Published in Mamm Genome on January 01, 2002
Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function. PLoS Genet (2005) 6.15
Dorsal-ventral patterning of the spinal cord requires Gli3 transcriptional repressor activity. Genes Dev (2002) 2.10
The Shh-independent activator function of the full-length Gli3 protein and its role in vertebrate limb digit patterning. Dev Biol (2007) 1.45
The Gli2 transcriptional activator is a crucial effector for Ihh signaling in osteoblast development and cartilage vascularization. Development (2009) 1.41
Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway. Hum Mol Genet (2009) 1.16
GLI3 constrains digit number by controlling both progenitor proliferation and BMP-dependent exit to chondrogenesis. Dev Cell (2012) 1.07
Gli3 coordinates three-dimensional patterning and growth of the tectum and cerebellum by integrating Shh and Fgf8 signaling. Development (2008) 1.06
The transcription factor Gli3 regulates differentiation of fetal CD4- CD8- double-negative thymocytes. Blood (2005) 1.04
Abnormal positioning of diencephalic cell types in neocortical tissue in the dorsal telencephalon of mice lacking functional Gli3. J Neurosci (2006) 1.02
Coordinated translocation of mammalian Gli proteins and suppressor of fused to the primary cilium. PLoS One (2010) 1.00
Direct and indirect requirements of Shh/Gli signaling in early pituitary development. Dev Biol (2010) 0.92
Limb anterior-posterior polarity integrates activator and repressor functions of GLI2 as well as GLI3. Dev Biol (2012) 0.91
Conserved cis-regulatory regions in a large genomic landscape control SHH and BMP-regulated Gremlin1 expression in mouse limb buds. BMC Dev Biol (2012) 0.90
Mouse thalamic differentiation: gli-dependent pattern and gli-independent prepattern. Front Neurosci (2012) 0.87
Ectodermal influx and cell hypertrophy provide early growth for all murine mammary rudiments, and are differentially regulated among them by Gli3. PLoS One (2011) 0.85
Penetrance of eye defects in mice heterozygous for mutation of Gli3 is enhanced by heterozygous mutation of Pax6. BMC Dev Biol (2006) 0.84
Sonic hedgehog acts cell-autonomously on muscle precursor cells to generate limb muscle diversity. Genes Dev (2012) 0.84
Sonic hedgehog-dependent synthesis of laminin alpha1 controls basement membrane assembly in the myotome. Development (2009) 0.83
Transcriptional analysis of Gli3 mutants identifies Wnt target genes in the developing hippocampus. Cereb Cortex (2012) 0.83
Shh and Gli3 regulate formation of the telencephalic-diencephalic junction and suppress an isthmus-like signaling source in the forebrain. Dev Biol (2011) 0.82
Prevention of premature fusion of calvarial suture in GLI-Kruppel family member 3 (Gli3)-deficient mice by removing one allele of Runt-related transcription factor 2 (Runx2). J Biol Chem (2012) 0.81
GLI3 Links Environmental Arsenic Exposure and Human Fetal Growth. EBioMedicine (2015) 0.80
Differential requirements for Gli2 and Gli3 in the regional specification of the mouse hypothalamus. Front Neuroanat (2015) 0.79
Loss-of-Function of Gli3 in Mice Causes Abnormal Frontal Bone Morphology and Premature Synostosis of the Interfrontal Suture. Front Physiol (2012) 0.79
Hedgehog and Gli signaling in embryonic mammary gland development. J Mammary Gland Biol Neoplasia (2013) 0.78
Wnt7b can replace Ihh to induce hypertrophic cartilage vascularization but not osteoblast differentiation during endochondral bone development. Bone Res (2014) 0.78
The pleiotropic mouse phenotype extra-toes spotting is caused by translation initiation factor Eif3c mutations and is associated with disrupted sonic hedgehog signaling. FASEB J (2011) 0.77
Spop regulates Gli3 activity and Shh signaling in dorsoventral patterning of the mouse spinal cord. Dev Biol (2017) 0.75
Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome. Proc Natl Acad Sci U S A (2009) 2.04
Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome. Proc Natl Acad Sci U S A (2012) 1.79
Blending addiction research and practice: strategies for technology transfer. J Subst Abuse Treat (2008) 1.30
Retinoic acid signaling identifies a distinct precursor population in the developing and adult forebrain. J Neurosci (2005) 1.06
22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome. Int J Dev Neurosci (2002) 1.00
22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development. Hum Mol Genet (2012) 0.99
Position and time specify the migration of a pioneering population of olfactory bulb interneurons. Dev Biol (2006) 0.98
Developmental and degenerative features in a complicated spastic paraplegia. Ann Neurol (2010) 0.93
Noses and neurons: induction, morphogenesis, and neuronal differentiation in the peripheral olfactory pathway. Dev Dyn (2005) 0.90
RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction. Mech Dev (2002) 0.85
No evidence for parental imprinting of mouse 22q11 gene orthologs. Mamm Genome (2006) 0.83
Loss of Gli3 and Shh function disrupts olfactory axon trajectories. J Comp Neurol (2004) 0.80
Methemoglobinemia from curing salt. CMAJ (2013) 0.75
Workplace-Based Assessment of Internal Medicine Resident Diagnostic Accuracy. J Grad Med Educ (2014) 0.75