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Molecular basis of specific inhibition of urokinase plasminogen activator by amiloride

Author
JANKUN, J1 2 ; SKRZYPCZAK-JANKUN, E1 3
[1] Urology Research Center, Department of Urology, Medical College of Ohio, Toledo, United States
[2] Department of Physiology and Molecular, Medicine, Medical College of Ohio, Toledo, United States
[3] Department of Chemistry, The University of Toledo, Toledo, United States
Source

Cancer biochemistry biophysics. 1999, Vol 17, Num 1-2, pp 109-123 ; ref : 16 ref

CODEN
CABCD4
ISSN
0305-7232
Scientific domain
Biochemistry, molecular biology, biophysics; Cell biology, histology; Medical oncology
Publisher
Gordon and Breach, London / Gordon and Breach, New York, NY / Gordon and Breach, Paris
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Activateur Amiloride Angiogenèse Anticancéreux Efficacité traitement Forme moléculaire Inhibiteur enzyme Peptidases Pharmacocinétique Plasminogène Activateur plasminogène urokinase Enzyme Hydrolases
Keyword (en)
Activator Amiloride Angiogenesis Antineoplastic agent Treatment efficiency Molecular form Enzyme inhibitor Peptidases Pharmacokinetics Plasminogen Enzyme Hydrolases
Keyword (es)
Activador Amilorida Angiogénesis Anticanceroso Eficacia tratamiento Forma molecular Inhibidor enzima Peptidases Farmacocinética Plasminógeno Enzima Hydrolases
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02R Antineoplastic agents / 002B02R02 Chemotherapy

Discipline
Pharmacological treatments
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
1965462

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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