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Cited by 952

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Death in Embryonic Systems: Death of cells is the usual accompaniment of embryonic growth and differentiation.

Saunders, John W.·1966·Science

Abstract

The principal conclusion to be drawn from the foregoing discussion is that the death of cells and the destruction of tissues, organs, and organ systems are programmed as normal morphogenetic events in the development of multicellular organisms. Death in embryonic systems may thus be explored within the same conceptual framework as growth and differentiation. The present exploration has revealed that death during embryogenesis serves utilitarian goals in some instances, at least, that its occurrence is subject to control by factors of the immediate cellular and humoral environment, and that aberrations in its normal pattern of expression provide the mechanism for realization of many mutant phenotypes. Hopefully, it has also pointed toward the appropriate formulation of some of the problems that confront us in understanding the control of death at the level of genetic transcription, the biochemical events which determine and accompany its occurrence, and the pathways of disposition and the developmental significance of disassembled cellular building blocks.

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Crossref · 10.1126/science.154.3749.604

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Metadata

Authors
Saunders, J. W.
Venue
Science
Published
1966-11-04
Volume
154
Issue
3749
Pages
604-612
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2024232113
Cited by
952
References
1
FWCI
9.18
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Death in Embryonic Systems: Death of cells is the usual accompaniment of embryonic growth and differentiation. https://app.cochat.ai/papers/10.1126/science.154.3749.604
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Saunders, J. W. (1966). Death in Embryonic Systems: Death of cells is the usual accompaniment of embryonic growth and differentiation. Science. https://doi.org/10.1126/science.154.3749.604

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.