"Cyclic AMP" 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.
An adenine nucleotide containing one phosphate group which is esterified to both the 3'- and 5'-positions of the sugar moiety. It is a second messenger and a key intracellular regulator, functioning as a mediator of activity for a number of hormones, including epinephrine, glucagon, and ACTH.
Descriptor ID |
D000242
|
MeSH Number(s) |
D03.633.100.759.646.138.395 D13.695.462.200 D13.695.667.138.395 D13.695.827.068.395
|
Concept/Terms |
Cyclic AMP- Cyclic AMP
- AMP, Cyclic
- Adenosine Cyclic-3',5'-Monophosphate
- Cyclic-3',5'-Monophosphate, Adenosine
- Adenosine Cyclic Monophosphate
- Cyclic Monophosphate, Adenosine
- Monophosphate, Adenosine Cyclic
- Adenosine Cyclic 3,5 Monophosphate
- Adenosine Cyclic 3',5'-Monophosphate
- 3',5'-Monophosphate, Adenosine Cyclic
- Adenosine Cyclic 3',5' Monophosphate
- Cyclic 3',5'-Monophosphate, Adenosine
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Below are MeSH descriptors whose meaning is more general than "Cyclic AMP".
Below are MeSH descriptors whose meaning is more specific than "Cyclic AMP".
This graph shows the total number of publications written about "Cyclic AMP" by people in this website by year, and whether "Cyclic AMP" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1992 | 2 | 1 | 3 |
1993 | 0 | 2 | 2 |
1994 | 0 | 1 | 1 |
1995 | 0 | 1 | 1 |
1996 | 0 | 4 | 4 |
1998 | 0 | 1 | 1 |
1999 | 0 | 1 | 1 |
2000 | 0 | 1 | 1 |
2001 | 0 | 1 | 1 |
2002 | 0 | 3 | 3 |
2003 | 1 | 3 | 4 |
2005 | 1 | 0 | 1 |
2007 | 1 | 2 | 3 |
2008 | 0 | 4 | 4 |
2009 | 0 | 1 | 1 |
2010 | 0 | 2 | 2 |
2011 | 1 | 3 | 4 |
2012 | 1 | 1 | 2 |
2013 | 1 | 1 | 2 |
2014 | 0 | 1 | 1 |
2016 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
2019 | 0 | 1 | 1 |
2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Cyclic AMP" by people in Profiles.
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Sah P, Derouen JT, Alexander JL, Zenewicz LA. Group 3 innate lymphocytes (ILC3s) upregulate IL-22 in response to elevated intracellular cAMP levels. Cytokine. 2022 05; 153:155862.
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Moss WJ, Patterson CE, Jochmans AK, Brown KM. Functional Analysis of the Expanded Phosphodiesterase Gene Family in Toxoplasma gondii Tachyzoites. mSphere. 2022 02 23; 7(1):e0079321.
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Roehrkasse AM, Warner ML, Booe JM, Pioszak AA. 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.
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Pan Z, Dumas EK, Lawrence C, Pate L, Longobardi S, Wang X, James JA, Kovats S, Farris AD. Bacillus anthracis Edema Toxin Inhibits Efferocytosis in Human Macrophages and Alters Efferocytic Receptor Signaling. Int J Mol Sci. 2019 Mar 07; 20(5).
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Larabee JL, Hauck G, Ballard JD. Unique, Intersecting, and Overlapping Roles of C/EBP ß and CREB in Cells of the Innate Immune System. Sci Rep. 2018 11 16; 8(1):16931.
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Blackwood BP, Wood DR, Yuan C, Nicolas J, De Plaen IG, Farrow KN, Chou P, Turner JR, Hunter CJ. A Role for cAMP and Protein Kinase A in Experimental Necrotizing Enterocolitis. Am J Pathol. 2017 Feb; 187(2):401-417.
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Singh N, Yadav M, Singh AK, Kumar H, Dwivedi SK, Mishra JS, Gurjar A, Manhas A, Chandra S, Yadav PN, Jagavelu K, Siddiqi MI, Trivedi AK, Chattopadhyay N, Sanyal S. Synthetic FXR agonist GW4064 is a modulator of multiple G protein-coupled receptors. Mol Endocrinol. 2014 May; 28(5):659-73.
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Ha JH, Ward JD, Varadarajalu L, Kim SG, Dhanasekaran DN. The gep proto-oncogene Ga12 mediates LPA-stimulated activation of CREB in ovarian cancer cells. Cell Signal. 2014 Jan; 26(1):122-32.
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Larabee JL, Shakir SM, Barua S, Ballard JD. Increased cAMP in monocytes augments Notch signaling mechanisms by elevating RBP-J and transducin-like enhancer of Split (TLE). J Biol Chem. 2013 Jul 26; 288(30):21526-36.
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Weems JC, Griesel BA, Olson AL. Class II histone deacetylases downregulate GLUT4 transcription in response to increased cAMP signaling in cultured adipocytes and fasting mice. Diabetes. 2012 Jun; 61(6):1404-14.