Free Access
Issue |
Med Sci (Paris)
Volume 33, Number 6-7, Juin-Juillet 2017
|
|
---|---|---|
Page(s) | 642 - 645 | |
Section | M/S Revues | |
DOI | https://doi.org/10.1051/medsci/20173306022 | |
Published online | 19 July 2017 |
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.