Editing the Human Genome with CRISPR/Cas: A Review of its Molecular Basis, Current Clinical Applications, and Bioethical Implications.

Autor: Ahumada-Ayala M; Hospital Angeles Pedregal, Mexico City, Mexico.; Department of Medicine, La Salle University School of Medicine, Mexico City, Mexico., Aguilar-López R; Department of Medicine, La Salle University School of Medicine, Mexico City, Mexico., González-Stoylov N; Department of Medicine, La Salle University School of Medicine, Mexico City, Mexico., Palacio-Sosa E; Department of Medicine, La Salle University School of Medicine, Mexico City, Mexico., Cervantes-Barragán DE; Department of Medicine, La Salle University School of Medicine, Mexico City, Mexico.; Department of Genetics and Molecular Biology, Hospital Central Sur Petróleos Mexicanos, Picacho, Mexico City, Mexico., Fernández-Hernández L; Molecular Biology Laboratory, National Institute of Pediatrics, Mexico City, Mexico.

Publikováno v: Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion [Rev Invest Clin] 2023; Vol. 75 (1), pp. 13-28.

Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy.

Autor: Ramos S; Laboratorio de Citogenética, Instituto Nacional de Pediatría, Ciudad de México, Mexico., Navarrete-Meneses P; Laboratorio de Genética y Cáncer, Instituto Nacional de Pediatría, Ciudad de México, Mexico., Molina B; Laboratorio de Citogenética, Instituto Nacional de Pediatría, Ciudad de México, Mexico., Cervantes-Barragán DE; Departamento de Genética, Hospital Central Sur Alta Especialidad, PEMEX, Ciudad de México, Mexico., Lozano V; Departamento de Hematología, Instituto Nacional de Cancerología, Ciudad de México, Mexico., Gallardo E; Servicio de Hematología, Hospital General de México, Ciudad de México, Mexico., Marchetti F; Department of Biology, Carleton University, Ottawa, Ontario, Canada., Frias S; Laboratorio de Citogenética, Instituto Nacional de Pediatría, Ciudad de México, Mexico.; Departamento de Medicina Genómica y Toxicología ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, Mexico.

Publikováno v: Environmental and molecular mutagenesis [Environ Mol Mutagen] 2018 Oct; Vol. 59 (8), pp. 755-768. Date of Electronic Publication: 2018 Sep 08.

Newborn screening for six lysosomal storage disorders in a cohort of Mexican patients: Three-year findings from a screening program in a closed Mexican health system.

Autor: Navarrete-Martínez JI; Department of Genetics, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Limón-Rojas AE; General Dictatorate, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Gaytán-García MJ; Department of Genetics, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Reyna-Figueroa J; Department of Medical Education and Research, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Wakida-Kusunoki G; General Dictatorate, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Delgado-Calvillo MDR; Department of Pediatrics, Hospital Regional de Villahermosa, PEMEX, Villahermosa, Tabasco, Mexico., Cantú-Reyna C; Genomi-k SAPI de CV. Monterrey, Nuevo León, Mexico; Escuela de Medicina Tecnológico de Monterrey, Monterrey, Nuevo León, Mexico., Cruz-Camino H; Genomi-k SAPI de CV. Monterrey, Nuevo León, Mexico; Escuela de Biotecnología y Ciencias de la Salud, Tecnológico de Monterrey, Monterrey, Nuevo León, Mexico., Cervantes-Barragán DE; Department of Genetics, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico; Facultad Mexicana de Medicina, Universidad La Salle, Mexico City, Mexico. Electronic address: david.eduardo.cervantes@pemex.com.

Publikováno v: Molecular genetics and metabolism [Mol Genet Metab] 2017 May; Vol. 121 (1), pp. 16-21. Date of Electronic Publication: 2017 Mar 09.

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome.

Autor: Nakamura K; From the Department of Human Genetics (K. Nakamura, K. Nishiyama, H.K., M.N., Y.T., N. Miyake, N. Matsumoto, H.S.), Yokohama City University Graduate School of Medicine, Yokohama; Department of Pediatrics (K. Nakamura, M.K., K. Hayasaka), Yamagata University Faculty of Medicine, Yamagata; Division of Neurology (H.O., S.Y., M. Okuda, T.W.), Clinical Research Institute, Kanagawa Children's Medical Center, Yokohama; Department of Child Neurology (E.N.), National Center Hospital, National Center of Neurology and Psychiatry, Tokyo; Department of Pediatric Neurology (K. Haginoya), Takuto Rehabilitation Center for Children, Sendai; Department of Pediatrics (J.T.), Epilepsy Center, Nishi-Niigata Chuo National Hospital, Niigata; Department of Pediatrics (S.S.), Osaka Medical College Hospital, Osaka; National Epilepsy Center (K.I.), Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka; Department of Pediatrics (S.T.), Yokohama City University Medical Center, Yokohama; Department of Pediatrics (H.I.), Tokyo Metropolitan Bokuto Hospital, Tokyo, Japan; Metabolic Neurogenetic Clinic (D.L., T.L.-S.), Wolfson Medical Center, Holon, Israel; Department of Human Genetics (D.E.C.-B., C.E.V.), National Institute of Pediatrics, Mexico City, Mexico; Division of Child Neurology (M. Ohfu), Okinawa Nanbu Medical Center and Children's Medical Center, Okinawa, Japan; Institute of Medical Genetics (K.W.), University Medical Center Ljubljana; Department of Child, Adolescent and Developmental Neurology (B.G.S.), University Children's Hospital, Ljubljana, Slovenia; Department of Neurology (S.H.), Nagano Children's Hospital, Nagano, Japan; Department of Obstetrics and Gynecology (D.C.), The Prenatal Diagnosis and Medical Genetics Program, Mount Sinai Hospital, University of Toronto; and Division of Clinical and Metabolic Genetics (D.C., D.M.R.), The Hospital for Sick Children, University of Toronto, Canada., Kato M, Osaka H, Yamashita S, Nakagawa E, Haginoya K, Tohyama J, Okuda M, Wada T, Shimakawa S, Imai K, Takeshita S, Ishiwata H, Lev D, Lerman-Sagie T, Cervantes-Barragán DE, Villarroel CE, Ohfu M, Writzl K, Gnidovec Strazisar B, Hirabayashi S, Chitayat D, Myles Reid D, Nishiyama K, Kodera H, Nakashima M, Tsurusaki Y, Miyake N, Hayasaka K, Matsumoto N, Saitsu H

Publikováno v: Neurology [Neurology] 2013 Sep 10; Vol. 81 (11), pp. 992-8. Date of Electronic Publication: 2013 Aug 09.