Titlebook: International Cell Biology 1980–1981; Papers Presented at H. G. Schweiger Book 1981 Springer-Verlag Berlin Heidelberg 1981 biology.cell.ce

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書目名稱International Cell Biology 1980–1981影響因子(影響力)




書目名稱International Cell Biology 1980–1981影響因子(影響力)學(xué)科排名




書目名稱International Cell Biology 1980–1981網(wǎng)絡(luò)公開度




書目名稱International Cell Biology 1980–1981網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱International Cell Biology 1980–1981被引頻次




書目名稱International Cell Biology 1980–1981被引頻次學(xué)科排名




書目名稱International Cell Biology 1980–1981年度引用




書目名稱International Cell Biology 1980–1981年度引用學(xué)科排名




書目名稱International Cell Biology 1980–1981讀者反饋




書目名稱International Cell Biology 1980–1981讀者反饋學(xué)科排名

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tympanometry

Transcription of Complex Structural Genes in the , Oocyte Systeminitiation. To follow this question, transcription systems are needed that allow to measure the template activity of native genes as well as of artificially modified DNA sequences. In the last few years, a whole series of such systems have been developed, such as injection of DNA into oocytes (Colma

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Structures of the U-snRNAsit became apparent that the nucleoli were very complex structures that contained a variety of enzymes, nonhistone proteins, the rDNA and precursors of rRNA. It was not known at that time that in addition to many species of macromolecules involved in ribosome synthesis, nucleoli also contained slowly

formula

The Association of Small Nuclear RNA Species with Rapidly Sedimenting Subnuclear StructuresDingman and Peacock, 1968; Weinberg and Penman, 1968; Hodnett and Busch, 1968). Studies using cell fractionation procedures demonstrated the existence of a cytoplasmic group (small cytoplasmic RNA, scRNA) and a nuclear group (small nuclear RNA, snRNA) among these low molecular weight RNA species (Zi

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RNA Processing in Frog Oocytes Microinjected with Cloned Genes or changed almost at will. In order to study the function of these cloned genes, it is however necessary to bring them “back to life” in an eukaryotic cellular environment. This can be done by various means, such as the recent in vitro transcription systems or, as will be discussed here, by the int

Grievance

Composition and Structural Organization of Nuclear Ribonucleoprotein in Amphibian Oocytesty, in sucrose, of 1.18 g cm. and containing most of the rapidly-labelled hnRNA in association with a population of heterogeneously-sized polypeptides. After further disruptive treatment, the nucleoplasmic fraction resolves into three distinct components: (i) a fibrillar network with a density, in s

Entropion

hnRNP Protein Distribution in Various Differentiated Vertebrate Cellsc polyribosomes, there have been far fewer attempts made to examine the native forms of nuclear RNA molecules undergoing processing (for review, see Martin et al. 1980). Electron microscope studies (Miller and Bakken 1972; Angelier and Lacroix 1975; Puvion-Dutilleul et al. 1977) suggest that as nucl

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