"Phosphoric Monoester Hydrolases" 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.
A group of hydrolases which catalyze the hydrolysis of monophosphoric esters with the production of one mole of orthophosphate.
Descriptor ID |
D010744
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MeSH Number(s) |
D08.811.277.352.650
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Phosphoric Monoester Hydrolases".
Below are MeSH descriptors whose meaning is more specific than "Phosphoric Monoester Hydrolases".
This graph shows the total number of publications written about "Phosphoric Monoester Hydrolases" by people in this website by year, and whether "Phosphoric Monoester Hydrolases" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2012 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
2021 | 2 | 0 | 2 |
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Below are the most recent publications written about "Phosphoric Monoester Hydrolases" by people in Profiles.
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An identical-by-descent novel splice-donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families. Ann Hum Genet. 2021 09; 85(5):186-195.
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Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes. J Gerontol A Biol Sci Med Sci. 2021 04 30; 76(5):786-795.
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Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1. Eur J Hum Genet. 2021 03; 29(3):411-421.
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Trehalose-6-Phosphate-Mediated Toxicity Determines Essentiality of OtsB2 in Mycobacterium tuberculosis In Vitro and in Mice. PLoS Pathog. 2016 Dec; 12(12):e1006043.
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Neu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathway. Am J Hum Genet. 2014 Sep 04; 95(3):285-93.
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A premature termination mutation in a patient with Lowe syndrome without congenital cataracts: dropping the "O" in OCRL. Klin Padiatr. 2013 Jan; 225(1):29-33.