| scholarly article | Q13442814 |
| P50 | author | Ian F. Musgrave | Q42211241 |
| P2093 | author name string | R Seifert | |
| K Wenzel-Seifert | |||
| D Krautwurst | |||
| P2860 | cites work | Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches | Q22337395 |
| A new generation of Ca2+ indicators with greatly improved fluorescence properties | Q27860793 | ||
| G-protein alpha-subunits in cytosolic and membranous fractions of human neutrophils | Q28243903 | ||
| Cyclophilin: a specific cytosolic binding protein for cyclosporin A | Q29620548 | ||
| The Ca2+ pump of the plasma membrane | Q35225011 | ||
| The superoxide-forming NADPH oxidase of phagocytes. An enzyme system regulated by multiple mechanisms. | Q36441621 | ||
| Role of Ca2(+)-ATPases in regulation of cellular Ca2+ signalling, as studied with the selective microsomal Ca2(+)-ATPase inhibitor, thapsigargin | Q37851724 | ||
| Signal transduction in cells following binding of chemoattractants to membrane receptors | Q39469822 | ||
| Immunophilins in protein folding and immunosuppression. | Q40388384 | ||
| Voltage-independent calcium channels. Regulation by receptors and intracellular calcium stores | Q40557340 | ||
| Receptor-activated Ca2+ influx: how many mechanisms for how many channels? | Q40752868 | ||
| Calcium influx and its control by calcium release | Q40857656 | ||
| The signal for capacitative calcium entry | Q40861260 | ||
| The class III antiarrhythmic drug amiodarone directly activates pertussis toxin-sensitive G proteins. | Q40995304 | ||
| The H1 receptor agonist 2-(3-chlorophenyl)histamine activates Gi proteins in HL-60 cells through a mechanism that is independent of known histamine receptor subtypes. | Q41038945 | ||
| Cyclopiazonic acid depletes intracellular Ca2+ stores and activates an influx pathway for divalent cations in HL-60 cells | Q41111892 | ||
| The Ca(2+)-mobilizing actions of a Jurkat cell extract on mammalian cells and Xenopus laevis oocytes | Q41351074 | ||
| Histamine receptor-dependent and/or -independent activation of guanine nucleotide-binding proteins by histamine and 2-substituted histamine derivatives in human leukemia (HL-60) and human erythroleukemia (HEL) cells | Q41358097 | ||
| Evidence for a direct interaction of thapsigargin with voltage-dependent Ca2+ channel | Q41396826 | ||
| Appearance of a novel Ca2+ influx pathway in Sf9 insect cells following expression of the transient receptor potential-like (trpl) protein of Drosophila | Q41461349 | ||
| Lipophilic beta-adrenoceptor antagonists and local anesthetics are effective direct activators of G-proteins | Q41467494 | ||
| The regulation of store-dependent Ca2+ influx in HL-60 granulocytes involves GTP-sensitive elements | Q41509037 | ||
| SK&F 96365, a novel inhibitor of receptor-mediated calcium entry | Q41771065 | ||
| Pharmacology of a Ca(2+)-influx pathway activated by emptying the intracellular Ca2+ stores in HL-60 cells: evidence that a cytochrome P-450 is not involved | Q41926739 | ||
| Maitotoxin activates cation channels distinct from the receptor-activated non-selective cation channels of HL-60 cells | Q42160913 | ||
| Formyl peptides and ATP stimulate Ca2+ and Na+ inward currents through non-selective cation channels via G-proteins in dibutyryl cyclic AMP-differentiated HL-60 cells. Involvement of Ca2+ and Na+ in the activation of beta-glucuronidase release and s | Q42161364 | ||
| Evaluation of calcium influx factors from stimulated Jurkat T-lymphocytes by microinjection into Xenopus oocytes | Q42490563 | ||
| Fluorescence ratio imaging of cytosolic free Na+ in individual fibroblasts and lymphocytes | Q42490771 | ||
| Characterization of the bradykinin-stimulated calcium influx pathway of cultured vascular endothelial cells. Saturability, selectivity, and kinetics | Q42493317 | ||
| Evidence from studies with hepatocyte suspensions that store-operated Ca2+ inflow requires a pertussis toxin-sensitive trimeric G-protein | Q42493654 | ||
| Reversible activation of NADPH oxidase in membranes of HL-60 human leukemic cells | Q42512078 | ||
| Thapsigargin inhibits Ca2+ entry into human neutrophil granulocytes | Q42823404 | ||
| Inhibition of L-type calcium-channel activity by thapsigargin and 2,5-t-butylhydroquinone, but not by cyclopiazonic acid | Q42828701 | ||
| Chemotactic peptide down-regulation of calcium mobilization induced by platelet-activating factor and by leukotriene B4 in human neutrophils is uncovered by protein phosphatase inhibitors | Q42829659 | ||
| Characterization of receptor-mediated and store-regulated Ca2+ influx in human neutrophils. | Q42832820 | ||
| Lack of effect of opioid peptides, morphine and naloxone on superoxide formation in human neutrophils and HL-60 leukemic cells | Q44340390 | ||
