Cation Transport Proteins
"Cation 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.
Membrane proteins whose primary function is to facilitate the transport of positively charged molecules (cations) across a biological membrane.
| Descriptor ID |
D027682
|
| MeSH Number(s) |
D12.776.157.530.450.250 D12.776.543.585.450.250
|
| Concept/Terms |
Cation Pump- Cation Pump
- Pump, Cation
- Cation Pumps
- Pumps, Cation
|
Below are MeSH descriptors whose meaning is more general than "Cation Transport Proteins".
Below are MeSH descriptors whose meaning is more specific than "Cation Transport Proteins".
This graph shows the total number of publications written about "Cation Transport Proteins" by people in this website by year, and whether "Cation 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 |
|---|
| 1999 | 1 | 0 | 1 |
| 2001 | 5 | 0 | 5 |
| 2002 | 1 | 0 | 1 |
| 2003 | 0 | 1 | 1 |
| 2004 | 3 | 1 | 4 |
| 2005 | 2 | 1 | 3 |
| 2006 | 3 | 1 | 4 |
| 2007 | 3 | 0 | 3 |
| 2008 | 2 | 1 | 3 |
| 2009 | 3 | 1 | 4 |
| 2010 | 3 | 3 | 6 |
| 2011 | 3 | 2 | 5 |
| 2012 | 2 | 0 | 2 |
| 2013 | 2 | 2 | 4 |
| 2014 | 2 | 1 | 3 |
| 2015 | 2 | 1 | 3 |
| 2016 | 2 | 4 | 6 |
| 2017 | 1 | 1 | 2 |
| 2018 | 1 | 0 | 1 |
| 2019 | 0 | 1 | 1 |
| 2020 | 1 | 1 | 2 |
| 2021 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
| 2023 | 2 | 0 | 2 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Cation Transport Proteins" by people in Profiles.
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Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload. Sci China Life Sci. 2025 Feb; 68(2):484-501.
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A dominant-negative Arabidopsis cation exchanger 1 (CAX1): N-terminal autoinhibition and membrane topology. Plant J. 2024 Sep; 119(6):2982-2999.
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Mechanism of Ca2+ transport by ferroportin. Elife. 2023 01 17; 12.
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Structural basis of ferroportin inhibition by minihepcidin PR73. PLoS Biol. 2023 01; 21(1):e3001936.
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The vacuolar H+/Ca transporter CAX1 participates in submergence and anoxia stress responses. Plant Physiol. 2022 11 28; 190(4):2617-2636.
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Characterization of two novel ammonia transporters, Hiat1a and Hiat1b, in the teleost model system Danio rerio. J Exp Biol. 2022 10 15; 225(20).
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De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. Am J Med Genet A. 2022 08; 188(8):2360-2366.
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De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures. Mol Autism. 2021 10 26; 12(1):69.
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Genomic, Transcriptomic, and Proteomic Profiling of Metastatic Breast Cancer. Clin Cancer Res. 2021 06 01; 27(11):3243-3252.
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Structural basis of ion transport and inhibition in ferroportin. Nat Commun. 2020 11 10; 11(1):5686.