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Modeling Smith-Lemli-Opitz syndrome with induced pluripotent stem cells reveals a causal role for Wnt/beta-catenin defects in neuronal cholesterol synthesis phenotypes

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作者： Francis, Kevin R. ^[1] ; Ton, Amy N. ^[2] ; Xin, Yao ^[3] ; O'Halloran, Peter E. ^[4] ; Wassif, Christopher A. ^[5] ; Malik, Nasir ; Williams, Ian M. ; Cluzeau, Celine V. ; Trivedi, Niraj S. ; Pavan, William J. ; Cho, Wonhwa ; Westphal, Heiner ; Porter, Forbes D.

作者单位： Univ Illinois, Dept Chem, Chicago, IL USA ^[1] NHGRI, Computat & Stat Genom Branch, NIH, Bethesda, MD 20892 USA ^[2] NHGRI, Genet Dis Res Branch, NIH, Bethesda, MD 20892 USA ^[3] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Program Dev Endocrinol & Genet, NIH, Bethesda ^[4] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Program Genom Differentiat, NIH, Bethesda, MD USA ^[5]

发布时间 2018-11-09

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Nature medicine

2016年22卷4期

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Modeling Smith-Lemli-Opitz syndrome with induced pluripotent stem cells reveals a causal role for Wnt/beta-catenin defects in neuronal cholesterol synthesis phenotypes

Nature medicine

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Modeling Smith-Lemli-Opitz syndrome with induced pluripotent stem cells reveals a causal role for Wnt/beta-catenin defects in neuronal cholesterol synthesis phenotypes

Nature medicine

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Nature medicine

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