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A MutSß-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice?
Zhao, Xiao-Nan; Lokanga, Rachel; Allette, Kimaada; Gazy, Inbal; Wu, Di; Usdin, Karen.
Afiliação
  • Zhao XN; Section on Gene Structure and Disease, Laboratory of Cell and Molecular Biology, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Lokanga R; Section on Gene Structure and Disease, Laboratory of Cell and Molecular Biology, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Allette K; Division of Medical Biochemistry, University of Cape Town Medical School, Cape Town, South Africa.
  • Gazy I; Section on Gene Structure and Disease, Laboratory of Cell and Molecular Biology, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Wu D; Section on Gene Structure and Disease, Laboratory of Cell and Molecular Biology, National Institute of Diabetes, Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, United States of America.
  • Usdin K; Section on Physical Biochemistry, Laboratory of Biochemistry and Genetics, National Institute of Diabetes, Digestive and Kidney Diseases. National Institutes of Health, Bethesda, Maryland, United States of America.
PLoS Genet ; 12(7): e1006190, 2016 07.
Article em En | MEDLINE | ID: mdl-27427765
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Proteínas de Ligação a DNA / Proteína MutS de Ligação de DNA com Erro de Pareamento / Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil Limite: Animals / Female / Humans / Male Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Proteínas de Ligação a DNA / Proteína MutS de Ligação de DNA com Erro de Pareamento / Proteína do X Frágil da Deficiência Intelectual / Síndrome do Cromossomo X Frágil Limite: Animals / Female / Humans / Male Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos