496 results on '"Nagao, Taku"'
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52. Gα 12/13 Mediates α 1 -Adrenergic Receptor–Induced Cardiac Hypertrophy
53. β1-Selective Agonist (−)-1-(3,4-Dimethoxyphenetylamino)-3-(3,4-dihydroxy)-2-propanol [(−)-RO363] Differentially Interacts with Key Amino Acids Responsible for β1-Selective Binding in Resting and Active States
54. Activation Mechanism of Gi and Go by Reactive Oxygen Species
55. Gβγ Counteracts Gαq Signaling upon α1-Adrenergic Receptor Stimulation
56. The quality of conduct in Japanese clinical trials
57. Contribution of pharmacology for new drug application in Japan
58. A Carbamate-Type Cholinesterase Inhibitor 2-sec-Butylphenyl N-Methylcarbamate Insecticide Blocks L-Type Ca2+ Channel in Guinea Pig Ventricular Myocytes
59. Enhanced cAMP Response of Naturally Occurring Mutant of Human β-Adrenergic Receptor
60. Infrastructure of Pharmaceutical Research and Development in Japan
61. Phosphatidylinositol is essential determinant for K+permeability involved in gastric proton pumping
62. Clathrin Box in G Protein-coupled Receptor Kinase 2
63. Reconstitution of Acid Secretion in Digitonin-permeabilized Rabbit Gastric Glands
64. Novel peptides from assassin bugs (Hemiptera: Reduviidae): isolation, chemical and biological characterization
65. Low affinity of β1-adrenergic receptor for β-arrestins explains the resistance to agonist-induced internalization
66. Ser1901 of α1C subunit is required for the PKA‐mediated enhancement of L‐type Ca2+ channel currents but not for the negative shift of activation
67. Diltiazem Ameliorates Contractile Dysfunction Without Shortening of Action Potential Duration in Ischemic Heart of Anesthetized Dogs
68. Serine Residue in the IIIS5-S6 Linker of the L-type Ca2+ Channel α1C Subunit Is the Critical Determinant of the Action of Dihydropyridine Ca2+Channel Agonists
69. Involvement of BKCa channels in the relaxation of detrusor muscle via β-adrenoceptors
70. Interaction with β-Arrestin Determines the Difference in Internalization Behavior between β1- and β2-Adrenergic Receptors
71. Molecular Cloning and Characterization of a Novel Chloride Intracellular Channel-related Protein, Parchorin, Expressed in Water-secreting Cells
72. Molecular cloning and characterization of a novel clic-related protein, parchorin, expressed in water-secreting cells
73. Translocation of HSP27 to Sarcomere Induced by Ischemic Preconditioning in Isolated Rat Hearts
74. Novel determinants of action of Ca2+ channel antagonists and agonists in L-type Ca2+ channel otic subunit
75. Simplified method for gene transfer and expression by recombinant adenoviruses.
76. Enhanced [Ca2+]i transients in rat ventricular myocytes after experimental myocardial infarction
77. Purification of the Intracellular Factors Essential for Acid Secretion Using Digitonin-permeabilized Rabbit Gastric Gland Model
78. The mechanism for beta-adrenoceptor-mediated relaxation of guinea-pig bladder smooth muscle
79. Localization and Expression of a Novel Chloride Intracellular Channel-related Protein, Parchorin, in Water-Secreting Cells
80. Gi and Go are target proteins of reactive oxygen species leading to activation of extracellular signal-regulated kinase (ERK)
81. Tissue specific expression of splice variants of the L-type Ca2+ channel α1C subunit in rats
82. Energy Preserving Effect of l-cis Diltiazem in Isolated Ischemic and Reperfused Guinea Pig Hearts. A 31P-NMR Study.
83. Affinity for β-arrestin determines differential behavior of agonist-induced internalization of β 1 and β 2-adrenergic receptors
84. Assessment of Affinities of Propranolol and Bopindolol to Membranes from COS-7 Cell Transiently Transfected with Beta-1- and Beta-2-Adrenoceptors Using a Radioligand-Binding Assay Method
85. Binding pocket of β1-adrenergic receptor responsible for high β1-selectivity of (-)-R0363
86. Analysis of Phenylephrine-induced hypertrophic response in cardiomyocytes of neonatal rats by adenovirus gene transfer method
87. l-cis Diltiazem attenuates intracellular Ca2+ overload by metabolic inhibition in guinea pig myocytes
88. Correlation between Ca2+ oscillation and cell proliferation via CCKB/gastrin receptor
89. Binding Pockets of the β1- and β2-Adrenergic Receptors for Subtype-Selective Agonists
90. Negative regulation of α2-adrenergic receptor-mediated Gi signalling by a novel pathway
91. Correlation between acid secretion and proton pump activity during inhibition by the proton pump inhibitors omeprazole and pantoprazole
92. Responsiveness of β-escin-permeabilized rabbit gastric gland model: effects of functional peptide fragments
93. Ser203as well as Ser204and Ser207in fifth transmembrane domain of the human β2-adrenoceptor contributes to agonist binding and receptor activation
94. Activation of Rac1 Increases c-Jun NH2-Terminal Kinase Activity and DNA Fragmentation in a Calcium-Dependent Manner in Rat Myoblast Cell Line H9c2
95. Nonspecific effects of the pharmacological probes commonly used to analyze signal transduction in rabbit parietal cells
96. Treatment With 1-cis Diltiazem Before Reperfusion Reduces Infarct Size in the Ischemic Rabbit Heart In Vivo
97. Involvement of racl in calcium-dependent activation of JNK and cell injury by oxidative stress in the rat myoblast cell line, H9c2
98. The Role of Pharmacology in the Globalization of Drug Development. Pharmacological evaluation of the development candidate.
99. Analysis of Domain Responsible for Desensitization of .BETA.1-Adrenergic Receptor.
100. The mechanism for the voltage-dependent block of diltiazem on L-type Ca2+ channels in guinea-pig ventricular myocytes.
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