000 01688 a2200421 4500
005 20250514160830.0
264 0 _c20031210
008 200312s 0 0 eng d
022 _a0022-3565
024 7 _a10.1124/jpet.102.052688
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aCarraway, Robert E
245 0 0 _aCa2+ channel blockers enhance neurotensin (NT) binding and inhibit NT-induced inositol phosphate formation in prostate cancer PC3 cells.
_h[electronic resource]
260 _bThe Journal of pharmacology and experimental therapeutics
_cNov 2003
300 _a640-50 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aBinding Sites
650 0 4 _aCalcium
_xpharmacology
650 0 4 _aCalcium Channel Blockers
_xpharmacology
650 0 4 _aEndocytosis
650 0 4 _aEnzyme Inhibitors
_xpharmacology
650 0 4 _aEpidermal Growth Factor
_xmetabolism
650 0 4 _aHumans
650 0 4 _aInositol Phosphates
_xmetabolism
650 0 4 _aIodine Radioisotopes
650 0 4 _aMale
650 0 4 _aNeurotensin
_xmetabolism
650 0 4 _aNifedipine
_xpharmacology
650 0 4 _aPhotoaffinity Labels
650 0 4 _aProstatic Neoplasms
_xpathology
650 0 4 _aProtein-Tyrosine Kinases
_xantagonists & inhibitors
650 0 4 _aReceptors, Neurotensin
_xmetabolism
650 0 4 _aTumor Cells, Cultured
700 1 _aGui, Xianyong
700 1 _aCochrane, David E
773 0 _tThe Journal of pharmacology and experimental therapeutics
_gvol. 307
_gno. 2
_gp. 640-50
856 4 0 _uhttps://doi.org/10.1124/jpet.102.052688
_zAvailable from publisher's website
999 _c14313337
_d14313337