{"id":10386,"date":"2017-11-22T00:00:00","date_gmt":"2017-11-21T23:00:00","guid":{"rendered":"https:\/\/idibell.cat\/es\/blog\/2017\/11\/22\/impulso-a-la-colaboracion-internacional-en-el-simposio-defectos-del-transporte-de-aminoacidos\/"},"modified":"2020-05-19T18:04:48","modified_gmt":"2020-05-19T16:04:48","slug":"impulso-a-la-colaboracion-internacional-en-el-simposio-defectos-del-transporte-de-aminoacidos","status":"publish","type":"post","link":"https:\/\/idibell.cat\/es\/2017\/11\/impulso-a-la-colaboracion-internacional-en-el-simposio-defectos-del-transporte-de-aminoacidos\/","title":{"rendered":"Impulso a la colaboraci\u00f3n internacional en el simposio \u201cDefectos del transporte de amino\u00e1cidos\u201d"},"content":{"rendered":"

Los pasados d\u00edas 20 y 21 de noviembre de 2017 tuvo lugar el
simposio \u201cDefectos del transporte de amino\u00e1cidos\u201d, organizado por el CIBER de Enfermedades Raras y la Fundaci\u00f3n Ram\u00f3n Areces,
en su sede de Madrid. Adem\u00e1s de investigadores nacionales, incluyendo el grupo de la Dra. Virgina Nunes de IDIBELL, que coorganizaba el simposio, han participado diecisiete de los principales especialistas en este campo, procedentes de Europa, Asia y Australia, que han cubierto aspectos relacionados con los mecanismos de patolog\u00eda y terapias desarrolladas para las enfermedades asociadas a defectos en el transporte de amino\u00e1cidos.
Las enfermedades cubiertas han sido principalmente hereditarias y raras, pero ha habido tambi\u00e9n contribuciones relevantes a enfermedades comunes como diabetes y c\u00e1ncer. El simposio se ha centrado en cuatro grupos principales de transportadores (heterom\u00e9ricos, mitocondriales y de la familia de transportadores de neurotransmisores, tanto en su vertiente neural como metab\u00f3lica). Se han presentado los \u00faltimos avances en el conocimiento sobre el mecanismo molecular de estos transportadores, espec\u00edficamente de los heterom\u00e9ricos, mitocondriales, de glutamato y de glicina. Paralelamente, se han descrito nuevos mecanismos de patolog\u00eda en aminoacidurias, enfermedades mitocondriales y de sinapsis neuronal. Entre las terapias presentadas han destacado nuevos tratamientos metab\u00f3licos para defectos de mielinizaci\u00f3n y bases moleculares de la acci\u00f3n de inhibidores de transportadores de glutamato.
El car\u00e1cter interdisciplinar del simposio ha beneficiado el flujo de informaci\u00f3n transversal entre los asistentes que trabajan en transporte de amino\u00e1cidos y sus patolog\u00edas asociadas.

<\/p>\n","protected":false},"excerpt":{"rendered":"

Los pasados d\u00edas 20 y 21 de noviembre de 2017 tuvo lugar el simposio \u201cDefectos del transporte de amino\u00e1cidos\u201d, organizado por el CIBER de Enfermedades Raras y la Fundaci\u00f3n Ram\u00f3n Areces, en su sede de Madrid. Adem\u00e1s de investigadores nacionales, incluyendo el grupo de la Dra. Virgina Nunes de IDIBELL, que coorganizaba el simposio, han […]<\/p>\n","protected":false},"author":6,"featured_media":10387,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"no-sidebar","site-content-layout":"page-builder","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":"default","adv-header-id-meta":"","stick-header-meta":"default","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":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"footnotes":""},"categories":[186,305,297],"tags":[275],"class_list":["post-10386","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-area-medicina-traslacional","category-genetica-molecular-humana-programa-de-genes-enfermedad-y-terapia","category-programa-de-genes-enfermedad-y-terapia","tag-medicina-traslacional"],"publishpress_future_action":{"enabled":false,"date":"2025-01-29 05:08:28","action":"change-status","newStatus":"draft","terms":[],"taxonomy":"category"},"publishpress_future_workflow_manual_trigger":{"enabledWorkflows":[]},"_links":{"self":[{"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/posts\/10386","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/users\/6"}],"replies":[{"embeddable":true,"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/comments?post=10386"}],"version-history":[{"count":0,"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/posts\/10386\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/media\/10387"}],"wp:attachment":[{"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/media?parent=10386"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/categories?post=10386"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/idibell.cat\/es\/wp-json\/wp\/v2\/tags?post=10386"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}