Published in Brain Res Dev Brain Res on November 09, 2005
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities. Mol Vis (2007) 1.12
Eye and neural defects associated with loss of GDF6. BMC Dev Biol (2006) 1.00
Impaired motor coordination and disrupted cerebellar architecture in Fgfr1 and Fgfr2 double knockout mice. Brain Res (2012) 0.89
Reelin signaling in development, maintenance, and plasticity of neural networks. Ageing Res Rev (2013) 0.87
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Conserved and differential gene interactions in dynamical biological systems. Bioinformatics (2011) 0.82
Genome-wide microarray comparison reveals downstream genes of Pax6 in the developing mouse cerebellum. Eur J Neurosci (2012) 0.81
Inhibition of the histone demethylase Kdm5b promotes neurogenesis and derepresses Reln (reelin) in neural stem cells from the adult subventricular zone of mice. Mol Biol Cell (2016) 0.79
Controlling the Regional Identity of hPSC-Derived Neurons to Uncover Neuronal Subtype Specificity of Neurological Disease Phenotypes. Stem Cell Reports (2015) 0.79
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Wls provides a new compartmental view of the rhombic lip in mouse cerebellar development. J Neurosci (2014) 0.77
Kruppel-Like Factor 4 Regulates Granule Cell Pax6 Expression and Cell Proliferation in Early Cerebellar Development. PLoS One (2015) 0.76
Regulation of Tlx3 by Pax6 is required for the restricted expression of Chrnα3 in Cerebellar Granule Neuron progenitors during development. Sci Rep (2016) 0.75
A Novel and Multivalent Role of Pax6 in Cerebellar Development. J Neurosci (2016) 0.75
Subtypes of medulloblastoma have distinct developmental origins. Nature (2010) 5.94
Prominin 1 marks intestinal stem cells that are susceptible to neoplastic transformation. Nature (2008) 5.59
Consensus paper: pathological role of the cerebellum in autism. Cerebellum (2012) 2.32
PolymiRTS Database: linking polymorphisms in microRNA target sites with complex traits. Nucleic Acids Res (2006) 1.96
An integrated in vitro and in vivo high-throughput screen identifies treatment leads for ependymoma. Cancer Cell (2011) 1.78
Siah regulation of Pard3A controls neuronal cell adhesion during germinal zone exit. Science (2010) 1.74
Genetics of the hippocampal transcriptome in mouse: a systematic survey and online neurogenomics resource. Front Neurosci (2009) 1.36
Huntingtin inhibits caspase-3 activation. EMBO J (2006) 1.17
Cellular localization and development of neuronal intranuclear inclusions in striatal and cortical neurons in R6/2 transgenic mice. J Comp Neurol (2002) 1.14
A transgenic mouse class-III beta tubulin reporter using yellow fluorescent protein. Genesis (2007) 1.11
Identification of 17 hearing impaired mouse strains in the TMGC ENU-mutagenesis screen. Hear Res (2006) 1.09
A deletion causing spontaneous fracture identified from a candidate region of mouse Chromosome 14. Mamm Genome (2005) 1.08
Repetitive behavior and increased activity in mice with Purkinje cell loss: a model for understanding the role of cerebellar pathology in autism. Eur J Neurosci (2010) 1.06
cDNA cloning and characterization of a novel gene encoding the MLF1-interacting protein MLF1IP. Oncogene (2004) 1.06
Connecting the dots of the cerebro-cerebellar role in cognitive function: neuronal pathways for cerebellar modulation of dopamine release in the prefrontal cortex. Synapse (2011) 1.05
Combining gene expression QTL mapping and phenotypic spectrum analysis to uncover gene regulatory relationships. Mamm Genome (2006) 1.04
The cerebellum and spatial ability: dissection of motor and cognitive components with a mouse model system. Eur J Neurosci (2003) 1.03
An integrative genomics strategy for systematic characterization of genetic loci modulating phenotypes. Hum Mol Genet (2007) 1.03
ClC-3 is required for LPA-activated Cl- current activity and fibroblast-to-myofibroblast differentiation. Am J Physiol Cell Physiol (2007) 1.01
Analysis of cerebellar development in math1 null embryos and chimeras. J Neurosci (2004) 1.01
