"AMP Deaminase" 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 enzyme that catalyzes the deamination of AMP to IMP. EC 3.5.4.6.
| Descriptor ID |
D000659
|
| MeSH Number(s) |
D08.811.277.151.653.060
|
| Concept/Terms |
AMP Deaminase- AMP Deaminase
- Deaminase, AMP
- Adenylate Deaminase
- Deaminase, Adenylate
- Myoadenylate Deaminase
- Deaminase, Myoadenylate
- AMP Aminohydrolase
- Aminohydrolase, AMP
- 5'-AMP Deaminase
- 5' AMP Deaminase
- Deaminase, 5'-AMP
- AMP Aminase
- Aminase, AMP
|
Below are MeSH descriptors whose meaning is more general than "AMP Deaminase".
Below are MeSH descriptors whose meaning is more specific than "AMP Deaminase".
This graph shows the total number of publications written about "AMP Deaminase" by people in this website by year, and whether "AMP Deaminase" 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 |
|---|
| 1998 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2003 | 1 | 1 | 2 |
| 2004 | 2 | 0 | 2 |
| 2005 | 3 | 0 | 3 |
| 2006 | 2 | 1 | 3 |
| 2007 | 2 | 0 | 2 |
| 2008 | 0 | 1 | 1 |
| 2009 | 1 | 3 | 4 |
| 2010 | 1 | 0 | 1 |
| 2011 | 2 | 2 | 4 |
| 2012 | 1 | 0 | 1 |
| 2013 | 2 | 1 | 3 |
| 2014 | 2 | 2 | 4 |
| 2015 | 2 | 1 | 3 |
| 2016 | 3 | 1 | 4 |
| 2017 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "AMP Deaminase" by people in Profiles.
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Teaching NeuroImages: Figure of 8: The clue to the diagnosis of AMPD2 pontocerebellar hypoplasia (PCH9). Neurology. 2017 10 03; 89(14):e172-e173.
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Insertion of a knockout-first cassette in Ampd1 gene leads to neonatal death by disruption of neighboring genes expression. Sci Rep. 2016 10 24; 6:35970.
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Genetic evaluation of AMPD1, CPT2, and PGYM metabolic enzymes in patients with chronic fatigue syndrome. Genet Mol Res. 2016 Jul 29; 15(3).
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Inflammation markers are associated with metabolic syndrome and ventricular arrhythmia in patients with coronary artery disease. Postepy Hig Med Dosw (Online). 2016 Feb 11; 70:56-66.
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Possible influence of AMPD1 on cholinergic neurotransmission and sleep. J Sleep Res. 2016 Feb; 25(1):124-6.
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Effects of the 34C>T Variant of the AMPD1 Gene on Immune Function, Multi-Organ Dysfunction, and Mortality in Sepsis Patients. Shock. 2015 Dec; 44(6):542-7.
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AMPD1 polymorphism and response to regadenoson. Pharmacogenomics. 2015 Nov; 16(16):1807-15.
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Effect of dipyridamole on myocardial reperfusion injury: A double-blind randomized controlled trial in patients undergoing elective coronary artery bypass surgery. Clin Pharmacol Ther. 2016 Apr; 99(4):381-9.
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AMPD1 functional variants associated with autism in Han Chinese population. Eur Arch Psychiatry Clin Neurosci. 2015 Sep; 265(6):511-7.
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Metformin in vitro and in vivo increases adenosine signaling in rabbit corpora cavernosa. J Sex Med. 2014 Jul; 11(7):1694-708.