Published in J Assoc Res Otolaryngol on January 30, 2008
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Survival of adult spiral ganglion neurons requires erbB receptor signaling in the inner ear. J Neurosci (2004) 1.88
Pathophysiology of Meniere's syndrome: are symptoms caused by endolymphatic hydrops? Otol Neurotol (2005) 1.74
Noncanonical Wnt signaling and neural polarity. Annu Rev Neurosci (2006) 1.63
Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution. Genome Res (2003) 1.62
Genetic interaction between Wnt/beta-catenin and BMP receptor signaling during formation of the AER and the dorsal-ventral axis in the limb. Genes Dev (2003) 1.55
Osteoprotegerin in the inner ear may inhibit bone remodeling in the otic capsule. Laryngoscope (2005) 1.53
Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations. Development (2006) 1.49
Distribution of gentamicin in the guinea pig inner ear after local or systemic application. J Assoc Res Otolaryngol (2003) 1.41
Suppression of neural fate and control of inner ear morphogenesis by Tbx1. Development (2004) 1.41
Identification of downstream genetic pathways of Tbx1 in the second heart field. Dev Biol (2008) 1.39
A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis. J Clin Invest (2011) 1.39
Regulation of outgrowth and apoptosis for the terminal appendage: external genitalia development by concerted actions of BMP signaling [corrected]. Development (2003) 1.38
Wnt signaling is sufficient to perturb oligodendrocyte maturation. Mol Cell Neurosci (2009) 1.37
Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field. Development (2006) 1.34
Signaling through BMP type 1 receptors is required for development of interneuron cell types in the dorsal spinal cord. Development (2004) 1.18
Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes. Hum Mol Genet (2003) 1.17
Loss of alpha CGRP reduces sound-evoked activity in the cochlear nerve. J Neurophysiol (2003) 1.15
Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome. Neurogenetics (2006) 1.14
Otic mesenchyme cells regulate spiral ganglion axon fasciculation through a Pou3f4/EphA4 signaling pathway. Neuron (2012) 1.14
The role of Brn4/Pou3f4 and Pax6 in forming the pancreatic glucagon cell identity. Dev Biol (2004) 1.14
Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients. Hum Mol Genet (2006) 1.13
Wolfram syndrome: a clinicopathologic correlation. Acta Neuropathol (2009) 1.11
T-genes and limb bud development. Am J Med Genet A (2006) 1.11
Pathology and pathophysiology of idiopathic sudden sensorineural hearing loss. Otol Neurotol (2005) 1.10
Sudden deafness: is it viral? ORL J Otorhinolaryngol Relat Spec (2008) 1.10
Bmp and Wnt/beta-catenin signals control expression of the transcription factor Olig3 and the specification of spinal cord neurons. Dev Biol (2006) 1.09
The closely related transcription factors Sox4 and Sox11 function as survival factors during spinal cord development. J Neurochem (2010) 1.08
Bone morphogenetic protein 4 (BMP4): a regulator of capsule chondrogenesis in the developing mouse inner ear. Dev Dyn (2003) 1.08
Osteoprotegrin knockout mice demonstrate abnormal remodeling of the otic capsule and progressive hearing loss. Laryngoscope (2006) 1.08
Bcl11a is required for neuronal morphogenesis and sensory circuit formation in dorsal spinal cord development. Development (2012) 1.07
Dual embryonic origin of the mammalian otic vesicle forming the inner ear. Development (2011) 1.07
BMP signaling mutant mice exhibit glial cell maturation defects. Mol Cell Neurosci (2007) 1.06
Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy. Hum Mol Genet (2006) 1.06
Genetic analyses demonstrate that bone morphogenetic protein signaling is required for embryonic cerebellar development. J Neurosci (2006) 1.05
Effects of fixative and embedding medium on morphology and immunostaining of the cochlea. Audiol Neurootol (2008) 1.04
Techniques of celloidin removal from temporal bone sections. Ann Otol Rhinol Laryngol (2009) 1.01
Isolation from cochlea of a novel human intronless gene with predominant fetal expression. J Assoc Res Otolaryngol (2004) 1.01
Genetic modifiers of the physical malformations in velo-cardio-facial syndrome/DiGeorge syndrome. Dev Disabil Res Rev (2008) 1.00
