of a human iPSC line from a patient with a defect of intergenomic communicationFrancisco Zurita, Teresa Galera, Cristina González-Páramos, et al.
Biochimica Et Biophysica Acta|June 30, 2006
Modeling human mitochondrial diseases in fliesAlvaro Sánchez-Martínez, Ningguang Luo, Paula Clemente, et al.
Archives of Neurology|April 13, 2005
Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 geneMiguel A Martín, Alberto Blázquez, Luis G Gutierrez-Solana, et al.
Stem Cell Research|August 11, 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 geneFrancisco Zurita-Díaz, María Del Carmen Ortuño-Costela, Ana Moreno-Izquierdo, et al.
Cytotherapy|March 17, 2021
Mitochondrial DNA from osteoarthritic patients drives functional impairment of mitochondrial activity: a study on transmitochondrial cybridsAndrea Dalmao-Fernández, Tamara Hermida-Gómez, Jenny Lund, et al.
Human Molecular Genetics|March 21, 2015
Cardiac deficiency of single cytochrome oxidase assembly factor scox induces p53-dependent apoptosis in a Drosophila cardiomyopathy modelLeticia Martínez-Morentin, Lidia Martínez, Sarah Piloto, et al.
Biochimica Et Biophysica Acta|August 7, 2013
Drosophila nuclear factor DREF regulates the expression of the mitochondrial DNA helicase and mitochondrial transcription factor B2 but not the mitochondrial translation factor B1Miguel A Fernández-Moreno, Rosana Hernández, Cristina Adán, et al.
Human Mutation|February 22, 2002
The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell linesBelén Bornstein, Jose Antonio Mas, Miguel Angel Fernández-Moreno, et al.
The Journal of Cell Biology|January 8, 2014
The thyroid hormone receptor β induces DNA damage and premature senescenceAlberto Zambrano, Verónica García-Carpizo, María Esther Gallardo, et al.
Neuromuscular Disorders : NMD|July 7, 2007
Mild ocular myopathy associated with a novel mutation in mitochondrial twinkle helicaseHenry Rivera, Alberto Blázquez, Julián Carretero, et al.
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