{"id":33631,"date":"2018-03-09T09:30:51","date_gmt":"2018-03-09T09:30:51","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/implicaciones-de-la-tirosinacinasa-p125fak-en-procesos-de-secrecion-pancreatica\/"},"modified":"2018-03-09T09:30:51","modified_gmt":"2018-03-09T09:30:51","slug":"implicaciones-de-la-tirosinacinasa-p125fak-en-procesos-de-secrecion-pancreatica","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/ciencias-de-la-vida\/implicaciones-de-la-tirosinacinasa-p125fak-en-procesos-de-secrecion-pancreatica\/","title":{"rendered":"Implicaciones de la tirosinacinasa p125fak en procesos de secrecion pancreatica."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Juan  Antonio Rosado Dionisio <\/strong><\/h2>\n<p>La ocupaci\u00f3n de los receptores de membrana ccka de alta y baja afinidad y de los muscarinicos m3 presentes en c\u00e9lulas acinares pancre\u00e1ticas de rata induce fosforilaci\u00f3n por vias dependientes e independientes de la activaci\u00f3n de la prote\u00edna cinasa c y de la movilizaci\u00f3n de calcio intracelular de residuos de tirosina presentes en la tirosina cinasa fak y en su sustrato paxilina. Dichas fosforilaciones requieren el mantenimiento de la organizaci\u00f3n del citoesqueleto de actina y son dependientes, al menos parcialmente, de la activaci\u00f3n de la gtpasa, rho. La fosforilaci\u00f3n de p125fak y paxilina no parece ser requisito necesario para el inicio y mantenimiento del proceso secretor enzim\u00e1tico que normalmente tiene lugar tras la activaci\u00f3n de los receptores m3 y ccka.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Implicaciones de la tirosinacinasa p125fak en procesos de secrecion pancreatica.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Implicaciones de la tirosinacinasa p125fak en procesos de secrecion pancreatica. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Juan  Antonio Rosado Dionisio <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Extremadura<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 22\/12\/1997<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Luis Jes\u00fas Garc\u00eda Mar\u00edn<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Jos\u00e9 Miguel Lopez novoa <\/li>\n<li>guillermo Alvarez de toledo naranjo (vocal)<\/li>\n<li>Antonio Farre viladrich (vocal)<\/li>\n<li>Jos\u00e9 Juli\u00e1n Calvo andres (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Juan Antonio Rosado Dionisio La ocupaci\u00f3n de los receptores de membrana ccka de alta y baja afinidad [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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