148 related articles for article (PubMed ID: 14623087)
1. Mitochondrial deoxyguanosine kinase mutations and mitochondrial DNA depletion syndrome.
Wang L; Eriksson S
FEBS Lett; 2003 Nov; 554(3):319-22. PubMed ID: 14623087
[TBL] [Abstract][Full Text] [Related]
2. Molecular insight into mitochondrial DNA depletion syndrome in two patients with novel mutations in the deoxyguanosine kinase and thymidine kinase 2 genes.
Wang L; Limongelli A; Vila MR; Carrara F; Zeviani M; Eriksson S
Mol Genet Metab; 2005 Jan; 84(1):75-82. PubMed ID: 15639197
[TBL] [Abstract][Full Text] [Related]
3. The Deoxynucleoside Triphosphate Triphosphohydrolase Activity of SAMHD1 Protein Contributes to the Mitochondrial DNA Depletion Associated with Genetic Deficiency of Deoxyguanosine Kinase.
Franzolin E; Salata C; Bianchi V; Rampazzo C
J Biol Chem; 2015 Oct; 290(43):25986-96. PubMed ID: 26342080
[TBL] [Abstract][Full Text] [Related]
4. The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA.
Mandel H; Szargel R; Labay V; Elpeleg O; Saada A; Shalata A; Anbinder Y; Berkowitz D; Hartman C; Barak M; Eriksson S; Cohen N
Nat Genet; 2001 Nov; 29(3):337-41. PubMed ID: 11687800
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mitochondrial DNA depletion and dGK gene mutations.
Salviati L; Sacconi S; Mancuso M; Otaegui D; Camaño P; Marina A; Rabinowitz S; Shiffman R; Thompson K; Wilson CM; Feigenbaum A; Naini AB; Hirano M; Bonilla E; DiMauro S; Vu TH
Ann Neurol; 2002 Sep; 52(3):311-7. PubMed ID: 12205643
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial DNA depletion can be prevented by dGMP and dAMP supplementation in a resting culture of deoxyguanosine kinase-deficient fibroblasts.
Taanman JW; Muddle JR; Muntau AC
Hum Mol Genet; 2003 Aug; 12(15):1839-45. PubMed ID: 12874104
[TBL] [Abstract][Full Text] [Related]
8. Substrate specificity of human recombinant mitochondrial deoxyguanosine kinase with cytostatic and antiviral purine and pyrimidine analogs.
Sjöberg AH; Wang L; Eriksson S
Mol Pharmacol; 1998 Feb; 53(2):270-3. PubMed ID: 9463485
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy.
Saada A; Shaag A; Mandel H; Nevo Y; Eriksson S; Elpeleg O
Nat Genet; 2001 Nov; 29(3):342-4. PubMed ID: 11687801
[TBL] [Abstract][Full Text] [Related]
12. Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genes.
Mancuso M; Filosto M; Tsujino S; Lamperti C; Shanske S; Coquet M; Desnuelle C; DiMauro S
Arch Neurol; 2003 Oct; 60(10):1445-7. PubMed ID: 14568816
[TBL] [Abstract][Full Text] [Related]
13. POS5 gene of Saccharomyces cerevisiae encodes a mitochondrial NADH kinase required for stability of mitochondrial DNA.
Strand MK; Stuart GR; Longley MJ; Graziewicz MA; Dominick OC; Copeland WC
Eukaryot Cell; 2003 Aug; 2(4):809-20. PubMed ID: 12912900
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Phosphorylation of anticancer nucleoside analogs by human mitochondrial deoxyguanosine kinase.
Zhu C; Johansson M; Permert J; Karlsson A
Biochem Pharmacol; 1998 Oct; 56(8):1035-40. PubMed ID: 9776315
[TBL] [Abstract][Full Text] [Related]
16. Hepatocerebral mitochondrial DNA depletion syndrome caused by deoxyguanosine kinase (DGUOK) mutations.
Freisinger P; Fütterer N; Lankes E; Gempel K; Berger TM; Spalinger J; Hoerbe A; Schwantes C; Lindner M; Santer R; Burdelski M; Schaefer H; Setzer B; Walker UA; Horváth R
Arch Neurol; 2006 Aug; 63(8):1129-34. PubMed ID: 16908739
[TBL] [Abstract][Full Text] [Related]
17. Mutations within the putative active site of heterodimeric deoxyguanosine kinase block the allosteric activation of the deoxyadenosine kinase subunit.
Park I; Ives DH
J Biochem Mol Biol; 2002 Mar; 35(2):244-7. PubMed ID: 12297037
[TBL] [Abstract][Full Text] [Related]
18. Directed mutagenesis of deoxyguanosine site at arginine 79 up-regulates turnover on deoxyadenosine kinase subunit of heterodimeric enzyme from Lactobacillus acidophilus R26.
Hong YS; Ma GT; Ives DH
J Biol Chem; 1995 Mar; 270(12):6602-6. PubMed ID: 7896799
[TBL] [Abstract][Full Text] [Related]
19. Molecular mechanisms of mitochondrial DNA depletion diseases caused by deficiencies in enzymes in purine and pyrimidine metabolism.
Eriksson S; Wang L
Nucleosides Nucleotides Nucleic Acids; 2008 Jun; 27(6):800-8. PubMed ID: 18600543
[TBL] [Abstract][Full Text] [Related]
20. Apoptosis induces efflux of the mitochondrial matrix enzyme deoxyguanosine kinase.
Jüllig M; Eriksson S
J Biol Chem; 2001 Jun; 276(26):24000-4. PubMed ID: 11294860
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
