Published in Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi on April 01, 2014
Encoding of movement fragments in the motor cortex. J Neurosci (2007) 2.41
Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. Am J Hum Genet (2003) 1.96
GJB2 mutation spectrum in 2,063 Chinese patients with nonsyndromic hearing impairment. J Transl Med (2009) 1.66
Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China. J Transl Med (2009) 1.62
Genetic basis of Y-linked hearing impairment. Am J Hum Genet (2013) 1.42
Population-based study evaluating and predicting the probability of death resulting from thyroid cancer and other causes among patients with thyroid cancer. J Clin Oncol (2012) 1.38
Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2. Am J Hum Genet (2010) 1.34
Inhibition of activated Stat3 reverses drug resistance to chemotherapeutic agents in gastric cancer cells. Cancer Lett (2011) 1.22
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness. Biochem Biophys Res Commun (2006) 1.19
Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss. Physiol Genomics (2009) 1.19
Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss. Nucleic Acids Res (2005) 1.11
Fate of mammalian cochlear hair cells and stereocilia after loss of the stereocilia. J Neurosci (2009) 1.10
Prestin forms oligomer with four mechanically independent subunits. Brain Res (2010) 1.09
Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss. Am J Med Genet A (2005) 1.03
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct. J Transl Med (2011) 1.03
Effects of alpha-tocopherol on noise-induced hearing loss in guinea pigs. Hear Res (2003) 1.02
Molecular etiology of hearing impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis. J Transl Med (2008) 1.02
Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss. Am J Med Genet A (2006) 1.02
Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China. PLoS One (2012) 1.01
Genetic mutations in nonsyndromic deafness patients of Chinese minority and Han ethnicities in Yunnan, China. J Transl Med (2013) 1.00
The prevalence of the 235delC GJB2 mutation in a Chinese deaf population. Genet Med (2007) 0.98
Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation. Am J Med Genet A (2005) 0.97
SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss. Genet Med (2008) 0.96
Color-tuning method by filling porous alumina membrane using atomic layer deposition based on metal-dielectric-metal structure. Appl Opt (2014) 0.96
VEGF-C promotes the development of esophageal cancer via regulating CNTN-1 expression. Cytokine (2011) 0.95
Design and simulation of omnidirectional reflective color filters based on metal-dielectric-metal structure. Opt Express (2014) 0.95
Usability of a CKD educational website targeted to patients and their family members. Clin J Am Soc Nephrol (2012) 0.95
Functional mutation of SMAC/DIABLO, encoding a mitochondrial proapoptotic protein, causes human progressive hearing loss DFNA64. Am J Hum Genet (2011) 0.94
Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusis. Acta Otolaryngol (2004) 0.94
Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment. PLoS One (2012) 0.93
Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2. J Transl Med (2010) 0.92
Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation. Biochem Biophys Res Commun (2005) 0.92
Design of reflective color filters with high angular tolerance by particle swarm optimization method. Opt Express (2013) 0.92
Directed use of the internet for health information by patients with chronic kidney disease: prospective cohort study. J Med Internet Res (2013) 0.91
Growth and fabrication of InAs/GaSb type II superlattice mid-wavelength infrared photodetectors. Nanoscale Res Lett (2011) 0.91
Deficiency in Six2 during prenatal development is associated with reduced nephron number, chronic renal failure, and hypertension in Br/+ adult mice. Am J Physiol Renal Physiol (2009) 0.90
Cochlear inner hair cell ribbon synapse is the primary target of ototoxic aminoglycoside stimuli. Mol Neurobiol (2013) 0.90
Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss. Biochem Biophys Res Commun (2005) 0.89
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss. J Genet Genomics (2010) 0.88
Programmed cell death 4 (PDCD4) mediates the sensitivity of gastric cancer cells to TRAIL-induced apoptosis by down-regulation of FLIP expression. Exp Cell Res (2010) 0.88
Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type II. PLoS One (2013) 0.87
Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation. Mitochondrion (2009) 0.87
A de novo GJB2 (connexin 26) mutation, R75W, in a Chinese pedigree with hearing loss and palmoplantar keratoderma. Am J Med Genet A (2009) 0.87
Phenotype and genotype of deaf patients with combined genomic and mitochondrial inheritance models. Mitochondrion (2013) 0.86
