Cited by 420Nitric Oxide and Endothelin EffectsPhosphodiesterase function and regulationReceptor Mechanisms and Signaling

Nitric Oxide and Cyclic GMP in Cell Signaling and Drug Development

Murad, Ferid·2006·New England Journal of Medicine

Abstract

In the 116th Shattuck Lecture, Nobel laureate Ferid Murad explains how nitric oxide was discovered to be a biologically important molecule and outlines its multiple roles.

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Crossref · 10.1056/nejmsa063904

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  • Constitutive eNOS/NOS3 and nNOS/NOS1 produce low cellular NO, generally for cGMP regulation and subsequent events.

    “The constitutive isoforms, endothelial and neuronal NOS (eNOS/NOS3 and nNOS/NOS1), produce low cellular levels of NO, generally for regulation of cGMP and subsequent events (for example, [15]).”

    From Signaling and stress: The redox landscape in NOS2 biology (2015) · cites this paper as [15]

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Authors
Murad, F.
Affiliations
The University of Texas Health Science Center at Houston (US)
Corresponding author
Murad, Ferid
Venue
New England Journal of Medicine
Published
2006-11-09
Volume
355
Issue
19
Pages
2003-2011
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W1973082528
Cited by
420
References
0
Citations by year
2026: 7 · 2025: 13 · 2024: 14 · 2023: 21 · 2022: 21 · 2021: 24 · 2020: 27 · 2019: 13 · 2018: 15 · 2017: 22 · 2016: 18 · 2015: 19 · 2014: 26 · 2013: 16 · 2012: 28
FWCI
3.07
Type
journal article
Language
en
Open access
closed
Locations
  • New England Journal of Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Phosphodiesterase function and regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
Keywords
nitric oxide, cyclic GMP, signal transduction, drug development, soluble guanylate cyclase
MeSH terms
Cyclic GMP, Guanylate Cyclase, Humans, Nitric Oxide, Drug Design, Signal Transduction, Reactive Oxygen Species, Nitric Oxide Synthase, Protein Isoforms

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