Published in Gene on August 17, 2013
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Identification of a novel homozygous mutation, TMPRSS3: c.535G>A, in a Tibetan family with autosomal recessive non-syndromic hearing loss. PLoS One (2014) 0.78
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The molecular basis of individual differences in phenylthiocarbamide and propylthiouracil bitterness perception. Curr Biol (2005) 3.41
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Interleukin-1 beta and tumor necrosis factor-alpha induce MUC5AC overexpression through a mechanism involving ERK/p38 mitogen-activated protein kinases-MSK1-CREB activation in human airway epithelial cells. J Biol Chem (2003) 1.55
Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p. Hum Genet (2003) 1.50
Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small families. Orphanet J Rare Dis (2012) 1.49
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Amplitude ratio of ulnar sensory nerve action potentials in segmental conduction study: reference values in healthy subjects and diagnostic usefulness in patients with ulnar neuropathy at the elbow. Am J Phys Med Rehabil (2008) 1.39
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Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice. J Physiol (2007) 1.21
Natural selection shapes nucleotide polymorphism across the genome of the nematode Caenorhabditis briggsae. Genome Res (2010) 1.21
Risk factors of developing new symptomatic vertebral compression fractures after percutaneous vertebroplasty in osteoporotic patients. Eur Spine J (2006) 1.14
Transcatheter closure of atrial septal defect: does age matter? Korean Circ J (2011) 1.10
Probing graphene grain boundaries with optical microscopy. Nature (2012) 1.10
Pathogenic effects of a novel mutation (c.664_681del) in KCNQ4 channels associated with auditory pathology. Biochim Biophys Acta (2010) 1.09
Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition. J Clin Invest (2011) 1.07
Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families. BMC Med Genet (2013) 1.07
A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss. Biochem Biophys Res Commun (2010) 1.05
Evidence for a founder mutation causing DFNA5 hearing loss in East Asians. J Hum Genet (2009) 0.98
Compositional difference in middle ear effusion: mucous versus serous. Laryngoscope (2002) 0.98
Mastoid and epitympanic obliteration in canal wall up mastoidectomy for prevention of retraction pocket. Otol Neurotol (2005) 0.97
Clinical outcome of transcatheter closure of patent ductus arteriosus in small children weighing 10 kg or less. Korean J Pediatr (2010) 0.97
Auditory neural pathway evaluation on sensorineural hearing loss using diffusion tensor imaging. Neuroreport (2004) 0.96
Dissemination of metallo-β-lactamase-producing Pseudomonas aeruginosa of sequence type 235 in Asian countries. J Antimicrob Chemother (2013) 0.96
Gender-specific association of the VEGF -2578C > A polymorphism in Korean patients with colon cancer. Anticancer Res (2007) 0.96
Idiopathic cardiomyopathies in Korean children. - 9-Year Korean Multicenter Study-. Circ J (2011) 0.96
Substance P stimulates CFTR-dependent fluid secretion by mouse tracheal submucosal glands. Pflugers Arch (2008) 0.96
Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss. Ann Clin Lab Sci (2010) 0.94
Mutations of acetylcholinesterase1 contribute to prothiofos-resistance in Plutella xylostella (L.). Biochem Biophys Res Commun (2006) 0.94
Kawasaki disease and hyponatremia. Pediatr Nephrol (2006) 0.94
Construction of a DNA chip for screening of genetic hearing loss. Clin Exp Otorhinolaryngol (2009) 0.93
The Autographa californica multiple nucleopolyhedrovirus ORF78 is essential for budded virus production and general occlusion body formation. J Virol (2013) 0.92
Transcatheter closure of perimembranous ventricular septal defect using Amplatzer ductal occluder. Catheter Cardiovasc Interv (2013) 0.92
Receptor-mediated gene delivery by folate-PEG-baculovirus in vitro. J Biotechnol (2007) 0.92
A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean population. PLoS One (2013) 0.91
CHD7 mutational analysis and clinical considerations for auditory rehabilitation in deaf patients with CHARGE syndrome. PLoS One (2011) 0.91
Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss. Int J Mol Med (2008) 0.91
Chronic epidural hematoma with rapid ossification. Childs Nerv Syst (2002) 0.91
Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein. Physiol Genomics (2009) 0.90
Interleukin-1beta upregulates Na+-K+-2Cl- cotransporter in human middle ear epithelia. J Cell Biochem (2007) 0.90
