Xenopus Cdc7 executes its essential function early in S phase and is counteracted by checkpoint-regulated protein phosphatase 1

• المؤلفون الرئيسيون: Poh, W.T, Chadha, G.S, Gillespie, P.J, Kaldis, P, Blow, J.J
• مؤلفون آخرون: BIOCHEMISTRY
• التنسيق: مقال
• منشور في: 2020
• الموضوعات: 4 amino 7 tert butyl 5 (4 methylphenyl)pyrazolo[3,4 d]pyrimidine; CDC7 protein, Xenopus; cell cycle protein; enzyme inhibitor; etoposide; pha 767491; phosphoprotein phosphatase 1; piperidone derivative; protein serine threonine kinase; pyrrole derivative; Xenopus protein; animal; article; Cdc7; CHO cell line; chromatin; Cricetulus; DNA replication; drug antagonism; drug effect; enzymology; growth, development and aging; hamster; metabolism; oocyte; PHA-767491; phosphorylation; S phase cell cycle checkpoint; Xenopus; PP1; Animals; Cell Cycle Proteins; CHO Cells; Chromatin; Cricetinae; DNA Replication; Enzyme Inhibitors; Etoposide; Ovum; Phosphorylation; Piperidones; Protein Phosphatase 1; Protein-Serine-Threonine Kinases; Pyrroles; S Phase Cell Cycle Checkpoints; Xenopus Proteins
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/182031
• المؤسسة: National University of Singapore

10.1098/rsob.130138