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Items: 14

1.

Grape Powder Improves Age-Related Decline in Mitochondrial and Kidney Functions in Fischer 344 Rats.

Pokkunuri I, Ali Q, Asghar M.

Oxid Med Cell Longev. 2016;2016:6135319. doi: 10.1155/2016/6135319.

2.

Leigh syndrome in Drosophila melanogaster: morphological and biochemical characterization of Surf1 post-transcriptional silencing.

Da-Rè C, von Stockum S, Biscontin A, Millino C, Cisotto P, Zordan MA, Zeviani M, Bernardi P, De Pittà C, Costa R.

J Biol Chem. 2014 Oct 17;289(42):29235-46. doi: 10.1074/jbc.M114.602938.

3.

SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors.

Renkema GH, Wortmann SB, Smeets RJ, Venselaar H, Antoine M, Visser G, Ben-Omran T, van den Heuvel LP, Timmers HJ, Smeitink JA, Rodenburg RJ.

Eur J Hum Genet. 2015 Feb;23(2):202-9. doi: 10.1038/ejhg.2014.80.

4.

SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease.

Echaniz-Laguna A, Ghezzi D, Chassagne M, Mayençon M, Padet S, Melchionda L, Rouvet I, Lannes B, Bozon D, Latour P, Zeviani M, Mousson de Camaret B.

Neurology. 2013 Oct 22;81(17):1523-30. doi: 10.1212/WNL.0b013e3182a4a518.

5.

SURF1 deficiency: a multi-centre natural history study.

Wedatilake Y, Brown RM, McFarland R, Yaplito-Lee J, Morris AA, Champion M, Jardine PE, Clarke A, Thorburn DR, Taylor RW, Land JM, Forrest K, Dobbie A, Simmons L, Aasheim ET, Ketteridge D, Hanrahan D, Chakrapani A, Brown GK, Rahman S.

Orphanet J Rare Dis. 2013 Jul 5;8:96. doi: 10.1186/1750-1172-8-96.

6.

The power of yeast to model diseases of the powerhouse of the cell.

Baile MG, Claypool SM.

Front Biosci (Landmark Ed). 2013 Jan 1;18:241-78. Review.

7.

Rescue of PINK1 protein null-specific mitochondrial complex IV deficits by ginsenoside Re activation of nitric oxide signaling.

Kim KH, Song K, Yoon SH, Shehzad O, Kim YS, Son JH.

J Biol Chem. 2012 Dec 28;287(53):44109-20. doi: 10.1074/jbc.M112.408146.

8.

Mitochondrial disorders of the nuclear genome.

Angelini C, Bello L, Spinazzi M, Ferrati C.

Acta Myol. 2009 Jul;28(1):16-23.

9.

Chromosome conformation capture of all 13 genomic Loci in the transcriptional regulation of the multisubunit bigenomic cytochrome C oxidase in neurons.

Dhar SS, Ongwijitwat S, Wong-Riley MT.

J Biol Chem. 2009 Jul 10;284(28):18644-50. doi: 10.1074/jbc.M109.019976.

10.

Light and electron microscopy characteristics of the muscle of patients with SURF1 gene mutations associated with Leigh disease.

Pronicki M, Matyja E, Piekutowska-Abramczuk D, Szymanska-Debinska T, Karkucinska-Wieckowska A, Karczmarewicz E, Grajkowska W, Kmiec T, Popowska E, Sykut-Cegielska J.

J Clin Pathol. 2008 Apr;61(4):460-6.

11.

Mutations in cytochrome c oxidase subunit VIa cause neurodegeneration and motor dysfunction in Drosophila.

Liu W, Gnanasambandam R, Benjamin J, Kaur G, Getman PB, Siegel AJ, Shortridge RD, Singh S.

Genetics. 2007 Jun;176(2):937-46.

12.

Defective splicing, disease and therapy: searching for master checkpoints in exon definition.

Buratti E, Baralle M, Baralle FE.

Nucleic Acids Res. 2006 Jul 19;34(12):3494-510. Review.

13.

Post-transcriptional silencing and functional characterization of the Drosophila melanogaster homolog of human Surf1.

Zordan MA, Cisotto P, Benna C, Agostino A, Rizzo G, Piccin A, Pegoraro M, Sandrelli F, Perini G, Tognon G, De Caro R, Peron S, Kronniè TT, Megighian A, Reggiani C, Zeviani M, Costa R.

Genetics. 2006 Jan;172(1):229-41.

14.

Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1.

Stiburek L, Vesela K, Hansikova H, Pecina P, Tesarova M, Cerna L, Houstek J, Zeman J.

Biochem J. 2005 Dec 15;392(Pt 3):625-32.

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