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Persistent hyperplastic primary vitreous due to somatic mosaic deletion of the arf tumor suppressor. Invest Ophthalmol Vis Sci (2007) 0.98
Developmental expression of PAM (protein associated with MYC) in the rodent brain. Brain Res Dev Brain Res (2002) 0.95
Pten deletion causes mTorc1-dependent ectopic neuroblast differentiation without causing uniform migration defects. Development (2012) 0.95
Neurobehavioral mutants identified in an ENU-mutagenesis project. Mamm Genome (2007) 0.92
Sustained attention in the mouse: a study of the relationship with the cerebellum. Behav Neurosci (2006) 0.92
Reorganization of circuits underlying cerebellar modulation of prefrontal cortical dopamine in mouse models of autism spectrum disorder. Cerebellum (2013) 0.92
Dissection of the cellular and molecular events that position cerebellar Purkinje cells: a study of the math1 null-mutant mouse. J Neurosci (2002) 0.91
The community effect and Purkinje cell migration in the cerebellar cortex: analysis of scrambler chimeric mice. J Neurosci (2002) 0.91
Studies on the hippocampal formation: From basic development to clinical applications: Studies on schizophrenia. Prog Neurobiol (2009) 0.87
Foxn3 is essential for craniofacial development in mice and a putative candidate involved in human congenital craniofacial defects. Biochem Biophys Res Commun (2010) 0.87
Clonal architecture of the mouse hippocampus. J Neurosci (2002) 0.87
Spatial and temporal requirements for huntingtin (Htt) in neuronal migration and survival during brain development. J Neurosci (2011) 0.84
Experimental Sey mouse chimeras reveal the developmental deficiencies of Pax6-null granule cells in the postnatal cerebellum. Dev Biol (2010) 0.84
A genome end-game: understanding gene function in the nervous system. Nat Neurosci (2004) 0.84
Genotype-dependent effects of adolescent nicotine exposure on dopamine functional dynamics in the nucleus accumbens shell in male and female mice: a potential mechanism underlying the gateway effect of nicotine. Psychopharmacology (Berl) (2011) 0.83
Kainic acid-induced neuronal degeneration in hippocampal pyramidal neurons is driven by both intrinsic and extrinsic factors: analysis of FVB/N↔C57BL/6 chimeras. J Neurosci (2012) 0.83
Acute mild footshock alters ethanol drinking and plasma corticosterone levels in C57BL/6J male mice, but not DBA/2J or A/J male mice. Alcohol (2008) 0.82
The expression of HDAC1 and HDAC2 during cerebellar cortical development. Cerebellum (2013) 0.82
The requirement of pax6 for postnatal eye development: evidence from experimental mouse chimeras. Invest Ophthalmol Vis Sci (2007) 0.82
Conserved and differential gene interactions in dynamical biological systems. Bioinformatics (2011) 0.82
Genome-wide microarray comparison reveals downstream genes of Pax6 in the developing mouse cerebellum. Eur J Neurosci (2012) 0.81
A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3. Pigment Cell Res (2007) 0.80
Phenotypic and genetic analysis of the cerebellar mutant tmgc26, a new ENU-induced ROR-alpha allele. Eur J Neurosci (2010) 0.79
Cellular retinol binding protein 1 modulates photoreceptor outer segment folding in the isolated eye. Dev Neurobiol (2010) 0.79
Use of the expanded panel of BXD mice narrow QTL regions in ethanol-induced locomotor activation and motor incoordination. Alcohol Clin Exp Res (2013) 0.79
Glutamate dysfunction associated with developmental cerebellar damage: relevance to autism spectrum disorders. Cerebellum (2014) 0.78
Dopamine dynamics associated with, and resulting from, schedule-induced alcohol self-administration: analyses in dopamine transporter knockout mice. Alcohol (2011) 0.78
Genetic mapping of vocalization to a series of increasing acute footshocks using B6.A consomic and B6.D2 congenic mouse strains. Behav Genet (2008) 0.78
Effects of age and strain on cell proliferation in the mouse rostral migratory stream. Neurobiol Aging (2013) 0.77
Inter-disciplinary research in the pediatric neurosciences: the NeuroDevNet model. Introduction. Semin Pediatr Neurol (2011) 0.77