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Cohesin Mutations Induce Chromatin Conformation Perturbation of the H19/IGF2 Imprinted Region and Gene Expression Dysregulation in Cornelia de Lange Syndrome Cell Lines.
Pileggi, Silvana; La Vecchia, Marta; Colombo, Elisa Adele; Fontana, Laura; Colapietro, Patrizia; Rovina, Davide; Morotti, Annamaria; Tabano, Silvia; Porta, Giovanni; Alcalay, Myriam; Gervasini, Cristina; Miozzo, Monica; Sirchia, Silvia Maria.
Afiliación
  • Pileggi S; Medical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milano, Italy.
  • La Vecchia M; Medical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milano, Italy.
  • Colombo EA; Medical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milano, Italy.
  • Fontana L; Medical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milano, Italy.
  • Colapietro P; Unit of Medical Genetics, ASST Santi Paolo e Carlo, 20142 Milano, Italy.
  • Rovina D; Department of Pathophysiology and Transplantation, Medical Genetics, Università degli Studi di Milano, 20122 Milan, Italy.
  • Morotti A; Medical Genetics, Department of Health Sciences, Università degli Studi di Milano, 20142 Milano, Italy.
  • Tabano S; Research Laboratories Coordination Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milano, Italy.
  • Porta G; Department of Pathophysiology and Transplantation, Medical Genetics, Università degli Studi di Milano, 20122 Milan, Italy.
  • Alcalay M; Laboratory of Medical Genetics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy.
  • Gervasini C; Centro di Medicina Genomica, Department of Medicine and Surgery, Università degli Studi dell'Insubria, 21100 Varese, Italy.
  • Miozzo M; Department of Experimental Oncology, IEO European Institute of Oncology IRCCS, 20139 Milan, Italy.
  • Sirchia SM; Department of Oncology and Hemato-Oncology, University of Milan, 20122 Milan, Italy.
Biomolecules ; 11(11)2021 11 02.
Article en En | MEDLINE | ID: mdl-34827619
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Cornelia de Lange Idioma: En Revista: Biomolecules Año: 2021 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Cornelia de Lange Idioma: En Revista: Biomolecules Año: 2021 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza