EDP Sciences logo
Authentification abonné
Rechercher
Menu
Accueil Tous les numéros Volume 33 / Numéro 6-7 (Juin-Juillet 2017) Med Sci (Paris), 33 6-7 (2017) 642-645 Références
Accès gratuit
Numéro
Med Sci (Paris)
Volume 33, Numéro 6-7, Juin-Juillet 2017
Page(s) 642 - 645
Section M/S Revues
DOI https://doi.org/10.1051/medsci/20173306022
Publié en ligne 19 juillet 2017
  1. Steffann J, Frydman N, Gigarel N, et al. Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis. J Med Genet 2006 ; 43 : 244–247. [CrossRef] [PubMed] [Google Scholar]
  2. Steffann J, Gigarel N, Corcos J, et al. Stability of the m.8993T->G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome. J Med Genet 2007 ; 44 : 664–669. [CrossRef] [PubMed] [Google Scholar]
  3. Bouchet C, Steffann J, Corcos J, et al. Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development. J Med Genet 2006 ; 43 : 788–792. [CrossRef] [PubMed] [Google Scholar]
  4. Monnot S, Gigarel N, Samuels DC, et al. Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system. Hum Mutat 2011 ; 32 : 116–125. [CrossRef] [PubMed] [Google Scholar]
  5. Reddy P, Ocampo A, Suzuki K, et al. Selective elimination of mitochondrial mutations in the germline by genome editing. Cell 2015 ; 161 : 459–469. [CrossRef] [PubMed] [Google Scholar]
  6. Jo A, Ham S, Lee GH, Lee YI, et al. Efficient Mitochondrial Genome Editing by CRISPR/Cas9. Biomed Res Int 2015 ; 2015 : 305716. [Google Scholar]
  7. Tonin Y, Heckel AM, Vysokikh M, et al. Modeling of antigenomic therapy of mitochondrial diseases by mitochondrially addressed RNA targeting a pathogenic point mutation in mitochondrial DNA. J Biol Chem 2014 ; 289 : 13323–13334. [CrossRef] [PubMed] [Google Scholar]
  8. Craven L, Tuppen HA, Greggains GD, et al. Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease. Nature 2010 ; 465 : 82–85. [CrossRef] [PubMed] [Google Scholar]
  9. Hyslop LA, Blakeley P, Craven L, et al. Towards clinical application of pronuclear transfer to prevent mitochondrial DNA disease. Nature 2016 ; 534 : 383–386. [CrossRef] [PubMed] [Google Scholar]
  10. Tachibana M, Sparman M, Sritanaudomchai H, et al. Mitochondrial gene replacement in primate offspring and embryonic stem cells. Nature 2009 ; 461 : 367–372. [CrossRef] [PubMed] [Google Scholar]
  11. Kang E, Wu J, Gutierrez NM, et al. Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations. Nature 2016 ; 540 : 270–275. [CrossRef] [PubMed] [Google Scholar]
  12. Roubertoux PL, Sluyter F, Carlier M, et al. Mitochondrial DNA modifies cognition in interaction with the nuclear genome and age in mice. Nat Genet 2003 ; 35 : 65–69. [Google Scholar]
  13. Latorre-Pellicer A, Moreno-Loshuertos R, Lechuga-Vieco AV, et al. Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing. Nature 2016 ; 535 : 561–565. [CrossRef] [PubMed] [Google Scholar]
  14. Johnson KR, Zheng QY, Bykhovskaya Y, et al. A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice. Nat Genet 2001 ; 27 : 191–194. [Google Scholar]
  15. Hudson G, Keers S, Yu Wai Man P, et al. Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder. Am J Hum Genet 2005 ; 77 : 1086–1091. [Google Scholar]
  16. Hauswirth WW, Laipis PJ. Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows. Proc Natl Acad Sci USA 1982 ; 79 : 4686–4690. [CrossRef] [Google Scholar]
  17. Koehler CM, Lindberg GL, Brown DR, et al. Replacement of bovine mitochondrial DNA by a sequence variant within one generation. Genetics 1991 ; 129 : 247–255. [PubMed] [Google Scholar]
  18. Marchington DR, Hartshorne GM, Barlow D, Poulton J. Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes: support for a genetic bottleneck. Am J Hum Genet 1997 ; 60 : 408–416. [PubMed] [Google Scholar]
  19. Acton BM, Lai I, Shang X, et al. Neutral mitochondrial heteroplasmy alters physiological function in mice. Biol Reprod 2007 ; 77 : 569–576. [CrossRef] [PubMed] [Google Scholar]
  20. Sharpley MS, Marciniak C, Eckel-Mahan K, et al. Heteroplasmy of mouse mtDNA is genetically unstable and results in altered behavior and cognition. Cell 2012 ; 151 : 333–343. [CrossRef] [PubMed] [Google Scholar]
  21. May-Panloup P, Boucret L, Chao de la Barca JM, et al. Ovarian ageing: the role of mitochondria in oocytes and follicles. Hum Reprod Update 2016 ; 22 : 725–743. [Google Scholar]
  22. Zhang J, Zhuang G, Zeng Y, et al. Pregnancy derived from human zygote pronuclear transfer in a patient who had arrested embryos after IVF. Reprod Biomed Online 2016 ; 33 : 529–533. [CrossRef] [PubMed] [Google Scholar]
  23. Tonin Y, Entelis N. Pathologies de l’ADN mitochondrial et stratégies thérapeutiques. Med Sci (Paris) 2014 ; 30 : 1101–1109. [CrossRef] [EDP Sciences] [PubMed] [Google Scholar]

Les statistiques affichées correspondent au cumul d'une part des vues des résumés de l'article et d'autre part des vues et téléchargements de l'article plein-texte (PDF, Full-HTML, ePub... selon les formats disponibles) sur la platefome Vision4Press.

Les statistiques sont disponibles avec un délai de 48 à 96 heures et sont mises à jour quotidiennement en semaine.

Le chargement des statistiques peut être long.