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Biomedical subjects

M Julian

Publications and source records attributed to M Julian.

92 records · Page 6Linked to original sources

[Dermal aging. Immunofluorescence study of collagens I and III and fibronectin].

In this study the authors have studied 10 young subjects and 10 old subjects. The biopsies are examined by light microscopy, and by immunofluorescence techniques with specific antibodies against collagen I, III and fibronectin. In this last case the authors used also immunoelectron microscopy with peroxidase labeling and immunofluorescence techniques in fibroblasts cultures. The results showed that there was no difference in collagen localization in young and old subjects. But the fibronectin was found decreased in papillary dermis of old subjects. These results are confirmed in culture, where the fibrillar extracellular fibronectin was abundant in culture of young subjects and very poor in old subjects. The role of fibronectin will be very important in ageing, its decrease will explain the morphological modifications of dermal connective tissue with age.

Adult↗

[Communicating acute aortic dissection (pathogenetic study)].

Thirty-five dissecting aneurisms of the aorta (D.A.). have been microscopically and ultramicroscopically examined. These data have been compared to those obtained from personal experiences on human aorta aging, as well as from Beta Aminopropionitrile treated rats. The authors conceive D.A. as a non-obligatory complication of a precocious and intense medianecrosis of the aortic wall, particularly characterized by a mucous imbibition and a loss elastic laminae. This medianecrosis is identical in dysplasic D.A. (Martan's syndrome for example) and in acquired D.A. (rapid aging or arteriosclerosis). The simultaneous occurence of a medianecrosis and conditions triggering tunica intima rupture, with blood afflux in the necrotic zone are undoubtedly rare. This explains the small number of observed D.A. in comparison to the large number of aortas with accentuated medial lesions.

Aged↗