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7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages.
Adamo, Antonio; Atashpaz, Sina; Germain, Pierre-Luc; Zanella, Matteo; D'Agostino, Giuseppe; Albertin, Veronica; Chenoweth, Josh; Micale, Lucia; Fusco, Carmela; Unger, Christian; Augello, Bartolomeo; Palumbo, Orazio; Hamilton, Brad; Carella, Massimo; Donti, Emilio; Pruneri, Giancarlo; Selicorni, Angelo; Biamino, Elisa; Prontera, Paolo; McKay, Ronald; Merla, Giuseppe; Testa, Giuseppe.
  • Adamo A; Department of Experimental Oncology, European Institute of Oncology (Istituto di Ricovero e Cura a Carattere Scientifico, IRCCS), Milan, Italy.
  • Atashpaz S; Department of Experimental Oncology, European Institute of Oncology (Istituto di Ricovero e Cura a Carattere Scientifico, IRCCS), Milan, Italy.
  • Germain PL; Department of Experimental Oncology, European Institute of Oncology (Istituto di Ricovero e Cura a Carattere Scientifico, IRCCS), Milan, Italy.
  • Zanella M; Department of Experimental Oncology, European Institute of Oncology (Istituto di Ricovero e Cura a Carattere Scientifico, IRCCS), Milan, Italy.
  • D'Agostino G; Department of Experimental Oncology, European Institute of Oncology (Istituto di Ricovero e Cura a Carattere Scientifico, IRCCS), Milan, Italy.
  • Albertin V; Department of Experimental Oncology, European Institute of Oncology (Istituto di Ricovero e Cura a Carattere Scientifico, IRCCS), Milan, Italy.
  • Chenoweth J; Lieber Institute for Brain Development, Baltimore, Maryland, USA.
  • Micale L; Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
  • Fusco C; Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
  • Unger C; Department of Biomedical Sciences, University of Sheffield, Sheffield, UK.
  • Augello B; Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
  • Palumbo O; Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
  • Hamilton B; Stemgent, Cambridge, Massachusetts, USA.
  • Carella M; Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
  • Donti E; Medical Genetics Unit, Hospital Santa Maria della Misericordia, University of Perugia, Perugia, Italy.
  • Pruneri G; Department of Experimental Oncology, European Institute of Oncology (Istituto di Ricovero e Cura a Carattere Scientifico, IRCCS), Milan, Italy.
  • Selicorni A; Unità Operativa Semplice (UOS) Genetica Clinica Pediatrica, Fondazione Monza e Brianza per il Bambino e la sua Mamma (Fondazione MBBM), Azienda Ospedaliera San Gerardo, Monza, Italy.
  • Biamino E; Department of Pediatrics, University of Turin, Turin, Italy.
  • Prontera P; Medical Genetics Unit, Hospital Santa Maria della Misericordia, University of Perugia, Perugia, Italy.
  • McKay R; Lieber Institute for Brain Development, Baltimore, Maryland, USA.
  • Merla G; Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
  • Testa G; 1] Department of Experimental Oncology, European Institute of Oncology (Istituto di Ricovero e Cura a Carattere Scientifico, IRCCS), Milan, Italy. [2] Department of Health Sciences, University of Milan, Milan, Italy.
Nat Genet ; 47(2): 132-41, 2015 Feb.
Article en En | MEDLINE | ID: mdl-25501393
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 7 / Regulación de la Expresión Génica / Síndrome de Williams / Factores de Transcripción TFII / Células Madre Pluripotentes / Variaciones en el Número de Copia de ADN Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article
Texto completo
Imprimir
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PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 7 / Regulación de la Expresión Génica / Síndrome de Williams / Factores de Transcripción TFII / Células Madre Pluripotentes / Variaciones en el Número de Copia de ADN Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article