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D. H. Williamson

Bio: D. H. Williamson is an academic researcher from Brewing Industry Research Foundation. The author has contributed to research in topics: Yeast & Protoplast. The author has an hindex of 5, co-authored 5 publications receiving 485 citations.

Papers
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Journal ArticleDOI
15 Jun 1957-Nature
TL;DR: Nečas3 showed that spontaneously autolysing yeast gave rise to a small extent to structures which, superficially at least, resembled protoplasts.
Abstract: A NEW approach to the structure and functions of the cell surface of certain bacteria was revealed when Weibull1 showed that, in the presence of sucrose, lysozyme dissolves the cell-wall, leaving the protoplast essentially intact. Various attempts have since been made to isolate protoplasts from bacteria normally insensitive to lysozyme2 and also from yeast. Thus Necas3 showed that spontaneously autolysing yeast gave rise to a small extent to structures which, superficially at least, resembled protoplasts.

215 citations

Journal ArticleDOI
TL;DR: The changes in dry mass, volume and oxygen uptake of synchronously dividing cultures of Saccharomyces cerevisiae were observed and a similar pattern of events was observed, except that cell volume started to increase soon after the start of the cell cycle.

55 citations


Cited by
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Julius Marmur1
TL;DR: A method has been described for the isolation of DNA from micro-organisms which yields stable, biologically active, highly polymerized preparations relatively free from protein and RNA, and Representative samples have been characterized for their thermal stability and sedimentation behaviour.

11,573 citations

Journal ArticleDOI
TL;DR: The bibliography is intended more as a guide to the literature than as a historically accurate record of the development of the field; the authors apologize to the earlier workers whose contributions thus get less explicit credit than they deserve.
Abstract: INTRODUCTION The cell cycle is the process of vegetative (asexual) cellular reproduction; in a normal cell cycle, one cell gives rise to two cells that are genetically identical to the original cell. Questions about the cell cycle can be conveniently divided into two categories. First, one can ask how a cell carries out a cell cycle, once it has undertaken to do so. Into this category fall questions about the morphological and biochemical aspects of cell-cycle events and about the mechanisms that ensure their temporal and functional coordination. Second, one can ask what determines when a cell will undertake a cell cycle, or how the overall control of cell proliferation is achieved. Into this category fall questions about the coordination of successive cell cycles, the coordination of growth with division, the coordination of cell proliferation with the availability of essential nutrients, and the selection of developmental alternatives. In the text that follows, we consider these two categories of questions in turn. Our bibliography is intended more as a guide to the literature than as a historically accurate record of the development of the field; we apologize to the earlier workers whose contributions thus get less explicit credit than they deserve. HOW DOES A CELL CARRY OUT A CELL CYCLE? As has often been noted, successful completion of a cell cycle requires a cell to integrate the processes that duplicate the cellular material with the processes that partition the duplicated material into two viable daughter cells. Another useful formulation of the...

1,099 citations

Journal ArticleDOI
TL;DR: It is proposed that the normal coordination of cell growth with cell division is a consequence of the following two relationships: growth, rather than progress through the DNA-division cycle, is normally rate-limiting for cell proliferation and a specific early event in G1 cannot be completed until a critical size is attained.

834 citations

Journal ArticleDOI

666 citations