Epigenetic mechanisms, including DNA methylation, histone modifications, and noncoding RNA expression, contribute to regulate islet cell development and function. Indeed, epigenetic mechanisms were recently shown to be involved in the control of endocrine cell fate decision, islet differentiation, beta-cell identity, proliferation, and mature function. Epigenetic mechanisms can also contribute to the pathogenesis of complex diseases. Emerging knowledge regarding epigenetic mechanisms suggest that they may be involved in beta-cell dysfunction and pathogenesis of diabetes. Epigenetic mechanisms could predispose to the diabetic phenotype such as decline of beta-cell proliferation ability and beta-cell failure, and account for complications associated with diabetes. Better understanding of epigenetic landscapes of islet differentiation and function may be useful to improve beta-cell differentiation protocols and discover novel therapeutic targets for prevention and treatment of diabetes.
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Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Chen, Hainan
Gu, Xueying
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Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Gu, Xueying
Su, I-hsin
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Rockefeller Univ, Lab Lymphocyte Signaling, New York, NY 10065 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Su, I-hsin
Bottino, Rita
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Univ Pittsburgh, Sch Med, Inst Diabet, Dept Pediat,Div Immunogenet, Pittsburgh, PA 15213 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Bottino, Rita
Contreras, Juan L.
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Univ Alabama Birmingham, Sch Med, Div Transplantat, Dept Surg, Birmingham, AL 35294 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Contreras, Juan L.
Tarakhovsky, Alexander
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Rockefeller Univ, Lab Lymphocyte Signaling, New York, NY 10065 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Tarakhovsky, Alexander
Kim, Seung K.
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Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
Stanford Univ, Sch Med, Dept Med, Div Oncol, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
机构:
Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Chen, Hainan
Gu, Xueying
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h-index: 0
机构:
Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Gu, Xueying
Su, I-hsin
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h-index: 0
机构:
Rockefeller Univ, Lab Lymphocyte Signaling, New York, NY 10065 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Su, I-hsin
Bottino, Rita
论文数: 0引用数: 0
h-index: 0
机构:
Univ Pittsburgh, Sch Med, Inst Diabet, Dept Pediat,Div Immunogenet, Pittsburgh, PA 15213 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Bottino, Rita
Contreras, Juan L.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Alabama Birmingham, Sch Med, Div Transplantat, Dept Surg, Birmingham, AL 35294 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Contreras, Juan L.
Tarakhovsky, Alexander
论文数: 0引用数: 0
h-index: 0
机构:
Rockefeller Univ, Lab Lymphocyte Signaling, New York, NY 10065 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Tarakhovsky, Alexander
Kim, Seung K.
论文数: 0引用数: 0
h-index: 0
机构:
Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
Stanford Univ, Sch Med, Dept Med, Div Oncol, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA