The scientist’s investigation covers issues in Voltage-dependent calcium channel, Calmodulin, Biophysics, Biochemistry and Cell biology. His Voltage-dependent calcium channel research incorporates elements of Genetics, Alternative splicing, Gene, Exon and splice. His research integrates issues of Endocrinology, Adenoviridae and Calcium signaling in his study of Calmodulin.
The study incorporates disciplines such as R-type calcium channel, Voltage-gated ion channel, Q-type calcium channel and Cardiac action potential in addition to Biophysics. His Biochemistry research is multidisciplinary, relying on both L-type calcium channel, Neuron and Signalling. His study in the field of Function is also linked to topics like Heartbeat.
David T. Yue focuses on Calmodulin, Biophysics, Voltage-dependent calcium channel, Cell biology and Biochemistry. His study in Calmodulin is interdisciplinary in nature, drawing from both Cav1.3, Mutagenesis, Ion channel, Intracellular and Allosteric regulation. His Cav1.3 research focuses on subjects like Alanine, which are linked to Alanine scanning.
His work on Depolarization as part of general Biophysics study is frequently linked to Sodium channel, therefore connecting diverse disciplines of science. As a member of one scientific family, David T. Yue mostly works in the field of Voltage-dependent calcium channel, focusing on Calcium channel and, on occasion, Calcium-binding protein. His studies in Cell biology integrate themes in fields like HEK 293 cells, Protein subunit and Mutant.
His primary areas of study are Calmodulin, Cell biology, Biophysics, Voltage-dependent calcium channel and Ion channel. His Calmodulin research includes themes of Plasma protein binding, Biochemistry and Calcium channel. His Cell biology research is multidisciplinary, incorporating elements of HEK 293 cells, Mutant, Gene knockdown and Gene isoform.
The various areas that David T. Yue examines in his Biophysics study include Nanotechnology, Open probability and Förster resonance energy transfer. His Voltage-dependent calcium channel study integrates concerns from other disciplines, such as Neuroscience, Ion channel gating, Protein kinase A and Calcium signaling. David T. Yue has included themes like Protein subunit and High homology in his Ion channel study.
His primary areas of study are Calmodulin, Voltage-dependent calcium channel, Ion channel, Neuroscience and Biophysics. His work carried out in the field of Calmodulin brings together such families of science as Long QT syndrome, Patch clamp and Pharmacology. His Voltage-dependent calcium channel study combines topics in areas such as Genetics, Homeostasis, Cell biology, Mutation and Ion channel gating.
His study focuses on the intersection of Cell biology and fields such as Cav1.3 with connections in the field of SK channel. His Neuroscience research includes elements of HEK 293 cells and Transduction. His Biophysics study combines topics from a wide range of disciplines, such as Plasma protein binding, Biochemistry, Ca2 channels, Fluorescence-lifetime imaging microscopy and Förster resonance energy transfer.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Calmodulin is the Ca2+ sensor for Ca2+ -dependent inactivation of L-type calcium channels.
Blaise Z Peterson;Carla D DeMaria;David T Yue.
Neuron (1999)
Preassociation of Calmodulin with Voltage-Gated Ca2+ Channels Revealed by FRET in Single Living Cells
Michael G. Erickson;Badr A. Alseikhan;Blaise Z. Peterson;David T. Yue.
Neuron (2001)
Calmodulin bifurcates the local Ca 2+ signal that modulates P/Q-type Ca 2+ channels
Carla D. DeMaria;Tuck Wah Soong;Badr A. Alseikhan;Rebecca S. Alvania.
Nature (2001)
Beta-adrenergic stimulation of calcium channels occurs by potentiation of high-activity gating modes
David T. Yue;Stefan Herzig;Eduardo Marban.
Proceedings of the National Academy of Sciences of the United States of America (1990)
Unified mechanisms of Ca2+ regulation across the Ca2+ channel family.
Haoya Liang;Carla D. DeMaria;Carla D. DeMaria;Michael G. Erickson;Masayuki X. Mori.
Neuron (2003)
Molecular localization of an ion-binding site within the pore of mammalian sodium channels.
Peter H. Backx;David T. Yue;John H. Lawrence;Eduardo Marban.
Science (1992)
Essential Ca2+-Binding Motif for Ca2+-Sensitive Inactivation of L-Type Ca2+ Channels
Marita de Leon;Yan Wang;Lisa Jones;Edward Perez-Reyes.
Science (1995)
Intracellular calcium transients underlying the short‐term force‐interval relationship in ferret ventricular myocardium.
W G Wier;D T Yue.
The Journal of Physiology (1986)
Contractility-dependent curvilinearity of end-systolic pressure-volume relations.
Daniel Burkhoff;Seiryo Sugiura;David T. Yue;Kiichi Sagawa.
American Journal of Physiology-heart and Circulatory Physiology (1987)
Mechanism of Ca2+-sensitive inactivation of L-type Ca2+ channels
John P. Imredy;David T. Yue.
Neuron (1994)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Cedars-Sinai Medical Center
MIT
Johns Hopkins University
Johns Hopkins University
Johns Hopkins University School of Medicine
York University
Harvard University
Mayo Clinic
Southern Medical University
Johns Hopkins University
National Bureau of Economic Research
Bank of Greece
Griffith University
Tsinghua University
Huazhong University of Science and Technology
University of Arizona
Aberystwyth University
Collège de France
Oregon State University
University of Copenhagen
University of Southampton
University of Exeter
George Mason University
Tufts University
Vrije Universiteit Amsterdam
New York University