Results 251 to 260 of about 188,322 (318)
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Annals of Internal Medicine, 1971
Excerpt To the editor: Schriebman, Goransky De Koliren, and Arky (Ann Intern Med74:399-403, 1971) reported on a patient with metastatic insulinoma who had been treated with streptozotocin.
E, Piroska, E, Kollin
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Excerpt To the editor: Schriebman, Goransky De Koliren, and Arky (Ann Intern Med74:399-403, 1971) reported on a patient with metastatic insulinoma who had been treated with streptozotocin.
E, Piroska, E, Kollin
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Toxicology Mechanisms and Methods, 2019
The present study investigated the protective effect of hesperidin on carbohydrate metabolizing enzymes in streptozotocin-induced diabetic rats. Hesperidin was administered to streptozotocin-induced (40 mg/kg b.w.) diabetic rats at different dosages of ...
S. R, Nandhakumar E, Haseena Banu H
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The present study investigated the protective effect of hesperidin on carbohydrate metabolizing enzymes in streptozotocin-induced diabetic rats. Hesperidin was administered to streptozotocin-induced (40 mg/kg b.w.) diabetic rats at different dosages of ...
S. R, Nandhakumar E, Haseena Banu H
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Studies on streptozotocin diabetes
Diabetes, 1976Both alloxan and streptozotocin produce β-cell necrosis in the rat. Previous studies have shown protection against alloxan toxicity by D-glucose, D-mannose, and the nonmetabolized analogue 3-0-methyl-D-glucose and removal of this protective effect by D-mannoheptulose. The effect of several agents (i.v.
O P, Ganda, A A, Rossini, A A, Like
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Chemico-Biological Interactions, 2016
Streptozotocin (STZ) has been extensively used over the last three decades to induce diabetes in various animal species and to help screen for hypoglycemic drugs.
S. Goyal +6 more
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Streptozotocin (STZ) has been extensively used over the last three decades to induce diabetes in various animal species and to help screen for hypoglycemic drugs.
S. Goyal +6 more
semanticscholar +1 more source
Helvetica Chimica Acta, 1974
Gemäss Formelschema werden die Synthesen modifizierter Streptozotocine der Struktur 5 aus N‐Nitroso‐carbamoylaziden 3 und D‐Glucosamin, ihre α‐1,3,4,6‐Tetra‐O‐acetyl‐Derivate 6 und die vergleichsweise aus 1,3,4,6‐Tetra‐O‐acetyl‐β‐D‐glucosamin 7 hergestellten zu 6 anomeren β‐Tetraacetyl‐Derivate 9, beschrieben.
Arthur Meier +4 more
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Gemäss Formelschema werden die Synthesen modifizierter Streptozotocine der Struktur 5 aus N‐Nitroso‐carbamoylaziden 3 und D‐Glucosamin, ihre α‐1,3,4,6‐Tetra‐O‐acetyl‐Derivate 6 und die vergleichsweise aus 1,3,4,6‐Tetra‐O‐acetyl‐β‐D‐glucosamin 7 hergestellten zu 6 anomeren β‐Tetraacetyl‐Derivate 9, beschrieben.
Arthur Meier +4 more
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Research Journal of Pharmacy and Technology, 2019
The aims of this study were to determine the effect of various fractions of okra pods extract (VOPE) to the changes of fasting blood glucose, serum insulin, and GLUT4 density on streptozotocin-induced type-2 diabetic mice.
A. A. Zuraidah +3 more
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The aims of this study were to determine the effect of various fractions of okra pods extract (VOPE) to the changes of fasting blood glucose, serum insulin, and GLUT4 density on streptozotocin-induced type-2 diabetic mice.
A. A. Zuraidah +3 more
semanticscholar +1 more source
Influence of Porphyromonas gingivalis in gut microbiota of streptozotocin-induced diabetic mice.
Oral Diseases, 2019OBJECTIVES Increasing evidence suggests that periodontitis can exacerbate diabetes, and gut bacterial dysbiosis appears to be linked with the diabetic condition.
Anri Ohtsu +10 more
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Mutagenic activity of streptozotocin
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 1968Abstract Streptozotocin plus “cofactor” has been shown to be mutagenic for histidine requiring Salmonella typhimurium strains. The cofactor has been shown to be nonessential to this activity. Revertant frequency data presented indicate that streptozotocin and N-nitrosoguanidine have comparable activity.
S M, Kolbye, M S, Legator
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Streptozotocin and Metastatic Insulinoma
Annals of Internal Medicine, 1971Excerpt The Chemotherapy Program of the National Cancer Institute has among its major goals the development of new antineoplastic drugs.
S K, Carter, L, Broder, M, Friedman
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