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Items: 1 to 20 of 100

1.

Lethal mitochondrial cardiomyopathy in a hypomorphic Med30 mouse mutant is ameliorated by ketogenic diet.

Krebs P, Fan W, Chen YH, Tobita K, Downes MR, Wood MR, Sun L, Li X, Xia Y, Ding N, Spaeth JM, Moresco EM, Boyer TG, Lo CW, Yen J, Evans RM, Beutler B.

Proc Natl Acad Sci U S A. 2011 Dec 6;108(49):19678-82. doi: 10.1073/pnas.1117835108. Epub 2011 Nov 21.

2.

Down-regulated energy metabolism genes associated with mitochondria oxidative phosphorylation and fatty acid metabolism in viral cardiomyopathy mouse heart.

Xu J, Nie HG, Zhang XD, Tian Y, Yu B.

Mol Biol Rep. 2011 Aug;38(6):4007-13. doi: 10.1007/s11033-010-0519-y. Epub 2010 Dec 3.

PMID:
21127995
3.

[Diagnosis of mitochondrial cardiomyopathies: the need for a multidisciplinary approach].

Santorelli FM, Bertini E.

G Ital Cardiol. 1999 Oct;29(10):1181-3. Italian. No abstract available.

PMID:
10546130
4.

Tissue-specific splicing of an Ndufs6 gene-trap insertion generates a mitochondrial complex I deficiency-specific cardiomyopathy.

Ke BX, Pepe S, Grubb DR, Komen JC, Laskowski A, Rodda FA, Hardman BM, Pitt JJ, Ryan MT, Lazarou M, Koleff J, Cheung MM, Smolich JJ, Thorburn DR.

Proc Natl Acad Sci U S A. 2012 Apr 17;109(16):6165-70. doi: 10.1073/pnas.1113987109. Epub 2012 Apr 2.

5.

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator.

Graham BH, Waymire KG, Cottrell B, Trounce IA, MacGregor GR, Wallace DC.

Nat Genet. 1997 Jul;16(3):226-34.

PMID:
9207786
6.

Cardiomyopathy in childhood, mitochondrial dysfunction, and the role of L-carnitine.

Winter SC, Buist NR.

Am Heart J. 2000 Feb;139(2 Pt 3):S63-9. Review.

PMID:
10650319
7.

Cardiomyocyte-Specific Ablation of Med1 Subunit of the Mediator Complex Causes Lethal Dilated Cardiomyopathy in Mice.

Jia Y, Chang HC, Schipma MJ, Liu J, Shete V, Liu N, Sato T, Thorp EB, Barger PM, Zhu YJ, Viswakarma N, Kanwar YS, Ardehali H, Thimmapaya B, Reddy JK.

PLoS One. 2016 Aug 22;11(8):e0160755. doi: 10.1371/journal.pone.0160755. eCollection 2016. Erratum in: PLoS One. 2016 Sep 30;11(9):e0164316.

8.

Mitochondrial defects in cardiomyopathy and neuromuscular disease.

Wallace DC.

Am Heart J. 2000 Feb;139(2 Pt 3):S70-85. Review.

PMID:
10650320
9.

Long-chain 3-hydroxy fatty acids accumulating in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial trifunctional protein deficiencies uncouple oxidative phosphorylation in heart mitochondria.

Tonin AM, Amaral AU, Busanello EN, Grings M, Castilho RF, Wajner M.

J Bioenerg Biomembr. 2013 Feb;45(1-2):47-57. doi: 10.1007/s10863-012-9481-9. Epub 2012 Oct 13.

PMID:
23065309
10.

Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is associated with mitochondrial myopathy and cardiomyopathy.

Palmieri L, Alberio S, Pisano I, Lodi T, Meznaric-Petrusa M, Zidar J, Santoro A, Scarcia P, Fontanesi F, Lamantea E, Ferrero I, Zeviani M.

Hum Mol Genet. 2005 Oct 15;14(20):3079-88. Epub 2005 Sep 9.

PMID:
16155110
11.

Ketogenic diet slows down mitochondrial myopathy progression in mice.

Ahola-Erkkilä S, Carroll CJ, Peltola-Mjösund K, Tulkki V, Mattila I, Seppänen-Laakso T, Oresic M, Tyynismaa H, Suomalainen A.

Hum Mol Genet. 2010 May 15;19(10):1974-84. doi: 10.1093/hmg/ddq076. Epub 2010 Feb 17.

PMID:
20167576
12.

Mitochondrial cardiomyopathy.

Ozawa T.

Herz. 1994 Apr;19(2):105-18, 125. Review.

PMID:
8194831
13.

Type 1 diabetic cardiomyopathy in the Akita (Ins2WT/C96Y) mouse model is characterized by lipotoxicity and diastolic dysfunction with preserved systolic function.

Basu R, Oudit GY, Wang X, Zhang L, Ussher JR, Lopaschuk GD, Kassiri Z.

Am J Physiol Heart Circ Physiol. 2009 Dec;297(6):H2096-108. doi: 10.1152/ajpheart.00452.2009. Epub 2009 Oct 2.

14.

Genotype and phenotype of severe mitochondrial cardiomyopathy: a recipient of heart transplantation and the genetic control.

Ozawa T, Katsumata K, Hayakawa M, Tanaka M, Sugiyama S, Tanaka T, Itoyama S, Nunoda S, Sekiguchi M.

Biochem Biophys Res Commun. 1995 Feb 15;207(2):613-20.

PMID:
7864851
15.

Regional absence of mitochondria causing energy depletion in the myocardium of muscle LIM protein knockout mice.

van den Bosch BJ, van den Burg CM, Schoonderwoerd K, Lindsey PJ, Scholte HR, de Coo RF, van Rooij E, Rockman HA, Doevendans PA, Smeets HJ.

Cardiovasc Res. 2005 Feb 1;65(2):411-8.

PMID:
15639480
16.

Knockdown of cytochrome P450 2E1 inhibits oxidative stress and apoptosis in the cTnT(R141W) dilated cardiomyopathy transgenic mice.

Lu D, Ma Y, Zhang W, Bao D, Dong W, Lian H, Huang L, Zhang L.

Hypertension. 2012 Jul;60(1):81-9. doi: 10.1161/HYPERTENSIONAHA.112.191478. Epub 2012 Jun 4.

17.

Transgenic mitochondrial superoxide dismutase and mitochondrially targeted catalase prevent antiretroviral-induced oxidative stress and cardiomyopathy.

Kohler JJ, Cucoranu I, Fields E, Green E, He S, Hoying A, Russ R, Abuin A, Johnson D, Hosseini SH, Raper CM, Lewis W.

Lab Invest. 2009 Jul;89(7):782-90. doi: 10.1038/labinvest.2009.39. Epub 2009 Apr 27.

18.

A case of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation.

Vallance HD, Jeven G, Wallace DC, Brown MD.

Pediatr Cardiol. 2004 Sep-Oct;25(5):538-40. Epub 2004 May 28.

PMID:
15164143
19.

Interdependence of Parkin-Mediated Mitophagy and Mitochondrial Fission in Adult Mouse Hearts.

Song M, Gong G, Burelle Y, Gustafsson ÅB, Kitsis RN, Matkovich SJ, Dorn GW 2nd.

Circ Res. 2015 Jul 31;117(4):346-51. doi: 10.1161/CIRCRESAHA.117.306859. Epub 2015 Jun 2.

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