Identification of neonatal grey lethal mice
β Scribed by Hollinshead, M. B. ;Schneider, L. C.
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 525 KB
- Volume
- 176
- Category
- Article
- ISSN
- 0003-276X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The grey lethal mouse is an osteopetrotic mutant which cannot be identified by its external appearance (grey fur) until eight days of age and dies within one month of birth. Techniques for the identification of neonatal mutants would greatly facilitate study of the pathogenesis of osteopetrosis and its early treatment.
Under hypothermal anesthesia, the left lower limbs of neonatal mice were amputated just above the knee joint. The external appearance of two day old amputated tibiae could be correlated with the external appearance of the mice at eight days of age. The diaphyses of normal tibiae appeared red under the dissecting microscope due to the presence of hemopoietic tissue occupying the central marrow cavity. Grey lethal tibiae appeared opaque because relatively more unresorbed bone occupied the center of the diaphysis.
Histologic examination showed that in normal mice at birth, the mandibular incisor extended posteriorly to the molar region of the jaw, but that in grey lethals dense bone prevented the incisor from growing posteriorly in this fashion.
π SIMILAR VOLUMES
## Abstract Many genes are known to function in a regionβspecific manner in the developing secondary palate. We have previously shown that __Shox2__βdeficient embryos die at midβgestation stage and develop an anterior clefting phenotype. Here, we show that mice carrying a conditional inactivation o
In addition to its proposed function in regulating serum IgG levels, the MHC class I-related neonatal Fc receptor (FcRn) is known to play a role in IgG transfer across rodent yolk sac and neonatal intestine. In contrast to humans, for which transplacental transfer of IgG appears to be the only mecha
## Communicated by Arnold Munnich Autosomal recessive malignant infantile osteopetrosis (ARO) is characterized by severe osteosclerosis, pathologic fractures, hepatosplenomegaly, and pancytopenia. The pathophysiological basis is inadequate bone resorption due to osteoclast dysfunction. In the major