Reversible Sensorineural Hearing Loss due to Pachymeningitis Associated with Elevated Serum MPO-ANCA. Clin Exp Otorhinolaryngol (2011) 0.90
Different functional consequences of two missense mutations in the GJB2 gene associated with non-syndromic hearing loss. Hum Mutat (2009) 0.90
Prostaglandin E2 induces MUC8 gene expression via a mechanism involving ERK MAPK/RSK1/cAMP response element binding protein activation in human airway epithelial cells. J Biol Chem (2004) 0.90
Membrane-specific expression of functional purinergic receptors in normal human nasal epithelial cells. Am J Physiol Lung Cell Mol Physiol (2004) 0.90
Evaluation of the pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss. Biochim Biophys Acta (2012) 0.89
Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation. PLoS One (2012) 0.89
Evaluation of white matter structures in patients with tinnitus using diffusion tensor imaging. J Clin Neurosci (2007) 0.89
Traumatic ventricular septal defect in a 4-year-old boy after blunt chest injury. Korean J Pediatr (2011) 0.88
The overexpression of acetylcholinesterase compensates for the reduced catalytic activity caused by resistance-conferring mutations in Tetranychus urticae. Insect Biochem Mol Biol (2011) 0.88
Significant association of SREBP-2 genetic polymorphisms with avascular necrosis in the Korean population. BMC Med Genet (2008) 0.88
Pou3f4 deficiency causes defects in otic fibrocytes and stria vascularis by different mechanisms. Biochem Biophys Res Commun (2010) 0.88
Developmental gene expression profiling along the tonotopic axis of the mouse cochlea. PLoS One (2012) 0.88
Local color vector binary patterns from multichannel face images for face recognition. IEEE Trans Image Process (2011) 0.88
Correlation of the aphicidal activity of Beauveria bassiana SFB-205 supernatant with enzymes. Fungal Biol (2009) 0.87
Genetic analysis of the CHD7 gene in Korean patients with CHARGE syndrome. Gene (2013) 0.87
An improved baculovirus insecticide producing occlusion bodies that contain Bacillus thuringiensis insect toxin. J Invertebr Pathol (2003) 0.87
Activation of epithelial sodium channel in human middle ear epithelial cells by dexamethasone. Eur J Pharmacol (2008) 0.86
Genomic sequence analysis of granulovirus isolated from the tobacco cutworm, Spodoptera litura. PLoS One (2011) 0.86
Functional evaluation of GJB2 variants in nonsyndromic hearing loss. Mol Med (2011) 0.85
Mucociliary differentiation according to time in human nasal epithelial cell culture. Differentiation (2002) 0.85
Purinergic stimulation induces Ca2+-dependent activation of Na+-K+-2Cl- cotransporter in human nasal epithelia. J Biol Chem (2004) 0.85
Enlarged cochlear aqueducts: a potential route for CSF gushers in patients with enlarged vestibular aqueducts. Otol Neurotol (2013) 0.84
Properties of substance P-stimulated mucus secretion from porcine tracheal submucosal glands. Am J Physiol Lung Cell Mol Physiol (2010) 0.84
Visualization of endolymphatic hydrops and correlation with audio-vestibular functional testing in patients with definite Meniere's disease. Auris Nasus Larynx (2012) 0.84
Genetic and epigenetic alterations of the NF2 gene in sporadic vestibular schwannomas. PLoS One (2012) 0.83
Human taste receptor-functionalized field effect transistor as a human-like nanobioelectronic tongue. Nano Lett (2012) 0.83
Production of classical swine fever virus envelope glycoprotein E2 as recombinant polyhedra in baculovirus-infected silkworm larvae. Mol Biotechnol (2012) 0.83
Three acetylcholinesterases of the pinewood nematode, Bursaphelenchus xylophilus: insights into distinct physiological functions. Mol Biochem Parasitol (2010) 0.83
House dust mite extract activates apical Cl(-) channels through protease-activated receptor 2 in human airway epithelia. J Cell Biochem (2010) 0.83
Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells. Hum Mol Genet (2013) 0.83
Role of postoperative magnetic resonance imaging after microvascular decompression of the facial nerve for the treatment of hemifacial spasm. Neurosurgery (2002) 0.83
NeuroBactrus, a novel, highly effective, and environmentally friendly recombinant baculovirus insecticide. Appl Environ Microbiol (2012) 0.83
Manganese-enhanced auditory tract-tracing MRI with cochlear injection. Magn Reson Imaging (2006) 0.82
AP2alpha is essential for MUC8 gene expression in human airway epithelial cells. J Cell Biochem (2010) 0.82
Morphologic Characteristics and Relating Factors to the Need of Technical Modification in Transcatheter Closure of Large Atrial Septal Defect (>/=25 mm). Korean Circ J (2010) 0.82