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References for PMC Articles for PubMed (Select 22701816)

1.

RALA and RALBP1 regulate mitochondrial fission at mitosis.

Kashatus DF, Lim KH, Brady DC, Pershing NL, Cox AD, Counter CM.

Nat Cell Biol. 2011 Aug 7;13(9):1108-15. doi: 10.1038/ncb2310.

2.

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.

3.

Transmission of mitochondrial DNA diseases and ways to prevent them.

Poulton J, Chiaratti MR, Meirelles FV, Kennedy S, Wells D, Holt IJ.

PLoS Genet. 2010 Aug 12;6(8). pii: e1001066. doi: 10.1371/journal.pgen.1001066. Review.

4.

174th ENMC international workshop: Applying pre-implantation genetic diagnosis to mtDNA diseases: implications of scientific advances 19-21 March 2010, Naarden, The Netherlands.

Poulton J, Bredenoord AL.

Neuromuscul Disord. 2010 Aug;20(8):559-63. doi: 10.1016/j.nmd.2010.05.008. No abstract available.

PMID:
20627569
5.

Mitochondrial DNA mutations in disease and aging.

Wallace DC.

Environ Mol Mutagen. 2010 Jun;51(5):440-50. doi: 10.1002/em.20586. Review.

PMID:
20544884
6.

Chromosome transfer in mature oocytes.

Tachibana M, Sparman M, Mitalipov S.

Nat Protoc. 2010 Jun;5(6):1138-47. doi: 10.1038/nprot.2010.75. Epub 2010 May 27.

7.

Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease.

Craven L, Tuppen HA, Greggains GD, Harbottle SJ, Murphy JL, Cree LM, Murdoch AP, Chinnery PF, Taylor RW, Lightowlers RN, Herbert M, Turnbull DM.

Nature. 2010 May 6;465(7294):82-5. doi: 10.1038/nature08958. Epub 2010 Apr 14.

8.

Previous estimates of mitochondrial DNA mutation level variance did not account for sampling error: comparing the mtDNA genetic bottleneck in mice and humans.

Wonnapinij P, Chinnery PF, Samuels DC.

Am J Hum Genet. 2010 Apr 9;86(4):540-50. doi: 10.1016/j.ajhg.2010.02.023. Epub 2010 Apr 1.

9.

Mitochondrial DNA mutations and human disease.

Tuppen HA, Blakely EL, Turnbull DM, Taylor RW.

Biochim Biophys Acta. 2010 Feb;1797(2):113-28. doi: 10.1016/j.bbabio.2009.09.005. Epub 2009 Sep 15. Review.

10.

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.

11.

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
12.

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
13.

Mitochondrial DNA heteroplasmy in ovine fetuses and sheep cloned by somatic cell nuclear transfer.

Burgstaller JP, Schinogl P, Dinnyes A, Müller M, Steinborn R.

BMC Dev Biol. 2007 Dec 21;7:141.

14.

Reprogramming following somatic cell nuclear transfer in primates is dependent upon nuclear remodeling.

Mitalipov SM, Zhou Q, Byrne JA, Ji WZ, Norgren RB, Wolf DP.

Hum Reprod. 2007 Aug;22(8):2232-42. Epub 2007 Jun 11.

15.

The development of novel quantification assay for mitochondrial DNA heteroplasmy aimed at preimplantation genetic diagnosis of Leigh encephalopathy.

Tajima H, Sueoka K, Moon SY, Nakabayashi A, Sakurai T, Murakoshi Y, Watanabe H, Iwata S, Hashiba T, Kato S, Goto Y, Yoshimura Y.

J Assist Reprod Genet. 2007 Jun;24(6):227-32. Epub 2007 Mar 8.

16.

The mitochondrial bottleneck occurs without reduction of mtDNA content in female mouse germ cells.

Cao L, Shitara H, Horii T, Nagao Y, Imai H, Abe K, Hara T, Hayashi J, Yonekawa H.

Nat Genet. 2007 Mar;39(3):386-90. Epub 2007 Feb 11.

PMID:
17293866
17.

Isolation and characterization of novel rhesus monkey embryonic stem cell lines.

Mitalipov S, Kuo HC, Byrne J, Clepper L, Meisner L, Johnson J, Zeier R, Wolf D.

Stem Cells. 2006 Oct;24(10):2177-86. Epub 2006 Jun 1.

18.

Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosis.

Steffann J, Frydman N, Gigarel N, Burlet P, Ray PF, Fanchin R, Feyereisen E, Kerbrat V, Tachdjian G, Bonnefont JP, Frydman R, Munnich A.

J Med Genet. 2006 Mar;43(3):244-7. Epub 2005 Sep 9.

19.
20.

Mitochondrial DNA mutations in human disease.

Taylor RW, Turnbull DM.

Nat Rev Genet. 2005 May;6(5):389-402. Review.

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