These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
9. Regulation of p53R2 and its role as potential target for cancer therapy. Wang X; Zhenchuk A; Wiman KG; Albertioni F Cancer Lett; 2009 Apr; 276(1):1-7. PubMed ID: 18760875 [TBL] [Abstract][Full Text] [Related]
10. [Effect of sturines A and B on DNA synthesis and ribonucleotide reductase and thymidine kinase activity in regenerating rat liver]. Silaeva SA; Khatsernova BIa; Danilova NI; Sheremet'evskaia TN; Iulikova EP Vopr Med Khim; 1980; 26(2):255-9. PubMed ID: 7006202 [TBL] [Abstract][Full Text] [Related]
11. Enzymatic property analysis of p53R2 subunit of human ribonucleotide reductase. Yen Y; Chu B; Yen C; Shih J; Zhou B Adv Enzyme Regul; 2006; 46():235-47. PubMed ID: 16846634 [No Abstract] [Full Text] [Related]
12. RRM2B-Mediated Regulation of Mitochondrial Activity and Inflammation under Oxidative Stress. Cho EC; Kuo ML; Cheng JH; Cheng YC; Hsieh YC; Liu YR; Hsieh RH; Yen Y Mediators Inflamm; 2015; 2015():287345. PubMed ID: 26089597 [TBL] [Abstract][Full Text] [Related]
13. Novel regulators and molecular mechanisms of p53R2 and its disease relevance. Cho EC; Yen Y Biochimie; 2016 Apr; 123():81-4. PubMed ID: 26796884 [TBL] [Abstract][Full Text] [Related]
14. [Molecular diagnosis of mitochondrial DNA deletion]. Murayama K Nihon Rinsho; 2002 Apr; 60 Suppl 4():261-5. PubMed ID: 12013861 [No Abstract] [Full Text] [Related]
15. Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene. Bornstein B; Area E; Flanigan KM; Ganesh J; Jayakar P; Swoboda KJ; Coku J; Naini A; Shanske S; Tanji K; Hirano M; DiMauro S Neuromuscul Disord; 2008 Jun; 18(6):453-9. PubMed ID: 18504129 [TBL] [Abstract][Full Text] [Related]
16. A genotoxicity test system based on p53R2 gene expression in human cells: assessment of its reactivity to various classes of genotoxic chemicals. Ohno K; Ishihata K; Tanaka-Azuma Y; Yamada T Mutat Res; 2008 Oct; 656(1-2):27-35. PubMed ID: 18674635 [TBL] [Abstract][Full Text] [Related]
18. Mitochondrial disorder with a common 4977-bp deletion presenting as a novel multisystem neurodegenerative disorder. Lane H; Bermingham N; Farrell MA; Redmond J; Connolly S; Brett FM Ir Med J; 2003 Sep; 96(8):249-50. PubMed ID: 14653385 [No Abstract] [Full Text] [Related]
19. Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system. Janssen AJ; Schuelke M; Smeitink JA; Trijbels FJ; Sengers RC; Lucke B; Wintjes LT; Morava E; van Engelen BG; Smits BW; Hol FA; Siers MH; Ter Laak H; van der Knaap MS; Van Spronsen FJ; Rodenburg RJ; van den Heuvel LP Ann Neurol; 2008 Apr; 63(4):473-81. PubMed ID: 18306232 [TBL] [Abstract][Full Text] [Related]
20. Excision of nucleoside analogs in mitochondria by p53 protein. Bakhanashvili M; Grinberg S; Bonda E; Rahav G AIDS; 2009 Apr; 23(7):779-88. PubMed ID: 19287302 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]