Please use this identifier to cite or link to this item: https://saber.ucv.ve/jspui/handle/10872/13853
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dc.contributor.authorVarndell, I.M.-
dc.contributor.authorHarris, A.-
dc.contributor.authorTapia, Félix J.-
dc.contributor.authorYanaihara, N.-
dc.contributor.authorDe Mey, J.-
dc.contributor.authorBloom, S.R-
dc.contributor.authorPolak, J.M.-
dc.date.accessioned2016-04-07T23:14:19Z-
dc.date.available2016-04-07T23:14:19Z-
dc.date.issued1983-07-
dc.identifier.issn0014-4754-
dc.identifier.urihttp://hdl.handle.net/10872/13853-
dc.description.abstractGastrin (G )-producing cells from the mammalian gastric antrum have been investigated using computer-assisted morphometry and a novel double colloidal gold-labeled-immunoglobulin electron immunocytochemical procedure. Correlation analysis of human antral G-cells indica tes (p < 0.001) that a single population of granules exists with small (160 nm) electron-dense and large (240 nm) electron-lucent forms representing the extremes. Non-crossreacting region-specific antisera have been used to visualize G-17 and G34 (progastrin) to the small electron-dense granules and G-17 lo the other intermediate forms. From the results we propose a topographic segregation of immunoreactive gastrins within 2 apparently distinct granule subclasses and suggest that this may represent the pathway of granule maturation.es_VE
dc.language.isoenes_VE
dc.publisherExperientiaes_VE
dc.relation.ispartofseriesVol. 15;Nº 39-
dc.subjectGastrin (G )es_VE
dc.subjectproducing cellses_VE
dc.subjectassisted morphometryes_VE
dc.subjectelectron-densees_VE
dc.subjectelectron-lucentes_VE
dc.titleIntracellular topography of immunoreactlve gastrin demonstrated using electron immunocytochemistry.es_VE
dc.typeArticlees_VE
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