標(biāo)題: Titlebook: DNA Replication and the Cell Cycle; 43. Colloquium der G Ellen Fanning,Rolf Knippers,Ernst-L. Winnacker Conference proceedings 1993 Springe [打印本頁(yè)] 作者: NO610 時(shí)間: 2025-3-21 17:25
書目名稱DNA Replication and the Cell Cycle影響因子(影響力)
書目名稱DNA Replication and the Cell Cycle影響因子(影響力)學(xué)科排名
書目名稱DNA Replication and the Cell Cycle網(wǎng)絡(luò)公開度
書目名稱DNA Replication and the Cell Cycle網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱DNA Replication and the Cell Cycle被引頻次
書目名稱DNA Replication and the Cell Cycle被引頻次學(xué)科排名
書目名稱DNA Replication and the Cell Cycle年度引用
書目名稱DNA Replication and the Cell Cycle年度引用學(xué)科排名
書目名稱DNA Replication and the Cell Cycle讀者反饋
書目名稱DNA Replication and the Cell Cycle讀者反饋學(xué)科排名
作者: CON 時(shí)間: 2025-3-21 23:49
https://doi.org/10.1007/978-981-13-2122-1ate for structure-function studies. Three amino acid segments (named Exo I, Exo II and Exo III), predicted to contain the critical amino acid residues forming the 3’–5’exonuclease active site, were identified in the N-terminal portion of ?29 DNA polymerase and other prokaryotic and eukaryotic DNA po作者: 切掉 時(shí)間: 2025-3-22 01:17 作者: 新鮮 時(shí)間: 2025-3-22 05:18 作者: 陳腐思想 時(shí)間: 2025-3-22 09:22
Protein-Primed Replication of Bacteriophage ?29 DNAate for structure-function studies. Three amino acid segments (named Exo I, Exo II and Exo III), predicted to contain the critical amino acid residues forming the 3’–5’exonuclease active site, were identified in the N-terminal portion of ?29 DNA polymerase and other prokaryotic and eukaryotic DNA po作者: lethal 時(shí)間: 2025-3-22 16:40 作者: lethal 時(shí)間: 2025-3-22 20:24 作者: 爆炸 時(shí)間: 2025-3-23 00:57 作者: 蛛絲 時(shí)間: 2025-3-23 01:40 作者: 老人病學(xué) 時(shí)間: 2025-3-23 07:30 作者: 繁忙 時(shí)間: 2025-3-23 11:07 作者: insomnia 時(shí)間: 2025-3-23 15:26 作者: 書法 時(shí)間: 2025-3-23 18:42 作者: Onerous 時(shí)間: 2025-3-24 00:48 作者: Banister 時(shí)間: 2025-3-24 03:27 作者: 美學(xué) 時(shí)間: 2025-3-24 09:52
M. F. Ahmed Shariff,Ruwan D. Nawarathnability to compare and contrast the mechanisms of DNA synthesis and the functions of the replicative enzymes. In much the same way, studies of the mammalian DNA viruses have contributed to an understanding of the enzymology of cellular DNA replication. The choice model system to date for understandin作者: Emmenagogue 時(shí)間: 2025-3-24 14:41 作者: Vasodilation 時(shí)間: 2025-3-24 18:11
Zeqi Chen,Yuehu Liu,Shaozhuo Zhai,Xinzhao Limation about protein phosphatases is available, a detailed understanding of the role of protein phosphorylation in modulating the function of cellular regulatory proteins has been difficult to achieve. Viral regulatory proteins, such as simian virus 40 (SV40) large tumor antigen (T Ag), represent an作者: Affectation 時(shí)間: 2025-3-24 21:14
Guanhong Zhang,Muyi Sun,Xiaoguang Zhoucell division (Pardee 1989). One such process is the activation of protein synthesis which is required not only for the G./G. transition, but also for cells to progress through G. and initiate DNA synthesis (Brooks 1977; Rossow et al. 1979). This event is associated with the phosphorylation of a num作者: flourish 時(shí)間: 2025-3-25 00:44
Zeqi Chen,Yuehu Liu,Shaozhuo Zhai,Xinzhao Litachment of ubiquitin, a small (8.5 kDa) and highly conserved protein, to proteolytic substrates prior to degradation (for reviews see Hershko 1991; Finley and Chau 1991; Jentsch et al. 1991, Jentsch 1992a; Jentsch 1992b). This pathway is highly selective and mediates the elimination of abnormal pro作者: 倔強(qiáng)不能 時(shí)間: 2025-3-25 03:35 作者: spinal-stenosis 時(shí)間: 2025-3-25 07:46 作者: Pudendal-Nerve 時(shí)間: 2025-3-25 13:33
