Showing results 1 to 10 of 10
A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation Chung, Juyong; Park, Sang Min; Chang, Sun O.; Chung, Taesu; Lee, Kyoung Yeul; Kim, Ah Reum; Park, Joo Hyun; et al, JOURNAL OF MOLECULAR MEDICINE-JMM, v.92, no.6, pp.651 - 663, 2014-06 |
BGN Mutations in X-Linked Spondyloepimetaphyseal Dysplasia Cho, Sung Yoon; Bae, Jun-Seok; Kim, Nayoung K. D.; Forzano, Francesca; Girisha, Katta Mohan; Baldo, Chiara; Faravelli, Francesca; et al, AMERICAN JOURNAL OF HUMAN GENETICS, v.98, no.6, pp.1243 - 1248, 2016-06 |
Destabilization and Mislocalization of POU3F4 by C-Terminal Frameshift Truncation and Extension Mutation Choi, Byung Yoon; Kim, Do-Hwan; Chung, Taesu; Chang, Mi; Kim, Eun-Hye; Kim, Ah Reum; Seok, Jungirl; et al, HUMAN MUTATION, v.34, no.2, pp.309 - 316, 2013-02 |
Downsloping High-Frequency Hearing Loss Due to Inner Ear Tricellular Tight Junction Disruption by a Novel ILDR1 Mutation in the Ig-Like Domain![]() Kim, Nayoung K. D.; Higashi, Tomohito; Lee, Kyoung Yeul; Kim, Ah Reum; Kitajiri, Shin-ichiro; Kim, Min Young; Chang, Mun Young; et al, PLOS ONE, v.10, no.2, 2015-02 |
G-RANK: an equivariant graph neural network for the scoring of protein-protein docking models Kim, Ha Young; Kim, Sungsik; Park, Woong-Yang; Kim, Dongsup, BIOINFORMATICS ADVANCES, v.3, no.1, 2023 |
Identification and Clinical Implications of Novel MY015A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing Chang, Mun Young; Kim, Ah Reum; Kim, Nayoung K. D.; Lee, Chung; Lee, Kyoung Yeul; Jeon, Woo-Sung; Koo, Ja-Won; et al, MOLECULES AND CELLS, v.38, no.9, pp.781 - 788, 2015-09 |
Lineage-dependent gene expression programs influence the immune landscape of colorectal cancer Lee, Hae-Ock; Hong, Yourae; Etlioglu, Hakki Emre; Cho, Yong Beom; Pomelle, Valentina; Van den Bosch, Ben; Vanhecke, Jasper; et al, NATURE GENETICS, v.52, no.6, pp.594 - +, 2020-06 |
Single-cell mapping of combinatorial target antigens for CAR switches using logic gates Kwon, Joonha; Kang, Junho; Jo, Areum; Seo, Kayoung; An, Dohyeon; Baykan, Mert Yakup; Lee, Jun Hyeong; et al, NATURE BIOTECHNOLOGY, v.41, no.11, pp.1593 - 1605, 2023-11 |
The mutational landscape of ocular marginal zone lymphoma identifies frequent alterations in TNFAIP3 followed by mutations in TBL1XR1 and CREBBP Jung, Hyunchul; Yoo, Hae Yong; Lee, Seung Ho; Shin, Sohyun; Kim, Sang Cheol; Lee, Sejoon; Joung, Je-Gun; et al, ONCOTARGET, v.8, no.10, pp.17038 - 17049, 2017-03 |
Whole-Exome Sequencing Identifies Mutations of KIF22 in Spondyloepimetaphyseal Dysplasia with Joint Laxity, Leptodactylic Type Min, Byung-Joo; Kim, Namshin; Chung, Taesu; Kim, Ok-Hwa; Nishimura, Gen; Chung, Chin Youb; Song, Hae Ryong; et al, AMERICAN JOURNAL OF HUMAN GENETICS, v.89, no.6, pp.760 - 766, 2011-12 |
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