Tatiana M. Vinogradova

National Institute on Aging — United States

Medicine · Health Sciences

29h-index4.9kcitations93works1.02yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Cardiac electrophysiology and arrhythmias(70), Ion channel regulation and function(48), Neuroscience and Neural Engineering(31), Receptor Mechanisms and Signaling(15), Phosphodiesterase function and regulation(11)

Publications93 total

Ca2+/Calmodulin-Dependent Protein Kinase II (CaMKII) Regulates Basal Cardiac Pacemaker Function: Pros and Cons
Cells·2024· 1 citedOpen Access
Mesenchymal stem cells in complex treatment of urinary tract diseases: a literature review and our own experience
Cellular Therapy and Transplantation·2023Open Access
Periphery Exploration Around 2,6-Diazaspiro[3.4]Octane Core Identifies Potent Nitrofuran Antitubercular Lead
SSRN Electronic Journal·2022Open Access
Phosphoprotein Phosphatase 1 but Not 2A Activity Modulates Coupled-Clock Mechanisms to Impact on Intrinsic Automaticity of Sinoatrial Nodal Pacemaker Cells
Cells·2021· 14 citedOpen Access
Ca2+ and Membrane Potential Transitions During Action Potentials Are Self-Similar to Each Other and to Variability of AP Firing Intervals Across the Broad Physiologic Range of AP Intervals During Autonomic Receptor Stimulation
Frontiers in Physiology·2021· 21 citedOpen Access
Dual Activation of Phosphodiesterase 3 and 4 Regulates Basal Cardiac Pacemaker Function and Beyond
International Journal of Molecular Sciences·2021· 25 citedOpen Access
Normal spontaneous firing of cardiac pacemaker cells is regulated by basal pkc delta activation
European Heart Journal·2020· 2 cited
Ca <sup>2+</sup> and Membrane Potential Transitions During Action Potentials are Self-Similar to Each Other and to Variability of AP Firing Intervals Across the Broad Physiologic Range of AP Intervals During Autonomic Receptor Stimulation
2020· 9 citedOpen Access
Self-similar action potential cycle-to-cycle variability of Ca2+ and current oscillators in cardiac pacemaker cells
2020· 7 cited
Sorafenib Suppresses Basal Spontaneous Beating of Rabbit Sinoatrial Node Cells (SANC) through Inhibition of Vascular Endothelial Growth Factor Receptor 1 (VEGFR1)
Biophysical Journal·2020· 1 citedOpen Access
Assessment of the impact of different therapeutic approaches on the urobiome changes in children with recurrent urinary tract infection
Ukrainian journal of Perinatology and Pediatrics·2019Open Access
P1593VEGFR1-PLC signaling is implicated in normal spontaneous firing of cardiac pacemaker cells
European Heart Journal·2019
The Anti-Cancer Drug Vatalanib (Ptk787/Zk222584) Suppresses Normal Spontaneous Firing of Rabbit Sinoatrial Node Cells (SANC)
Biophysical Journal·2019Open Access
Rhythm and Rate of Action Potential Firing of Single Cardiac Pacemaker Cells Emerge from Concordant Beat to Beat Variability of Coupled Calcium and Membrane Potential Functions
Biophysical Journal·2019· 1 citedOpen Access
Dual Activation of Phosphodiesterases 3 and 4 Regulates Basal Spontaneous Beating Rate of Cardiac Pacemaker Cells: Role of Compartmentalization?
Frontiers in Physiology·2018· 21 citedOpen Access
Unique Ca2+-Cycling Protein Abundance and Regulation Sustains Local Ca2+ Releases and Spontaneous Firing of Rabbit Sinoatrial Node Cells
International Journal of Molecular Sciences·2018· 17 citedOpen Access
Basal Spontaneous Firing of Rabbit Sinoatrial Node Cells Is Regulated by Dual Activation of PDEs (Phosphodiesterases) 3 and 4
Circulation Arrhythmia and Electrophysiology·2018· 28 citedOpen Access
Protein Phosphatase-1 Modulates Basal Spontaneous Beating Rate of Sinoatrial Node Cells (SANC)
Biophysical Journal·2018Open Access
Abstract 15188: Basal Epac2 Activation Regulates Spontaneous Beating of Cardiac Pacemaker Cells
Circulation·2017
Cycling Proteins Generates Robust Rhythmic Local Ca 2+ Releases in Cardiac Pacemaker Cells
2017
page 1 of 5Next →

Frequent Co-authors

Edward G. Lakatta(40), Victor A. Maltsev(22), Alexey E. Lyashkov(16), Syevda Sirenko(12), K. Yu. Bogdanov(11), Dongmei Yang(11), Harold A. Spurgeon(10), Michael D. Stern(7), Yevgeniya Lukyanenko(6), Ihor Zahanich(6), Bruce D. Ziman(6), Antoine Younès(5), Alexey Khodjakov(4), A. Ruknudin(4), Yael Yaniv(4), Yue Li(3), Yue Li(3), Christopher H. Morrell(3), Weizhong Zhu(2), Ying-Ying Zhou(2)