Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits

By Ramakers Ger J.A.   Wolfer David   Rosenberger Georg   Kuchenbecker Kerstin   Kreienkamp Hans-Jürgen   Prange-Kiel Janine   Rune Gabriele   Richter Karin   Langnaese Kristina   Masneuf Sophie   Bösl Michael R.   Fischer Klaus-Dieter   Krugers Harm J.   Lipp Hans-Peter   van Galen Elly   Kutsche Kerstin  

Human Molecular Genetics, Vol. 21, Iss. 2, 2012-01 ,pp. : 268-286

Oxford University Press

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Interaction between krit1 and icap1 α infers perturbation of integrin β 1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation

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Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2953-2960

Oxford University Press

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Homozygous α6 Integrin Mutation in Junctional Epidermolysis Bullosa with Congenital Duodenal Atresia

By Pulkkinen Leena  

Human Molecular Genetics, Vol. 6, Iss. 5, 1997-05 ,pp. : 669-674

Oxford University Press

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Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia

By Massinen Satu   Tammimies Kristiina   Tapia-Pez Isabel   Matsson Hans   Hokkanen Marie-Estelle   Sderberg Ola   Landegren Ulf   Castrn Eero   Gustafsson Jan-ke   Treuter Eckardt   Kere Juha  

Human Molecular Genetics, Vol. 18, Iss. 15, 2009-08 ,pp. : 2802-2812

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Absence of α7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy

By Guo Chun   Willem Michael   Raivich Gennadij   Emerson Michael   Neyses Ludwig   Mayer Ulrike  

Human Molecular Genetics, Vol. 15, Iss. 6, 2006-03 ,pp. : 989-998

Oxford University Press

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