Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 87

1.

MT-CYB mutations in hypertrophic cardiomyopathy.

Hagen CM, Aidt FH, Havndrup O, Hedley PL, Jespersgaard C, Jensen M, Kanters JK, Moolman-Smook JC, Møller DV, Bundgaard H, Christiansen M.

Mol Genet Genomic Med. 2013 May;1(1):54-65. doi: 10.1002/mgg3.5. Epub 2013 Apr 12. Erratum in: Mol Genet Genomic Med. 2013 Sep;1(3):187.

2.

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

Hagen CM, Aidt FH, Havndrup O, Hedley PL, Jensen MK, Kanters JK, Pham TT, Bundgaard H, Christiansen M.

PLoS One. 2015 Apr 29;10(4):e0124540. doi: 10.1371/journal.pone.0124540. eCollection 2015.

3.

Human Mitochondrial Cytochrome b Variants Studied in Yeast: Not All Are Silent Polymorphisms.

Song Z, Laleve A, Vallières C, McGeehan JE, Lloyd RE, Meunier B.

Hum Mutat. 2016 Sep;37(9):933-41. doi: 10.1002/humu.23024. Epub 2016 Jun 27.

4.

Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny.

Zaragoza MV, Brandon MC, Diegoli M, Arbustini E, Wallace DC.

Eur J Hum Genet. 2011 Feb;19(2):200-7. doi: 10.1038/ejhg.2010.169. Epub 2010 Oct 27.

5.

Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population.

Hagen CM, Aidt FH, Hedley PL, Jensen MK, Havndrup O, Kanters JK, Moolman-Smook JC, Larsen SO, Bundgaard H, Christiansen M.

PLoS One. 2013 Aug 5;8(8):e71904. doi: 10.1371/journal.pone.0071904. Print 2013.

6.

Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure.

Arbustini E, Fasani R, Morbini P, Diegoli M, Grasso M, Dal Bello B, Marangoni E, Banfi P, Banchieri N, Bellini O, Comi G, Narula J, Campana C, Gavazzi A, Danesino C, Viganò M.

Heart. 1998 Dec;80(6):548-58. Erratum in: Heart 1999 Mar;81(3):330.

7.

Novel m.15434C>A (p.230L>I) Mitochondrial Cytb Gene Missense Mutation Associated with Dilated Cardiomyopathy.

Zarrouk Mahjoub S, Mehri S, Ourda F, Finsterer J, Ben Arab S.

ISRN Cardiol. 2012;2012:251723. doi: 10.5402/2012/251723. Epub 2012 Jul 3.

8.

Mitochondrial DNA variations associated with hypertrophic cardiomyopathy.

Govindaraj P, Khan NA, Rani B, Rani DS, Selvaraj P, Jyothi V, Bahl A, Narasimhan C, Rakshak D, Premkumar K, Khullar M, Thangaraj K.

Mitochondrion. 2014 May;16:65-72. doi: 10.1016/j.mito.2013.10.006. Epub 2013 Nov 9.

PMID:
24215792
9.

Evidence for the presence of somatic mitochondrial DNA mutations in right atrial appendage tissues of coronary artery disease patients.

Matam K, Shaik NA, Aggarwal S, Diwale S, Banaganapalli B, Al-Aama JY, Elango R, Rao P, Hasan Q.

Mol Genet Genomics. 2014 Aug;289(4):533-40. doi: 10.1007/s00438-014-0828-2. Epub 2014 Mar 7.

PMID:
24604425
10.

Novel mitochondrial DNA mutations associated with Chinese familial hypertrophic cardiomyopathy.

Wei YL, Yu CA, Yang P, Li AL, Wen JY, Zhao SM, Liu HX, Ke YN, Campbell W, Zhang YG, Li XH, Liao WQ.

Clin Exp Pharmacol Physiol. 2009 Sep;36(9):933-9. doi: 10.1111/j.1440-1681.2009.05183.x. Epub 2009 Mar 26.

PMID:
19473338
11.

Diagnostic disparity and identification of two TNNI3 gene mutations, one novel and one arising de novo, in South African patients with restrictive cardiomyopathy and focal ventricular hypertrophy.

Mouton JM, Pellizzon AS, Goosen A, Kinnear CJ, Herbst PG, Brink PA, Moolman-Smook JC.

Cardiovasc J Afr. 2015 Mar-Apr;26(2):63-9. doi: 10.5830/CVJA-2015-019.

12.

Polymorphisms in the MT-ATP6 and MT-CYB genes in in vitro fertilization failure.

Mao GH, Wang YN, Xu M, Wang WL, Tan L, Tao SB.

Mitochondrial DNA. 2015 Feb;26(1):20-4. doi: 10.3109/19401736.2013.840612. Epub 2013 Oct 9.

PMID:
24102627
13.

Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes.

Alila OF, Rebai EM, Tabebi M, Tej A, Chamkha I, Tlili A, Bouguila J, Tilouche S, Soyah N, Boughamoura L, Fakhfakh F.

Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Jul;27(4):2873-80. doi: 10.3109/19401736.2015.1060417. Epub 2015 Aug 10.

PMID:
26258512
14.

Clinical characterization and mitochondrial DNA sequence variations in Leber hereditary optic neuropathy.

Kumar M, Kaur P, Kumar M, Saxena R, Sharma P, Dada R.

Mol Vis. 2012;18:2687-99. Epub 2012 Nov 12.

15.

Molecular genetic and functional characterization implicate muscle-restricted coiled-coil gene (MURC) as a causal gene for familial dilated cardiomyopathy.

Rodriguez G, Ueyama T, Ogata T, Czernuszewicz G, Tan Y, Dorn GW 2nd, Bogaev R, Amano K, Oh H, Matsubara H, Willerson JT, Marian AJ.

Circ Cardiovasc Genet. 2011 Aug 1;4(4):349-58. doi: 10.1161/CIRCGENETICS.111.959866. Epub 2011 Jun 3.

16.

Genetic diagnosis of hypertrophic cardiomyopathy using mass spectrometry DNA arrays and high resolution melting.

Santos S, Lança V, Oliveira H, Branco P, Silveira L, Marques V, Brito D, Madeira H, Bicho M, Fernandes AR.

Rev Port Cardiol. 2011 Jan;30(1):7-18.

17.

Mitochondrial DNA depletion, mitochondrial mutations and high TFAM expression in hepatocellular carcinoma.

Qiao L, Ru G, Mao Z, Wang C, Nie Z, Li Q, Huang-Yang Y, Zhu L, Liang X, Yu J, Jiang P.

Oncotarget. 2017 Sep 16;8(48):84373-84383. doi: 10.18632/oncotarget.21033. eCollection 2017 Oct 13.

18.

Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathy.

Zarrouk-Mahjoub S, Mehri S, Ouarda F, Finsterer J, Boussaada R.

Herz. 2015 May;40(3):436-41. doi: 10.1007/s00059-013-3950-8. Epub 2013 Sep 27.

PMID:
24068026
19.

Gene mutations in apical hypertrophic cardiomyopathy.

Arad M, Penas-Lado M, Monserrat L, Maron BJ, Sherrid M, Ho CY, Barr S, Karim A, Olson TM, Kamisago M, Seidman JG, Seidman CE.

Circulation. 2005 Nov 1;112(18):2805-11.

20.

Molecular genetics and pathogenesis of hypertrophic cardiomyopathy.

Marian AJ, Salek L, Lutucuta S.

Minerva Med. 2001 Dec;92(6):435-51. Review.

Supplemental Content

Support Center