102 results on '"Wu, Chen-Chi"'
Search Results
2. Machine learning-based longitudinal prediction for GJB2-related sensorineural hearing loss
3. Application of Genetic Information to Cochlear Implantation in Clinical Practice
4. Synthesis of Pigmented Parylene Coatings and Control of the Chromatism Based on Chemical Vapor Deposition Copolymerization
5. Otoprotection against aminoglycoside- and cisplatin-induced ototoxicity focusing on the upstream drug uptake pathway
6. Genetic Factors Contribute to the Phenotypic Variability in GJB2-Related Hearing Impairment
7. Generation of induced pluripotent stem cells (IBMSi027-A) from a patient with hearing loss carrying WFS1 c.2051C > T (p.Ala684Val) variant
8. Genetic Underpinnings and Audiological Characteristics in Children With Unilateral Sensorineural Hearing Loss
9. Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population
10. Emergence and Persistent Dominance of SARS-CoV-2 Omicron BA.2.3.7 Variant, Taiwan
11. Otoprotective Effects of Fucoidan Reduce Cisplatin-Induced Ototoxicity in Mouse Cochlear UB/OC-2 Cells
12. Simulation-predicted and -explained inheritance model of pathogenicity confirmed by transgenic mice models
13. Outbreak investigation in a COVID-19 designated hospital: The combination of phylogenetic analysis and field epidemiology study suggesting airborne transmission
14. Genetic Underpinnings and Audiological Characteristics in Children with Unilateral Sensorineural Hearing Loss
15. Effects of Diet and Lifestyle on Audio-Vestibular Dysfunction in the Elderly: A Literature Review
16. Identification of nine novel variants acrossPAX3,SOX10,EDNRB, andMITFgenes in Waardenburg syndrome with next‐generation sequencing
17. Gene therapy with a synthetic adeno-associated viral vector improves audiovestibular phenotypes in Pjvk-mutant mice
18. Generation of induced pluripotent stem cells from a patient with hearing loss carrying OPA1 c.1468T>C (p.Cys490Arg) variant
19. Emergence and Persistent Dominance of Omicron BA.2.3.7 Variant in Community Outbreaks in Taiwan
20. Comprehensive Etiologic Analyses in Pediatric Cochlear Implantees and the Clinical Implications
21. Cochlear Implantation Outcomes in Patients with Auditory Neuropathy Spectrum Disorder of Genetic and Non-Genetic Etiologies: A Multicenter Study
22. Computer simulations reveal pathogenicity and inheritance modes of hearing loss-causing germinal variants
23. Prognostic determinants of hearing outcomes in children with congenital cytomegalovirus infection
24. Identification of eight novel variants across PAX3, SOX10, EDNRB and MITF genes in Waardenburg syndrome with next-generation sequencing
25. Helical structure motifs made searchable for functional peptide design
26. Bisdemethoxycurcumin-mediated Attenuation of Apoptosis Prevents Gentamicin-induced Ototoxicity in Mouse Cochlear UB/OC-2 Cells
27. Hearing Features and Cochlear Implantation Outcomes in Patients With PathogenicMYO15AVariants: a Multicenter Observational Study
28. Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment
29. Cochlear implantation in LEOPARD syndrome: Our experience with three patients
30. Insights into phenotypic differences between humans and mice with p.T721M and other C-terminal variants of the SLC26A4 gene
31. Hearing Impairment with Monoallelic GJB2 Variants
32. Low intensity ultrasound enhances cisplatin uptake in vitro by cochlear hair cells
33. Seroprevalence Surveys for Anti-SARS-CoV-2 Antibody in Different Populations in Taiwan With Low Incidence of COVID-19 in 2020 and Severe Outbreaks of SARS in 2003
34. FGF23 ameliorates ischemia-reperfusion induced acute kidney injury via modulation of endothelial progenitor cells: targeting SDF-1/CXCR4 signaling
35. The prevalence and demographic features of congenital cytomegalovirus infection in an urban area of East Asia: A population-based study
36. Toward the Pathogenicity of the SLC26A4 p.C565Y Variant Using a Genetically Driven Mouse Model
37. Hereditary Hearing Impairment with Cutaneous Abnormalities
38. Performance Evaluation of BONET with PCI Express 2.0
39. Detecting VoIP Traffic Based on Human Conversation Patterns
40. Generation and pathological characterization of a transgenic mouse model carrying a missense PJVK mutation
41. Altered expression of genes regulating inflammation and synaptogenesis during regrowth of afferent neurons to cochlear hair cells
42. Efficient In Utero Gene Transfer to the Mammalian Inner Ears by the Synthetic Adeno-Associated Viral Vector Anc80L65
43. An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response
44. Establishment of an induced pluripotent stem cell (iPSC) line from a 7-year-old male patient with profound hearing loss carrying c.235delC in GJB2 gene
45. Toward the pathogenicity of the SLC26A4 p.C565Y variant using a genetically driven mouse model
46. Endoscopic Resection of Middle-Ear Lymphatic Malformation in a Child
47. Vohwinkel syndrome associated with a p.Gly59Arg missense mutation in GJB2
48. Consumption of betel quid contributes to sensorineural hearing impairment through arecoline-induced oxidative stress
49. Generation of a human iPS cell line (CGMH.SLC26A4919-2) from a Pendred syndrome patient carrying SLC26A4 c.919-2A>G splice-site mutation
50. Can Nutritional Intervention for Obesity and Comorbidities Slow Down Age-Related Hearing Impairment?
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