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A kainate receptor is an ionotropic receptor activated by the neurotransmitter glutamate. Activation opens an ion channel, coupling chemical recognition to an electrical response. The family is named after kainic acid, an experimental agonist. Kainate receptors and AMPA receptors are distinct receptor families even though some experimental agonists can activate both, making pharmacological responses alone difficult to interpret.[ref]
Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice by C. Mulle and others. Abstract: ionotropic receptor classes and difficulty separating kainate from AMPA responses.
A genetic experiment helped isolate the kainate component. C. Mulle and colleagues generated mice lacking the subunit then called GluR6. Neurons in the hippocampal CA3 region became much less sensitive to kainic acid; a postsynaptic kainate current evoked by a train of mossy-fibre stimulation was absent in the mutants. This linked a molecular subunit to a synaptically evoked response, rather than merely to a response produced by bathing tissue in an agonist.[ref]
Altered synaptic physiology and reduced susceptibility to kainate-induced seizures in GluR6-deficient mice by C. Mulle and others. Nature392,601–605(1998), abstract: deletion, CA3 responses and mossy-fibre stimulation.
The subunit's current name is GluK2.[ref]https://www.ncbi.nlm.nih.gov/mesh/2106638. NLM GluK2 nomenclature record, entry terms include GluR6
For example, a current produced by an agonist that also activates AMPA receptors cannot be assigned wholly to kainate receptors. Comparing selective perturbations with synaptic stimulation supplies stronger evidence for the receptor responsible. In another experimental setting, paired recordings in ground-squirrel retina showed that AMPA receptors and kainate receptors could route cone signals into OFF retinal bipolar cells with different temporal filtering properties.[ref]
Bipolar cells use kainate and AMPA receptors to filter visual information into separate channels by S. H. DeVries. Abstract and Results: paired cone/bipolar recordings, pharmacology and distinct temporal filtering.
Electron-ion recombination combines a free electron with a positive ion, reducing the number of free charge carriers. The released binding energy must be carried away, for example by a photon or another particle.
In an ionization chamber, recombination before charge collection reduces the measured signal. A simplified local model has loss rate , with coefficient depending on the species and conditions. Increasing the collection field can reduce the time available for recombination, but complete collection must be established experimentally rather than assumed from the applied voltage alone.
Pinned article: Introduction to the OurBigBook Project
Welcome to the OurBigBook Project! Our goal is to create the perfect publishing platform for STEM subjects, and get university-level students to write the best free STEM tutorials ever.
Everyone is welcome to create an account and play with the site: ourbigbook.com/go/register. We belive that students themselves can write amazing tutorials, but teachers are welcome too. You can write about anything you want, it doesn't have to be STEM or even educational. Silly test content is very welcome and you won't be penalized in any way. Just keep it legal!
Intro to OurBigBook
. Source. We have two killer features:
- topics: topics group articles by different users with the same title, e.g. here is the topic for the "Fundamental Theorem of Calculus" ourbigbook.com/go/topic/fundamental-theorem-of-calculusArticles of different users are sorted by upvote within each article page. This feature is a bit like:
- a Wikipedia where each user can have their own version of each article
- a Q&A website like Stack Overflow, where multiple people can give their views on a given topic, and the best ones are sorted by upvote. Except you don't need to wait for someone to ask first, and any topic goes, no matter how narrow or broad
This feature makes it possible for readers to find better explanations of any topic created by other writers. And it allows writers to create an explanation in a place that readers might actually find it.Figure 1. Screenshot of the "Derivative" topic page. View it live at: ourbigbook.com/go/topic/derivativeVideo 2. OurBigBook Web topics demo. Source. - local editing: you can store all your personal knowledge base content locally in a plaintext markup format that can be edited locally and published either:This way you can be sure that even if OurBigBook.com were to go down one day (which we have no plans to do as it is quite cheap to host!), your content will still be perfectly readable as a static site.
- to OurBigBook.com to get awesome multi-user features like topics and likes
- as HTML files to a static website, which you can host yourself for free on many external providers like GitHub Pages, and remain in full control
Figure 2. You can publish local OurBigBook lightweight markup files to either OurBigBook.com or as a static website.Figure 3. Visual Studio Code extension installation.Figure 5. . You can also edit articles on the Web editor without installing anything locally. Video 3. Edit locally and publish demo. Source. This shows editing OurBigBook Markup and publishing it using the Visual Studio Code extension. - Infinitely deep tables of contents:
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Further documentation can be found at: docs.ourbigbook.com
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