Matches in SemOpenAlex for { <https://semopenalex.org/work/W2000682050> ?p ?o ?g. }
- W2000682050 endingPage "33" @default.
- W2000682050 startingPage "26" @default.
- W2000682050 abstract "Abstract Inward and, depending on activation state, outward potassium currents are the dominant ion channels in microglial cells in culture. During transition between resting and activated phases, there is also an upregulated expression of stretch/swelling‐activated chloride currents. Pharmacological blockade of the specific potassium channels does not prevent the transition, whereas blockade of chloride channels does, suggesting that this current may be involved in phase changes. Interestingly, this chloride current is far less studied than the potassium currents with regard to the different microglial phases. One puzzling finding when studying microglial state is that despite changes in current densities and membrane oscillations during transition, there is no evidence of an accompanying change in membrane potential. In other cells of the immune system, membrane oscillations and alterations in membrane potential are correlated with transitions in cellular phases. This discrepancy in microglia may be a result of the fact that almost all ion channel and membrane potential studies in culture are undertaken with concomitant dialysis of cytoplasm with pipette solution. Further complicating matters is that the few studies that use microglia in situ, find fundamental differences in ion channel current patterns of “resting” microglia as well as different temporal changes to pathological events or stimuli. Microsc. Res. Tech. 54:26–33, 2001. © 2001 Wiley‐Liss, Inc." @default.
- W2000682050 created "2016-06-24" @default.
- W2000682050 creator A5017992417 @default.
- W2000682050 creator A5083634411 @default.
- W2000682050 date "2001-06-05" @default.
- W2000682050 modified "2023-09-23" @default.
- W2000682050 title "Ion channels in cultured microglia" @default.
- W2000682050 cites W1519817425 @default.
- W2000682050 cites W1864129699 @default.
- W2000682050 cites W1901115290 @default.
- W2000682050 cites W1930803389 @default.
- W2000682050 cites W1934467632 @default.
- W2000682050 cites W1974210405 @default.
- W2000682050 cites W1985973215 @default.
- W2000682050 cites W1992593796 @default.
- W2000682050 cites W1992967280 @default.
- W2000682050 cites W1999827700 @default.
- W2000682050 cites W1999862704 @default.
- W2000682050 cites W2001226049 @default.
- W2000682050 cites W2005772981 @default.
- W2000682050 cites W2007284527 @default.
- W2000682050 cites W2011094963 @default.
- W2000682050 cites W2012210144 @default.
- W2000682050 cites W2013923694 @default.
- W2000682050 cites W2015962290 @default.
- W2000682050 cites W2017305833 @default.
- W2000682050 cites W2026627501 @default.
- W2000682050 cites W2031186076 @default.
- W2000682050 cites W2032505238 @default.
- W2000682050 cites W2043589327 @default.
- W2000682050 cites W2043794976 @default.
- W2000682050 cites W2050361888 @default.
- W2000682050 cites W2051148897 @default.
- W2000682050 cites W2052926870 @default.
- W2000682050 cites W2059091065 @default.
- W2000682050 cites W2064329226 @default.
- W2000682050 cites W2068830996 @default.
- W2000682050 cites W2071779846 @default.
- W2000682050 cites W2077475030 @default.
- W2000682050 cites W2080455120 @default.
- W2000682050 cites W2084255043 @default.
- W2000682050 cites W2092547166 @default.
- W2000682050 cites W2123326490 @default.
- W2000682050 cites W2141892357 @default.
- W2000682050 cites W2141977404 @default.
- W2000682050 cites W2142820562 @default.
- W2000682050 cites W2144042798 @default.
- W2000682050 cites W2151497893 @default.
- W2000682050 cites W2157660452 @default.
- W2000682050 cites W2162693284 @default.
- W2000682050 cites W2170785039 @default.
- W2000682050 cites W2183920111 @default.
- W2000682050 cites W2189016339 @default.
- W2000682050 cites W2268145670 @default.
- W2000682050 cites W2465134749 @default.
- W2000682050 cites W2734291336 @default.
- W2000682050 cites W4245476301 @default.
- W2000682050 cites W4313324522 @default.
- W2000682050 cites W963922907 @default.
- W2000682050 doi "https://doi.org/10.1002/jemt.1117" @default.
- W2000682050 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/11526954" @default.
- W2000682050 hasPublicationYear "2001" @default.
- W2000682050 type Work @default.
- W2000682050 sameAs 2000682050 @default.
- W2000682050 citedByCount "22" @default.
- W2000682050 countsByYear W20006820502012 @default.
- W2000682050 countsByYear W20006820502013 @default.
- W2000682050 countsByYear W20006820502015 @default.
- W2000682050 countsByYear W20006820502016 @default.
- W2000682050 countsByYear W20006820502022 @default.
- W2000682050 crossrefType "journal-article" @default.
- W2000682050 hasAuthorship W2000682050A5017992417 @default.
- W2000682050 hasAuthorship W2000682050A5083634411 @default.
- W2000682050 hasBestOaLocation W20006820501 @default.
- W2000682050 hasConcept C12554922 @default.
- W2000682050 hasConcept C145822097 @default.
- W2000682050 hasConcept C169760540 @default.
- W2000682050 hasConcept C170493617 @default.
- W2000682050 hasConcept C178790620 @default.
- W2000682050 hasConcept C181911157 @default.
- W2000682050 hasConcept C185263204 @default.
- W2000682050 hasConcept C185592680 @default.
- W2000682050 hasConcept C203014093 @default.
- W2000682050 hasConcept C2776914184 @default.
- W2000682050 hasConcept C2779830541 @default.
- W2000682050 hasConcept C41625074 @default.
- W2000682050 hasConcept C50254741 @default.
- W2000682050 hasConcept C517785266 @default.
- W2000682050 hasConcept C55493867 @default.
- W2000682050 hasConcept C83743174 @default.
- W2000682050 hasConcept C86803240 @default.
- W2000682050 hasConcept C95444343 @default.
- W2000682050 hasConceptScore W2000682050C12554922 @default.
- W2000682050 hasConceptScore W2000682050C145822097 @default.
- W2000682050 hasConceptScore W2000682050C169760540 @default.
- W2000682050 hasConceptScore W2000682050C170493617 @default.
- W2000682050 hasConceptScore W2000682050C178790620 @default.
- W2000682050 hasConceptScore W2000682050C181911157 @default.