Kyu-Yup Lee

发表

Effective PEI-mediated delivery of CRISPR-Cas9 complex for targeted gene therapy.

Kyu-Yup Lee, Dongsik Park, Won Jong Kim, 2018, Nanomedicine : nanotechnology, biology, and medicine.

Pannexin 3 is required for normal progression of skeletal development in vertebrates

T. Huh, J. Bok, Z. Ryoo, 2015, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Methionine Sulfoxide Reductase A, B1 and B2 Are Likely to Be Involved in the Protection against Oxidative Stress in the Inner Ear

Jaetae Lee, U. Kim, Byeonghyeon Lee, 2014, Cells Tissues Organs.

The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss

G. Vriend, H. Venselaar, J. Bok, 2014, Open Biology.

Genetic analysis of TMPRSS3 gene in the Korean population with autosomal recessive nonsyndromic hearing loss.

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

Evaluation of the pathogenicity of GJB3 and GJB6 variants associated with nonsyndromic hearing loss.

C. Jeon, U. Kim, Kyu-Yup Lee, 2013, Biochimica et biophysica acta.

Fursultiamine Prevents Drug-Induced Ototoxicity by Reducing Accumulation of Reactive Oxygen Species in Mouse Cochlea

In-kyu Lee, U. Kim, Ye-Ri Kim, 2021, Antioxidants.

Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

J. Bok, U. Kim, P. Wangemann, 2019, Theranostics.

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.

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.

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.

Galangin prevents aminoglycoside-induced ototoxicity by decreasing mitochondrial production of reactive oxygen species in mouse cochlear cultures.

In-kyu Lee, U. Kim, Min-A Kim, 2016, Toxicology letters.

Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.

Y. Bae, J. Bok, Z. Ryoo, 2014, Human molecular genetics.

Molecular and Clinical Characterization of the Variable Phenotype in Korean Families with Hearing Loss Associated with the Mitochondrial A1555G Mutation

U. Kim, Jong Dae Lee, Kyu-Yup Lee, 2012, PloS one.

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.

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 analysis of auditory neuropathy spectrum disorder in the Korean population.

U. Kim, Jong Dae Lee, Jeong-In Baek, 2013, Gene.

Identification and functional characterization of novel compound heterozygotic mutations in the TECTA gene.

U. Kim, Kyu-Yup Lee, B. Sagong, 2012, Gene.

A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss.

U. Kim, Kyu-Yup Lee, R. Park, 2010, Biochemical and biophysical research communications.

KL1333, a derivative of β-lapachone, protects against cisplatin-induced ototoxicity in mouse cochlear cultures.

In-kyu Lee, U. Kim, Ye-Ri Kim, 2020, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.