Aldo A. Rodríguez-Menchaca

发表

The molecular basis of chloroquine block of the inward rectifier Kir2.1 channel

Frank B. Sachse, Martin Tristani-Firouzi, F. Sachse, 2008, Proceedings of the National Academy of Sciences.

Modulation of Kv2.1 channels inactivation by curcumin

A. Rodríguez-Menchaca, Aldo A. Rodríguez-Menchaca, Mayra Delgado-Ramírez, 2015, Pharmacological reports : PR.

Dual Regulation of Voltage-Sensitive Ion Channels by PIP2

Lei Zhou, D. Logothetis, A. Rodríguez-Menchaca, 2012, Front. Pharmacol..

Regulation of Kv2.1 channel inactivation by phosphatidylinositol 4,5-bisphosphate

J. Arreola, D. Logothetis, C. Villalba-Galea, 2018, Scientific Reports.

Mechanisms for Kir channel inhibition by quinacrine: acute pore block of Kir2.x channels and interference in PIP2 interaction with Kir2.x and Kir6.2 channels

Daniela Ponce-Balbuena, J. Sánchez-Chapula, A. Lopez-Izquierdo, 2011, Pflügers Archiv - European Journal of Physiology.

The anti-tumor drug 2-hydroxyoleic acid regulates the oncogenic potassium channel Kv10.1

A. Rodríguez-Menchaca, Aldo A. Rodríguez-Menchaca, Rita Morán-Zendejas, 2023, Beni-Suef University Journal of Basic and Applied Sciences.

Inhibition of Kir4.1 potassium channels by quinacrine

J. Sánchez-Chapula, T. Ferrer, Eloy G. Moreno-Galindo, 2017, Brain Research.

Inhibition of CaV2.3 channels by NK1 receptors is sensitive to membrane cholesterol but insensitive to caveolin-1

Aldo A. Rodríguez-Menchaca, U. Meza, S. Sánchez‐Armass, 2014, Pflügers Archiv - European Journal of Physiology.

Revealing the activation pathway for TMEM16A chloride channels from macroscopic currents and kinetic models

H. C. Hartzell, S. Cruz-Rangel, J. Arreola, 2016, Pflügers Archiv - European Journal of Physiology.

Voltage-induced structural modifications on M2 muscarinic receptor and their functional implications when interacting with iperoxo.

M. Tristani-Firouzi, José J. De Jesús-Pérez, T. Ferrer, 2020, Biochemical pharmacology.

Hypercholesterolemia Induces Up-regulation of KACh Cardiac Currents via a Mechanism Independent of Phosphatidylinositol 4,5-Bisphosphate and Gβγ*

D. Logothetis, C. Baumgarten, A. Bukiya, 2011, The Journal of Biological Chemistry.

Hypercholesterolemia Induces Up-regulation of K ACh Cardiac Currents via a Mechanism Independent of Phosphatidylinositol 4,5-Bisphosphate and G (cid:1)(cid:2) *

Zhe Zhang, D. Logothetis, C. Baumgarten, 2020 .

Functional marriage in plasma membrane: Critical cholesterol level–optimal protein activity

S. Sánchez-Armáss, A. Rodríguez-Menchaca, Aldo A. Rodríguez-Menchaca, 2020, British journal of pharmacology.

Distant Cytosolic Residues Mediate a Two-way Molecular Switch That Controls the Modulation of Inwardly Rectifying Potassium (Kir) Channels by Cholesterol and Phosphatidylinositol 4,5-Bisphosphate (PI(4,5)P2)*

D. Logothetis, S. Noskov, I. Levitan, 2012, The Journal of Biological Chemistry.

Molecular Mechanisms of Chloroquine Inhibition of Heterologously Expressed Kir6.2/SUR2A Channels

Daniela Ponce-Balbuena, J. Sánchez-Chapula, T. Ferrer, 2012, Molecular Pharmacology.

The D3-dopaminergic Agonist 7-hydroxy-dipropylaminotetralin (7-OH-DPAT) Increases Cardiac Action Potential Duration and Blocks Human Ether-a-go-go-related Gene K+ Channel

J. Sánchez-Chapula, R. Navarro-Polanco, Aldo A. Rodríguez-Menchaca, 2006, Journal of cardiovascular pharmacology.

Extracellular protons enable activation of the calcium‐dependent chloride channel TMEM16A

H. C. Hartzell, S. Cruz-Rangel, J. Arreola, 2017, The Journal of physiology.

Phytochemicals genistein and capsaicin modulate Kv2.1 channel gating

A. Rodríguez-Menchaca, Aldo A. Rodríguez-Menchaca, Mayra Delgado-Ramírez, 2017, Pharmacological reports : PR.

Modulation of the voltage-gated potassium channel Kv2.1 by the anti-tumor alkylphospholipid perifosine

Aldo A. Rodríguez-Menchaca, Mayra Delgado-Ramírez, I. Aréchiga-Figueroa, 2016, Pharmacological reports : PR.

Phosphatidylinositol 4,5-Bisphosphate and Cholesterol Regulators of the Calcium-Activated Chloride Channels TMEM16A and TMEM16B.

J. Arreola, P. Pérez-Cornejo, Aldo A. Rodríguez-Menchaca, 2023, Advances in Experimental Medicine and Biology.

Impact of the whole-cell patch-clamp configuration on the pharmacological assessment of the hERG channel: trazodone as a case example.

J. Sánchez-Chapula, T. Ferrer, Eloy G. Moreno-Galindo, 2014, Journal of pharmacological and toxicological methods.

Inhibition of cardiac HERG potassium channels by antidepressant maprotiline.

J. Sánchez-Chapula, R. Navarro-Polanco, Tania Ferrer-Villada, 2006, European journal of pharmacology.

Kir4.1/Kir5.1 channels possess strong intrinsic inward rectification determined by a voltage-dependent K+-flux gating mechanism

J. Sánchez-Chapula, T. Ferrer, Eloy G. Moreno-Galindo, 2021, The Journal of general physiology.

In vitro and in silico characterization of the inhibition of Kir4.1 channels by aminoglycoside antibiotics

A. Rodríguez-Menchaca, Aldo A. Rodríguez-Menchaca, Mayra Delgado-Ramírez, 2020, British journal of pharmacology.

in coronary macro-, not microcirculation Hypercholesterolemia inhibits L-type calcium current

K. K. Maddali, C. Heaps, D. Logothetis, 2015 .

S(+)amphetamine induces a persistent leak in the human dopamine transporter: molecular stent hypothesis

A. Rodríguez-Menchaca, Aldo A. Rodríguez-Menchaca, L. D. De Felice, 2012, British journal of pharmacology.

Riluzole inhibits Kv4.2 channels acting on the closed and closed inactivated states.

J. Sánchez-Chapula, T. Ferrer, Eloy G. Moreno-Galindo, 2021, European journal of pharmacology.

Cytoskeleton disruption affects Kv2.1 channel function and its modulation by PIP2

A. Rodríguez-Menchaca, Aldo A. Rodríguez-Menchaca, Mayra Delgado-Ramírez, 2019, The Journal of Physiological Sciences.

PIP2 controls voltage-sensor movement and pore opening of Kv channels through the S4–S5 linker

Meng Cui, Diomedes E Logothetis, D. Logothetis, 2012, Proceedings of the National Academy of Sciences.