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Plos One|October 21, 2016
Generating Rho-0 Cells Using Mesenchymal Stem Cell LinesMercedes Fernández-Moreno, Tamara Hermida-Gómez, M Esther Gallardo, et al.Plos One|September 7, 2012
Modeling pathogenic mutations of human twinkle in Drosophila suggests an apoptosis role in response to mitochondrial defectsAlvaro Sanchez-Martinez, Manuel Calleja, Susana Peralta, et al.Oncotarget|March 28, 2020
Correction: Enhanced tumorigenicity by mitochondrial DNA mild mutationsAlberto Cruz-Bermúdez, Carmen G Vallejo, Ramiro J Vicente-Blanco, et al.Stem Cell Research|June 28, 2016
Generation of a human iPSC line from a patient with Leigh syndromeTeresa Galera, Francisco Zurita, Cristina González-Páramos, et al.Stem Cell Research|June 28, 2016
Generation of a human control iPSC line with a European mitochondrial haplogroup U backgroundTeresa Galera, Francisco Zurita, Cristina González-Páramos, et al.Medicina Clinica|June 26, 2010
[Mitochondrial DNA depletion and POLG mutations in a patient with sensory ataxia, dysarthria and ophthalmoplegia]Ignacio J Posada, María Esther Gallardo, Cristina Domínguez, et al.Oncotarget|April 25, 2015
Enhanced tumorigenicity by mitochondrial DNA mild mutationsAlberto Cruz-Bermúdez, Carmen G Vallejo, Ramiro J Vicente-Blanco, et al.Stem Cell Research|March 22, 2019
Derivation of an aged mouse induced pluripotent stem cell line, IISHDOi005-AMaría Del Carmen Ortuño-Costela, Victoria Cerrada, Marta García-López, et al.Stem Cell Research|June 28, 2016
Generation of a human iPSC line from a patient with a mitochondrial encephalopathy due to mutations in the GFM1 geneFrancisco Zurita-Díaz, Teresa Galera-Monge, Ana Moreno-Izquierdo, et al.Stem Cell Research|June 28, 2016
Generation of a human iPSC line from a patient with an optic atrophy 'plus' phenotype due to a mutation in the OPA1 geneTeresa Galera-Monge, Francisco Zurita-Díaz, Ana Moreno-Izquierdo, et al.Pageof 7