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注意：仅列出部分参考文献，下载原文获取全部文献信息。Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
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DYRK1A mutations in two unrelated patients
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The Down syndrome-related protein kinase DYRK1A phosphorylates p27Kip1 and Cyclin D1 and induces cell cycle exit and neuronal differentiation
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Structures of Down Syndrome Kinases, DYRKs, Reveal Mechanisms of Kinase Activation and Substrate Recognition
Meera Soundararajan et al.
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Dyrk1A Influences Neuronal Morphogenesis Through Regulation of Cytoskeletal Dynamics in Mammalian Cortical Neurons
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Molecular cytogenetic characterization of an interstitial deletion of chromosome 21 (21q22.13q22.3) in a patient with dysmorphic features, intellectual disability and severe generalized epilepsy
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The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy
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Rate of de novo mutations and the importance of father's age to disease risk
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Clinical Manifestations of the Deletion of Down Syndrome Critical Region Including DYRK1A and KCNJ6
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Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly
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Microdeletion of the Down Syndrome Critical Region at 21q22
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Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A
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Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly
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DYRK1A accumulates in splicing speckles through a novel targeting signal and induces speckle disassembly
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