Titlebook: Cell Dynamics; Molecular Aspects of Masashi Tazawa Book 1989 Springer-Verlag/Wien 1989 cell

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書(shū)目名稱(chēng)Cell Dynamics影響因子(影響力)




書(shū)目名稱(chēng)Cell Dynamics影響因子(影響力)學(xué)科排名




書(shū)目名稱(chēng)Cell Dynamics網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱(chēng)Cell Dynamics網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




書(shū)目名稱(chēng)Cell Dynamics被引頻次




書(shū)目名稱(chēng)Cell Dynamics被引頻次學(xué)科排名




書(shū)目名稱(chēng)Cell Dynamics年度引用




書(shū)目名稱(chēng)Cell Dynamics年度引用學(xué)科排名




書(shū)目名稱(chēng)Cell Dynamics讀者反饋




書(shū)目名稱(chēng)Cell Dynamics讀者反饋學(xué)科排名

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Construction and Analysis of , Mutants with Defects in Actin-Binding Proteinsctive in specific components of the cytoskeleton. By a colony blot technique three mutants were detected that were defective in the F-actin crosslinking proteins aactinin and 120 kDa gelation factor and the F-actin fragmenting protein severin, respectively. Here we focus on the description of the a-

flutter

Condyle

Domain Structure of , Myosin Heavy Chainnhibited by physiological levels of Ca.. The involvement of the Ca-inhibition in regulating plasmodial motility is suggested by the Ca-dependent contraction of demembranated plasmodial cells (... 1981, . and . 1984, . and . 1986, 1986 a)..The domain structure of this myosin HC (230 K Mr) was studied

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Immunoelectron Microscopic Localization of the , 36,000-Dalton Actin Binding Protein on the Surface luble fraction prepared from the endoplasm at the electron microscopic resolution using immunogold reagents. The ABP-36 was specifically localized on the surfaces of vesicles of 0.5 to 1.0 μm in diameter, and the vesicles are often clustered. This Triton insoluble fraction binds exogenous added acti

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Manipulating Single Microtubulesotubules (which are only 25 nm in width) and other submicroscopic filaments with the light microscope. We then describe the asymmetric growth and shortening of freshly exposed micro-tubule ends observed with video-enhanced DIC microscopy. Plus and minus ends were exposed by cutting the microtubule w

外形

Cytochalasin-Induced Ultrastructural Alterations in , Pollen Tubess that occur in pollen tubes of . following treatment with cytochalasins. We utilize rapid freeze fixation and freeze substitution as a method superior to conventional chemical fixation for the preservation of cytoskeletal elements and membrane systems. The results show that either cytochalasin B or

Impugn

Pinocytosis and Locomotion of , XVII. Different Morphodynamic Forms of Endocytosis and Microfilament and to study the mode of membrane-microfilament interaction in .. The chemical nature of all applied substances has a distinct influence on the size and shape of pinocytotic invaginations in that channels are formed ranging from 16 ± 3 μm (divalent cations) to 47 ± 8 μm (monovalent cations) in leng

arrhythmic

Diffusion of Substances in the Cytoplasm and Across the Nuclear Envelope in Egg Cells protoplasm in sand dollar eggs and starfish and mouse oocytes microinjected with fluorescent substances. The diffusion rates of fluorescein (M.W.: 408.5) and FITC-dextran (M.W.: 39,000) in sand dollar egg cytoplasm were 20–30%, respectively of the diffusion rates of these substances in water. In st