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Items: 1 to 20 of 119

1.

Rapid mitochondrial DNA segregation in primate preimplantation embryos precedes somatic and germline bottleneck.

Lee HS, Ma H, Juanes RC, Tachibana M, Sparman M, Woodward J, Ramsey C, Xu J, Kang EJ, Amato P, Mair G, Steinborn R, Mitalipov S.

Cell Rep. 2012 May 31;1(5):506-15.

2.

Limitations of preimplantation genetic diagnosis for mitochondrial DNA diseases.

Mitalipov S, Amato P, Parry S, Falk MJ.

Cell Rep. 2014 May 22;7(4):935-7. doi: 10.1016/j.celrep.2014.05.004. No abstract available.

3.

Data from artificial models of mitochondrial DNA disorders are not always applicable to humans.

Steffann J, Gigarel N, Samuels DC, Monnot S, Borghese R, Hesters L, Frydman N, Burlet P, Frydman R, Benachi A, Rotig A, Munnich A, Bonnefont JP.

Cell Rep. 2014 May 22;7(4):933-4. doi: 10.1016/j.celrep.2014.05.005. No abstract available.

4.

A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes.

Cree LM, Samuels DC, de Sousa Lopes SC, Rajasimha HK, Wonnapinij P, Mann JR, Dahl HH, Chinnery PF.

Nat Genet. 2008 Feb;40(2):249-54. doi: 10.1038/ng.2007.63. Epub 2008 Jan 27.

PMID:
18223651
5.

A systematic analysis of the suitability of preimplantation genetic diagnosis for mitochondrial diseases in a heteroplasmic mitochondrial mouse model.

Neupane J, Vandewoestyne M, Heindryckx B, Ghimire S, Lu Y, Qian C, Lierman S, Van Coster R, Gerris J, Deroo T, Deforce D, De Sutter P.

Hum Reprod. 2014 Apr;29(4):852-9. doi: 10.1093/humrep/deu016. Epub 2014 Feb 12.

PMID:
24524987
6.

The kinetics of donor cell mtDNA in embryonic and somatic donor cell-derived bovine embryos.

Ferreira CR, Meirelles FV, Yamazaki W, Chiaratti MR, Méo SC, Perecin F, Smith LC, Garcia JM.

Cloning Stem Cells. 2007 Winter;9(4):618-29.

PMID:
18154521
7.

Poor correlations in the levels of pathogenic mitochondrial DNA mutations in polar bodies versus oocytes and blastomeres in humans.

Gigarel N, Hesters L, Samuels DC, Monnot S, Burlet P, Kerbrat V, Lamazou F, Benachi A, Frydman R, Feingold J, Rotig A, Munnich A, Bonnefont JP, Frydman N, Steffann J.

Am J Hum Genet. 2011 Apr 8;88(4):494-8. doi: 10.1016/j.ajhg.2011.03.010.

8.

The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes.

Wai T, Teoli D, Shoubridge EA.

Nat Genet. 2008 Dec;40(12):1484-8. doi: 10.1038/ng.258.

PMID:
19029901
9.

Mitochondrial gene replacement in primate offspring and embryonic stem cells.

Tachibana M, Sparman M, Sritanaudomchai H, Ma H, Clepper L, Woodward J, Li Y, Ramsey C, Kolotushkina O, Mitalipov S.

Nature. 2009 Sep 17;461(7262):367-72. doi: 10.1038/nature08368. Epub 2009 Aug 26. Erratum in: Nature. 2014 Dec;516(7530):276.

10.

Mitochondrial DNA and the mammalian oocyte.

Shoubridge EA, Wai T.

Curr Top Dev Biol. 2007;77:87-111. Review.

PMID:
17222701
11.

New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice.

Cao L, Shitara H, Sugimoto M, Hayashi J, Abe K, Yonekawa H.

