{"id":31549,"date":"1997-01-01T00:00:00","date_gmt":"1997-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/caracterizacion-de-un-nuevo-factor-pou-en-placenta-humana\/"},"modified":"1997-01-01T00:00:00","modified_gmt":"1997-01-01T00:00:00","slug":"caracterizacion-de-un-nuevo-factor-pou-en-placenta-humana","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/caracterizacion-de-un-nuevo-factor-pou-en-placenta-humana\/","title":{"rendered":"Caracterizacion de un nuevo factor pou en placenta humana."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Oscar Jimenez Mateo <\/strong><\/h2>\n<p>Se han clonado 1805 pares de bases correspondientes al adn complementario de un nuevo factor de transcripcion pou humano. Este factor, hpla-1, es homologo del factor skn-1\/epoc-1\/oct-11, clonado inicialmente en rata y raton, y no habia sido identificado previamente, en humanos. El gen de hpla-1 se expresa especificamente, en placenta, tiroides, e hipofisis humana. El pre-arn mensajero de hpla-1 presenta multiples opciones de procesamiento, generando distintas poblaciones de arn mensajeros maduros (hpla-1, hpla-1ar, y hpla-1tt).  el arn mensajero de hpla-1 codifica para una proteina de 436 aa y 47.4 kda. Los arn mensajeros de hp1a-1ar y hp1a-1tt generan isoformas de la proteina truncadas en el extremo n-terminal. La proteina hpla-1, pero no su isoforma hpla-1 ar, es capaz de transactivar, in vitro, el promotor minimo del gen hp1-3. La isoforma hpla-1ar carece de la region rica en aminoacidos cargados presente en hpla-1. Es la primera vez que una region de estas caracteristicas se implica en transactivacion en la familia pou.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Caracterizacion de un nuevo factor pou en placenta humana.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Caracterizacion de un nuevo factor pou en placenta humana. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Oscar Jimenez Mateo <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Aut\u00f3noma de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/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> Castrillo Diez Jos\u00e9 Luis<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Ana Aranda Iriarte <\/li>\n<li> Mayor De La Torre Pilar (vocal)<\/li>\n<li>Mar\u00eda  Jes\u00fas Lopez Zabalza (vocal)<\/li>\n<li>Pilar Santisteban Sanz (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Oscar Jimenez Mateo Se han clonado 1805 pares de bases correspondientes al adn complementario de un nuevo [&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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