Congenital hydrocephalus associated with abnormal subcommissural organ in mice lacking huntingtin in Wnt1 cell lineages

By Dietrich Paula   Shanmugasundaram Revathi   E Shuyu   Dragatsis Ioannis  

Human Molecular Genetics, Vol. 18, Iss. 1, 2009-01 ,pp. : 142-150

Oxford University Press

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In vivo misregulation of genes involved in apoptosis, development and oxidative stress in mice lacking both functional Werner syndrome protein and poly(ADP-ribose) polymerase-1

By Deschênes François   Massip Laurent   Lebel Michel  

Human Molecular Genetics, Vol. 14, Iss. 21, 2005-11 ,pp. : 3293-3308

Oxford University Press

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mbryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1

By Gridley T.  

Human Molecular Genetics, Vol. 8, Iss. 5, 1999-05 ,pp. : 723-730

Oxford University Press

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Down-regulation of the dopamine receptor D2 in mice lacking ataxin 1

By Goold Robert   Hubank Michael   Hunt Abigail   Holton Janice   Menon Rajesh P.   Revesz Tamas   Pandolfo Massimo   Matilla-Dueas Antoni  

Human Molecular Genetics, Vol. 16, Iss. 17, 2007-09 ,pp. : 2122-2134

Oxford University Press

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DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation

By Morris J.A.   Kandpal G.   Ma L.   Austin C.P.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1591-1608

Oxford University Press

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