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By Amano Kenji   Sago Haruhiko   Uchikawa Chiharu   Suzuki Taishi   Kotliarova Svetlana E.   Nukina Nobuyuki   Epstein Charles J.   Yamakawa Kazuhiro  

Human Molecular Genetics, Vol. 13, Iss. 13, 2004-07 ,pp. : 1333-1340

Oxford University Press

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DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: implications for Down syndrome and Alzheimer's disease

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Human Molecular Genetics, Vol. 17, Iss. 7, 2008-04 ,pp. : 1020-1030

Oxford University Press

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OLIG2 over-expression impairs proliferation of human Down syndrome neural progenitors

By Lu Jie   Lian Gewei   Zhou Hui   Esposito Giuseppe   Steardo Luca   Delli-Bovi Laurent C.   Hecht Jonathan L.   Lu Q. Richard   Sheen Volney  

Human Molecular Genetics, Vol. 21, Iss. 10, 2012-05 ,pp. : 2330-2340

Oxford University Press

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De novo SHANK3 mutation causes Rett syndrome‐like phenotype in a female patient

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 7, 2015-07 ,pp. : 1593-1596

John Wiley & Sons Inc

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Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in mice

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Human Molecular Genetics, Vol. 18, Iss. 20, 2009-10 ,pp. : 3914-3925

Oxford University Press

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