In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila.

Harnish, J Michael; Deal, Samantha L; Chao, Hsiao-Tuan; Wangler, Michael F; Yamamoto, Shinya

Harnish, J Michael; Deal, Samantha L; Chao, Hsiao-Tuan; Wangler, Michael F; Yamamoto, Shinya.

Afiliação

Harnish JM; Department of Molecular and Human Genetics, Baylor College of Medicine.
Deal SL; Program in Developmental Biology, Baylor College of Medicine.
Chao HT; Department of Molecular and Human Genetics, Baylor College of Medicine; Department of Pediatrics, Section of Neurology and Developmental Neuroscience, Baylor College of Medicine; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital; Department of Neuroscience, Baylor College
Wangler MF; Department of Molecular and Human Genetics, Baylor College of Medicine; Program in Developmental Biology, Baylor College of Medicine; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital.
Yamamoto S; Department of Molecular and Human Genetics, Baylor College of Medicine; Program in Developmental Biology, Baylor College of Medicine; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital; Department of Neuroscience, Baylor College of Medicine; yamamoto@bcm.edu.

J Vis Exp ; (150)2019 08 20.

Article em En | MEDLINE | ID: mdl-31498321

Assuntos

Drosophila melanogaster/fisiologia; Genes/genética; Genômica/métodos; Mutação; Fenótipo; Algoritmos; Alelos; Animais; Drosophila melanogaster/genética; Exoma; Testes Genéticos; Humanos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Genômica / Drosophila melanogaster / Genes / Mutação Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: J Vis Exp Ano de publicação: 2019 Tipo de documento: Article

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