{"id":21025,"date":"2011-09-14T23:19:08","date_gmt":"2011-09-15T02:19:08","guid":{"rendered":"http:\/\/www.inclusive.org.br\/?p=21025"},"modified":"2011-09-14T23:19:08","modified_gmt":"2011-09-15T02:19:08","slug":"mais-um-medicamento-para-melhorar-a-cognicao-em-sindrome-de-down-esta-sendo-estudado-na-franca","status":"publish","type":"post","link":"https:\/\/inclusivenews.com.br\/?p=21025","title":{"rendered":"Mais um medicamento para melhorar a cogni\u00e7\u00e3o em s\u00edndrome de Down est\u00e1 sendo estudado na Fran\u00e7a"},"content":{"rendered":"<p><img loading=\"lazy\" decoding=\"async\" class=\"alignleft size-full wp-image-21026\" title=\"lejeune\" src=\"http:\/\/inclusivenews.com.br\/wp-content\/uploads\/lejeune.jpg\" alt=\"Logotipo da Funda\u00e7\u00e3o J\u00earome Lejeune.\" width=\"231\" height=\"62\" \/>O laborat\u00f3rio NovAliX anunciou que estabelecer\u00e1 uma parceria para colabora\u00e7\u00e3o em pesquisas sobre s\u00edndrome de Down com a Funda\u00e7\u00e3o francesa J\u00earome Lejeune.<\/p>\n<p>O laborat\u00f3rio usar\u00e1 seus conhecimentos e capacidades em qu\u00edmica medicinal e biologia estrutural para desenvolver uma pequena mol\u00e9cula que poder\u00e1 afetar a s\u00edntese de beta-cistationina (CBS). A inibi\u00e7\u00e3o de CBS que existe em maior quantidade em pessoas com s\u00eddrome de Down tem sido associada com a restaura\u00e7\u00e3o de comprometimento cognitivo em modelos animais que apresentam a trissomia.<\/p>\n<p>&#8220;Estamos entusiasmados para avan\u00e7ar com os nossos programas de pesquisa para o tratamento da trissomia 21, tirando proveito da especialidade do NovAlix no desenho de estrutura de medicamentos e capacidade de trabalhar com metodologias de \u00faltima gera\u00e7\u00e3o\u201d, disse o Dr. Henri Bl\u00e9haut, Diretor Cient\u00edfico da Funda\u00e7\u00e3o J\u00e9r\u00f4me Lejeune.<\/p>\n<p>Stephan Jenn, presidente da NovAliX, disse: &#8220;estamos muito satisfeitos em investigar uma abordagem nova de pesquisa em s\u00edndrome de Down (trissomia 21) e apoiar a Funda\u00e7\u00e3o J\u00e9r\u00f4me Lejeune em seus esfor\u00e7os para melhorar a qualidade de vida das pessoas com s\u00edndrome de Down&#8221;.<\/p>\n<p>Sobre a s\u00edndrome de Down (Trissomia 21)<br \/>\nTrissomia 21, \u00e9 a mais comum de defici\u00eancia gen\u00e9tica intelectual, produzindo defici\u00eancia intelectual em n\u00edveis variados. \u00c9 causada por uma irregularidade cromoss\u00f4mica: Enquanto a maioria dos seres humanos t\u00eam 46 cromossomos divididos em 23 pares, na Trissomia 21 as pessoas t\u00eam um terceiro cromossomo adicionado ao par 21. O cromossomo extra produz uma superabund\u00e2ncia de elementos qu\u00edmicos, causando desequil\u00edbrios funcionais por todo o corpo. Agora sabemos como tratar e curar muitas quest\u00f5es de sa\u00fade associadas a trissomia 21, mas ainda precisamos combater as causas da defici\u00eancia intelectual.<\/p>\n<p>A Funda\u00e7\u00e3o J\u00e9r\u00f4me Lejeune<br \/>\nCriada em 1996 e reconhecida como sendo de Interesse P\u00fablico, a Funda\u00e7\u00e3o J\u00e9r\u00f4me Lejeune trabalha na pesquisa de gen\u00e9tica em defici\u00eancia intelectual: Trissomia 21 (S\u00edndrome de Down), s\u00edndrome de &#8220;Cri du chat&#8221;, S\u00edndrome do X Fr\u00e1gil, monossomias &#8230; A fim de encontrar um tratamento no futuro para curar pacientes com defici\u00eancias intelectuais, a Funda\u00e7\u00e3o J\u00e9r\u00f4me Lejeune financia cerca de 40 programas de pesquisa em todo o mundo a cada ano. Na Fran\u00e7a, \u00e9 o maior provedor de fundos para pesquisas sobre Trissomia 21 (S\u00edndrome de Down). A Funda\u00e7\u00e3o tamb\u00e9m criou o Instituto J\u00e9r\u00f4me Lejeune considerado como o principal elo entre pacientes e pesquisas de doen\u00e7as gen\u00e9ticas da intelig\u00eancia. O instituto oferece consultas m\u00e9dicas especializadas para a defici\u00eancia intelectual gen\u00e9tica: diagn\u00f3stico, tratamento, preven\u00e7\u00e3o de defici\u00eancias m\u00faltiplas, informa\u00e7\u00e3o \u00e0s fam\u00edlias e forma\u00e7\u00e3o profissional. A Funda\u00e7\u00e3o J\u00e9r\u00f4me Lejeune \u00e9 totalmente mantida por doa\u00e7\u00f5es privadas. Esta colabora\u00e7\u00e3o com NovAliX ocorre atrav\u00e9s do programa CiBleS21.<\/p>\n<p>Sobre NovAliX<br \/>\nO laborat\u00f3rio NovAliX desenvolve tecnologias de base qu\u00edmica e biof\u00edsica para apoiar as necessidades da ind\u00fastria farmac\u00eautica da descoberta \u00e0 fabrica\u00e7\u00e3o. Com tecnologia SPR, cristalografia de raios X de prote\u00ednas, espectrometria de massa e qu\u00edmica supramolecular, o NovAliX oferece servi\u00e7os integrados abrangentes para a descoberta de pequenas mol\u00e9culas de drogas. Com avan\u00e7adas tecnologias de RMN, o NovAliX fornece caracteriza\u00e7\u00e3o de produtos biol\u00f3gicos, an\u00e1lise minuciosa de APIs e estudos de polimorfismo para apoiar o desenvolvimento farmac\u00eautico e equipes de fabrica\u00e7\u00e3o. O NovAliX Group, uma equipe de 120 cientistas, est\u00e1 localizado em Strasbourg-Illkirch (Fran\u00e7a) e Heidelberg (Alemanha).<\/p>\n","protected":false},"excerpt":{"rendered":"<p>O laborat\u00f3rio NovAliX anunciou que estabelecer\u00e1 uma parceria para colabora\u00e7\u00e3o em pesquisas sobre s\u00edndrome de Down com a Funda\u00e7\u00e3o francesa J\u00earome Lejeune.<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-container-style":"default","site-container-layout":"default","site-sidebar-layout":"default","disable-article-header":"default","disable-site-header":"default","disable-site-footer":"default","disable-content-area-spacing":"default","footnotes":""},"categories":[38,4],"tags":[],"class_list":["post-21025","post","type-post","status-publish","format-standard","hentry","category-deficiencia","category-noticias"],"yoast_head":"<!-- This site is optimized 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