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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|March 24, 2020
KL1333, a derivative of β-lapachone, protects against cisplatin-induced ototoxicity in mouse cochlear culturesHan-Sol Lee, Ye-Ri Kim, In-Kyu Lee, et al.Genes & Genomics|November 20, 2021
Protective effect of berberine chloride against cisplatin-induced ototoxicityJong-Heun Kim, Jeong-In Baek, In-Kyu Lee, et al.Genes & Genetic Systems|December 23, 2016
A novel missense variant in the DIAPH1 gene in a Korean family with autosomal dominant nonsyndromic hearing lossTae-Hun Kang, Jeong-In Baek, Borum Sagong, et al.Genes & Genomics|January 11, 2023
Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGSYe-Ri Kim, Hye-Min Kim, Byeonghyeon Lee, et al.BMC Medical Genetics|July 20, 2013
Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean familiesHae-Mi Woo, Hong-Joon Park, Jeong-In Baek, et al.The Indian Journal of Medical Research|August 14, 2009
Identification of novel variants in the COL4A4 gene in Korean patients with thin basement membrane nephropathyJeong-In Baek, Su-Jin Choi, Sun-Hee Park, et al.Orphanet Journal of Rare Diseases|September 4, 2012
Targeted massive parallel sequencing: the effective detection of novel causative mutations associated with hearing loss in small familiesJeong-In Baek, Se-Kyung Oh, Dong-Bin Kim, et al.Journal of Human Genetics|November 14, 2009
Evidence for a founder mutation causing DFNA5 hearing loss in East AsiansHong-Joon Park, Hyun-Ju Cho, Jeong-In Baek, et al.Annals of Clinical and Laboratory Science|November 2, 2014
Identification of causative mutation in a Korean family with Crouzon syndrome using whole exome sequencingBorum Sagong, Da Jung Jung, Jeong-In Baek, et al.Plos One|July 11, 2013
Mutational analysis of EYA1, SIX1 and SIX5 genes and strategies for management of hearing loss in patients with BOR/BO syndromeMee Hyun Song, Tae-Jun Kwon, Hui Ram Kim, et al.Pageof 4