Concepedia

Author

Saul Maayani

Icahn School of Medicine at Mount Sinai

Also Known As

S Maayani, S. MAAYANI, S. Maayani, S. Ma’ayani, SAUL MAAYANI, Saul MAAYANI, Saul Maayani

130

Publications

5.3K

Citations

39

H-Index

90

Concepts

All Affiliations

Icahn School of Medicine at Mount SinaiCity University of New YorkTel Aviv UniversityAndrija Stampar Teaching Institute of Public HealthMount Sinai Hospital
SM

About

Saul Maayani is an author at Icahn School of Medicine at Mount Sinai specializing in medicine, pharmacology, and neuropharmacology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

29

45

2.3K

2

Natural Sciences

6

6

220

3

Health Sciences

3

3

52

4

Engineering

2

2

110

5

Education

1

1

27

Saul Maayani

×

79

Publications

4.8K

Citations

38

H-Index

YearCitations

Effector Pathway-Dependent Relative Efficacy at Serotonin Type 2A and 2C Receptors: Evidence for Agonist-Directed Trafficking of Receptor Stimulus

Kelly A. Berg, Saul Maayani, Joseph Goldfarb,

Molecular Pharmacology

1998

512

Characterization of the 5-hydroxytryptamine1a receptor-mediated inhibition of forskolin-stimulated adenylate cyclase activity in guinea pig and rat hippocampal membranes.

Michael De Vivo, Saul Maayani

Journal of Pharmacology and Experimental Therapeutics

1986

424

Tricyclic antidepressant drugs block histamine H2 receptor in brain

J P Green, Saul Maayani

Nature

1977

233

Multiple and interrelated functional asymmetries in rat brain

S.D. Glick, Richard C. Meibach, Russell D. Cox,

Life Sciences

1979

181

Pharmacological studies of human erectile tissue: characteristics of spontaneous contractions and alterations in α‐adrenoceptor responsiveness with age and disease in isolated tissues

George J. Christ, Saul Maayani, Mira Valcic,

British Journal of Pharmacology

1990

158

Psychotomimetics as anticholinergic agents—I

Saul Maayani, Harel Weinstein, N. BEN-ZVI,

Biochemical Pharmacology

1974

142

Signal transduction differences between 5-hydroxytryptamine type 2A and type 2C receptor systems.

Kelly A. Berg, William P. Clarke, Cynthia Sailstad,

Molecular Pharmacology

1994

132

BMY 7378, a buspirone analog with high affinity, selectivity and low intrinsic activity at the 5-HT1A receptor in rat and guinea pig hippocampal membranes

Frank D. Yocca, Deborah K. Hyslop, David W. Smith,

European Journal of Pharmacology

1987

128

Pharmacological characterization of two 5-hydroxytryptamine receptors coupled to adenylate cyclase in guinea pig hippocampal membranes.

Andrew Shenker, Saul Maayani, Harel Weinstein,

Molecular Pharmacology

1987

126

A Locus of the Gonadotropin-releasing Hormone Receptor That Differentiates Agonist and Antagonist Binding Sites

Wei Zhou, Vladimir Rodic, Smiljka Kitanovic,

Journal of Biological Chemistry

1995

113

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