Výsledky vyhledávání

Histoenzymatic study of human renal tissue preservation: II--Catalase activity in proximal tubular cells is uncorrelated with transplant evolution

Autor: L, Benkoël, A, Chamlian, V, di Marino, J, Brisse, A, Chollat-Namy, J M, Gulian, P, Bongrand

Publikováno v: Cellular and molecular biology (Noisy-le-Grand, France). 40(6)

Enzyme histochemical activity of catalase, a peroxisomal enzyme involved in cellular antioxidant systems, was studied in proximal tubular cells of human renal transplants as a marker of ischemia-reperfusion injury in the prediction of the evolution o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::eda914530eb3c017939075bd2235eb67
https://pubmed.ncbi.nlm.nih.gov/7812189

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24 Hour-Hypothermic Preservation of Rat Liver with Euro-Collins and UW Solutions. Comparative Evaluation by 31P NMR Spectroscopy, Biochemical Assays and Light Microscopy

Autor: F. Desmoulin, C. Scheiner, Patrick J. Cozzone, Michel Charrel, S. Masson, J-M. Gulian, C. Dalmasso

Publikováno v: Drugs and the Liver: High Risk Patients and Transplantation ISBN: 9789401057486

Advances in liver preservation had been slow, until Jamieson et al. (1) described a successful long-term cold-preservation of the dog liver based on the use of a lactobionatecontaining solution. However, additional progress has remained limited for t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::65996ddc5052b1c4ccdc6e8b185e44ee
https://doi.org/10.1007/978-94-011-1994-8_13

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Loss of endoplasmic reticulum membrane integrity: an image analysis of the glucose-6-phosphatase system in human hepatocyte

Autor: A, Chamlian, L, Benkoel, J M, Gulian, P, Bongrand, J, Brisse, C, Dalmasso, A M, Benoliel

Publikováno v: Cellular and molecular biology. 38(3)

Histochemical and cytochemical methods induce a loss of endoplasmic reticulum (ER) membrane integrity in hepatocytes. In order to evaluate the degree of ER membrane integrity, glucose-6-phosphatase (G6P-A) was localized in light and electron microsco

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::90511f81e4d4ab256c120acb108f99b1
https://pubmed.ncbi.nlm.nih.gov/1319283

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[Comparative study of LpAI lipoparticles, HDL cholesterol and apolipoprotein AI in a control population, in a group of subjects with coronary diseases, and in a group of subjects with angiographically normal coronary vessels]

Autor: J P, Ardissone, A, Cohen-Billiemaz, M, Heim, J M, Gulian, J P, Giordanella, M, Bory, M, Charrel

Publikováno v: Annales de biologie clinique. 50(3)

A new method for directly measuring LpAI lipoparticles containing apolipoprotein AI, but not apolipoprotein AII, is now disponible for laboratories. Concentrations of LpAI were measured in serum from 158 presumably healthy normolipidemic subjects (72

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::44b4443867a9c097016b955b7269f4e7
https://pubmed.ncbi.nlm.nih.gov/1456494

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Quantitative histochemical study of glucose-6-phosphatase in periportal and perivenous human hepatocytes

Autor: A, Chamlian, L, Benkoel, P, Bongrand, J M, Gulian, J, Brisse

Publikováno v: Cellular and molecular biology. 37(2)

The glucose-6-phosphatase activity of periportal and perivenous human hepatocytes was studied with a quantitative method. The results obtained with histogram of light intensity distributions indicate that the enzyme reaction was 1.3 to 2.5 fold highe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bda07353bd957454704b0e874c07835a
https://pubmed.ncbi.nlm.nih.gov/1652360

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[Acquired von Willebrand's disease, cryoglobulinemia and pseudoanalbuminemia in monoclonal dysglobulinemia]

Autor: J R, Harlé, P, Lefevre, M, Pesquié, M F, Aillaud, C, Dalmasso, J, Boucraut, J M, Gulian, J M, Karsenti, D, Bernard, M, Charrel

Publikováno v: Presse medicale (Paris, France : 1983). 19(36)

The authors report an exceptional case of complex monoclonal dysglobulinaemia characterized by cryoglobulinaemia, pseudoanalbuminaemia and acquired type 1 Von Willebrand's disease. All these biological abnormalities are consecutive to the formation o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3e1470c4a4dbc03c02ef4e06b3c1f591
https://pubmed.ncbi.nlm.nih.gov/2147267

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