PLoS Genet. 2009 Dec;5(12):e1000756. doi: 10.1371/journal.pgen.1000756. Epub 2009 Dec 4.

12.

Prospect of preimplantation genetic diagnosis for heritable mitochondrial DNA diseases.

Dean NL, Battersby BJ, Ao A, Gosden RG, Tan SL, Shoubridge EA, Molnar MJ.

Mol Hum Reprod. 2003 Oct;9(10):631-8. Erratum in: Mol Hum Reprod. 2004 Aug;10(8):621.

PMID:
12970401
13.

Development of bovine-ovine interspecies cloned embryos and mitochondria segregation in blastomeres during preimplantation.

Hua S, Zhang Y, Song K, Song J, Zhang Z, Zhang L, Zhang C, Cao J, Ma L.

Anim Reprod Sci. 2008 May;105(3-4):245-57. Epub 2007 Mar 6.

PMID:
17399920
14.

Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations.

Kang E, Wu J, Gutierrez NM, Koski A, Tippner-Hedges R, Agaronyan K, Platero-Luengo A, Martinez-Redondo P, Ma H, Lee Y, Hayama T, Van Dyken C, Wang X, Luo S, Ahmed R, Li Y, Ji D, Kayali R, Cinnioglu C, Olson S, Jensen J, Battaglia D, Lee D, Wu D, Huang T, Wolf DP, Temiakov D, Belmonte JC, Amato P, Mitalipov S.

Nature. 2016 Dec 8;540(7632):270-275. doi: 10.1038/nature20592. Epub 2016 Nov 30.

PMID:
27919073
15.

Sequential comprehensive chromosome analysis on polar bodies, blastomeres and trophoblast: insights into female meiotic errors and chromosomal segregation in the preimplantation window of embryo development.

Capalbo A, Bono S, Spizzichino L, Biricik A, Baldi M, Colamaria S, Ubaldi FM, Rienzi L, Fiorentino F.

Hum Reprod. 2013 Feb;28(2):509-18. doi: 10.1093/humrep/des394. Epub 2012 Nov 11.

PMID:
23148203
16.

Towards germline gene therapy of inherited mitochondrial diseases.

Tachibana M, Amato P, Sparman M, Woodward J, Sanchis DM, Ma H, Gutierrez NM, Tippner-Hedges R, Kang E, Lee HS, Ramsey C, Masterson K, Battaglia D, Lee D, Wu D, Jensen J, Patton P, Gokhale S, Stouffer R, Mitalipov S.

Nature. 2013 Jan 31;493(7434):627-31. doi: 10.1038/nature11647. Epub 2012 Oct 24.

17.

Differences in Strength and Timing of the mtDNA Bottleneck between Zebrafish Germline and Non-germline Cells.

Otten AB, Theunissen TE, Derhaag JG, Lambrichs EH, Boesten IB, Winandy M, van Montfoort AP, Tarbashevich K, Raz E, Gerards M, Vanoevelen JM, van den Bosch BJ, Muller M, Smeets HJ.

Cell Rep. 2016 Jul 19;16(3):622-30. doi: 10.1016/j.celrep.2016.06.023. Epub 2016 Jun 30.

18.
19.

Spatiotemporal dynamics of OCT4 protein localization during preimplantation development in mice.

Fukuda A, Mitani A, Miyashita T, Kobayashi H, Umezawa A, Akutsu H.

Reproduction. 2016 Nov;152(5):417-30. doi: 10.1530/REP-16-0277. Epub 2016 Aug 5.

20.

Segregation of mtDNA throughout human embryofetal development: m.3243A>G as a model system.

Monnot S, Gigarel N, Samuels DC, Burlet P, Hesters L, Frydman N, Frydman R, Kerbrat V, Funalot B, Martinovic J, Benachi A, Feingold J, Munnich A, Bonnefont JP, Steffann J.

Hum Mutat. 2011 Jan;32(1):116-25. doi: 10.1002/humu.21417.

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