UP 202-56, an adenosine analogue, selectively acts via A1 receptors to significantly decrease noxiously-evoked spinal c-Fos protein expression.
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| Title: | UP 202-56, an adenosine analogue, selectively acts via A1 receptors to significantly decrease noxiously-evoked spinal c-Fos protein expression. |
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| Authors: | Honoré P; Physiopharmacologie du Système Nerveux, INSERM U.161 and EPHE, Paris, France., Buritova J, Chapman V, Besson JM |
| Source: | Pain [Pain] 1998 Apr; Vol. 75 (2-3), pp. 281-93. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 7508686 Publication Model: Print Cited Medium: Print ISSN: 0304-3959 (Print) Linking ISSN: 03043959 NLM ISO Abbreviation: Pain Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 9583764 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: UP 202-56, an adenosine analogue, selectively acts via A1 receptors to significantly decrease noxiously-evoked spinal c-Fos protein expression. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Honoré+P%22">Honoré P</searchLink>; Physiopharmacologie du Système Nerveux, INSERM U.161 and EPHE, Paris, France.<br /><searchLink fieldCode="AU" term="%22Buritova+J%22">Buritova J</searchLink><br /><searchLink fieldCode="AU" term="%22Chapman+V%22">Chapman V</searchLink><br /><searchLink fieldCode="AU" term="%22Besson+JM%22">Besson JM</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%227508686%22">Pain</searchLink> [Pain] 1998 Apr; Vol. 75 (2-3), pp. 281-93. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lippincott+Williams+%26+Wilkins%22">Lippincott Williams & Wilkins </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>7508686 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>0304-3959 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2203043959%22">03043959 </searchLink><i>NLM ISO Abbreviation: </i>Pain <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=9583764 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/s0304-3959(98)00006-2 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 281 Titles: – TitleFull: UP 202-56, an adenosine analogue, selectively acts via A1 receptors to significantly decrease noxiously-evoked spinal c-Fos protein expression. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Honoré P – PersonEntity: Name: NameFull: Buritova J – PersonEntity: Name: NameFull: Chapman V – PersonEntity: Name: NameFull: Besson JM IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 04 Text: 1998 Apr Type: published Y: 1998 Identifiers: – Type: issn-print Value: 0304-3959 Numbering: – Type: volume Value: 75 – Type: issue Value: 2-3 Titles: – TitleFull: Pain Type: main |
| ResultId | 1 |