Mitochondrial stress triggers a pro-survival response through epigenetic modifications of nuclear DNA.

Autor: Mayorga L; Instituto de Histología y Embriología de Mendoza (IHEM, Universidad Nacional de Cuyo, CONICET)-Centro Universitario UNCuyo, 5500, Mendoza, Argentina. liamayorga@fcm.uncu.edu.ar., Salassa BN; Instituto de Histología y Embriología de Mendoza (IHEM, Universidad Nacional de Cuyo, CONICET)-Centro Universitario UNCuyo, 5500, Mendoza, Argentina.; Facultad de Odontología, Univeridad Nacional de Cuyo- Centro Universitario UNCuyo, 5500, Mendoza, Argentina., Marzese DM; John Wayne Cancer Institute, 2200 Santa Monica Boulevard, Santa Monica, CA, 90404, USA., Loos MA; Hospital de Pediatría J.P. Garrahan, Combate de los Pozos 1881, 1245, Buenos Aires, Argentina., Eiroa HD; Hospital de Pediatría J.P. Garrahan, Combate de los Pozos 1881, 1245, Buenos Aires, Argentina., Lubieniecki F; Hospital de Pediatría J.P. Garrahan, Combate de los Pozos 1881, 1245, Buenos Aires, Argentina., García Samartino C; Facultad de Ciencias Médicas, Universidad Nacional de Cuyo-Centro Universitario UNCuyo, 5500, Mendoza, Argentina., Romano PS; Instituto de Histología y Embriología de Mendoza (IHEM, Universidad Nacional de Cuyo, CONICET)-Centro Universitario UNCuyo, 5500, Mendoza, Argentina.; Facultad de Ciencias Médicas, Universidad Nacional de Cuyo-Centro Universitario UNCuyo, 5500, Mendoza, Argentina., Roqué M; Instituto de Histología y Embriología de Mendoza (IHEM, Universidad Nacional de Cuyo, CONICET)-Centro Universitario UNCuyo, 5500, Mendoza, Argentina.; Facultad de Ciencias Exactas y Naturales, Universidad Nacional de Cuyo-Centro Universitario UNCuyo, 5500, Mendoza, Argentina.

Publikováno v: Cellular and molecular life sciences : CMLS [Cell Mol Life Sci] 2019 Apr; Vol. 76 (7), pp. 1397-1417. Date of Electronic Publication: 2019 Jan 23.

[The importance of a law on time: presentation of a girl with biotinidase deficiency who was not picked up through the neonatal screening].

Autor: Bay LB; Unidad de Errores Congénitos del Metabolismo, Hospital Nacional de Pediatría Prof. Dr. Juan P. Garrahan. bay.luisa@gmail.com, de Pinho S, Eiroa HD, Otegui I, Rodríguez R

Publikováno v: Archivos argentinos de pediatria [Arch Argent Pediatr] 2010 Feb; Vol. 108 (1), pp. e13-6.

Datamining approaches for examining the low prevalence of N-acetylglutamate synthase deficiency and understanding transcriptional regulation of urea cycle genes.

Autor: Caldovic L; Center for Genetic Medicine Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA.; Department of Genomics and Precision Medicine, School of Medicine and Health Sciences, The George Washington University, Washington, DC, USA., Ahn JJ; Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA., Andricovic J; Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA., Balick VM; Department of Biochemistry and Molecular Medicine, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA., Brayer M; Department of Biological Sciences, The George Washington University, Washington, DC, USA., Chansky PA; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA., Dawson T; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.; AMPEL BioSolutions LLC, Charlottesville, Virginia, USA., Edwards AC; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.; Center for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA., Felsen SE; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.; Center for Neuroscience Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA., Ismat K; Center for Genetic Medicine Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA.; Department of Genomics and Precision Medicine, School of Medicine and Health Sciences, The George Washington University, Washington, DC, USA., Jagannathan SV; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA., Mann BT; Department of Microbiology, Immunology, and Tropical Medicine, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA., Medina JA; The Institute for Biomedical Science, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA., Morizono T; College of Science and Engineering, University of Minnesota, Minneapolis, Minnesota, USA., Morizono M; College of Science and Engineering, University of Minnesota, Minneapolis, Minnesota, USA., Salameh S; Department of Pharmacology & Physiology, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA.; Sheikh Zayed Institute for Pediatric Surgical Innovation, Children's National Hospital, Washington, DC, USA., Vashist N; Center for Genetic Medicine Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA.; Department of Genomics and Precision Medicine, School of Medicine and Health Sciences, The George Washington University, Washington, DC, USA., Williams EC; Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.; The George Washington University Cancer Center, School of Medicine and Health Sciences, George Washington University, Washington, DC, USA., Zhou Z; Department of Civil and Environmental Engineering, The George Washington University, Washington, DC, USA., Morizono H; Center for Genetic Medicine Research, Children's National Research Institute, Children's National Hospital, Washington, DC, USA.; Department of Genomics and Precision Medicine, School of Medicine and Health Sciences, The George Washington University, Washington, DC, USA.

Publikováno v: Journal of inherited metabolic disease [J Inherit Metab Dis] 2024 Nov; Vol. 47 (6), pp. 1175-1193. Date of Electronic Publication: 2023 Nov 05.

Hippocampal tau oligomerization early in tau pathology coincides with a transient alteration of mitochondrial homeostasis and DNA repair in a mouse model of tauopathy.

Autor: Zheng, Jin¹ (AUTHOR), Akbari, Mansour¹ (AUTHOR), Schirmer, Claire² (AUTHOR), Reynaert, Marie-Line² (AUTHOR), Loyens, Anne² (AUTHOR), Lefebvre, Bruno² (AUTHOR), Buée, Luc² (AUTHOR), Croteau, Deborah L.³ (AUTHOR), Galas, Marie-Christine² (AUTHOR), Bohr, Vilhelm A.^1,3 (AUTHOR) vbohr@nih.gov

Publikováno v: Acta Neuropathologica Communications. 3/4/2020, Vol. 8 Issue 1, p1-23. 23p.

The effect of mitochondrial transplantation therapy from different gender on inhibiting cell proliferation of malignant melanoma.

Autor: Zhenyao Yu, Yixue Hou, Wei Zhou, Zizhen Zhao, Zesheng Liu, Ailing Fu

Publikováno v: International Journal of Biological Sciences; 2021, Vol. 17 Issue 8, p2021-2033, 13p