"Second Messenger Systems" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Systems in which an intracellular signal is generated in response to an intercellular primary messenger such as a hormone or neurotransmitter. They are intermediate signals in cellular processes such as metabolism, secretion, contraction, phototransduction, and cell growth. Examples of second messenger systems are the adenyl cyclase-cyclic AMP system, the phosphatidylinositol diphosphate-inositol triphosphate system, and the cyclic GMP system.
|Second Messenger Systems
- Second Messenger Systems
- Second Messenger System
- System, Second Messenger
- Systems, Second Messenger
- Intracellular Second Messengers
- Intracellular Second Messenger
- Messengers, Intracellular Second
- Second Messenger, Intracellular
- Second Messengers, Intracellular
- Second Messengers
- Messenger, Second
- Messengers, Second
- Second Messenger
Below are MeSH descriptors whose meaning is more general than "Second Messenger Systems".
Below are MeSH descriptors whose meaning is more specific than "Second Messenger Systems".
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Below are the most recent publications written about "Second Messenger Systems" by people in Profiles.
Biochemical characterization of G protein coupling to calcitonin gene-related peptide and adrenomedullin receptors using a native PAGE assay. J Biol Chem. 2020 07 10; 295(28):9736-9751.
Collybolide is a novel biased agonist of ?-opioid receptors with potent antipruritic activity. Proc Natl Acad Sci U S A. 2016 May 24; 113(21):6041-6.
Cystathionine ß-synthase regulates endothelial function via protein S-sulfhydration. FASEB J. 2016 Jan; 30(1):441-56.
Insulin receptor regulates photoreceptor CNG channel activity. Am J Physiol Endocrinol Metab. 2012 Dec 01; 303(11):E1363-72.
Focus on molecules: phosphatidylinositol-4,5-bisphosphate (PIP2). Exp Eye Res. 2010 Sep; 91(3):324-5.
Basic FGF-induced down-regulation of IGF-I mRNA in cultured rat Müller cells. Exp Eye Res. 1999 Jan; 68(1):19-27.
Extracellular matrix proteins are potent agonists of human smooth muscle cell migration. J Vasc Surg. 1996 Jul; 24(1):25-32; discussion 32-3.
Regulation of genetic expression in shear stress-stimulated endothelial cells. Ann N Y Acad Sci. 1992 Oct 13; 665:94-104.
Shear stress increases inositol trisphosphate levels in human endothelial cells. Biochem Biophys Res Commun. 1990 Jul 16; 170(1):281-7.
T lymphocyte activation: a biological model of signal transduction. Crit Rev Immunol. 1990; 10(4):347-91.