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Titlebook: Biology of Aging and Development; G. Jeanette Thorbecke Book 1975 Springer Science+Business Media New York 1975 aging.biology.cancer.devel

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发表于 2025-3-21 19:31:00 | 显示全部楼层 |阅读模式
期刊全称Biology of Aging and Development
影响因子2023G. Jeanette Thorbecke
视频video
学科分类FASEB Monographs
图书封面Titlebook: Biology of Aging and Development;  G. Jeanette Thorbecke Book 1975 Springer Science+Business Media New York 1975 aging.biology.cancer.devel
影响因子"e of the reasons for all the F ASEB Societies to meet yearly is the possibility O to interrelate recent progress in diverse areas of research. The F ASEB Conferences have been organized to promote such interdisciplinary approaches. They center around a basic theme with the aim of discussing active research, in­ cluding widely divergent approaches, towards a better understanding of a general biological phenomenon. Because of the mounting interest in the subject of aging and development, this has been chosen as the theme for this year‘s symposia. We have necessarily been limited in the number of topics that could be covered. In our choice we have attempted to‘ select those facets of the main subject which at this time are gen­ erating active research interest among our membership. We have included invited speakers from abroad, such as Drs. Goldstein, Liew and Miller from Canada and Drs. Wolpert, Holliday and Williamson from England. I am sorry to say that the two speakers that we had invited from Russia, Dr. Frolkis, and from Czechoslovakia, Dr. Sterzl, were unable to attend.
Pindex Book 1975
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Current theories of biological aging genetic or epigenetic level. The error theory, the redundant message theory, the codon restriction theory, and the transcriptional event theory represent the major current conceptualizations of biological aging as held by most gerontologists. The finding that cultured normal human and animal cells
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Towards a theory of developmenthed by viewing the egg as containing a program for development, and considering the logical nature of the program by treating cells as automata and ignoring the details of molecular mechanisms. It is suggested that development is essentially a simple process, the cells having a limited repertoire of
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Expression of specific clones during B cell developmentese specificities were found to be present in slightly higher frequency in neonatal than in adult spleens. The parameters of stimulation of neonatal B cells were similar to those of adult B cells but the antibody-forming cell progeny of neonatal B cells produce predominantly .M rather than .G antibo
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