Borum Sagong

发表

Molecular cloning, characterization, and expression of pannexin genes in chicken.

U. Kim, J. Bae, Tae-Jun Kwon, 2014, Poultry science.

Alpha-lipoic acid protects against cisplatin-induced ototoxicity via the regulation of MAPKs and proinflammatory cytokines.

Jaetae Lee, Se-Jin Kim, In-kyu Lee, 2014, Biochemical and biophysical research communications.

A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct

U. Kim, Jeong-In Baek, Kyu-Yup Lee, 2016, Clinical and experimental otorhinolaryngology.

Identification of causative mutation in a Korean family with Crouzon syndrome using whole exome sequencing.

Jaetae Lee, U. Kim, Min-A Kim, 2014, Annals of clinical and laboratory science.

Genetic association of MYH genes with hereditary hearing loss in Korea.

U. Kim, J. Choi, Se‐Kyung Oh, 2016, Gene.

Multiplex minisequencing screening for PTC genotype associated with bitter taste perception

M. Rhyu, U. Kim, Mi-Kyung Ye, 2014, Molecular Biology Reports.

A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome.

U. Kim, Kyu-Yup Lee, Sang-Heun Lee, 2012, Gene.

Genetic analysis of COL11A2 in Korean patients with autosomal dominant non-syndromic hearing loss

U. Kim, J. Choi, Se‐Kyung Oh, 2016, Genes & Genomics.

A Systematic Survey of Carbonic Anhydrase mRNA Expression During Mammalian Inner Ear Development

J. Bok, U. Kim, J. Choi, 2013, Developmental dynamics : an official publication of the American Association of Anatomists.

Evaluation of the Contribution of the EYA4 and GRHL2 Genes in Korean Patients with Autosomal Dominant Non-Syndromic Hearing Loss

U. Kim, Hyo-Jeong Lee, Min-A Kim, 2015, PloS one.

Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndrome.

M. B. Duz, M. Seven, U. Kim, 2016, Gene.

Identification of a nonsense mutation in the STRC gene in a Korean family with moderate hearing loss.

J. Bok, U. Kim, Jeong‐In Baek, 2016, International journal of pediatric otorhinolaryngology.

Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

U. Kim, Mihyun Park, Hae-Mi Woo, 2013, BMC Medical Genetics.

Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans

U. Kim, Nari Ryu, Min-A Kim, 2016, BMC Medical Genetics.

Genetic Analysis of Genes Related to Tight Junction Function in the Korean Population with Non-Syndromic Hearing Loss

U. Kim, Min-A Kim, Ye-Ri Kim, 2014, PloS one.

Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss.

U. Kim, Sang-Heun Lee, Hyun-joo Cho, 2010, Annals of clinical and laboratory science.

A mutation of the succinate dehydrogenase B gene in a Korean family with paraganglioma

Mi Joo Kim, U. Kim, Y. Seo, 2016, Familial Cancer.

A1555G homoplasmic mutation from A1555G heteroplasmic mother with Pendred syndrome.

U. Kim, Byeonghyeon Lee, M. Park, 2014, International journal of pediatric otorhinolaryngology.

A Rapid Method for Simultaneous Screening of Multi-Gene Mutations Associated with Hearing Loss in the Korean Population

U. Kim, Jeong-In Baek, Kyu-Yup Lee, 2013, PloS one.

Genetic Polymorph isms and Haplotype Analysis of Sweet Taste Receptor TAS1R2 Gene in the Korean Population

U. Kim, J. Bae, Tae-Jun Kwon, 2010 .

Molecular analysis of TMC1 gene in the Korean patients with nonsyndromic hearing loss

U. Kim, Sang-Heun Lee, Tae-Jun Kwon, 2011, Genes & Genomics.

A Novel Frameshift Mutation of SLC26A4 in a Korean Family With Nonsyndromic Hearing Loss and Enlarged Vestibular Aqueduct

U. Kim, Jeong‐In Baek, Kyu‐Yup Lee, 2016, Clinical and experimental otorhinolaryngology.

Spatiotemporal expression patterns of clusterin in the mouse inner ear

J. Bok, U. Kim, Jeong-Oh Shin, 2017, Cell and Tissue Research.

Spatiotemporal expression patterns of clusterin in the mouse inner ear

J. Bok, U. Kim, Jeong-Oh Shin, 2017, Cell and Tissue Research.