Genetic variants in GRHL3 and risk for neural tube defects: A case-control and case-parent triad/control study.

Yang, Wenlei; Xiao, Yanhui; Tian, Tian; Jin, Lei; Wang, Linlin; Ren, Aiguo

Yang, Wenlei; Xiao, Yanhui; Tian, Tian; Jin, Lei; Wang, Linlin; Ren, Aiguo.

Afiliação

Yang W; Institute of Reproductive and Child Health, NHC Key Laboratory of Reproductive Health, Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing, China.
Xiao Y; Institute of Reproductive and Child Health, NHC Key Laboratory of Reproductive Health, Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing, China.
Tian T; Institute of Reproductive and Child Health, NHC Key Laboratory of Reproductive Health, Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing, China.
Jin L; Institute of Reproductive and Child Health, NHC Key Laboratory of Reproductive Health, Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing, China.
Wang L; Institute of Reproductive and Child Health, NHC Key Laboratory of Reproductive Health, Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing, China.
Ren A; Institute of Reproductive and Child Health, NHC Key Laboratory of Reproductive Health, Department of Epidemiology and Biostatistics, School of Public Health, Peking University Health Science Center, Beijing, China.

Birth Defects Res ; 111(19): 1468-1478, 2019 11 15.

Article em En | MEDLINE | ID: mdl-31332962

Assuntos

Proteínas de Ligação a DNA/genética; Defeitos do Tubo Neural/genética; Fatores de Transcrição/genética; Adulto; Povo Asiático; Estudos de Casos e Controles; China; Proteínas de Ligação a DNA/metabolismo; Encefalocele/genética; Família; Feminino; Predisposição Genética para Doença; Genótipo; Humanos; Recém-Nascido; Masculino; Mutação de Sentido Incorreto; Tubo Neural/metabolismo; Defeitos do Tubo Neural/metabolismo; Polimorfismo de Nucleotídeo Único/genética; Disrafismo Espinal/genética; Fatores de Transcrição/metabolismo

Palavras-chave

case-parent triads; common variants; grainyhead like transcription factor 3; neural tube defects; single nucleotide polymorphisms

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Proteínas de Ligação a DNA / Defeitos do Tubo Neural Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Newborn País/Região como assunto: Asia Idioma: En Revista: Birth Defects Res Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

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