[2T14] Cell Structure and Function / Cycle, Development 02

2:04 PM - 2:13 PM JST(5:04 AM - 5:13 AM UTC)

[2T14-07] Molecular mechanism underlying ciliopathy (Meckel syndrome) caused by defects in thioredoxin domain of TXNDC15

^○Shingo Yamazaki¹, Taiju Fujii¹, Hye-Won Shin¹, Yohei Katoh², Kazuhisa Nakayama¹ (1.Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto University, 2.Hiroshima University Genome Editing Innovation Center)

キーテクノロジー：CRISPR/Cas9

Keywords:

一次繊毛、トランジションゾーン、PDIファミリー、繊毛病、チオレドキシン・ドメイン

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