Efficacy of Varenicline, an 42 Nicotinic Acetylcholine Receptor Partial Agonist, vs Placebo or Sustained-Release Bupropion for Smoking Cessation A Randomized Controlled Trial
By D. Jorenby, J. Hays, N. Rigotti, S. Azoulay, E. Watsky, K. Williams, C. Billing, J. Gong, K. Reeves. 2006
1,321 citations recorded by the source corpus.
Subfields: Epidemiology, Molecular Biology, Physiology
View Paper: https://www.semanticscholar.org/paper/15c02edd50c9e2e1733e2a16ec555c60e77bd697
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In Molecular Biology
- A. Garcia-Romeu
- J. Lindstrom
- Roland R. Griffiths
- Matthew W. Johnson
- A. Kuryatov
- Mary P Cosimano
- L. Tapia
In Physiology
Citations in the corpus
- Ca2+ Permeability of the (α4)3(β2)2 Stoichiometry Greatly Exceeds That of (α4)2(β2)3 Human Acetylcholine Receptors (2006, background): “The newly approved drug for smoking cessation, varenicline, is believed to act like cytisine as a partial agonist on 4 2 AChRs in oocytes and on dopaminergic neurons (Coe et al., 2005; Jorenby et al., 2006).”
- Pilot Study of the 5-HT2AR Agonist Psilocybin in the Treatment of Tobacco Addiction (2014, background): “For example, when paired with 12 brief weekly counseling meetings, pharmacotherapies have shown seven-day point prevalence abstinence rates of 24.9% to 26.3% (bupropion) and 33.5% to 35.2% (varenicline) at approximately 6 months post-TQD (Gonzales et al., 2006; Jorenby et al., 2006).”