{"id":3,"date":"2010-04-06T12:12:20","date_gmt":"2010-04-06T16:12:20","guid":{"rendered":"http:\/\/medicina.udd.cl\/centro-genetica-humana\/proyectos\/"},"modified":"2016-03-28T10:50:38","modified_gmt":"2016-03-28T13:50:38","slug":"proyectos","status":"publish","type":"page","link":"https:\/\/medicina.udd.cl\/centro-genetica-genomica\/investigacion\/proyectos\/","title":{"rendered":"Proyectos"},"content":{"rendered":"

2016-2020<\/strong> A connectomic neuroimaging study of the 22q11 deletion syndrome: a window into schizophrenia and its genetic causes. Fondecyt Regular 116. Investigador responsable N Crossley (PUC), Co investigadora G Repetto<\/p>\n

2016-2019<\/strong> Understanding host response to ANDV infection, immunological and transcriptomics approach. Fondecyt Regular 2016. Investigador respondable: Cecilia Vial.<\/p>\n

2015-2016<\/strong> \u201cDesarrollo de l\u00edneas celulares de c\u00e1ncer de vejiga relacionado a exposici\u00f3n a ars\u00e9nico\u201d. (IR: Mario Fern\u00e1ndez). PMI. CoInvestigadora: A Ziegler<\/p>\n

2015-2017<\/strong> \u00abFortalecimiento y desarrollo de la investigaci\u00f3n en biomedicina mediante la adquisici\u00f3n de un claster computacional\u00bb. Fondequip. Luis Le\u00f3n.<\/p>\n

2015-2016<\/strong> Proyecto Interno UDD \u201cStructural analysis of missense mutations in the SHP2 protein using molecular dynamics\u201d. IR: LL<\/p>\n

2015<\/strong> \u201cHands-on training in targeted proteomics techniques and data analysis at the leading German Cancer Research Center \u201cREDES 140051. IR: A Ziegler<\/p>\n

2014-2017<\/strong> Determining the genetic basis of Epidermolysis bullosa symptoms through Genotype-Phenotype associations using Next Generation Sequencing.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Fondecyt de Iniciaci\u00f3n 11140440 IR: Ignacia Fuentes<\/p>\n

2014-2017 <\/strong>\u201cThe Role of Cyclin D1 Activity In The Regulation Of Autophagy And Senescence In Mammary And Gastric Epithelial Cells\u201d. (IR: Nelson Brown). Fondecyt\u00a0 1140389.<\/p>\n

2014-2017<\/strong> FONDECYT, Lecannelier A (PI), Funding Source: Fondecyt (March 2014 \u2013 March 2017), EXPLORANDO LA SENSIBILIDAD AL ESTRES EN INFANTES: UN ESTUDIO GENETICO, PSICOBIOLOGICO Y VINCULAR The goal of this project is to analyze the stress response in infants from the mother factors (care, introspection and sensitivity to stress) and child\u00b4s factors (genetics and patterns of attachment). Role: Co-investigator<\/p>\n

2014-2015<\/strong>\u00a0\u00a0\u00a0 Chromosome 22q11.2 microdeletion syndrome: a window into understanding developmental diseases of the heart and brain.\u00a0 Canada-Latin America and the Caribbean Research Exchange Grants (LACREG) IR: G Repetto<\/p>\n

2014-2015<\/strong> Proyecto PMI \u201cDesarrollo de un panel de mutaciones para el diagn\u00f3stico molecular de fibrosis qu\u00edstica espec\u00edfico para la poblaci\u00f3n chilena\u201d IR: LL CoI: GL<\/p>\n

2014-2015<\/strong> Proyecto PMI \u201cIdentificaci\u00f3n de microRNAs como potenciales biomarcadores en el diagn\u00f3stico precoz de cardiomiopat\u00eda diab\u00e9tica asociada a la obesidad\u201d CoI:LL<\/p>\n

