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大鼠视网膜发育过程中增殖和细胞周期长度的定量分析。

Quantitative analysis of proliferation and cell cycle length during development of the rat retina.

作者信息

Alexiades M R, Cepko C

机构信息

Department of Genetics and Howard Hughes Medical Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Dev Dyn. 1996 Mar;205(3):293-307. doi: 10.1002/(SICI)1097-0177(199603)205:3<293::AID-AJA9>3.0.CO;2-D.

Abstract

The rat retina has been a useful model system for the study of the development of the central nervous system (CNS). In order to facilitate future studies on the mechanisms that control retinal growth, we have quantified the proliferation of retinal cells and the length of the cell cycle throughout development. For each day during development, the number of mitotic and postmitotic cells per retina, the proportion of cycling cells, S phase length, and cell cycle length were determined through quantification of cell numbers and 3H-thymidine labeling. As retinal development proceeds, the proportion of cycling cells decreases, and cell cycle length increases, in part due to an increase in S phase length.

摘要

大鼠视网膜一直是研究中枢神经系统(CNS)发育的有用模型系统。为了便于今后对控制视网膜生长机制的研究,我们在整个发育过程中对视网膜细胞的增殖和细胞周期长度进行了量化。在发育过程中的每一天,通过对细胞数量的量化和3H-胸腺嘧啶核苷标记,确定每个视网膜中有丝分裂和有丝分裂后细胞的数量、循环细胞的比例、S期长度和细胞周期长度。随着视网膜发育的进行,循环细胞的比例下降,细胞周期长度增加,部分原因是S期长度增加。

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