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Kohei Omachi

Washington University in St. Louis

5

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17

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Defining cellular complexity in human autosomal dominant polycystic kidney disease by multimodal single cell analysis

2021 bioRxiv
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Aminoglycoside-induced premature termination codon readthrough of COL4A5 nonsense mutations that cause Alport syndrome

2021 bioRxiv
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Comparative Analysis and Rational Design of dCas9-VP64 Variants for CRISPR Activation

2021 bioRxiv
- Kohei Omachi
- Jeffrey H. Miner
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Trimerization and genotype-phenotype correlation of COL4A5 mutants in Alport syndrome

2020 Kidney International Reports
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Alport Syndrome Therapeutics: Ready for Prime-Time Players

2019 Trends in Pharmacological Sciences
- Kohei Omachi
- Jeffrey H. Miner
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