Published in Behav Brain Res on October 31, 2010
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The preparation of reach to grasp movements in adults with Down syndrome. Hum Mov Sci (2001) 0.84
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A genome-wide investigation of SNPs and CNVs in schizophrenia. PLoS Genet (2009) 5.01
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The SYK tyrosine kinase: a crucial player in diverse biological functions. Nat Rev Immunol (2010) 4.26
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A novel Syk-dependent mechanism of platelet activation by the C-type lectin receptor CLEC-2. Blood (2005) 2.90
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Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project. Mamm Genome (2012) 2.12
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans. PLoS Genet (2007) 2.09
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CLEC-2 and Syk in the megakaryocytic/platelet lineage are essential for development. Blood (2011) 1.30
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Down syndrome: searching for the genetic culprits. Dis Model Mech (2011) 1.28
Superoxide dismutase 1 and tgSOD1 mouse spinal cord seed fibrils, suggesting a propagative cell death mechanism in amyotrophic lateral sclerosis. PLoS One (2010) 1.25
Heme oxygenase-1 accelerates cutaneous wound healing in mice. PLoS One (2009) 1.23
An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Dis Model Mech (2009) 1.22
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Genomically humanized mice: technologies and promises. Nat Rev Genet (2011) 1.18
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Rac GTPases play critical roles in early T-cell development. Blood (2008) 1.13
Down's syndrome-like cardiac developmental defects in embryos of the transchromosomic Tc1 mouse. Cardiovasc Res (2010) 1.13
Function of the nucleotide exchange activity of vav1 in T cell development and activation. Sci Signal (2009) 1.13
Down syndrome: from understanding the neurobiology to therapy. J Neurosci (2010) 1.13
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Essential role of Rac1 and Rac3 GTPases in neuronal development. FASEB J (2009) 1.10
Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome. Hum Mol Genet (2009) 1.09
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