Pradeep Reddy, Felipe Vilella, Juan Carlos Izpisua Belmonte, Carlos Simón. Genes (Basel) 2020
Times Cited: 6
Times Cited: 6
Times Cited
Times Co-cited
Similarity
Mitochondrially targeted ZFNs for selective degradation of pathogenic mitochondrial genomes bearing large-scale deletions or point mutations.
Payam A Gammage, Joanna Rorbach, Anna I Vincent, Edward J Rebar, Michal Minczuk. EMBO Mol Med 2014
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Targeted elimination of mutant mitochondrial DNA in MELAS-iPSCs by mitoTALENs.
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MitoTALEN: A General Approach to Reduce Mutant mtDNA Loads and Restore Oxidative Phosphorylation Function in Mitochondrial Diseases.
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REST suppression mediates neural conversion of adult human fibroblasts via microRNA-dependent and -independent pathways.
Janelle Drouin-Ouellet, Shong Lau, Per Ludvik Brattås, Daniella Rylander Ottosson, Karolina Pircs, Daniela A Grassi, Lucy M Collins, Romina Vuono, Annika Andersson Sjöland, Gunilla Westergren-Thorsson,[...]. EMBO Mol Med 2017
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Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects.
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Maintenance of age in human neurons generated by microRNA-based neuronal conversion of fibroblasts.
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Exploring mTOR inhibition as treatment for mitochondrial disease.
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Parkin-mediated mitophagy and autophagy flux disruption in cellular models of MERRF syndrome.
Marina Villanueva-Paz, Suleva Povea-Cabello, Irene Villalón-García, Mónica Álvarez-Córdoba, Juan M Suárez-Rivero, Marta Talaverón-Rey, Sandra Jackson, Rafael Falcón-Moya, Antonio Rodríguez-Moreno, José A Sánchez-Alcázar. Biochim Biophys Acta Mol Basis Dis 2020
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Pathophysiological characterization of MERRF patient-specific induced neurons generated by direct reprogramming.
Marina Villanueva-Paz, Suleva Povea-Cabello, Irene Villalón-García, Juan M Suárez-Rivero, Mónica Álvarez-Córdoba, Mario de la Mata, Marta Talaverón-Rey, Sandra Jackson, José A Sánchez-Alcázar. Biochim Biophys Acta Mol Cell Res 2019
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A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations.
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Development of a single-chain, quasi-dimeric zinc-finger nuclease for the selective degradation of mutated human mitochondrial DNA.
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Mitochondrial Donation: A Boon or Curse for the Treatment of Incurable Mitochondrial Diseases.
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Simple Generation of a High Yield Culture of Induced Neurons from Human Adult Skin Fibroblasts.
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Specific elimination of mutant mitochondrial genomes in patient-derived cells by mitoTALENs.
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A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing.
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Selective elimination of mitochondrial mutations in the germline by genome editing.
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Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system.
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Multiplex genome engineering using CRISPR/Cas systems.
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Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations.
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Mutations causing mitochondrial disease: What is new and what challenges remain?
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The Reproductive Journey in the Genomic Era: From Preconception to Childhood.
Sandra Garcia-Herrero, Blanca Simon, Javier Garcia-Planells. Genes (Basel) 2020
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Preimplantation Genetic Testing for Monogenic Disorders.
Martine De Rycke, Veerle Berckmoes. Genes (Basel) 2020
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National, regional, and global trends in infertility prevalence since 1990: a systematic analysis of 277 health surveys.
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Optimized NGS Approach for Detection of Aneuploidies and Mosaicism in PGT-A and Imbalances in PGT-SR.
Carmen M García-Pascual, Luis Navarro-Sánchez, Roser Navarro, Lucía Martínez, Jorge Jiménez, Lorena Rodrigo, Carlos Simón, Carmen Rubio. Genes (Basel) 2020
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Identification and Characterization of Extracellular Vesicles and Its DNA Cargo Secreted During Murine Embryo Development.
Blanca Simon, David Bolumar, Alicia Amadoz, Jorge Jimenez-Almazán, Diana Valbuena, Felipe Vilella, Inmaculada Moreno. Genes (Basel) 2020
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Preimplantation Genetic Testing for Chromosomal Abnormalities: Aneuploidy, Mosaicism, and Structural Rearrangements.
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Preimplantation Genetic Testing for Polygenic Disease Relative Risk Reduction: Evaluation of Genomic Index Performance in 11,883 Adult Sibling Pairs.
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Characteristics of the IVF Cycle that Contribute to the Incidence of Mosaicism.
Lorena Rodrigo, Mónica Clemente-Císcar, Inmaculada Campos-Galindo, Vanessa Peinado, Carlos Simón, Carmen Rubio. Genes (Basel) 2020
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Combined Preimplantation Genetic Testing for Autosomal Dominant Polycystic Kidney Disease: Consequences for Embryos Available for Transfer.
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Concise Review: Induced Pluripotent Stem Cell-Based Drug Discovery for Mitochondrial Disease.
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New Structures Reveal Interaction Dynamics in Respiratory Supercomplexes.
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Mitochondrial DNA mutation-elicited oxidative stress, oxidative damage, and altered gene expression in cultured cells of patients with MERRF syndrome.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.