Search Results - Nakhro, Khriezhanuo

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  1. 1
    Haploid selection within a single ejaculate increases offspring fitness

    Haploid selection within a single ejaculate increases offspring fitness by Alavioon, Ghazal, Hotzy, Cosima, Nakhro, Khriezhanuo, Rudolf, Sandra, Scofield, Douglas G., Zajitschek, Susanne, Maklakov, Alexei A., Immler, Simone

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  2. 2
    Two de novo mutations of MFN2 associated with early-onset Charcot-Marie-Tooth disease type 2A neuropathy

    Two de novo mutations of MFN2 associated with early-onset Charcot-Marie-Tooth disease type 2A neuropathy by Nakhro, Khriezhanuo, Kongju National University, Kongju, Republic of Korea, Kim, Y.J., Kongju National University, Kongju, Republic of Korea, Lee, J.H., Kongju National University, Kongju, Republic of Korea, Koo, H.S., Ewha Womans University, Seoul, Republic of Korea, Choi, B.O., Ewha Womans University, Seoul, Republic of Korea, Chung, K.W., Kongju National University, Kongju, Republic of Korea

    Published in Genes & genomics
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  3. 3
    Large-scale generation and phenotypic characterization of zebrafish CRISPR mutants of DNA repair genes

    Large-scale generation and phenotypic characterization of zebrafish CRISPR mutants of DNA repair genes by Shin, Unbeom, Nakhro, Khriezhanuo, Oh, Chang-Kyu, Carrington, Blake, Song, HeaIn, Varshney, Gaurav K., Kim, Yeongjae, Song, Hyemin, Jeon, Sangeun, Robbins, Gabrielle, Kim, Sangin, Yoon, Suhyeon, Choi, Yong Jun, Kim, Yoo Jung, Burgess, Shawn, Kang, Sukhyun, Sood, Raman, Lee, Yoonsung, Myung, Kyungjae

    Published in DNA repair
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  4. 4
    Compound mutations of PEO1 and TYMP in a progressive external ophthalmoplegia patient with incomplete mitochondrial neurogastrointestinal encephalomyopathy phenotype

    Compound mutations of PEO1 and TYMP in a progressive external ophthalmoplegia patient with incomplete mitochondrial neurogastrointestinal encephalomyopathy phenotype by Nakhro, Khriezhanuo, Chung, Ki Wha, Kim, Seung-Min, Sunwoo, Il-Nam, Cho, Eun Min, Park, Sun Wha, Hwang, Jung Hee, Choi, Byung-Ok

    Published in Genes & genomics
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  5. 5
    A novel Lys141Thr mutation in small heat shock protein 22 ( HSPB8 ) gene in Charcot–Marie–Tooth disease type 2L

    A novel Lys141Thr mutation in small heat shock protein 22 ( HSPB8 ) gene in Charcot–Marie–Tooth disease type 2L by Nakhro, Khriezhanuo, Park, Jin-Mo, Kim, Ye Jin, Yoon, Bo Ram, Yoo, Jeong Hyun, Koo, Heasoo, Choi, Byung-Ok, Chung, Ki Wha

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