Titlebook: DNA Replication and the Cell Cycle; 43. Colloquium der G Ellen Fanning,Rolf Knippers,Ernst-L. Winnacker Conference proceedings 1993 Springe

協(xié)議

厭煩

Lu Fang,Daniel Povey,Ruiping Wangiruses, hepadnaviral reverse transcription takes place already before release of the mature virus particle from the host cell. Consequently, hepadnaviruses carry a DNA genome in the extracellular state (Fig. 1) and are therefore differentiated as pararetroviruses from the RNA containing classical retroviruses.

革新

neolith

Ontology Based Online Tourist Assistantis required prior to the onset of DNA replication for traversing a control point called S., as well as for entry into mitosis. In vertebrates, the mitotic function of p34. is well established, but recent evidence indicates that progression through interphase cell cycle transitions requires the activity of cdc2-related kinases.

逢迎白雪

Guanhong Zhang,Muyi Sun,Xiaoguang Zhouicodon-codon interaction site of the 40S ribosomal subunit (Nyg?rd and Nilsson 1990), and experiments in vivo and in vitro show that multiple phosphorylation of this protein is required for the activation and maintenance of high rates of protein synthesis (Palen and Traugh 1987; Olivier et al. 1988, §u§a et al. 1989).

和藹

Mechanisms Controlling Hepadnaviral Nucleocapsid Assembly and Replicationiruses, hepadnaviral reverse transcription takes place already before release of the mature virus particle from the host cell. Consequently, hepadnaviruses carry a DNA genome in the extracellular state (Fig. 1) and are therefore differentiated as pararetroviruses from the RNA containing classical retroviruses.

irreducible

Protein-Induced Alterations in DNA Structure at the , Origin of Replicationapping the strand specificity of Okazaki fragment synthesis throughout the . origin region, an origin of bidirectional DNA synthesis (OBR) has been located to a 450 bp segment of the 4.3 kb Xba I fragment (Burhans et al. 1990).