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Items: 1 to 20 of 30

1.

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. Erratum in: Nature. 2014 Dec;516(7530):276.

2.

Prevalence of mitochondrial 1555A-->G mutation in adults of European descent.

Vandebona H, Mitchell P, Manwaring N, Griffiths K, Gopinath B, Wang JJ, Sue CM.

N Engl J Med. 2009 Feb 5;360(6):642-4. doi: 10.1056/NEJMc0806397. No abstract available.

3.

Prevalence of mitochondrial 1555A-->G mutation in European children.

Bitner-Glindzicz M, Pembrey M, Duncan A, Heron J, Ring SM, Hall A, Rahman S.

N Engl J Med. 2009 Feb 5;360(6):640-2. doi: 10.1056/NEJMc0806396. No abstract available.

4.

Pathogenic mitochondrial DNA mutations are common in the general population.

Elliott HR, Samuels DC, Eden JA, Relton CL, Chinnery PF.

Am J Hum Genet. 2008 Aug;83(2):254-60. doi: 10.1016/j.ajhg.2008.07.004.

5.

Mitochondrial disorders in the nervous system.

DiMauro S, Schon EA.

Annu Rev Neurosci. 2008;31:91-123. doi: 10.1146/annurev.neuro.30.051606.094302. Review.

PMID:
18333761
6.

Prevalence of mitochondrial DNA disease in adults.

Schaefer AM, McFarland R, Blakely EL, He L, Whittaker RG, Taylor RW, Chinnery PF, Turnbull DM.

Ann Neurol. 2008 Jan;63(1):35-9.

PMID:
17886296
7.

A multiplex real-time PCR method to detect and quantify mitochondrial DNA deletions in individual cells.

Krishnan KJ, Bender A, Taylor RW, Turnbull DM.

Anal Biochem. 2007 Nov 1;370(1):127-9. No abstract available.

PMID:
17662684
8.
9.

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.

10.

Can 'abnormally' fertilized zygotes give rise to viable embryos?

Feenan K, Herbert M.

Hum Fertil (Camb). 2006 Sep;9(3):157-69. Review.

PMID:
17008268
11.

Transmission of mitochondrial DNA disorders: possibilities for the future.

Brown DT, Herbert M, Lamb VK, Chinnery PF, Taylor RW, Lightowlers RN, Craven L, Cree L, Gardner JL, Turnbull DM.

Lancet. 2006 Jul 1;368(9529):87-9. No abstract available.

PMID:
16815383
12.

Treatment for mitochondrial disorders.

Chinnery P, Majamaa K, Turnbull D, Thorburn D.

Cochrane Database Syst Rev. 2006 Jan 25;(1):CD004426. Review. Update in: Cochrane Database Syst Rev. 2012;4:CD004426.

PMID:
16437486
13.

Gene therapy for progeny of mito-mice carrying pathogenic mtDNA by nuclear transplantation.

Sato A, Kono T, Nakada K, Ishikawa K, Inoue S, Yonekawa H, Hayashi J.

Proc Natl Acad Sci U S A. 2005 Nov 15;102(46):16765-70.

14.

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.

15.

Mitochondrial DNA mutations in human disease.

Taylor RW, Turnbull DM.

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

16.

Familial myopathy: new insights into the T14709C mitochondrial tRNA mutation.

McFarland R, Schaefer AM, Gardner JL, Lynn S, Hayes CM, Barron MJ, Walker M, Chinnery PF, Taylor RW, Turnbull DM.

Ann Neurol. 2004 Apr;55(4):478-84.

PMID:
15048886
17.

Comparison of mitochondrial DNA contents in human embryos with good or poor morphology at the 8-cell stage.

Lin DP, Huang CC, Wu HM, Cheng TC, Chen CI, Lee MS.

Fertil Steril. 2004 Jan;81(1):73-9.

PMID:
14711547
18.

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

Taylor RW, Giordano C, Davidson MM, d'Amati G, Bain H, Hayes CM, Leonard H, Barron MJ, Casali C, Santorelli FM, Hirano M, Lightowlers RN, DiMauro S, Turnbull DM.

J Am Coll Cardiol. 2003 May 21;41(10):1786-96.

19.

Quantification of human ooplasmic mitochondria.

Barritt JA, Kokot M, Cohen J, Steuerwald N, Brenner CA.

Reprod Biomed Online. 2002 May-Jun;4(3):243-7.

PMID:
12709274
20.

The epidemiology of Leber hereditary optic neuropathy in the North East of England.

Y-W-Man P, Griffiths PG, Brown DT, Howell N, Turnbull DM, Chinnery PF.

Am J Hum Genet. 2003 Feb;72(2):333-9.

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