pubmed-article:14749428 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C0027882 | lld:lifeskim |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C0038588 | lld:lifeskim |
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pubmed-article:14749428 | lifeskim:mentions | umls-concept:C1171362 | lld:lifeskim |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C0120285 | lld:lifeskim |
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pubmed-article:14749428 | lifeskim:mentions | umls-concept:C0036849 | lld:lifeskim |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C1442518 | lld:lifeskim |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C0205463 | lld:lifeskim |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C1552652 | lld:lifeskim |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C2348519 | lld:lifeskim |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C1552685 | lld:lifeskim |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C1704788 | lld:lifeskim |
pubmed-article:14749428 | lifeskim:mentions | umls-concept:C1705195 | lld:lifeskim |
pubmed-article:14749428 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:14749428 | pubmed:dateCreated | 2004-1-29 | lld:pubmed |
pubmed-article:14749428 | pubmed:abstractText | The spinal substantia gelatinosa (SG) is known to be involved in the manipulation of nociceptive and thermal primary afferent input; however, the interrelationships of its neuronal components are poorly understood. As a step toward expanding understanding, we took a relatively unique approach by concentrating on a set of SG neurons selectively labeled by green fluorescent protein (GFP) in a transgenic mouse. These GFP-expressing SG neurons prove to have homogenous morphological and electrophysiological properties, are systematically spaced in the SG, contain GABA, receive C-fiber primary afferent input, and upregulate c-Fos protein in response to noxious stimuli. Together, the properties established for these GFP-labeled neurons are consistent with a modular SG organization in which afferent activity related to nociception or other C-fiber signaling are subject to integration/modulation by repeating, similar circuits of neurons. | lld:pubmed |
pubmed-article:14749428 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14749428 | pubmed:language | eng | lld:pubmed |
pubmed-article:14749428 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14749428 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:14749428 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:14749428 | pubmed:month | Jan | lld:pubmed |
pubmed-article:14749428 | pubmed:issn | 1529-2401 | lld:pubmed |
pubmed-article:14749428 | pubmed:author | pubmed-author:van den... | lld:pubmed |
pubmed-article:14749428 | pubmed:author | pubmed-author:PerlEdward... | lld:pubmed |
pubmed-article:14749428 | pubmed:author | pubmed-author:HantmanAdam... | lld:pubmed |
pubmed-article:14749428 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:14749428 | pubmed:day | 28 | lld:pubmed |
pubmed-article:14749428 | pubmed:volume | 24 | lld:pubmed |
pubmed-article:14749428 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:14749428 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:14749428 | pubmed:pagination | 836-42 | lld:pubmed |
pubmed-article:14749428 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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pubmed-article:14749428 | pubmed:meshHeading | pubmed-meshheading:14749428... | lld:pubmed |
pubmed-article:14749428 | pubmed:year | 2004 | lld:pubmed |
pubmed-article:14749428 | pubmed:articleTitle | Morphological and physiological features of a set of spinal substantia gelatinosa neurons defined by green fluorescent protein expression. | lld:pubmed |
pubmed-article:14749428 | pubmed:affiliation | Department of Cell and Molecular Physiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA. | lld:pubmed |
pubmed-article:14749428 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:14749428 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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