Initiation of Bacteriophage λ DNA Replication in Vitro in a System Reconstituted with Purified ProteExtensive genetic and biochemical studies during the past three decades have established bacteriophage λ as a prototype for elucidation of the fundamental molecular mechanisms responsible for initiation and regulation of chromosomal DNA replication (see Keppel et al. 1988) for a recent review of λ DNA replication).作者: 制造 時(shí)間: 2025-3-25 18:43
https://doi.org/10.1007/978-3-642-77040-1Cell Cycle Control; DNA; Protein Phosphorylation; Proteinphosphorylierung; Replication, DNA; Replikation,作者: rheumatology 時(shí)間: 2025-3-25 21:46
978-3-642-77042-5Springer-Verlag Berlin Heidelberg 1993作者: Condense 時(shí)間: 2025-3-26 03:59
Colloquium der Gesellschaft für Biologische Chemie in Mosbach Badenhttp://image.papertrans.cn/d/image/260192.jpg作者: llibretto 時(shí)間: 2025-3-26 06:07 作者: 使入迷 時(shí)間: 2025-3-26 08:27 作者: Mumble 時(shí)間: 2025-3-26 15:59
Protein-Primed Replication of Bacteriophage ?29 DNAn which the ?29 DNA polymerase catalyzes the covalent linkage of dAMP to the OH group of serine 232 in the terminal protein. The ?29 DNA polymerase also catalyzes elongation, that proceeds by a strand-displacement mechanism (Blanco et al. 1989). In addition to initiation and DNA polymerization activ作者: 換話題 時(shí)間: 2025-3-26 20:33 作者: 可觸知 時(shí)間: 2025-3-26 23:54 作者: 慷慨援助 時(shí)間: 2025-3-27 03:30 作者: Fillet,Filet 時(shí)間: 2025-3-27 08:33
Eukaryotic Origins of DNA Replicationntral to control of the eukaryotic cell cycle (Laskey et al. 1989). In addition, initiation of DNA replication is coupled to programmed changes in gene expression that occur during the life of a single cell as well as during the development of multicellular organisms (Villarreal 1991). Therefore, un作者: 共棲 時(shí)間: 2025-3-27 11:47
Protein-Induced Alterations in DNA Structure at the , Origin of Replication the DNA sequences that encompass the origin of replication associated with the Chinese hamster dihydrofolate reductase . gene. A variety of experimental approaches suggests that replication of amplified . genes in die methotrexate-resistant variant of CHO cells, CHOC 400, initiates within a 4.3 kb 作者: MAIZE 時(shí)間: 2025-3-27 15:10
Mechanism and Control of Cellular DNA Replicationbility to compare and contrast the mechanisms of DNA synthesis and the functions of the replicative enzymes. In much the same way, studies of the mammalian DNA viruses have contributed to an understanding of the enzymology of cellular DNA replication. The choice model system to date for understandin作者: 放縱 時(shí)間: 2025-3-27 18:02 作者: 流出 時(shí)間: 2025-3-28 00:38 作者: amenity 時(shí)間: 2025-3-28 04:34
The Mitogen/Oncogene-Activated p70s6k: Its Role in the G0/G1 Transitioncell division (Pardee 1989). One such process is the activation of protein synthesis which is required not only for the G./G. transition, but also for cells to progress through G. and initiate DNA synthesis (Brooks 1977; Rossow et al. 1979). This event is associated with the phosphorylation of a num作者: 悠然 時(shí)間: 2025-3-28 06:47
