Syngeneic transplantation of rat pancreatic islets into the spleen. Light and electron microscopical findings
International Journal of Pancreatology, ISSN: 1537-3649, Vol: 3, Issue: 1, Page: 59-72
1988
- 4Citations
- 4Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations4
- Citation Indexes4
- CrossRef4
- Captures4
- Readers4
Article Description
An islet transplantation model was established with the two congeneic Lewis rat strains LEW.1W and LEW.1A, which were made diabetic by a single i.p. injection of 50 mg/kg b.w. streptozotocin. Isolated neonatal islets of the two strains served as a graft. Syngeneic transplantation into the spleen resulted in permanent graft survival and in normoglycemia of streptozotocin diabetic rats of the two strains. 200 days after transplantation functionally intact islets were demonstrable in the spleen by histological, histochemical and electron microscopical investigations. Histochemical findings indicate an activation of interdigitating reticular cells in the white pulp and of macrophages in the red pulp of the spleen as consequences of the islet transplantation. In addition a few electron microscopical findings concerning possible interactions between host plasma cells, lymphocytes and transplanted beta cells of islets are described and discussed. © 1988 Elsevier Science Publishers B.V. (Biomedical Division).
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0023878436&origin=inward; http://dx.doi.org/10.1007/bf02788224; http://www.ncbi.nlm.nih.gov/pubmed/3127496; https://link.springer.com/10.1007/BF02788224; https://dx.doi.org/10.1007/bf02788224; https://link.springer.com/article/10.1007/BF02788224
Springer Science and Business Media LLC
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