In a previous paper it was shown that the respiratory power of the cartilage cell declines with advancing age while the glycolytic power does not change (Rosentlial, Bowie and Wagoner, '41). I n the present communication data are presented concerning the structure of the respiratory system in articu
The dehydrogenatic ability of bovine articular cartilage in relation to its age
β Scribed by Rosenthal, Otto ;Bowie, Morris A. ;Wagoner, George
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1942
- Tongue
- English
- Weight
- 380 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0095-9898
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β¦ Synopsis
I n two previous papers the decline of the respiratory power of bovine articular cartilage ('41 a ) and the structure of the dehydrogenatic component of the respiratory system ('42) have been described. I n the present communication data are presented concerning the dehydrogenatic activity of bovine articular cartilage in different ages. I n particular, we shall deal with the question of whether the deterioration of the respiratory power in aging cartilage i s due to a diminution of the entire respiratory system or only of one of its two main components.
The experimental procedure has been described in the preceding papers.
π SIMILAR VOLUMES
The phenomenon of "growing old" is the summation of the degenerative changes which occur in all tissues. Some tissues undergo demonstrable degeneration at earlier ages than others. The degenerative changes are grossly apparent in some tissues and afford a definite index of the structural age of the
## Abstract The arcuate fasciculus is a major white matter tract involved in language processing that has also been repeatedly implicated in intelligence and reasoning tasks. Language in the human brain is lateralized in terms of both function and structure, and while the arcuate fasciculus reflect
## Objective: To determine the sites of cleavage and denaturation of type ii collagen (cii) by collagenase(s) in healthy and osteoarthritic (oa) human articular cartilage and their relationship to the distribution of matrix metalloproteinase 1 (mmp-1) and mmp-13. ## Methods: Single (per subject)