"Shab Potassium Channels" 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 subfamily of shaker potassium channels that shares homology with its founding member, Shab protein, Drosophila. They regulate delayed rectifier currents in the NERVOUS SYSTEM of DROSOPHILA and in the SKELETAL MUSCLE and HEART of VERTEBRATES.
|Shab Potassium Channels
- Shab Potassium Channels
- Potassium Channels, Shab
- Kv2 Potassium Channels
- Potassium Channels, Kv2
Kv2.2 Potassium Channel
- Kv2.2 Potassium Channel
- Potassium Channel, Kv2.2
- KCNB2 Potassium Channel
- Potassium Channel, KCNB2
- CDRK Potassium Channel
- Potassium Channel, CDRK
Kv2.1 Potassium Channel
- Kv2.1 Potassium Channel
- Potassium Channel, Kv2.1
- DRK1 Potassium Channel
- Potassium Channel, DRK1
Below are MeSH descriptors whose meaning is more general than "Shab Potassium Channels".
Below are MeSH descriptors whose meaning is more specific than "Shab Potassium Channels".
This graph shows the total number of publications written about "Shab Potassium Channels" by people in this website by year, and whether "Shab Potassium Channels" 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|
To return to the timeline, click here.
Below are the most recent publications written about "Shab Potassium Channels" by people in Profiles.
Determining the correct stoichiometry of Kv2.1/Kv6.4 heterotetramers, functional in multiple stoichiometrical configurations. Proc Natl Acad Sci U S A. 2020 04 28; 117(17):9365-9376.
Regulation of Kv2.1 channel inactivation by phosphatidylinositol 4,5-bisphosphate. Sci Rep. 2018 01 29; 8(1):1769.
Dromedary immune response and specific Kv2.1 antibody generation using a specific immunization approach. Int J Biol Macromol. 2016 Dec; 93(Pt A):167-171.
Voltage-sensor conformation shapes the intra-membrane drug binding site that determines gambierol affinity in Kv channels. Neuropharmacology. 2016 08; 107:160-167.
Modulation of Closed-State Inactivation in Kv2.1/Kv6.4 Heterotetramers as Mechanism for 4-AP Induced Potentiation. PLoS One. 2015; 10(10):e0141349.
Quantitative single-cell ion-channel gene expression profiling through an improved qRT-PCR technique combined with whole cell patch clamp. J Neurosci Methods. 2012 Jul 30; 209(1):227-34.
The electrically silent Kv6.4 subunit confers hyperpolarized gating charge movement in Kv2.1/Kv6.4 heterotetrameric channels. PLoS One. 2012; 7(5):e37143.
SUMO modification of cell surface Kv2.1 potassium channels regulates the activity of rat hippocampal neurons. J Gen Physiol. 2011 May; 137(5):441-54.
Functional interactions between residues in the S1, S4, and S5 domains of Kv2.1. Eur Biophys J. 2011 Jun; 40(6):783-93.
Conserved negative charges in the N-terminal tetramerization domain mediate efficient assembly of Kv2.1 and Kv2.1/Kv6.4 channels. J Biol Chem. 2009 Nov 13; 284(46):31625-34.