49 results on '"Moreno-Galindo, Eloy G."'
Search Results
2. Synergistic antidepressant-like effect of capsaicin and citalopram reduces the side effects of citalopram on anxiety and working memory in rats
3. The voltage-sensitive cardiac M2 muscarinic receptor modulates the inward rectification of the G protein-coupled, ACh-gated K+ current
4. Developmental light deprivation transiently reduces the expression of vGluT2 and GluN2B in the rat ventral suprachiasmatic nucleus
5. Impact of the whole-cell patch-clamp configuration on the pharmacological assessment of the hERG channel: Trazodone as a case example
6. The agonist-specific voltage dependence of M2 muscarinic receptors modulates the deactivation of the acetylcholine-gated K+ current (I KACh)
7. Developmental light deprivation transiently reduces the expression of vGluT2 and GluN2B in the rat ventral suprachiasmatic nucleus.
8. Differential voltage-dependent modulation of the ACh-gated K+ current by adenosine and acetylcholine
9. GABA Neurotransmission of the Suprachiasmatic Nucleus Is Modified During Rat Postnatal Development
10. The principal conductance in Giardia lamblia trophozoites possesses functional properties similar to the mammalian ClC-2 current
11. Tamoxifen Inhibits Cardiac ATP-Sensitive and Acetylcholine-Activated K+ Currents in Part by Interfering With Phosphatidylinositol 4,5-Bisphosphate–Channel Interaction
12. Light stimulation during postnatal development is not determinant for glutamatergic neurotransmission from the retinohypothalamic tract to the suprachiasmatic nucleus in rats
13. Riluzole inhibits Kv4.2 channels acting on the closed and closed inactivated states
14. sj-pdf-2-jbr-10.1177_07487304211048052 – Supplemental material for GABA Neurotransmission of the Suprachiasmatic Nucleus Is Modified During Rat Postnatal Development
15. sj-pdf-1-jbr-10.1177_07487304211048052 – Supplemental material for GABA Neurotransmission of the Suprachiasmatic Nucleus Is Modified During Rat Postnatal Development
16. Kir4.1/Kir5.1 channels possess strong intrinsic inward rectification determined by a voltage-dependent K+-flux gating mechanism
17. 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
18. Muscarinic-activated potassium current mediates the negative chronotropic effect of pilocarpine on the rabbit sinoatrial node
19. Kv1.5 Open Channel Block by the Antiarrhythmic Drug Disopyramide: Molecular Determinants of Block
20. Voltage sensitivity of M2 muscarinic receptors underlies the delayed rectifier-like activation of ACh-gated K+ current by choline in feline atrial myocytes
21. Differential voltage-dependent modulation of the ACh-gated K+ current by adenosine and acetylcholine.
22. Relaxation gating of the acetylcholine-activated inward rectifier K+ current is mediated by intrinsic voltage sensitivity of the muscarinic receptor
23. Voltage-induced structural modifications on M2 muscarinic receptor and their functional implications when interacting with the superagonist iperoxo
24. Functional Pre- and Postsynaptic Changes between the Retinohypothalamic Tract and Suprachiasmatic Nucleus during Rat Postnatal Development
25. Development-Dependent Changes in the NR2 Subtype of the N-Methyl-D-Aspartate Receptor in the Suprachiasmatic Nucleus of the Rat
26. Modeling effects of voltage dependent properties of the cardiac muscarinic receptor on human sinus node function
27. Capsaicin produces antidepressant-like effects in the forced swimming test and enhances the response of a sub-effective dose of amitriptyline in rats
28. Functional Pre- and Postsynaptic Changes between the Retinohypothalamic Tract and Suprachiasmatic Nucleus during Rat Postnatal Development.
29. Molecular determinants of Kv7.1/KCNE1 channel inhibition by amitriptyline
30. Voltage-Dependent Activation of M2 Muscarinic Receptors-IKACH by the Superagonist Iperoxo in Cardiac Myocytes
31. Inhibition of Kir4.1 potassium channels by quinacrine
32. Chloroquine blocks the Kir4.1 channels by an open-pore blocking mechanism
33. The voltage-sensitive cardiac M2 muscarinic receptor modulates the inward rectification of the G protein-coupled, ACh-gated K+ current.
34. Pharmacological Conversion of a Cardiac Inward Rectifier into an Outward Rectifier Potassium Channel
35. Corrigendum to “Mechanosensitive Ca2+-permeable channels in human leukemic cells: pharmacological and molecular evidence for TRPV2” [Biochim. Biophys. Acta (1848/1PA) (2015) 51–59]
36. Voltage sensitivity of M2 muscarinic receptors underlies the delayed rectifier-like activation of ACh-gated K+ current by choline in feline atrial myocytes
37. Relaxation gating of the acetylcholine-activated inward rectifier K+ current is mediated by intrinsic voltage sensitivity of the muscarinic receptor
38. Mechanosensitive Ca2+-permeable channels in human leukemic cells: Pharmacological and molecular evidence for TRPV2
39. The principal conductance in Giardia lamblia trophozoites possesses functional properties similar to the mammalian ClC-2 current
40. Voltage sensitivity of M2muscarinic receptors underlies the delayed rectifier-like activation of ACh-gated K+current by choline in feline atrial myocytes
41. The Antimalarial Drug Mefloquine Inhibits Cardiac Inward Rectifier K+ Channels: Evidence for Interference in PIP2-Channel Interaction
42. Molecular Basis for a High-Potency Open-Channel Block of Kv1.5 Channel by the Endocannabinoid Anandamide
43. Voltage sensitivity of M2 muscarinic receptors underlies the delayed rectifier-like activation of ACh-gated K+ current by choline in feline atrial myocytes.
44. The Antimalarial Drug Mefloquine Inhibits Cardiac Inward Rectifier K+ Channels: Evidence for Interference in PIP2-Channel Interaction.
45. The Antimalarial Drug Mefloquine Inhibits Cardiac Inward Rectifier K+Channels Evidence for Interference in PIP2-Channel Interaction
46. Tamoxifen Inhibits Cardiac ATP-Sensitive and Acetylcholine-Activated K+Currents in Part by Interfering With Phosphatidylinositol 4,5-Bisphosphate–Channel Interaction
47. Mechanosensitive Ca2 +-permeable channels in human leukemic cells: Pharmacological and molecular evidence for TRPV2.
48. Corrigendum to “Mechanosensitive Ca2 +-permeable channels in human leukemic cells: pharmacological and molecular evidence for TRPV2” [Biochim. Biophys. Acta (1848/1PA) (2015) 51–59].
49. Conformational changes in the M2 muscarinic receptor induced by membrane voltage and agonist binding.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.