Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome

By Till Sally M.   Wijetunge Lasani S.   Seidel Viktoria G.   Harlow Emily   Wright Ann K.   Bagni Claudia   Contractor Anis   Gillingwater Thomas H.   Kind Peter C.  

Human Molecular Genetics, Vol. 21, Iss. 10, 2012-05 ,pp. : 2143-2156

Oxford University Press

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Reproductive dysfunction and decreased GnRH neurogenesis in a mouse model of CHARGE syndrome

By Layman Wanda S.   Hurd Elizabeth A.   Martin Donna M.  

Human Molecular Genetics, Vol. 20, Iss. 16, 2011-08 ,pp. : 3138-3150

Oxford University Press

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Inhibition of RhoA pathway rescues the endocytosis defects in Oligophrenin1 mouse model of mental retardation

By Khelfaoui Malik   Pavlowsky Alice   Powell Andrew D.   Valnegri Pamela   Cheong Kenneth W.   Blandin Yann   Passafaro Maria   Jefferys John G.R.   Chelly Jamel   Billuart Pierre  

Human Molecular Genetics, Vol. 18, Iss. 14, 2009-07 ,pp. : 2575-2583

Oxford University Press

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Astroglial FMRP-dependent translational down-regulation of mGluR5 underlies glutamate transporter GLT1 dysregulation in the fragile X mouse

By Higashimori Haruki   Morel Lydie   Huth James   Lindemann Lothar   Dulla Chris   Taylor Amaro   Freeman Mike   Yang Yongjie  

Human Molecular Genetics, Vol. 22, Iss. 10, 2013-05 ,pp. : 2041-2054

Oxford University Press

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Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP

By Linder Bastian   Plttner Oliver   Kroiss Matthias   Hartmann Enno   Laggerbauer Bernhard   Meister Gunter   Keidel Eva   Fischer Utz  

Human Molecular Genetics, Vol. 17, Iss. 20, 2008-10 ,pp. : 3236-3246

Oxford University Press

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