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Page 1
The metabolism and disposition of the oral dipeptidyl peptidase-4 inhibitor, linagliptin, in humans.
Drug Metab Dispos. 2010 Apr;38(4):667-78. doi: 10.1124/dmd.109.031476. Epub 2010 Jan 19.
Drug Metab Dispos. 2010.
PMID: 20086031
Clinical Trial.
Fecal excretion was the dominant excretion pathway with 84.7% (p.o.) and 58.2% (i.v.) of the dose. Renal excretion accounted for 5.4% (p.o.) and 30.8% (i.v.) of the dose. ...The exposure (area under the curve 0-24 h) to the parent compound in plasma accounted for 19 …
Fecal excretion was the dominant excretion pathway with 84.7% (p.o.) and 58.2% (i.v.) of the dose. Renal excretion accounted for 5.4% …
[Ribonuclease activity following partial hepatectomy in the liver of healthy and alloxan diabetic rats and histological findings in the islets of Langerhans (author's transl)].
Blech W, Weiss I.
Blech W, et al.
Exp Pathol (Jena). 1975;10(1-2):28-38.
Exp Pathol (Jena). 1975.
PMID: 786709
German.
Protein measurement was performed after the method of LOWREY (LOWREY et al. 1951) as modified by GLASER and KLEINE (1962); blood sugar was determined in tail vein blood by means of o-toluidine technique. In the liver homogenate with ethyl alcohol the RNA extraction was mod …
Protein measurement was performed after the method of LOWREY (LOWREY et al. 1951) as modified by GLASER and KLEINE (1962); blood sugar was d …
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[Degradation and association of glucagon by intact human erythrocytes].
Hildebrandt W, Dudek S, Blech W.
Hildebrandt W, et al.
Biomed Biochim Acta. 1989;48(8):509-15.
Biomed Biochim Acta. 1989.
PMID: 2619724
German.
This degrading activity was quantitatively inhibited by Contrykal, EDTA, and o-phenanthroline. Both glucagon degradation and association by human red cells were quantitatively inhibited by bacitracin. ...
This degrading activity was quantitatively inhibited by Contrykal, EDTA, and o-phenanthroline. Both glucagon degradation and associat …
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[Proteolytic degradation of glucagon by human erythrocytes].
Hildebrandt W, Wiederanders B, Brömme HJ, Blech W.
Hildebrandt W, et al.
Biomed Biochim Acta. 1985;44(11-12):1599-608.
Biomed Biochim Acta. 1985.
PMID: 3911953
German.
The enzyme which likely belongs to the class of insulin-glucagon-proteinases, can be inhibited by chelating agents, such as ethylenediamine tetraacetic acid and o-phenanthroline, thiol blocking reagents, such as p-chloromercuribenzoate and N-ethylmaleimide as well as by pr …
The enzyme which likely belongs to the class of insulin-glucagon-proteinases, can be inhibited by chelating agents, such as ethylenediamine …
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