| Literature DB >> 31492507 |
Jihwan Park1, Chang Linda Liu1, Junhyong Kim2, Katalin Susztak3.
Abstract
A revolution in cellular measurement technology is underway. Whereas prior studies have been able to analyze only the averaged outputs from renal tissue, we now can accurately monitor genome-wide gene expression, regulation, function, cellular history, and cellular interactions in thousands of individual cells in a single experiment. These methods are key drivers in changing our previous morphotype-based organ and disease descriptions to unbiased genomic definitions and therefore improving our understanding of kidney development, homeostasis, and disease.Entities:
Keywords: RNA-seq; epigenome; kidney disease; single cell
Mesh:
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Year: 2019 PMID: 31492507 PMCID: PMC6777841 DOI: 10.1016/j.kint.2019.03.035
Source DB: PubMed Journal: Kidney Int ISSN: 0085-2538 Impact factor: 10.612