"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 |
|---|
| 1991 | 0 | 1 | 1 |
| 1996 | 2 | 0 | 2 |
| 1998 | 2 | 0 | 2 |
| 1999 | 0 | 3 | 3 |
| 2001 | 1 | 1 | 2 |
| 2002 | 4 | 0 | 4 |
| 2003 | 2 | 1 | 3 |
| 2004 | 1 | 0 | 1 |
| 2005 | 3 | 0 | 3 |
| 2006 | 3 | 1 | 4 |
| 2007 | 2 | 0 | 2 |
| 2008 | 1 | 1 | 2 |
| 2009 | 1 | 2 | 3 |
| 2010 | 2 | 1 | 3 |
| 2011 | 2 | 2 | 4 |
| 2012 | 2 | 0 | 2 |
| 2013 | 3 | 2 | 5 |
| 2014 | 4 | 2 | 6 |
| 2015 | 6 | 0 | 6 |
| 2016 | 4 | 2 | 6 |
| 2017 | 0 | 3 | 3 |
| 2018 | 2 | 0 | 2 |
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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Functional genomics identifies AMPD2 as a new prognostic marker for undifferentiated pleomorphic sarcoma. Int J Cancer. 2019 02 15; 144(4):859-867.
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Multicopy integrants of crt genes and co-expression of AMP deaminase improve lycopene production in Yarrowia lipolytica. J Biotechnol. 2019 Jan 10; 289:46-54.
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Clinical and genetic spectrum of AMPD2-related pontocerebellar hypoplasia type 9. Eur J Hum Genet. 2018 05; 26(5):695-708.
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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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Relationship Between Polymorphisms in Methotrexate Pathway Genes and Outcome of Methotrexate Treatment in a Cohort of 119 Patients with Juvenile Idiopathic Arthritis. J Rheumatol. 2017 08; 44(8):1216-1223.
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Genetic contribution to lipid levels in early life based on 158 loci validated in adults: the FAMILY study. Sci Rep. 2017 03 06; 7(1):68.
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The role of microorganisms in the degradation of adenosine triphosphate (ATP) in chill-stored common carp (Cyprinus carpio) fillets. Food Chem. 2017 Jun 01; 224:347-352.
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Dissociation of muscle insulin sensitivity from exercise endurance in mice by HDAC3 depletion. Nat Med. 2017 Feb; 23(2):223-234.
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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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Overproduction, Purification and Characterization of Adenylate Deaminase from Aspergillus oryzae. Appl Biochem Biotechnol. 2016 Dec; 180(8):1635-1643.