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6. Wolfram Syndrome protein, Miner1, regulates sulphydryl redox status, the unfolded protein response, and Ca2+ homeostasis. Wiley SE; Andreyev AY; Divakaruni AS; Karisch R; Perkins G; Wall EA; van der Geer P; Chen YF; Tsai TF; Simon MI; Neel BG; Dixon JE; Murphy AN EMBO Mol Med; 2013 Jun; 5(6):904-18. PubMed ID: 23703906 [TBL] [Abstract][Full Text] [Related]
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8. The mitochondrial genome in Wolfram syndrome. Barrett TG; Scott-Brown M; Seller A; Bednarz A; Poulton K; Poulton J J Med Genet; 2000 Jun; 37(6):463-6. PubMed ID: 10928858 [No Abstract] [Full Text] [Related]
9. Role of Mitochondrial Dynamics in Neuronal Development: Mechanism for Wolfram Syndrome. Cagalinec M; Liiv M; Hodurova Z; Hickey MA; Vaarmann A; Mandel M; Zeb A; Choubey V; Kuum M; Safiulina D; Vasar E; Veksler V; Kaasik A PLoS Biol; 2016 Jul; 14(7):e1002511. PubMed ID: 27434582 [TBL] [Abstract][Full Text] [Related]
10. Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease. Rigoli L; Bramanti P; Di Bella C; De Luca F Pediatr Res; 2018 May; 83(5):921-929. PubMed ID: 29774890 [TBL] [Abstract][Full Text] [Related]
11. Do mtDNA deletions drive premature aging in mtDNA mutator mice? Kraytsberg Y; Simon DK; Turnbull DM; Khrapko K Aging Cell; 2009 Aug; 8(4):502-6. PubMed ID: 19416127 [TBL] [Abstract][Full Text] [Related]
12. Ageing: mice and mitochondria. Martin GM; Loeb LA Nature; 2004 May; 429(6990):357-9. PubMed ID: 15164048 [No Abstract] [Full Text] [Related]
13. Mitochondrial wrinkles: the first signs of ageing? Raftopoulou M Nat Cell Biol; 2005 Sep; 7(9):853. PubMed ID: 16136182 [No Abstract] [Full Text] [Related]
14. Accumulating mitochondrial DNA mutations drive premature hematopoietic aging phenotypes distinct from physiological stem cell aging. Norddahl GL; Pronk CJ; Wahlestedt M; Sten G; Nygren JM; Ugale A; Sigvardsson M; Bryder D Cell Stem Cell; 2011 May; 8(5):499-510. PubMed ID: 21549326 [TBL] [Abstract][Full Text] [Related]
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18. Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome. La Morgia C; Maresca A; Amore G; Gramegna LL; Carbonelli M; Scimonelli E; Danese A; Patergnani S; Caporali L; Tagliavini F; Del Dotto V; Capristo M; Sadun F; Barboni P; Savini G; Evangelisti S; Bianchini C; Valentino ML; Liguori R; Tonon C; Giorgi C; Pinton P; Lodi R; Carelli V Sci Rep; 2020 Mar; 10(1):4785. PubMed ID: 32179840 [TBL] [Abstract][Full Text] [Related]
19. Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy and deafness (DIDMOAD, Wolfram syndrome). Rötig A; Cormier V; Chatelain P; Francois R; Saudubray JM; Rustin P; Munnich A J Inherit Metab Dis; 1993; 16(3):527-30. PubMed ID: 7609443 [No Abstract] [Full Text] [Related]
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