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Transmembrane Domain Mediates Tetramerization of α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid (AMPA) Receptors.
Stoichiometric relationship among clock proteins determines robustness of circadian rhythms.
Replication Initiation Protein Sld3/Treslin Orchestrates the Assembly of the Replication Fork Helicase during S Phase.
replication initiation protein Sld2 regulates helicase assembly.
Positive Amplification Mechanism Involving a Kinase and Replication Initiation Factor Helps Assemble the Replication Fork Helicase.
Long term ablation of protein kinase A (PKA)-mediated cardiac troponin I phosphorylation leads to excitation-contraction uncoupling and diastolic dysfunction in a knock-in mouse model of hypertrophic cardiomyopathy.
Intracellular regions of the Eag potassium channel play a critical role in generation of voltage-dependent currents.
Dpb11 protein helps control assembly of the Cdc45·Mcm2-7·GINS replication fork helicase.
DNA sequences proximal to human mitochondrial DNA deletion breakpoints prevalent in human disease form G-quadruplexes, a class of DNA structures inefficiently unwound by the mitochondrial replicative Twinkle helicase.
DNA Interactions Probed by Hydrogen-Deuterium Exchange (HDX) Fourier Transform Ion Cyclotron Resonance Mass Spectrometry Confirm External Binding Sites on the Minichromosomal Maintenance (MCM) Helicase.
Constitutive phosphorylation of cardiac myosin regulatory light chain in vivo.
Cdc45 protein-single-stranded DNA interaction is important for stalling the helicase during replication stress.
Allosteric Transmission along a Loosely Structured Backbone Allows a Cardiac Troponin C Mutant to Function with Only One Ca Ion.
14-3-3τ promotes surface expression of Cav2.2 (α1B) Ca2+ channels.