Monosaccharide Transport Proteins
"Monosaccharide 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 large group of membrane transport proteins that shuttle MONOSACCHARIDES across CELL MEMBRANES.
| Descriptor ID |
D009004
|
| MeSH Number(s) |
D12.776.157.530.500 D12.776.543.585.500
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Monosaccharide Transport Proteins".
Below are MeSH descriptors whose meaning is more specific than "Monosaccharide Transport Proteins".
This graph shows the total number of publications written about "Monosaccharide Transport Proteins" by people in this website by year, and whether "Monosaccharide Transport Proteins" 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 |
|---|
| 1994 | 1 | 0 | 1 |
| 1995 | 1 | 0 | 1 |
| 1997 | 2 | 0 | 2 |
| 1998 | 1 | 1 | 2 |
| 1999 | 1 | 0 | 1 |
| 2000 | 0 | 2 | 2 |
| 2001 | 4 | 3 | 7 |
| 2002 | 1 | 5 | 6 |
| 2003 | 1 | 1 | 2 |
| 2004 | 2 | 1 | 3 |
| 2007 | 2 | 0 | 2 |
| 2010 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Monosaccharide Transport Proteins" by people in Profiles.
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SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals. Hum Mutat. 2019 07; 40(7):908-925.
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The Autoimmune Disorder Susceptibility Gene CLEC16A Restrains NK Cell Function in YTS NK Cell Line and Clec16a Knockout Mice. Front Immunol. 2019; 10:68.
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CLEC16A regulates splenocyte and NK cell function in part through MEK signaling. PLoS One. 2018; 13(9):e0203952.
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Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy. Ann Neurol. 2018 06; 83(6):1133-1146.
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Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet. PLoS One. 2017; 12(9):e0184022.
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Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein. Nat Commun. 2017 01 20; 8:14152.
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Toward high-resolution computational design of the structure and function of helical membrane proteins. Nat Struct Mol Biol. 2016 06 07; 23(6):475-80.
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Clinical reasoning: novel GLUT1-DS mutation: refractory seizures and ataxia. Neurology. 2015 Apr 14; 84(15):e111-4.
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Triheptanoin for glucose transporter type I deficiency (G1D): modulation of human ictogenesis, cerebral metabolic rate, and cognitive indices by a food supplement. JAMA Neurol. 2014 Oct; 71(10):1255-65.
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The diabetes susceptibility gene Clec16a regulates mitophagy. Cell. 2014 Jun 19; 157(7):1577-90.