Compounds > 1,4-dihydropyridine
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1,4-dihydropyridine and serine

1,4-dihydropyridine has been researched along with serine in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (25.00)18.2507
2000's3 (75.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Eisfeld, J; Klöckner, U; Mikala, G; Schwartz, A; Varadi, G; Varadi, M1
Adachi-Akahane, S; Nagao, T; Okamura, Y; Yamaguchi, S1
Armstrong, DL; Birnbaumer, L; Darden, T; Erxleben, C; Gomez-Alegria, C; Mori, Y1
Adachi-Akahane, S; Ichijo, H; Nagao, T; Yamaguchi, S; Yoshioka, K; Zhorov, BS1

Other Studies

4 other study(ies) available for 1,4-dihydropyridine and serine

ArticleYear
cAMP-dependent phosphorylation sites and macroscopic activity of recombinant cardiac L-type calcium channels.
    Molecular and cellular biochemistry, 1998, Volume: 185, Issue:1-2

    Topics: Alanine; Amino Acid Substitution; Barium; Binding Sites; Calcium Channel Blockers; Calcium Channels; Calcium Channels, L-Type; Cells, Cultured; Cyclic AMP; Cyclic AMP-Dependent Protein Kinases; Dihydropyridines; Humans; Kidney; Membrane Proteins; Muscle Proteins; Mutagenesis, Site-Directed; Myocardium; Patch-Clamp Techniques; Phosphorylation; Recombinant Proteins; Serine; Transfection

1998
Serine residue in the IIIS5-S6 linker of the L-type Ca2+ channel alpha 1C subunit is the critical determinant of the action of dihydropyridine Ca2+ channel agonists.
    The Journal of biological chemistry, 2000, Dec-29, Volume: 275, Issue:52

    Topics: Amino Acid Sequence; Animals; Calcium Channel Blockers; Calcium Channels, L-Type; Cricetinae; Dihydropyridines; Molecular Sequence Data; Point Mutation; Protein Conformation; Protein Subunits; Rats; Serine; Structure-Activity Relationship

2000
Modulation of cardiac Ca(V)1.2 channels by dihydropyridine and phosphatase inhibitor requires Ser-1142 in the domain III pore loop.
    Proceedings of the National Academy of Sciences of the United States of America, 2003, Mar-04, Volume: 100, Issue:5

    Topics: 3-Pyridinecarboxylic acid, 1,4-dihydro-2,6-dimethyl-5-nitro-4-(2-(trifluoromethyl)phenyl)-, Methyl ester; Adenosine Triphosphate; Animals; Calcium Channel Agonists; Calcium Channels; Calcium Channels, L-Type; Cell Line; Cell Membrane; Cricetinae; Dihydropyridines; Electrophysiology; Enzyme Inhibitors; Models, Molecular; Mutagenesis, Site-Directed; Mutation; Okadaic Acid; Phosphoric Monoester Hydrolases; Phosphorylation; Protein Binding; Protein Structure, Secondary; Protein Structure, Tertiary; Rabbits; Serine; Threonine; Time Factors; Transfection

2003
Key roles of Phe1112 and Ser1115 in the pore-forming IIIS5-S6 linker of L-type Ca2+ channel alpha1C subunit (CaV 1.2) in binding of dihydropyridines and action of Ca2+ channel agonists.
    Molecular pharmacology, 2003, Volume: 64, Issue:2

    Topics: Alanine; Animals; Calcium Channel Agonists; Calcium Channel Blockers; Calcium Channels, L-Type; Dihydropyridines; Isradipine; Phenylalanine; Point Mutation; Protein Subunits; Pyrroles; Rats; Repetitive Sequences, Nucleic Acid; Serine

2003