2014-2015<\/strong> Proyecto PMI \u00abDesarrollo de una novedosa plataforma tecnol\u00f3gica para diagnosticar enfermedades gen\u00e9ticas: uso de Epidermolisis Bulosa como prueba de concepto.\u00bb IR: Ignacia Fuentes<\/p>\n

2014-2015<\/strong> Proyecto PMI \u00abImplementaci\u00f3n del m\u00e9todo de inmunofluorescencia para EB: Posicionando a Chile como foco regional en diagn\u00f3stico de EB\u00bb IR: Ignacia Fuentes<\/p>\n

2014-2015<\/strong> Proyecto Interno UDD \u00abCaracterizaci\u00f3n gen\u00e9tica de pacientes chilenos con Epidermolisis Bulosa de la Uni\u00f3n: b\u00fasqueda de mutaciones frecuentes y desarrollo de un test r\u00e1pido de diagn\u00f3stico \u00bb IR: Ignacia Fuentes<\/p>\n

2013-2017<\/strong> Genetic modifiers of the cardiovascular phenotype of 22q11 microdeletion syndrome: Next generation sequencing of candidate regions identified by genome-wide association analysis. Fondecyt 1130392. IR G Repetto\/ CoI UDD G Lay-Son, C Vial<\/p>\n

2013-2017<\/strong> International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome. NIH grant 1U01MH101723-01 (EEUU). Co Investigadora en Chile G Repetto<\/p>\n

2013-2015<\/strong> \u201cAnomal\u00edas cong\u00e9nitas y trastornos del desarrollo: Evaluaci\u00f3n de costo-efectividad de las nuevas herramientas diagn\u00f3sticas\u201d. Financiamiento: FONIS \u2013 2013 \u2013 SA13I20321. IR: G Lay-Son; IA: C Vial; Col: G Repetto<\/p>\n

2012-2015<\/strong> Genetic variants related to presence of bladder urothelial carcinoma in a high-risk, arsenic-exposed population in northern Chile (Antofagasta): a genome-wide association study\u201d. IR: Mario Fern\u00e1ndez. Fondecyt Regular 1120987. CoInvestigadora: A Ziegler<\/p>\n

2012-2013<\/strong> PROYECTO INTERNO UDD Financiamiento: UDD \u2013 2012 \u2013 23400070, \u201cAN\u00c1LISIS MUTACIONAL DEL GEN CFTR EN PACIENTES CHILENOS CON FIBROSIS QU\u00cdSTICA\u201d. IR: G Lay-Son<\/p>\n

2011-2014<\/strong> FONDECYT 11110397 Vial, C (PI), Funding Source: FONDECYT HOST GENETIC FACTORS AND SEVERITY OF ANDES HANTAVIRUS INFECTION: A GENOME WIDE ASSOCIATION STUDYThe goal of this project is to genotipified patients with hantavirus cardiopulmonary syndrome that has a mild or severe clinical course, to search for association of SNPs or CNVs with the disease severity. Role: Principal Investigator<\/p>\n

2011-2012<\/strong> PROYECTO INTERNO UDD Funding Source: Universidad del Desarrollo (March 2011-February 2012) OSTEOCLAST PARTICIPATION ON PHENOTYPIC DIFFERENCES OF OSTEOGENESIS IMPERFECTA PATIENTS. The main goal of this project is to study if the phenotypic differences of OI patients can be explained by differences on the osteoclastogenesis process. Role: PI<\/p>\n

2010-2015<\/strong> NIH U19 AI045452 Mertz, G (PI) Funding Source: NIH\/NIAID (UNM\/Chile ICIDR),\u00a0 ANDES VIRUS TRANSMISSION AND PATHOGENESIS IN CHILE. The goals of this project are the study of index cases with HCPS and their household contacts for person to person transmission evaluation; study of viral variants from human index, secondary cases and rodents; and to develop anti-Andes virus vaccine evaluation capacity.\u00a0 Role: Co-Investigator<\/p>\n

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

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