Distribution of type IV collagen in the cochlea in Alport syndrome. Arch Otolaryngol Head Neck Surg (2005) 1.00
Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairment. Am J Med Genet A (2007) 0.98
Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome. Laryngoscope (2006) 0.97
CARMA3 mediates lysophosphatidic acid-stimulated cytokine secretion by bronchial epithelial cells. Am J Respir Cell Mol Biol (2008) 0.96
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. Am J Hum Genet (2013) 0.96
Traffic of genetic information between segmental duplications flanking the typical 22q11.2 deletion in velo-cardio-facial syndrome/DiGeorge syndrome. Genome Res (2005) 0.95
Changes in cytochemistry of sensory and nonsensory cells in gentamicin-treated cochleas. J Assoc Res Otolaryngol (2003) 0.94
Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis. BMC Dev Biol (2009) 0.94
Hominoid lineage specific amplification of low-copy repeats on 22q11.2 (LCR22s) associated with velo-cardio-facial/digeorge syndrome. Hum Mol Genet (2007) 0.92
Polyester wax: a new embedding medium for the histopathologic study of human temporal bones. Laryngoscope (2006) 0.91
Mesodermal Tbx1 is required for patterning the proximal mandible in mice. Dev Biol (2010) 0.91
Mutational analysis of HOXA2 and SIX2 in a Bronx population with isolated microtia. Int J Pediatr Otorhinolaryngol (2010) 0.91
Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle. Dev Dyn (2010) 0.90
Mutation of the POU-domain gene Brn4/Pou3f4 affects middle-ear sound conduction in the mouse. Hear Res (2005) 0.88
3p-- syndrome defines a hearing loss locus in 3p25.3. Hear Res (2007) 0.88
Differences in gene expression between the otic capsule and other bones. Hear Res (2010) 0.88
Harvest: an open platform for developing web-based biomedical data discovery and reporting applications. J Am Med Inform Assoc (2013) 0.86
AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12. Genome Res (2007) 0.85
Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams-Beuren syndrome. Am J Med Genet A (2013) 0.84
Temporal bone histopathology in alport syndrome. Laryngoscope (2004) 0.84
Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: a phenotype correlation study. Int J Pediatr Otorhinolaryngol (2011) 0.84
Otic mesenchyme expression of Cre recombinase directed by the inner ear enhancer of the Brn4/Pou3f4 gene. Genesis (2009) 0.84
Temporal bone histopathology in a case of sensorineural hearing loss caused by superficial siderosis of the central nervous system and treated by cochlear implantation. Otol Neurotol (2011) 0.82
GJB2 mutation spectrum in 209 hearing impaired individuals of predominantly Caribbean Hispanic and African descent. Int J Pediatr Otorhinolaryngol (2010) 0.81
Studies of otic capsule morphology and gene expression in the Mov13 mouse--an animal model of type I osteogenesis imperfecta. Audiol Neurootol (2007) 0.81
Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes. Psychiatr Genet (2014) 0.81
Human temporal bone consortium for research resource enhancement. Otol Neurotol (2008) 0.80
Extralabyrinthine manifestations of DFNA9. J Assoc Res Otolaryngol (2010) 0.80
Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development. Dev Dyn (2012) 0.79
Human temporal bone consortium for research resource enhancement. J Assoc Res Otolaryngol (2008) 0.79
Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients. Am J Med Genet A (2012) 0.79
Genetic evaluation of American minority pediatric cochlear implant recipients. Int J Pediatr Otorhinolaryngol (2008) 0.78
Abnormal mesenchymal differentiation in the superior semicircular canal of brn4/pou3f4 knockout mice. Arch Otolaryngol Head Neck Surg (2005) 0.78
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients. Int J Pediatr Otorhinolaryngol (2012) 0.77
Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice. BMC Dev Biol (2013) 0.76
Innervation of supporting cells in the guinea pig cochlea detected in bloc-surface preparations. Neuroreport (2002) 0.76
Correction: A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family. PLoS One (2015) 0.75
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A novel, single nucleotide polymorphism-based assay to detect 22q11 deletions. Genet Test (2007) 0.75