The suppression of premature termination codons and the repair of splicing mutations in CFTR.

Oren, Yifat S; Pranke, Iwona M; Kerem, Batsheva; Sermet-Gaudelus, Isabelle

Oren, Yifat S; Pranke, Iwona M; Kerem, Batsheva; Sermet-Gaudelus, Isabelle.

Afiliação

Oren YS; Department of Genetics, The Life Sciences Institute, The Hebrew University, Jerusalem, Israel; SpliSense Therapeutics, Givat Ram Campus, Hebrew University, Jerusalem, Israel.
Pranke IM; INSERM U 1151, Institut Necker Enfants Malades, Paris, France; Université Paris Sorbonne, France.
Kerem B; Department of Genetics, The Life Sciences Institute, The Hebrew University, Jerusalem, Israel. Electronic address: batshevak@savion.huji.ac.il.
Sermet-Gaudelus I; INSERM U 1151, Institut Necker Enfants Malades, Paris, France; Unité de Pneumo-Allergologie Pédiatrique, Centre de Ressources et de Compétence de la Mucoviscidose, Hôpital Necker Enfants Malades, Paris, France; Université Paris Sorbonne, France. Electronic address: isabelle.sermet@aphp.fr.

Curr Opin Pharmacol ; 34: 125-131, 2017 06.

Article em En | MEDLINE | ID: mdl-29128743

Assuntos

Códon sem Sentido; Regulador de Condutância Transmembrana em Fibrose Cística/genética; Fibrose Cística/terapia; Splicing de RNA; Fibrose Cística/genética; Humanos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Splicing de RNA / Códon sem Sentido / Regulador de Condutância Transmembrana em Fibrose Cística / Fibrose Cística Limite: Humans Idioma: En Revista: Curr Opin Pharmacol Ano de publicação: 2017 Tipo de documento: Article

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