Design of Lightweight CFRP Automotive Part as an Alternative for Steel Part by Thickness and Lay-Up Optimization von Lee, Jeong-Min, Min, Byeong-Jin, Park, Joon-Hong, Kim, Dong-Hwan, Kim, Byung-Min, Ko, Dae-Cheol

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Prediction of the Delamination at the Steel and CFRP Interface of Hybrid Composite Part von Park, Jun-Su, Kim, Jae-Hong, Park, Joon-Hong, Ko, Dae-Cheol

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Performance comparison and erosion prediction of jet pumps by using a numerical method von Song, Xue-Guan, Park, Joon-Hong, Kim, Seung-Gyu, Park, Young-Chul

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Identification of novel missense mutation related with non-syndromic sensorineural deafness, DFNA11 in korean family by NGS von Kim, Ye-Ri, Kim, Hye-Min, Lee, Byeonghyeon, Baek, Jeong-In, Lee, Kyu-Yup, Park, Hong-Joon, Kim, Un-Kyung

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Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss von Kim, Min-A, Kim, Ye-Ri, Sagong, Borum, Cho, Hyun-Ju, Bae, Jae Woong, Kim, Jeongho, Lee, Jinwook, Park, Hong-Joon, Choi, Jae Young, Lee, Kyu-Yup, Kim, Un-Kyung

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A novel missense variant in the DIAPH1 gene in a Korean family with autosomal dominant nonsyndromic hearing loss von Kang, Tae-Hun, Baek, Jeong-In, Sagong, Borum, Park, Hong-Joon, Park, Chan Ik, Lee, Kyu-Yup, Kim, Un-Kyung

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Glycoalkaloids and Metabolites Inhibit the Growth of Human Colon (HT29) and Liver (HepG2) Cancer Cells von Lee, Kap-Rang, Kozukue, Nobuyuki, Han, Jae-Sook, Park, Joon-Hong, Chang, Eun-young, Baek, Eun-Jung, Chang, Jong-Sun, Friedman, Mendel

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Structural analysis of woven-fabric composite considering changes in degrees of in-plane shear deformation during manufacturing process von Lee, Jeong-Min, Jeong, Ki-Hyeon, Moon, Young-Hoon, Park, Joon-Hong, Ko, Dae-Cheol

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Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population von Han, Sung-Hee, Park, Hong-Joon, Kang, Eun-Joo, Ryu, Jae-Song, Lee, Anna, Yang, Young-Ho, Lee, Kyoung-Ryul

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Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation von Bae, Jae Woong, Kim, Dong-Bin, Choi, Jae Young, Park, Hong-Joon, Lee, Jong Dae, Hur, Dong Gu, Bae, Seung-Hyun, Jung, Da Jung, Lee, Sang Heun, Kim, Un-Kyung, Lee, Kyu Yup

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Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families von Woo, Hae-Mi, Park, Hong-Joon, Baek, Jeong-In, Park, Mi-Hyun, Kim, Un-Kyung, Sagong, Borum, Koo, Soo Kyung

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Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans von Ryu, Nari, Sagong, Borum, Park, Hong-Joon, Kim, Min-A, Lee, Kyu-Yup, Choi, Jae Young, Kim, Un-Kyung

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A mesh-based disparity representation method for view interpolation and stereo image compression von Park, Joon Hong, Park, Hyun Wook

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Development of a partition panel of an Al6061 sheet metal part for the improvement of formability and mechanical properties by hot forming quenching von Ko, Dae-Cheol, Ko, Dae-Hoon, Kim, Jae-Hong, Park, Joon-Hong

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Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations von Song, Mee Hyun, Shin, Joong-Wook, Park, Hong-Joon, Lee, Kyung-A, Kim, Yoonjung, Kim, Un-Kyung, Jeon, Ju Hyun, Choi, Jae Young

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Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians von YAN, Denise, PARK, Hong-Joon, XUE ZHONG LIU, XIAO MEI OUYANG, PANDYA, Arti, DOI, Katsumi, ERDENETUNGALAG, Raadnabazar, LI LIN DU, MATSUSHIRO, Naoki, NANCE, Walter E, GRIFFITH, Andrew J

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Functional evaluation of GJB2 variants in nonsyndromic hearing loss von Choi, Soo-Young, Lee, Kyu Yup, Kim, Hyun-Jin, Kim, Hyo-Kyeong, Chang, Qing, Park, Hong-Joon, Jeon, Chang-Jin, Lin, Xi, Bok, Jinwoong, Kim, Un-Kyung

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Connexin26 Mutations Associated With Nonsyndromic Hearing Loss von Park, Hong-Joon, Houn Hahn, Si, Chun, Young-Myoung, Park, Keehyun, Kim, Hee-Nam

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Surgical and Audiologic Comparison Between Sophono and Bone-Anchored Hearing Aids Implantation von Shin, Joong-Wook, Kim, Sung Huhn, Choi, Jae Young, Park, Hong-Joon, Lee, Seung-Chul, Choi, Jee-Sun, Park, Han Q, Lee, Ho-Ki

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The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss von Kwon, Tae-Jun, Oh, Se-Kyung, Park, Hong-Joon, Sato, Osamu, Venselaar, Hanka, Choi, Soo Young, Kim, SungHee, Lee, Kyu-Yup, Bok, Jinwoong, Lee, Sang-Heun, Vriend, Gert, Ikebe, Mitsuo, Kim, Un-Kyung, Choi, Jae Young

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