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New PDF release: Biomembranes: Volume 2

By Arthur B. Pardee (auth.), Lionel A. Manson (eds.)

This quantity comprises the contributions to a symposium held at Gatlinburg, Tennessee, below the auspices of the Oak Ridge nationwide Laboratory, in April, 1971. some time past, those lawsuits had seemed as a complement to the magazine of mobile body structure. as a result of the nature of the topic ma­ terial and the relevance of the subject of the symposium to the readers of BIOMEMBRANES, it used to be agreed by means of the organizers of the symposium to put up the contributions of the partici­ pants as a separate quantity in BIOMEMBRANES. It were initially envisaged that, at times, the complaints of a convention whose subject material was once without delay on the topic of the scope of this sequence will be integrated. The lawsuits are being released precisely as they've been submitted to the Editor with no the standard editorial re­ V1S10n. this is often being performed to extend the rate of publica­ tion. for a similar rOeason, no indices were supplied because the time had to organize an sufficient topic index might have unnecessarily not on time booklet. integrated within the court cases are brief studies of a few workshops that have been held through the convention. The editor has bought first-class cooperation from either the organizers of the convention and the various participants to this quantity. If the scan is a hit, it truly is due to their promptness.

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Extra info for Biomembranes: Volume 2

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X2 C. Giller The very low surface tension (13) of Muller and Rudin type artificial bilayers « 1 dyn/cm) would indicate very close packing of the phospholipids in the bilayer. 2 at)40 dyn/cm and the number of phospholipid and cholesterol molecules per erythrocyte used by Korn (10), results in roughly 60-65% of the erythrocyte surface area (153 ~2) covered by the lipid bilayer. It is then clear that if this packing arrangement is assumed, there is not sufficient lipid to cover the total erythrocyte surface (see also 14).

The outer element consists of irregularly anastomosing tubules. Other materials appear to be transported from Nissl bodies to a highly-structured region of smooth ER which lies close to the innermost element of the Golgi stack. , flattened) portions and numerous long, irregularly anastomosing tubules. At least two types of lysosomes, dense bodies and coated vesicles, apparently form from GERL. GERL shows acid phosphatase activity but not the NDPase or TPPase activity characteristic of the innermost element of the Golgi stack.

Siccardi, Y. Hirota, and F. Jacob. 1910. On the process of cellular division in Escherichia coli. II. Membrane protein alterations associated with mutations affecting the initiation of DNA synthesis. , 52 : 15-89. , A. Lazdunski, and B. Shapiro. The interrelationship between membrane protein alteration and DNA synthesis in Escherichia coli. Biochemistry, in press. , B. Shapiro, Y. Hirota, and F. Jacob. 1911. On the process of cellular division in Escherichia coli. IV. Altered protein composition and turnover of the membrane of thermosensitive mutants defective in chromosome replication.

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