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The Challenges of Mitochondrial Replacement
article has not abstract
Vyšlo v časopise: The Challenges of Mitochondrial Replacement. PLoS Genet 10(4): e32767. doi:10.1371/journal.pgen.1004315
Kategorie: Viewpoints
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.pgen.1004315Souhrn
article has not abstract
Zdroje
1. HFEA, Mitochondria public consultation (2012) Available: http://www.hfea.gov.uk/6896.html. Accessed 29 March 2014.
2. KoopmanWJ, WillemsPH, SmeitinkJA (2012) Monogenic mitochondrial disorders. N Engl J Med 366 : 1132–1141.
3. Wellcome Trust Centre for Mitochondrial Research (2014) Patient Care Guidelines. Available: http://www.newcastle-mitochondria.com/service/patient-care-guidelines/. Accessed 29 March 2014.
4. SteffannJ, FrydmanN, GigarelN, BurletP, RayPF, et al. (2006) Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis. J Med Genet 43 : 244–247.
5. SteffannJ, GigarelN, CorcosJ, BonnièreM, Encha-RazaviF, et al. (2007) 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 44 : 664–669.
6. TachibanaM, SparmanM, SritanaudomchaiH, MaH, ClepperL, et al. (2009) Mitochondrial gene replacement in primate offspring and embryonic stem cells. Nature 461 : 367–372.
7. TachibanaM, AmatoP, SparmanM, WoodwardJ, SanchisDM, et al. (2013) Towards germline gene therapy of inherited mitochondrial diseases. Nature 493 : 627–631.
8. CravenL, TuppenHA, GreggainsGD, HarbottleSJ, MurphyJL, et al. (2010) Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease. Nature 465 : 82–85.
9. HFEA (2011) Review of scientific methods to avoid mitochondrial disease 2011 (including 2013 update). Available: http://www.hfea.gov.uk/6372.html. Accessed 29 March 2014.
10. ReinhardtK, DowlingDK, MorrowEH (2013) Mitochondrial replacement, evolution, and the clinic. Science 341 : 1345–1346.
11. Yu-Wai-ManP, GriffithsPG, HudsonG, ChinneryPF (2009) Inherited mitochondrial optic neuropathies. J Med Genet 46 : 145–158.
12. GiordanoC, MontopoliM, PerliE, OrlandiM, FantinM, et al. (2011) Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy. Brain 134 : 220–234.
13. PereiraL, GonçalvesJ, Franco-DuarteR, SilvaJ, RochaT, et al. (2007) No evidence for an mtDNA role in sperm motility: data from complete sequencing of asthenozoospermic males. Mol Biol Evol 24 : 868–874.
14. MossmanJA, SlateJ, BirkheadTR, MooreHD, PaceyAA (2012) Mitochondrial haplotype does not influence sperm motility in a UK population of men. Hum Reprod 27 : 641–651.
15. LeeHS, MaH, JuanesRC, TachibanaM, SparmanM, et al. (2012) Rapid mitochondrial DNA segregation in primate preimplantation embryos precedes somatic and germline bottleneck. Cell Rep 1 : 506–515.
16. BattersbyBJ, ShoubridgeEA (2001) Selection of a mtDNA sequence variant in hepatocytes of heteroplasmic mice is not due to differences in respiratory chain function or efficiency of replication. Hum Mol Genet 10 : 2469–2479.
17. CannonMV, DunnDA, IrwinMH, BrooksAI, BartolFF, et al. (2011) Xenomitochondrial mice: investigation into mitochondrial compensatory mechanisms. Mitochondrion 11 : 33–39.
18. GregorováS, DivinaP, StorchovaR, TrachtulecZ, FotopulosovaV, et al. (2008) Mouse consomic strains: exploiting genetic divergence between Mus m. musculus and Mus m. domesticus subspecies. Genome Res 18 : 509–515.
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Genetika Reprodukčná medicína
Článok vyšiel v časopisePLOS Genetics
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