| Use of manganese to discriminate between calcium influx and mobilization from internal stores in stimulated human neutrophils. | Q44789184 | ||
| Differential inhibition of human neutrophil activation by cyclosporins A, D, and H. Cyclosporin H is a potent and effective inhibitor of formyl peptide-induced superoxide formation | Q45296977 | ||
| Uptake and intracellular sequestration of divalent cations in resting and methacholine-stimulated mouse lacrimal acinar cells. Dissociation by Sr2+ and Ba2+ of agonist-stimulated divalent cation entry from the refilling of the agonist-sensitive intr | Q45971523 | ||
| Characterization of the plasma membrane bound GTPase from rabbit neutrophils. I. Evidence for an Ni-like protein coupled to the formyl peptide, C5a, and leukotriene B4 chemotaxis receptors | Q46874581 | ||
| Degradation of a calcium influx factor (CIF) can be blocked by phosphatase inhibitors or chelation of Ca2+. | Q49069256 | ||
| Partial inhibition of human neutrophil activation by FK-506 at supratherapeutic concentrations | Q53022050 | ||
| Okadaic acid uncouples calcium entry from depletion of intracellular stores. | Q53022473 | ||
| The roles of extracellular and intracellular calcium in lysosomal enzyme release and superoxide anion generation by human neutrophils | Q57731264 | ||
| Subcellular localization of Gi alpha in human neutrophils | Q57908518 | ||
| Replenishing the stores | Q59076136 | ||
| Basic methods for the study of phagocytosis | Q69760996 | ||
| Arachidonate and other fatty acids mobilize Ca2+ ions and stimulate beta-glucuronidase release in a Ca(2+)-dependent fashion from undifferentiated HL-60 cells | Q70787077 | ||
| Differential distribution of neuronal markers and neuropeptides in the human lacrimal gland | Q71885199 | ||
| Novel potent inhibitor of receptor-activated nonselective cation currents in HL-60 cells | Q72082143 | ||
| Phosphorylation down-regulates the store-operated Ca2+ entry pathway of human neutrophils | Q72772757 | ||
| Activation by chemotactic peptide of a receptor-operated Ca2+ entry pathway in differentiated HL60 cells | Q72809134 | ||
| Cyclosporin H is a potent and selective formyl peptide receptor antagonist. Comparison with N-t-butoxycarbonyl-L-phenylalanyl-L-leucyl-L-phenylalanyl-L- leucyl-L-phenylalanine and cyclosporins A, B, C, D, and E | Q72967745 | ||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 679-686 | |
| P577 | publication date | 1996-03-01 | |
| P1433 | published in | Biochemical Journal | Q864221 |
| P1476 | title | Thapsigargin activates univalent- and bivalent-cation entry in human neutrophils by a SK&F I3 96365- and Gd3+-sensitive pathway and is a partial secretagogue: involvement of pertussis-toxin-sensitive G-proteins and protein phosphatases 1/2A and 2B in the signal-transduction pathway | |
| P478 | volume | 314 ( Pt 2) |
| Q42470152 | 2-Benzyloxybenzaldehyde inhibits formyl peptide-stimulated increase in intracellular Ca2+ in neutrophils mainly by blocking Ca2+ entry. |
| Q46630908 | A store-operated nonselective cation channel in human lymphocytes |
| Q27313547 | Calpain 2 controls turnover of LFA-1 adhesions on migrating T lymphocytes |
| Q44466208 | Characterization of maleimide-activated Ca2+ entry in neutrophils |
| Q43882504 | Cholesterol-modulating agents selectively inhibit calcium influx induced by chemoattractants in human neutrophils |
| Q44264306 | GEA3162 stimulates Ca2+ entry in neutrophils |
| Q41010992 | High constitutive activity of the human formyl peptide receptor |
| Q43733608 | Inhibition of extracellular Ca(2+) entry by YC-1, an activator of soluble guanylyl cyclase, through a cyclic GMP-independent pathway in rat neutrophils |
| Q73375412 | Inhibition of interleukin-8-activated human neutrophil chemotaxis by thapsigargin in a calcium- and cyclic AMP-dependent way |
| Q73396326 | Inhibition of store-dependent capacitative Ca2+ influx by unsaturated fatty acids |
| Q33406546 | Intracellular free calcium mediates glioma cell detachment and cytotoxicity after photodynamic therapy |
| Q42837762 | LFA-1-mediated adhesion is regulated by cytoskeletal restraint and by a Ca2+-dependent protease, calpain |
| Q77587549 | Protein phosphatase inhibitors exert specific and nonspecific effects on calcium influx in thapsigargin-treated human neutrophils |
| Q45159213 | Stimulation of cellular free Ca2+ elevation and inhibition of store-operated Ca2+ entry by kazinol B in neutrophils |
| Q46651587 | The immunostimulatory peptide WKYMVm-NH activates bone marrow mouse neutrophils via multiple signal transduction pathways |
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