Browsing Artículos by Author "Young, Juan I."

Correct developmental expression level of rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memory

Autor: Cao, Lei; Molina, Jessica; Abad, Clemer; Carmona-Mora, Paulina; Cardenas Oyarzo, Areli; Young, Juan I.; Walz, Katherina Año: 2014N° de proyecto: 1061067Tipo: ArticuloPrograma: FONDECYT

Defective cell-cell adhesion in hyh mutant mice: a pathogenic mechanism underlying cerebral ventricular surface disruption and hydrocephalus?

Autor: Kerr, Bredford; Alvarez-Saavedra, Matias; Saez, Mauricio A.; Saona, Alexandra; Young, Juan I. Año: 2009N° de proyecto: 1070241Tipo: ArticuloPrograma: FONDECYT

Elevated expression of mecp2 in cardiac and skeletal tissues is detrimental for normal development

Autor: Alvarez-Saavedra, Matias; Carrasco, Loreto; Sura-Trueba, Sylvia; Aiello, Vera Demarchi; Walz, Katherina; Xavier Neto, Jose; Young, Juan I. Año: 2010N° de proyecto: 1061067Tipo: ArticuloPrograma: FONDECYT

Elevated expression of mecp2 in cardiac and skeletal tissues is detrimental for normal development

Autor: Alvarez-Saavedra, Matias; Carrasco, Loreto; Sura-Trueba, Sylvia; Aiello, Vera Demarchi; Walz, Katherina; Xavier Neto, Jose; Young, Juan I. Año: 2010N° de proyecto: 1051079Tipo: ArticuloPrograma: FONDECYT

Functional and cellular characterization of human retinoic acid induced 1 (rai1) mutations associated with smith-magenis syndrome

Autor: Carmona-Mora, Paulina; Encina, Carolina A.; Canales, Cesar P.; Cao, Lei; Molina, Jessica; Kairath, Pamela; Young, Juan I.; Walz, Katherina Año: 2010N° de proyecto: 1051079Tipo: ArticuloPrograma: FONDECYT

Functional and cellular characterization of human retinoic acid induced 1 (rai1) mutations associated with smith-magenis syndrome

Autor: Carmona-Mora, Paulina; Encina, Carolina A.; Canales, Cesar P.; Cao, Lei; Molina, Jessica; Kairath, Pamela; Young, Juan I.; Walz, Katherina Año: 2010N° de proyecto: 1061067Tipo: ArticuloPrograma: FONDECYT

Phenotypic consequences of copy number variation: insights from smith-magenis and potocki-lupski syndrome mouse models

Autor: Ricard, Guenola; Molina, Jessica; Chrast, Jacqueline; Gu, Wenli; Gheldof, Nele; Pradervand, Sylvain; Schuetz, Frederic; Young, Juan I.; Lupski, James R.; Reymond, Alexandre; Walz, Katherina Año: 2010N° de proyecto: 1051079Tipo: ArticuloPrograma: FONDECYT

Phenotypic consequences of copy number variation: insights from smith-magenis and potocki-lupski syndrome mouse models

Autor: Ricard, Guenola; Molina, Jessica; Chrast, Jacqueline; Gu, Wenli; Gheldof, Nele; Pradervand, Sylvain; Schuetz, Frederic; Young, Juan I.; Lupski, James R.; Reymond, Alexandre; Walz, Katherina Año: 2010N° de proyecto: 1061067Tipo: ArticuloPrograma: FONDECYT

Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease

Autor: Krall, Paola; Canales, Cesar P.; Kairath, Pamela; Carmona-Mora, Paulina; Molina, Jessica; Carpio, J. Daniel; Ruiz, Phillip; Mezzano, Sergio A.; Li, Jing; Wei, Changli; Reiser, Jochen; Young, Juan I.; Walz, Katherina Año: 2010N° de proyecto: 1080083Tipo: ArticuloPrograma: FONDECYT

Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease

Autor: Krall, Paola; Canales, Cesar P.; Kairath, Pamela; Carmona-Mora, Paulina; Molina, Jessica; Carpio, J. Daniel; Ruiz, Phillip; Mezzano, Sergio A.; Li, Jing; Wei, Changli; Reiser, Jochen; Young, Juan I.; Walz, Katherina Año: 2010N° de proyecto: 1051079Tipo: ArticuloPrograma: FONDECYT

Podocyte-specific overexpression of wild type or mutant trpc6 in mice is sufficient to cause glomerular disease

Autor: Krall, Paola; Canales, Cesar P.; Kairath, Pamela; Carmona-Mora, Paulina; Molina, Jessica; Carpio, J. Daniel; Ruiz, Phillip; Mezzano, Sergio A.; Li, Jing; Wei, Changli; Reiser, Jochen; Young, Juan I.; Walz, Katherina Año: 2010N° de proyecto: 1061067Tipo: ArticuloPrograma: FONDECYT

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