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Journal of Molecular Medicine (Berlin, Germany)|February 15, 2014
A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitationJuyong Chung, Sang Min Park, Sun O Chang, et al.Mycoses|January 21, 2016
Isolation and identification of Malassezia species from Chinese and Korean patients with seborrheic dermatitis and in vitro studies on their bioactivity on sebaceous lipids and IL-8 productionSoo Young Kim, Se Hyun Kim, Su Na Kim, et al.Plos One|February 11, 2015
Downsloping high-frequency hearing loss due to inner ear tricellular tight junction disruption by a novel ILDR1 mutation in the Ig-like domainNayoung K D Kim, Tomohito Higashi, Kyoung Yeul Lee, et al.Journal of Translational Medicine|November 29, 2018
Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinicsBong Jik Kim, Jeong Hun Jang, Jin Hee Han, et al.BMC Nephrology|December 5, 2012
Risk factors affecting seroconversion after influenza A/H1N1 vaccination in hemodialysis patientsSung Jin Moon, Sang Hun Lee, Young-Ho Byun, et al.Plos One|October 30, 2016
Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in KoreansBong Jik Kim, Ah Reum Kim, Chung Lee, et al.Human Mutation|February 12, 2019
Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafnessBong Jik Kim, Dong-Kyu Kim, Jin Hee Han, et al.Scientific Reports|February 9, 2019
Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric populationJae Joon Han, Pham Dinh Nguyen, Doo-Yi Oh, et al.Human Mutation|January 17, 2020
POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic featuresDoo-Yi Oh, Yoshihiro Matsumoto, Shin-Ichiro Kitajiri, et al.Journal of Medical Genetics|September 2, 2019
Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human DIAPH1-related cytoskeletopathyBong Jik Kim, Takehiko Ueyama, Takushi Miyoshi, et al.Pageof 8