This article deals with and compares cell cycle information obtained in mouse and in human epidermis in vivo. In order to compare data in mouse and in man, DNA labeling and mitotic index experiments were performed to obtain cell cycle information in normal human epidermis in vivo. Experiments were also performed on genetically inbred and outbred strains of mice—to provide a clue to the differences observed between mouse and man. The article makes the following points:1. In contrast to mouse epidermis, there are no consistent diurnal fluctuations in and there is no cell kinetic relationship between mitotic and DNA-labeling indices in normal human epidermis in vivo. The variability from individual to individual in human subjects and the lack ...
Epidermal cells were separated from newborn mouse skin and grown on glass chamber slides or in plast...
In previous studies, the rates of epidermal glycolysis and amino acid incorporation were found to pa...
The purpose of this investigation was to characterize the [3H]thymidine label-retaining and the “mat...
This article deals with and compares cell cycle information obtained in mouse and in human epidermis...
Labeling and mitotic index data and estimates for the length of the S and M phases of the cell cycle...
Cell kinetic perturbations that resulted in a wave of increased cell division during the 6-8hr lag p...
In order to obtain information on the distribution of total cell cycle times in hairless mouse epide...
Cell kinetic perturbations that resulted in a wave of increased cell division during the 6–8hr lag p...
In order to obtain information on the distribution of total cell cycle times in hairless mouse epide...
Includes bibliographical references."Research supported by the United States Atomic Energy Commissio...
A detailed examination of cell proliferation kinetics in normal human epidermis is presented. Using ...
The data from published studies of circadian rhythms in epidermal cell proliferation in mice, rats, ...
Cantharidin application to mouse skin induces cell injury followed by a regenerative wave of cells e...
Cell kinetic perturbations that resulted in a wave of increased cell division during the 6–8hr lag p...
A heavy water (2H2O) labeling method recently developed to measure cell proliferation in vivo is app...
Epidermal cells were separated from newborn mouse skin and grown on glass chamber slides or in plast...
In previous studies, the rates of epidermal glycolysis and amino acid incorporation were found to pa...
The purpose of this investigation was to characterize the [3H]thymidine label-retaining and the “mat...
This article deals with and compares cell cycle information obtained in mouse and in human epidermis...
Labeling and mitotic index data and estimates for the length of the S and M phases of the cell cycle...
Cell kinetic perturbations that resulted in a wave of increased cell division during the 6-8hr lag p...
In order to obtain information on the distribution of total cell cycle times in hairless mouse epide...
Cell kinetic perturbations that resulted in a wave of increased cell division during the 6–8hr lag p...
In order to obtain information on the distribution of total cell cycle times in hairless mouse epide...
Includes bibliographical references."Research supported by the United States Atomic Energy Commissio...
A detailed examination of cell proliferation kinetics in normal human epidermis is presented. Using ...
The data from published studies of circadian rhythms in epidermal cell proliferation in mice, rats, ...
Cantharidin application to mouse skin induces cell injury followed by a regenerative wave of cells e...
Cell kinetic perturbations that resulted in a wave of increased cell division during the 6–8hr lag p...
A heavy water (2H2O) labeling method recently developed to measure cell proliferation in vivo is app...
Epidermal cells were separated from newborn mouse skin and grown on glass chamber slides or in plast...
In previous studies, the rates of epidermal glycolysis and amino acid incorporation were found to pa...
The purpose of this investigation was to characterize the [3H]thymidine label-retaining and the “mat...