Ubiquitin-Dependent Protein Degradationtachment of ubiquitin, a small (8.5 kDa) and highly conserved protein, to proteolytic substrates prior to degradation (for reviews see Hershko 1991; Finley and Chau 1991; Jentsch et al. 1991, Jentsch 1992a; Jentsch 1992b). This pathway is highly selective and mediates the elimination of abnormal pro作者: Osteoporosis 時(shí)間: 2025-3-28 14:09
Ternary Complex Formation at the Human c-, Serum Response Elementellular signalling pathway that leads to the rapid and transient transcriptional activation of a large family of genes, the so-called “immediate-early” genes (Almendrai et al. 1988; Bravo 1990). To attain a comprehensive understanding of cellular growth control will require the elucidation of the me作者: libertine 時(shí)間: 2025-3-28 15:01 作者: OVER 時(shí)間: 2025-3-28 20:17
M. F. Ahmed Shariff,Ruwan D. NawarathnaFurthermore, SV40 DNA exists in a chromatin structure that resembles the structure of cellular chromatin and therefore could be a useful model for chromosome, as well as DNA replication (Stillman 1986; DePamphilis and Bradley 1986; Cheng and Kelly 1989; Smith and Stillman 1989).作者: 雄偉 時(shí)間: 2025-3-29 01:58
Mechanism and Control of Cellular DNA ReplicationFurthermore, SV40 DNA exists in a chromatin structure that resembles the structure of cellular chromatin and therefore could be a useful model for chromosome, as well as DNA replication (Stillman 1986; DePamphilis and Bradley 1986; Cheng and Kelly 1989; Smith and Stillman 1989).作者: 繼而發(fā)生 時(shí)間: 2025-3-29 04:37
Protein-DNA Interaction at Yeast Replication Origins: An ARS Consensus Binding Protein from two-dimensional gel electrophoresis systems (Brewer and Fangman 1987; Huberman et al. 1987) that allow the separation of replication intermediates and the subsequent mapping of initiation sites for DNA replication.作者: 委派 時(shí)間: 2025-3-29 09:44 作者: 完全 時(shí)間: 2025-3-29 15:23
Ubiquitin-Dependent Protein Degradationteins and controls the half-lives of some regulatory proteins. Known targets include transcriptional regulators (Hochstrasser et al. 1991) p53 (Scheffner et al. 1990) and cyclins (Glotzer et al. 1991). In a number of eukaryotes, cyclin degradation is required to exit from mitosis.作者: Lipoprotein(A) 時(shí)間: 2025-3-29 19:33 作者: mechanical 時(shí)間: 2025-3-29 20:28 作者: TIGER 時(shí)間: 2025-3-30 03:30
Hong Tao,Chenping Hou,Dongyun Yi,Jubo Zhuparticipants as well as cyclin proteins that regulate the activity of the kinases (see E. Nigg and coworkers, this Vol., p 147). But other enzyme systems may also participate in signal transmission as, for example components of the ubiquitin-dependent protein degradation pathway (see S. Jentsch et al., this Vol., p. 177).作者: 并入 時(shí)間: 2025-3-30 07:59
Tao Tang,Yingxuan You,Ti Wang,Hong Liuadvancing replication fork requires the coordinate collaboration of different types of enzymes and other proteins which appear to be in a higher order structure to ensure the precise and rapid duplication of the more than 10. base pairs in higher eukaryotic cells.作者: 協(xié)議 時(shí)間: 2025-3-30 10:14 作者: 厭煩 時(shí)間: 2025-3-30 13:42
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.作者: 革新 時(shí)間: 2025-3-30 16:57 作者: neolith 時(shí)間: 2025-3-31 00:01
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.作者: 逢迎白雪 時(shí)間: 2025-3-31 02:44
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).作者: 和藹 時(shí)間: 2025-3-31 05:17
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.作者: irreducible 時(shí)間: 2025-3-31 09:13
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).
