Titlebook: Nucleocytoplasmic Transport; Reiner Peters,Michael Trendelenburg Conference proceedings 1986 Springer-Verlag, Berlin Heidelberg 1986 bioch

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Identification of a Sequence in Influenza Virus Nucleoprotein Which Specifies Nuclear Accumulation est has focussed on two aspects of the accumulation process. First, studies have been directed at understanding the cellular mechanisms which underlie the observed nuclear accumulation. The selectivity of the uptake process (Bonner, 1975a,b; De Robertis et al., 1973; De Robertis and Black, 1981; Dab

isotope

Adenovirus E1A: Implications of a Post-Translational Modification for Nuclear Localization and Stimto the E1A gene product which include the . activation of other viral genes (1–3) and certain cellular genes (4,5), the immortalization and partial transformation of cells (6), and, when acting in concert with other oncogenes, the complete transformation of cells (7). Two mRNAs which are encoded by

CLAMP

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Modulation Methods and Slow Molecular Rotations,of the experiment. For example, a finding that D. for a membrane protein measured over a distance of a micron or more is exceeding slow (<. cm. s.) does not indicate whetehr the protein is trapped by anchorage to some immobile structrure (in which case D. would be low) or merely confined by a limiti

Torrid

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Giant Polysome Formation in , Salivary Gland Cells as Studied by Microdissection Techniques,. In another approach (2) cytoplasm with different amounts of endoplasmic reticulum (Fig. 2) is isolated (Fig. 3). The information obtained by these techniques can be used to draw conclusions regarding the mode of formation and function of the giant, GO ribosome-polysomes dominating the polysome pop

chandel

Hdl348

Intracellular Transport of a Karyophilic Protein,acterized and designated as N1-N4 and nucleoplasmin. Karyophilic proteins are also present in oocytes from amphibians other than Xenopus (Dabauvalle and Franke, 1982). However, their occurance in somatic cells is largely unresolved.

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