324 related articles for article (PubMed ID: 26773591)
21. Novel deoxyguanosine kinase gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndrome.
Sezer T; Ozçay F; Balci O; Alehan F
J Child Neurol; 2015 Jan; 30(1):124-8. PubMed ID: 24423689
[TBL] [Abstract][Full Text] [Related]
22. [Digestive system disease as manifestation of the pleiotropic action of genes in mitochondrial dysfunction].
Hrechanina OIa; Hrechanina IuB; Husar VA; Molodan LV
Lik Sprava; 2014 Nov; (11):29-39. PubMed ID: 25528830
[TBL] [Abstract][Full Text] [Related]
23. The first founder DGUOK mutation associated with hepatocerebral mitochondrial DNA depletion syndrome.
Brahimi N; Jambou M; Sarzi E; Serre V; Boddaert N; Romano S; de Lonlay P; Slama A; Munnich A; Rötig A; Bonnefont JP; Lebre AS
Mol Genet Metab; 2009 Jul; 97(3):221-6. PubMed ID: 19394258
[TBL] [Abstract][Full Text] [Related]
24. Mitochondrial respiratory dysfunction-elicited oxidative stress and posttranslational protein modification in mitochondrial diseases.
Wu YT; Wu SB; Lee WY; Wei YH
Ann N Y Acad Sci; 2010 Jul; 1201():147-56. PubMed ID: 20649551
[TBL] [Abstract][Full Text] [Related]
25. [Redox state of the electron-transport carriers in cardiac mitochondria: a study by the method of low-temperature EPR spectroscopy].
Ruuge EK; Lakomkin VL; Timoshin AA
Biofizika; 1997; 42(6):1240-6. PubMed ID: 9490110
[TBL] [Abstract][Full Text] [Related]
26. Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions.
Ronchi D; Garone C; Bordoni A; Gutierrez Rios P; Calvo SE; Ripolone M; Ranieri M; Rizzuti M; Villa L; Magri F; Corti S; Bresolin N; Mootha VK; Moggio M; DiMauro S; Comi GP; Sciacco M
Brain; 2012 Nov; 135(Pt 11):3404-15. PubMed ID: 23043144
[TBL] [Abstract][Full Text] [Related]
27. In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromes.
Bulst S; Abicht A; Holinski-Feder E; Müller-Ziermann S; Koehler U; Thirion C; Walter MC; Stewart JD; Chinnery PF; Lochmüller H; Horvath R
Hum Mol Genet; 2009 May; 18(9):1590-9. PubMed ID: 19221117
[TBL] [Abstract][Full Text] [Related]
28. [Diagnosis and therapy of mitochondrial diseases].
Pál E
Ideggyogy Sz; 2012 Jul; 65(7-8):229-37. PubMed ID: 23074842
[TBL] [Abstract][Full Text] [Related]
29. Kinetic properties of mutant deoxyguanosine kinase in a case of reversible hepatic mtDNA depletion.
Mousson de Camaret B; Taanman JW; Padet S; Chassagne M; Mayençon M; Clerc-Renaud P; Mandon G; Zabot MT; Lachaux A; Bozon D
Biochem J; 2007 Mar; 402(2):377-85. PubMed ID: 17073823
[TBL] [Abstract][Full Text] [Related]
30. Deoxyribonucleoside kinases in mitochondrial DNA depletion.
Saada-Reisch A
Nucleosides Nucleotides Nucleic Acids; 2004 Oct; 23(8-9):1205-15. PubMed ID: 15571232
[TBL] [Abstract][Full Text] [Related]
31. Increased Electron Paramagnetic Resonance Signal Correlates with Mitochondrial Dysfunction and Oxidative Stress in an Alzheimer's disease Mouse Brain.
Fang D; Zhang Z; Li H; Yu Q; Douglas JT; Bratasz A; Kuppusamy P; Yan SS
J Alzheimers Dis; 2016; 51(2):571-80. PubMed ID: 26890765
[TBL] [Abstract][Full Text] [Related]
32. Mitochondrial hepatopathy in adults: a case series and review of the literature.
Cloots K; Verbeek J; Orlent H; Meersseman W; Cassiman D
Eur J Gastroenterol Hepatol; 2013 Aug; 25(8):892-8. PubMed ID: 23426270
[TBL] [Abstract][Full Text] [Related]
33. Mutation analysis in 16 patients with mtDNA depletion.
Carrozzo R; Bornstein B; Lucioli S; Campos Y; de la Pena P; Petit N; Dionisi-Vici C; Vilarinho L; Rizza T; Bertini E; Garesse R; Santorelli FM; Arenas J
Hum Mutat; 2003 Apr; 21(4):453-4. PubMed ID: 12655576
[TBL] [Abstract][Full Text] [Related]
34. Mitochondrial deoxyguanosine kinase is required for female fertility in mice.
Gao Y; Dong R; Yan J; Chen H; Sang L; Yao X; Fan D; Wang X; Zuo X; Zhang X; Yang S; Wu Z; Sun J
Acta Biochim Biophys Sin (Shanghai); 2024 Mar; 56(3):427-439. PubMed ID: 38327186
[TBL] [Abstract][Full Text] [Related]
35. Deoxyguanosine kinase deficiency: a report of four patients.
Ünal Ö; Hişmi B; Kılıç M; Gülşen HH; Coşkun T; Sivri SH; Dursun A; Yüce A; Tokatlı A
J Pediatr Endocrinol Metab; 2017 May; 30(6):697-702. PubMed ID: 28493820
[TBL] [Abstract][Full Text] [Related]
36. Does the patient have a mitochondrial encephalomyopathy?
DiMauro S; Bonilla E; De Vivo DC
J Child Neurol; 1999 Nov; 14 Suppl 1():S23-35. PubMed ID: 10593563
[TBL] [Abstract][Full Text] [Related]
37. Re-evaluation of the dysfunction of mitochondrial respiratory chain in skeletal muscle of patients with Parkinson's disease.
Winkler-Stuck K; Kirches E; Mawrin C; Dietzmann K; Lins H; Wallesch CW; Kunz WS; Wiedemann FR
J Neural Transm (Vienna); 2005 Apr; 112(4):499-518. PubMed ID: 15340872
[TBL] [Abstract][Full Text] [Related]
38. Incidence of Primary Mitochondrial Disease in Children Younger Than 2 Years Presenting With Acute Liver Failure.
McKiernan P; Ball S; Santra S; Foster K; Fratter C; Poulton J; Craig K; McFarland R; Rahman S; Hargreaves I; Gupte G; Sharif K; Taylor RW
J Pediatr Gastroenterol Nutr; 2016 Dec; 63(6):592-597. PubMed ID: 27482763
[TBL] [Abstract][Full Text] [Related]
39. Disorders of the mitochondria.
Treem WR; Sokol RJ
Semin Liver Dis; 1998; 18(3):237-53. PubMed ID: 9773424
[TBL] [Abstract][Full Text] [Related]
40. The clinical diagnosis of POLG disease and other mitochondrial DNA depletion disorders.
Cohen BH; Naviaux RK
Methods; 2010 Aug; 51(4):364-73. PubMed ID: 20558295
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
