Molecular basis of ciliary defects caused by compound heterozygous variations of dynein-2 DYNC2LI1 subunit found in skeletal ciliopathies

Hantian Qiu

[P-392(1T14a-11)] Molecular basis of ciliary defects caused by compound heterozygous variations of dynein-2 DYNC2LI1 subunit found in skeletal ciliopathies

^○Hantian Qiu¹, Yuta Tsurumi², Yohei Katoh¹, Kazuhisa Nakayama¹ (1.Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, Kyoto University, 2.General Research Institute, Hoyu Co., Ltd.)

キーテクノロジー：CRISPR-Cas9 免疫沈降免疫染色

Cilia、Dynein-2、DYNC2LI1、Ciliopathy

qiu.hantian.x48@kyoto-u.jp

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The 94th Annual Meeting of JBS

[P-392(1T14a-11)] Molecular basis of ciliary defects caused by compound heterozygous variations of dynein-2 DYNC2LI1 subunit found in skeletal ciliopathies

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