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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Experimental and Mol...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Experimental and Molecular Pathology
Article . 1967 . Peer-reviewed
License: Elsevier TDM
Data sources: Crossref
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Morphogenesis of human aortic coarctation

Authors: John U. Balis; An Soo Chan; Patrick E. Conen;

Morphogenesis of human aortic coarctation

Abstract

Abstract The congenital medial lesion of sortic coarctation was studied by light and electron microscopy. In aortas of young infants prominent morphological features of this lesion were interstitial edema, increased ground substance and proliferation of poorly differentiated smooth muscle cells. The latter contained large aggregates of glycogen granules and frequent profiles of dilated endoplasmic reticulum. Characteristic changes were observed in aortic coarctation with age. Thus, there was progressive accumulation of fibroelastic tissue in the extracellular space. Moreover, autophagic vacuoles, suggestive of focal cytoplasmic degradation, appeared in smooth muscle cells, which also revealed a gradual decrease in their glycogen content. Subsequently, there were frequent vacuolated areas in the cytoplasm which contained thin myofilaments associated with numerous clusters of ribosome particles. Elastic elements often showed evidence of degeneration in coarctations obtained from children older than 5 years. At this time, smooth muscle cells appeared well differentiated and contained scanty ergastoplasmic membranes. These observations suggest that the morphogenesis of arterial fibroelastosis is interrelated with various phases of cytodifferentiation. It is further suggested that aging of the arterial tissue is accelerated in areas of structural disorganization.

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Keywords

Male, Aging, Microscopy, Adolescent, Histocytochemistry, Infant, Newborn, Infant, Blood Pressure, Elastic Tissue, Endoplasmic Reticulum, Aortic Coarctation, Basement Membrane, Mitochondria, Microscopy, Electron, Child, Preschool, Humans, Female, Collagen, Extracellular Space, Glycogen

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    22
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
22
Average
Top 10%
Top 10%
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