Quantitative evaluation of monocyte transmigration into the brain following chemical opening of the blood-brain barrier in mice. Brain Res (2006) 0.86
Familial auditory neuropathy. Laryngoscope (2003) 0.85
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss. Biochem Biophys Res Commun (2007) 0.85
Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genes. Int J Pediatr Otorhinolaryngol (2012) 0.85
Effective transduction of primary mouse blood- and bone marrow-derived monocytes/macrophages by HIV-based defective lentiviral vectors. J Virol Methods (2006) 0.85
Contactin-1 (CNTN-1) overexpression is correlated with advanced clinical stage and lymph node metastasis in oesophageal squamous cell carcinomas. Jpn J Clin Oncol (2012) 0.85
Cochlear mitochondrial DNA3867bp deletion in aged mice. Chin Med J (Engl) (2002) 0.84
POT1 deficiency alters telomere length and telomere-associated gene expression in human gastric cancer cells. Eur J Cancer Prev (2010) 0.84
Expression of VEGF-C correlates with a poor prognosis based on analysis of prognostic factors in 73 patients with esophageal squamous cell carcinomas. Jpn J Clin Oncol (2009) 0.83
Expression and clinical significance of cathepsin B and stefin A in laryngeal cancer. Oncol Rep (2011) 0.83
Bone marrow-derived cells contribute to NDEA-induced lung squamous cell carcinoma. Tumour Biol (2012) 0.83
Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss. Mitochondrion (2008) 0.83
Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China. J Hum Genet (2010) 0.82
Primary tumours of the facial nerve: diagnostic and surgical treatment experience in Chinese PLA General Hospital. Acta Otolaryngol (2007) 0.82
Timing of intracranial hypertension following severe traumatic brain injury. Neurocrit Care (2013) 0.81
Clue to a new deafness gene: a large Chinese nonsyndromic hearing loss family linked to DFNA4. J Genet Genomics (2012) 0.81
Upregulation of PAX2 promotes the metastasis of esophageal cancer through interleukin-5. Cell Physiol Biochem (2015) 0.81
Mutations in the mitochondrial 12S rRNA gene in elderly Chinese people. Acta Otolaryngol (2014) 0.81
A 360-degree floating 3D display based on light field regeneration. Opt Express (2013) 0.81
Diagnosis and treatment of giant cell granuloma of the temporal bone: Report of eight cases. Acta Otolaryngol (2012) 0.81
Epidemiological survey on the relationship between different iodine intakes and the prevalence of hyperthyroidism. Eur J Endocrinol (2002) 0.81
Deletions are easy detectable in cochlear mitochondrial DNA of Cu/Zn superoxide dismutase gene knockout mice. Chin Med J (Engl) (2002) 0.80
Ultralong-range phase imaging with orthogonal dispersive spectral-domain optical coherence tomography. Opt Lett (2012) 0.80
[Meta-analysis on effectiveness of prelingually deaf patients at different ages following cochlear implantation]. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi (2015) 0.80
Tonotopic reorganization and spontaneous firing in inferior colliculus during both short and long recovery periods after noise overexposure. J Biomed Sci (2013) 0.80
[Demethylation in the promoter area by the antisense of human DNA MTase gene]. Zhonghua Zhong Liu Za Zhi (2002) 0.79
Efficacy and safety of combined radiotherapy with EGFR inhibitors and chemotherapy for laryngeal organ preservation in patients with locally advanced hypopharyngeal carcinomas. Curr Cancer Drug Targets (2014) 0.79
Intracranial pressure response after pharmacologic treatment of intracranial hypertension. J Trauma Acute Care Surg (2014) 0.79
Silencing of the HCCR2 gene induces apoptosis and suppresses the aggressive phenotype of hepatocellular carcinoma cells in culture. J Gastrointest Surg (2011) 0.79
Geniculate ganglion decompression of facial nerve by transmastoid-epitympanum approach. Acta Otolaryngol (2013) 0.79
Selective expression of Huntingtin-associated protein 1 in {beta}-cells of the rat pancreatic islets. J Histochem Cytochem (2009) 0.79
Chalcogenide coatings of Ge15Sb20S65 and Te20As30Se50. Appl Opt (2008) 0.79
Expression and role of V1A subunit of V-ATPases in gastric cancer cells. Int J Clin Oncol (2015) 0.79
A systematically combined genotype and functional combination analysis of CYP2E1, CYP2D6, CYP2C9, CYP2C19 in different geographic areas of mainland China--a basis for personalized therapy. PLoS One (2013) 0.79
Prognostic models to predict overall and cause-specific survival for patients with middle ear cancer: a population-based analysis. BMC Cancer (2014) 0.79
E2F1: a potential negative regulator of hTERT transcription in normal cells upon activation of oncogenic c-Myc. Med Sci Monit (2012) 0.79
[Significance of some otologic function tests in diagnosis of Meniere's disease]. Lin Chuang Er Bi Yan Hou Ke Za Zhi (2006) 0.79
Mitochondria toxin-induced acute cochlear cell death indicates cellular activity-correlated energy consumption. Eur Arch Otorhinolaryngol (2012) 0.79