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Molecular Neurobiology|January 15, 2019
Correction to: Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of HearingByeonghyeon Lee, Jeong-In Baek, Hyehyun Min, et al.Molecular Neurobiology|January 13, 2018
Exocyst Complex Member EXOC5 Is Required for Survival of Hair Cells and Spiral Ganglion Neurons and Maintenance of HearingByeonghyeon Lee, Jeong-In Baek, Hyehyun Min, et al.Plos One|March 8, 2013
A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean populationBorum Sagong, Jeong-In Baek, Se-Kyung Oh, et al.Journal of Molecular Medicine (Berlin, Germany)|May 22, 2012
A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domainHyun-Ju Cho, Hong-Joon Park, Maria Trexler, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 18, 2015
Pannexin 3 is required for normal progression of skeletal development in vertebratesSe-Kyung Oh, Jeong-Oh Shin, Jeong-In Baek, et al.American Journal of Physiology. Renal Physiology|October 10, 2014
Exocyst Sec10 protects renal tubule cells from injury by EGFR/MAPK activation and effects on endocytosisBen Fogelgren, Xiaofeng Zuo, Janine M Buonato, et al.Plos One|May 8, 2015
A post-developmental genetic screen for zebrafish models of inherited liver diseaseSeok-Hyung Kim, Shu-Yu Wu, Jeong-In Baek, et al.European Journal of Human Genetics : EJHG|August 21, 2014
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraineSe-Kyung Oh, Jeong-In Baek, Karl M Weigand, et al.Redox Biology|December 4, 2018
Therapeutic potential of the mitochondria-targeted antioxidant MitoQ in mitochondrial-ROS induced sensorineural hearing loss caused by Idh2 deficiencyYe-Ri Kim, Jeong-In Baek, Sung Hwan Kim, et al.Pageof 4