Single-cell genomics and gene editing: implications for nephrology

Parker C Wilson¹, Benjamin D Humphreys^{2

3}

Affiliations

¹ Department of Pathology and Immunology, Washington University in Saint Louis School of Medicine, St. Louis, MO, USA.
² Division of Nephrology, Department of Medicine, Washington University in Saint Louis School of Medicine, St. Louis, MO, USA. humphreysbd@wustl.edu.
³ Department of Developmental Biology, Washington University in Saint Louis School of Medicine, St. Louis, MO, USA. humphreysbd@wustl.edu.

Review

Parker C Wilson et al. Nat Rev Nephrol. 2019 Feb.

. 2019 Feb;15(2):63-64.

doi: 10.1038/s41581-018-0094-3.

Parker C Wilson¹, Benjamin D Humphreys^{2

3}

¹ Department of Pathology and Immunology, Washington University in Saint Louis School of Medicine, St. Louis, MO, USA.
² Division of Nephrology, Department of Medicine, Washington University in Saint Louis School of Medicine, St. Louis, MO, USA. humphreysbd@wustl.edu.
³ Department of Developmental Biology, Washington University in Saint Louis School of Medicine, St. Louis, MO, USA. humphreysbd@wustl.edu.

No abstract available

References

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1. Young, M. D. et al. Single-cell transcriptomes from human kidneys reveal the cellular identity of renal tumors. Science 361, 594–599 (2018). - DOI
1. Qiu, C. et al. Renal compartment-specific genetic variation analyses identify new pathways in chronic kidney disease. Nat. Med. 24, 1721–1731 (2018). - DOI
1. Gillies, C. E. et al. An eQTL landscape of kidney tissue in human nephrotic syndrome. Am. J. Hum. Genet. 103, 232–244 (2018). - DOI
1. Park, J. et al. Single-cell transcriptomics of the mouse kidney reveals potential cellular targets of kidney disease. Science 360, 758–763 (2018). - DOI