| pubmed-article:7507337 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7507337 | lifeskim:mentions | umls-concept:C0035316 | lld:lifeskim |
| pubmed-article:7507337 | lifeskim:mentions | umls-concept:C1171362 | lld:lifeskim |
| pubmed-article:7507337 | lifeskim:mentions | umls-concept:C0007447 | lld:lifeskim |
| pubmed-article:7507337 | lifeskim:mentions | umls-concept:C0600437 | lld:lifeskim |
| pubmed-article:7507337 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
| pubmed-article:7507337 | lifeskim:mentions | umls-concept:C1515670 | lld:lifeskim |
| pubmed-article:7507337 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:7507337 | pubmed:dateCreated | 1994-3-1 | lld:pubmed |
| pubmed-article:7507337 | pubmed:abstractText | We have identified a putative cGMP-gated cation conductance in rat retinal ganglion cells. Both in situ hybridization and polymerase chain reaction amplification detected transcripts in ganglion cells that were highly homologous to the cGMP-gated cation channel expressed in rod photoreceptors. Whole-cell patch-clamp recordings detected a current stimulated by cGMP due to activation of nonselective cation channels. This current had a reversal potential near 0 mV, showed some outward rectification, and could be blocked by Cd2+. The current could also be activated by a phosphodiesterase inhibitor and the nitric oxide donors sodium nitroprusside and S-nitrosocysteine. We propose that nitric oxide released from an identified subpopulation of amacrine cells may activate this channel to modulate ganglion cell activity. | lld:pubmed |
| pubmed-article:7507337 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:7507337 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:7507337 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7507337 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:7507337 | pubmed:issn | 0896-6273 | lld:pubmed |
| pubmed-article:7507337 | pubmed:author | pubmed-author:AhmadII | lld:pubmed |
| pubmed-article:7507337 | pubmed:author | pubmed-author:BarnstableC... | lld:pubmed |
| pubmed-article:7507337 | pubmed:author | pubmed-author:KocsisJ DJD | lld:pubmed |
| pubmed-article:7507337 | pubmed:author | pubmed-author:ShepherdG MGM | lld:pubmed |
| pubmed-article:7507337 | pubmed:author | pubmed-author:ZufallFF | lld:pubmed |
| pubmed-article:7507337 | pubmed:author | pubmed-author:Leinders-Zufa... | lld:pubmed |
| pubmed-article:7507337 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7507337 | pubmed:volume | 12 | lld:pubmed |
| pubmed-article:7507337 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7507337 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7507337 | pubmed:pagination | 155-65 | lld:pubmed |
| pubmed-article:7507337 | pubmed:dateRevised | 2008-11-21 | lld:pubmed |
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| pubmed-article:7507337 | pubmed:year | 1994 | lld:pubmed |
| pubmed-article:7507337 | pubmed:articleTitle | Retinal ganglion cells express a cGMP-gated cation conductance activatable by nitric oxide donors. | lld:pubmed |
| pubmed-article:7507337 | pubmed:affiliation | Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, Connecticut 06510. | lld:pubmed |
| pubmed-article:7507337 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7507337 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:7507337 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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