Plasma Membrane Neurotransmitter Transport Proteins
"Plasma Membrane Neurotransmitter Transport Proteins" 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 family of neurotransmitter transporter proteins that facilitate NEUROTRANSMITTER reuptake into PRESYNAPTIC TERMINALS. They may play a role in regulating the intensity and duration of neurotransmission.
MeSH Number(s)
D12.776.157.530.562.374
D12.776.543.585.562.374
Concept/Terms
Plasma Membrane Neurotransmitter Transport Proteins- Plasma Membrane Neurotransmitter Transport Proteins
- Plasma Membrane Neurotransmitter Transporters
- Plasma Membrane Neurotransmitter Transporter Proteins
- Neurotransmitter Transport Proteins, Plasma Membrane
- Neurotransmitter Transporters, Plasma Membrane
Below are MeSH descriptors whose meaning is more general than "Plasma Membrane Neurotransmitter Transport Proteins".
Below are MeSH descriptors whose meaning is more specific than "Plasma Membrane Neurotransmitter Transport Proteins".
This graph shows the total number of publications written about "Plasma Membrane Neurotransmitter Transport Proteins" by people in Harvard Catalyst Profiles by year, and whether "Plasma Membrane Neurotransmitter Transport Proteins" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 0 | 1 | 1 |
| 2005 | 1 | 0 | 1 |
| 2006 | 0 | 1 | 1 |
| 2008 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 2 | 0 | 2 |
| 2017 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
Below are the most recent publications written about "Plasma Membrane Neurotransmitter Transport Proteins" by people in Profiles.
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Creatine Transporter Deficiency Presenting as Failure to Thrive: A Case Report of a Novel SLC6A8 Variant Causing a Treatable but Likely Underdiagnosed Genetic Disorder. J Investig Med High Impact Case Rep. 2023 Jan-Dec; 11:23247096231154438.
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Person Ability Scores as an Alternative to Norm-Referenced Scores as Outcome Measures in Studies of Neurodevelopmental Disorders. Am J Intellect Dev Disabil. 2020 11 01; 125(6):475-480.
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Laboratory diagnosis of creatine deficiency syndromes: a technical standard and guideline of the American College of Medical Genetics and Genomics. Genet Med. 2017 02; 19(2):256-263.
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Structural dynamics of the monoamine transporter homolog LeuT from accelerated conformational sampling and channel analysis. Proteins. 2014 Oct; 82(10):2289-302.
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Genotype-phenotype correlation of contiguous gene deletions of SLC6A8, BCAP31 and ABCD1. Clin Genet. 2015 Feb; 87(2):141-7.
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Phenotype and genotype in 101 males with X-linked creatine transporter deficiency. J Med Genet. 2013 Jul; 50(7):463-72.
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LeuT conformational sampling utilizing accelerated molecular dynamics and principal component analysis. Biophys J. 2012 Jul 03; 103(1):L1-3.
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Molecular analysis of guanidinoacetate-n-methyltransferase (GAMT) and creatine transporter (SLC6A8) gene by using denaturing high pressure liquid chromatography (DHPLC) as a possible source of human male infertility. Pak J Pharm Sci. 2011 Jan; 24(1):75-9.
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Cardiac manifestations in a child with a novel mutation in creatine transporter gene SLC6A8. Neurology. 2008 Apr 29; 70(18):1642-4.
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Prenatal choline deficiency increases choline transporter expression in the septum and hippocampus during postnatal development and in adulthood in rats. Brain Res. 2007 Jun 02; 1151:1-11.