alanine and isradipine

alanine has been researched along with isradipine in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (50.00)18.2507
2000's2 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Acheson, M; Catterall, WA; Hockerman, GH; Johnson, BD; Peterson, BZ; Scheuer, T1
Grabner, M; Hering, S; Kraus, RL; Ostler, D; Striessnig, J1
Glossmann, H; Mitterdorfer, J; Striessnig, J; Wappl, E1
Adachi-Akahane, S; Ichijo, H; Nagao, T; Yamaguchi, S; Yoshioka, K; Zhorov, BS1

Other Studies

4 other study(ies) available for alanine and isradipine

ArticleYear
Analysis of the dihydropyridine receptor site of L-type calcium channels by alanine-scanning mutagenesis.
    The Journal of biological chemistry, 1997, Jul-25, Volume: 272, Issue:30

    Topics: Alanine; Amino Acid Sequence; Animals; Binding Sites; Calcium Channel Blockers; Calcium Channels; Calcium Channels, L-Type; Cell Line; Humans; Isradipine; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Peptide Mapping; Protein Structure, Secondary; Rabbits

1997
Molecular mechanism of diltiazem interaction with L-type Ca2+ channels.
    The Journal of biological chemistry, 1998, Oct-16, Volume: 273, Issue:42

    Topics: Alanine; Animals; Binding Sites; Calcium Channel Blockers; Calcium Channels; Calcium Channels, L-Type; Dihydropyridines; Diltiazem; DNA Mutational Analysis; Electric Conductivity; Electrophysiology; Ion Channel Gating; Isradipine; Muscle, Skeletal; Mutagenesis

1998
Mechanism of dihydropyridine interaction with critical binding residues of L-type Ca2+ channel alpha 1 subunits.
    The Journal of biological chemistry, 2001, Apr-20, Volume: 276, Issue:16

    Topics: Alanine; Amino Acid Sequence; Amino Acid Substitution; Animals; Binding Sites; Calcium Channel Blockers; Calcium Channels, L-Type; Dihydropyridines; Female; Isoleucine; Isradipine; Kinetics; Methionine; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Oocytes; Phenylalanine; Protein Structure, Secondary; Protein Subunits; Recombinant Proteins; Valine; Xenopus laevis

2001
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