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Publications by Galya R. Abdrakhmanova
3′-Fluoro Substitution in the Pyridine Ring of Epibatidine Improves Selectivity and Efficacy for Α4β2 Versus Α3β4 nAChRs
Neuropharmacology
Molecular Neuroscience
Cellular
Pharmacology
Related publications
Epibatidine Induces Long-Term Potentiation (LTP) via Activation of Α4β2 Nicotinic Acetylcholine Receptors (nAChRs) in Vivo in the Intact Mouse Dentate Gyrus: Both Α7 and Α4β2 nAChRs Essential to Nicotinic LTP
Journal of Pharmacological Sciences
Molecular Medicine
Pharmacology
Functional Characterization of AT-1001, an Α3β4 Nicotinic Acetylcholine Receptor Ligand, at Human Α3β4 and Α4β2 nAChR
Nicotine and Tobacco Research
Environmental
Public Health
Occupational Health
Pharmacological and Functional Comparisons of Α6/Α3β2β3-nAChRs and Α4β2-nAChRs Heterologously Expressed in the Human Epithelial SH-EP1 Cell Line
Acta Pharmacologica Sinica
Medicine
Pharmacology
Selectivity of ABT-089 for Α4β2* and Α6β2* Nicotinic Acetylcholine Receptors in Brain
Biochemical Pharmacology
Biochemistry
Pharmacology
Synthesis and Nucleophilic Aromatic Substitution of 3-Fluoro-5-Nitro-1-(Pentafluorosulfanyl)benzene
Beilstein Journal of Organic Chemistry
Organic Chemistry
Asymmetric Agonist Selectivity of Agonist Sites in (Α4β2)2α4 Nicotinic Acetylcholine Receptors: A Key Determinant of Agonist Efficacy
Biophysical Journal
Biophysics
[3H]Epibatidine Photolabels Non-Equivalent Amino Acids in the Agonist Binding Site ofTorpedoand Α4β2 Nicotinic Acetylcholine Receptors
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
L-Histidinol Improves the Selectivity and Efficacy of Alkylating Agents and Daunomycin in Mice With P388 Leukaemia
British Journal of Cancer
Cancer Research
Oncology
Synthesis and Evaluation of 3-123i-Iodo-5-[2-(S)-3-Pyrrolinylmethoxy]-Pyridine (Niodene) as a Potential Nicotinic Α4β2 Receptor Imaging Agent
Bioorganic and Medicinal Chemistry Letters
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
