{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,22]],"date-time":"2026-10-22T01:16:26Z","timestamp":1792631786142,"version":"4.5.0"},"reference-count":62,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JASN"],"published-print":{"date-parts":[[2018,3]]},"abstract":"<jats:p>\n                    Human kidney function is underpinned by approximately 1,000,000 nephrons, although the number varies substantially, and low nephron number is linked to disease. Human kidney development initiates around 4 weeks of gestation and ends around 34\u201337 weeks of gestation. Over this period, a reiterative inductive process establishes the nephron complement. Studies have provided insightful anatomic descriptions of human kidney development, but the limited histologic views are not readily accessible to a broad audience. In this first paper in a series providing comprehensive insight into human kidney formation, we examined human kidney development in 135 anonymously donated human kidney specimens. We documented kidney development at a macroscopic and cellular level through histologic analysis, RNA\n                    <jats:italic toggle=\"yes\">in situ<\/jats:italic>\n                    hybridization, immunofluorescence studies, and transcriptional profiling, contrasting human development (4\u201323 weeks) with mouse development at selected stages (embryonic day 15.5 and postnatal day 2). The high-resolution histologic interactive atlas of human kidney organogenesis generated can be viewed at the GUDMAP database (www.gudmap.org) together with three-dimensional reconstructions of key components of the data herein. At the anatomic level, human and mouse kidney development differ in timing, scale, and global features such as lobe formation and progenitor niche organization. The data also highlight differences in molecular and cellular features, including the expression and cellular distribution of anchor gene markers used to identify key cell types in mouse kidney studies. These data will facilitate and inform\n                    <jats:italic toggle=\"yes\">in vitro<\/jats:italic>\n                    efforts to generate human kidney structures and comparative functional analyses across mammalian species.\n                  <\/jats:p>","DOI":"10.1681\/asn.2017080887","type":"journal-article","created":{"date-parts":[[2018,2,15]],"date-time":"2018-02-15T14:15:23Z","timestamp":1518704123000},"page":"785-805","source":"Crossref","is-referenced-by-count":224,"title":["Conserved and Divergent Features of Human and Mouse Kidney Organogenesis"],"prefix":"10.1681","volume":"29","author":[{"given":"Nils O.","family":"Lindstr\u00f6m","sequence":"first","affiliation":[{"name":"Department of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine,"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jill A.","family":"McMahon","sequence":"additional","affiliation":[{"name":"Department of Stem Cell Biology and Regenerative Medicine, Keck 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