Ca2+ channel blockers enhance neurotensin (NT) binding and inhibit NT-induced inositol phosphate formation in prostate cancer PC3 cells. [electronic resource]
Producer: 20031210Description: 640-50 p. digitalISSN:- 0022-3565
- Binding Sites
- Calcium -- pharmacology
- Calcium Channel Blockers -- pharmacology
- Endocytosis
- Enzyme Inhibitors -- pharmacology
- Epidermal Growth Factor -- metabolism
- Humans
- Inositol Phosphates -- metabolism
- Iodine Radioisotopes
- Male
- Neurotensin -- metabolism
- Nifedipine -- pharmacology
- Photoaffinity Labels
- Prostatic Neoplasms -- pathology
- Protein-Tyrosine Kinases -- antagonists & inhibitors
- Receptors, Neurotensin -- metabolism
- Tumor Cells, Cultured
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Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
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