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The novel Cln1(R151X) mouse model of infantile neuronal ceroid lipofuscinosis (INCL) for testing nonsense suppression therapy.
Miller, Jake N; Kovács, Attila D; Pearce, David A.
Afiliação
  • Miller JN; Division of Basic Biomedical Sciences, Sanford School of Medicine of the University of South Dakota, Vermillion, SD, USA Sanford Children's Health Research Center, Sanford Research, Sioux Falls, SD, USA and.
  • Kovács AD; Sanford Children's Health Research Center, Sanford Research, Sioux Falls, SD, USA and.
  • Pearce DA; Division of Basic Biomedical Sciences, Sanford School of Medicine of the University of South Dakota, Vermillion, SD, USA Sanford Children's Health Research Center, Sanford Research, Sioux Falls, SD, USA and Department of Pediatrics, Sanford School of Medicine of the University of South Dakota, Sioux Falls, SD, USA david.pearce@sanfordhealth.org.
Hum Mol Genet ; 24(1): 185-96, 2015 Jan 01.
Article em En | MEDLINE | ID: mdl-25205113
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Códon sem Sentido / Proteínas de Membrana / Lipofuscinoses Ceroides Neuronais Limite: Animals / Humans / Infant / Male / Newborn Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Códon sem Sentido / Proteínas de Membrana / Lipofuscinoses Ceroides Neuronais Limite: Animals / Humans / Infant / Male / Newborn Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2015 Tipo de documento: Article