"Acyltransferases" 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.
Enzymes from the transferase class that catalyze the transfer of acyl groups from donor to acceptor, forming either esters or amides. (From Enzyme Nomenclature 1992) EC 2.3.
Descriptor ID |
D000217
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MeSH Number(s) |
D08.811.913.050
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Acyltransferases".
Below are MeSH descriptors whose meaning is more specific than "Acyltransferases".
This graph shows the total number of publications written about "Acyltransferases" by people in this website by year, and whether "Acyltransferases" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1994 | 1 | 0 | 1 |
1996 | 0 | 1 | 1 |
1997 | 1 | 0 | 1 |
2001 | 0 | 1 | 1 |
2009 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2015 | 1 | 1 | 2 |
2016 | 0 | 1 | 1 |
2020 | 1 | 0 | 1 |
2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Acyltransferases" by people in Profiles.
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Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis. Genes (Basel). 2023 03 15; 14(3).
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Loss of hepatic Mboat7 leads to liver fibrosis. Gut. 2021 05; 70(5):940-950.
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CDK5RAP2 interaction with components of the Hippo signaling pathway may play a role in primary microcephaly. Mol Genet Genomics. 2017 Apr; 292(2):365-383.
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A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis. Nat Genet. 2015 Dec; 47(12):1443-8.
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Tentative clinical diagnosis of Lujan-Fryns syndrome--A conglomeration of different genetic entities? Am J Med Genet A. 2016 Jan; 170A(1):94-102.
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Theoretical study of lipid biosynthesis in wild-type Escherichia coli and in a protoplast-type L-form using elementary flux mode analysis. FEBS J. 2010 Feb; 277(4):1023-34.
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Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap. Eur J Hum Genet. 2009 Oct; 17(10):1207-15.
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Lysophosphatidic acid, a novel lipid growth factor for human thyroid cells: over-expression of the high-affinity receptor edg4 in differentiated thyroid cancer. Int J Cancer. 2001 Apr 15; 92(2):249-56.
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PcMYB1, a novel plant protein containing a DNA-binding domain with one MYB repeat, interacts in vivo with a light-regulatory promoter unit. Plant J. 1997 May; 11(5):1079-93.
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The transcriptional regulator CPRF1: expression analysis and gene structure. Mol Gen Genet. 1996 Jul 26; 251(6):619-27.