395 related articles for article (PubMed ID: 30848931)
1. Increased dNTP pools rescue mtDNA depletion in human POLG-deficient fibroblasts.
Blázquez-Bermejo C; Carreño-Gago L; Molina-Granada D; Aguirre J; Ramón J; Torres-Torronteras J; Cabrera-Pérez R; Martín MÁ; Domínguez-González C; de la Cruz X; Lombès A; García-Arumí E; Martí R; Cámara Y
FASEB J; 2019 Jun; 33(6):7168-7179. PubMed ID: 30848931
[TBL] [Abstract][Full Text] [Related]
2. Deoxyribonucleoside treatment rescues EtBr-induced mtDNA depletion in iPSC-derived neural stem cells with POLG mutations.
Kristiansen CK; Furriol J; Chen A; Sullivan GJ; Bindoff LA; Liang KX
FASEB J; 2023 Sep; 37(9):e23139. PubMed ID: 37584631
[TBL] [Abstract][Full Text] [Related]
3. POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts.
Stewart JD; Schoeler S; Sitarz KS; Horvath R; Hallmann K; Pyle A; Yu-Wai-Man P; Taylor RW; Samuels DC; Kunz WS; Chinnery PF
Biochim Biophys Acta; 2011 Mar; 1812(3):321-5. PubMed ID: 21138766
[TBL] [Abstract][Full Text] [Related]
4. Mammalian ribonucleotide reductase subunit p53R2 is required for mitochondrial DNA replication and DNA repair in quiescent cells.
Pontarin G; Ferraro P; Bee L; Reichard P; Bianchi V
Proc Natl Acad Sci U S A; 2012 Aug; 109(33):13302-7. PubMed ID: 22847445
[TBL] [Abstract][Full Text] [Related]
5. Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population.
González-Vioque E; Blázquez A; Fernández-Moreira D; Bornstein B; Bautista J; Arpa J; Navarro C; Campos Y; Fernández-Moreno MA; Garesse R; Arenas J; Martín MA
Arch Neurol; 2006 Jan; 63(1):107-11. PubMed ID: 16401742
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial deoxyribonucleotide pools in deoxyguanosine kinase deficiency.
Saada A
Mol Genet Metab; 2008 Nov; 95(3):169-73. PubMed ID: 18723380
[TBL] [Abstract][Full Text] [Related]
7. Genetic and chemical rescue of the Saccharomyces cerevisiae phenotype induced by mitochondrial DNA polymerase mutations associated with progressive external ophthalmoplegia in humans.
Baruffini E; Lodi T; Dallabona C; Puglisi A; Zeviani M; Ferrero I
Hum Mol Genet; 2006 Oct; 15(19):2846-55. PubMed ID: 16940310
[TBL] [Abstract][Full Text] [Related]
8. Limited dCTP availability accounts for mitochondrial DNA depletion in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
González-Vioque E; Torres-Torronteras J; Andreu AL; Martí R
PLoS Genet; 2011 Mar; 7(3):e1002035. PubMed ID: 21483760
[TBL] [Abstract][Full Text] [Related]
9. Combined use of Saccharomyces cerevisiae, Caenorhabditis elegans and patient fibroblasts leads to the identification of clofilium tosylate as a potential therapeutic chemical against POLG-related diseases.
Pitayu L; Baruffini E; Rodier C; Rötig A; Lodi T; Delahodde A
Hum Mol Genet; 2016 Feb; 25(4):715-27. PubMed ID: 26692522
[TBL] [Abstract][Full Text] [Related]
10. The molecular characterisation of mitochondrial DNA deficient oocytes using a pig model.
Tsai TS; Tyagi S; St John JC
Hum Reprod; 2018 May; 33(5):942-953. PubMed ID: 29546367
[TBL] [Abstract][Full Text] [Related]
11. No correlation between mtDNA amount and methylation levels at the CpG island of
Steffann J; Pouliet A; Adjal H; Bole C; Fourrage C; Martinovic J; Rolland-Galmiche L; Rotig A; Tores F; Munnich A; Bonnefont JP
J Med Genet; 2017 May; 54(5):324-329. PubMed ID: 28069933
[TBL] [Abstract][Full Text] [Related]
12. Mitochondrial deoxyribonucleoside triphosphate pools in thymidine kinase 2 deficiency.
Saada A; Ben-Shalom E; Zyslin R; Miller C; Mandel H; Elpeleg O
Biochem Biophys Res Commun; 2003 Oct; 310(3):963-6. PubMed ID: 14550298
[TBL] [Abstract][Full Text] [Related]
13. In vivo functional analysis of the human mitochondrial DNA polymerase POLG expressed in cultured human cells.
Spelbrink JN; Toivonen JM; Hakkaart GA; Kurkela JM; Cooper HM; Lehtinen SK; Lecrenier N; Back JW; Speijer D; Foury F; Jacobs HT
J Biol Chem; 2000 Aug; 275(32):24818-28. PubMed ID: 10827171
[TBL] [Abstract][Full Text] [Related]
14. Depletion of the other genome-mitochondrial DNA depletion syndromes in humans.
Elpeleg O; Mandel H; Saada A
J Mol Med (Berl); 2002 Jul; 80(7):389-96. PubMed ID: 12110944
[TBL] [Abstract][Full Text] [Related]
15. The mtDNA mutation spectrum in the PolG mutator mouse reveals germline and somatic selection.
Maclaine KD; Stebbings KA; Llano DA; Havird JC
BMC Genom Data; 2021 Nov; 22(1):52. PubMed ID: 34823474
[TBL] [Abstract][Full Text] [Related]
16. The Saccharomyces cerevisiae mitochondrial DNA polymerase and its contribution to the knowledge about human POLG-related disorders.
Gilea AI; Magistrati M; Notaroberto I; Tiso N; Dallabona C; Baruffini E
IUBMB Life; 2023 Dec; 75(12):983-1002. PubMed ID: 37470284
[TBL] [Abstract][Full Text] [Related]
17. The mitochondrial DNA polymerase gamma degrades linear DNA fragments precluding the formation of deletions.
Nissanka N; Bacman SR; Plastini MJ; Moraes CT
Nat Commun; 2018 Jun; 9(1):2491. PubMed ID: 29950568
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic study.
Müller-Höcker J; Horvath R; Schäfer S; Hessel H; Müller-Felber W; Kühr J; Copeland WC; Seibel P
J Cell Mol Med; 2011 Feb; 15(2):445-56. PubMed ID: 19538466
[TBL] [Abstract][Full Text] [Related]
19. Increased burden of mitochondrial DNA deletions and point mutations in early-onset age-related hearing loss in mitochondrial mutator mice.
Kim MJ; Haroon S; Chen GD; Ding D; Wanagat J; Liu L; Zhang Y; White K; Park HJ; Han C; Boyd K; Caicedo I; Evans K; Linser PJ; Tanokura M; Prolla T; Salvi R; Vermulst M; Someya S
Exp Gerontol; 2019 Oct; 125():110675. PubMed ID: 31344454
[TBL] [Abstract][Full Text] [Related]
20. De Novo Development of mtDNA Deletion Due to Decreased POLG and SSBP1 Expression in Humans.
Lee Y; Kim T; Lee M; So S; Karagozlu MZ; Seo GH; Choi IH; Lee PCW; Kim CJ; Kang E; Lee BH
Genes (Basel); 2021 Feb; 12(2):. PubMed ID: 33671400
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
