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Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations.
Bantounas I, Rooney KM, Lopes FM, Tengku F, Woods S, Zeef LAH, Lin IH, Kuba SY, Bates N, Hummelgaard S, Hillman KA, Cereghini S, Woolf AS, Kimber SJ. Bantounas I, et al. Among authors: hillman ka. Stem Cell Reports. 2024 Jun 11;19(6):859-876. doi: 10.1016/j.stemcr.2024.04.011. Epub 2024 May 23. Stem Cell Reports. 2024. PMID: 38788724 Free PMC article.
P2 receptors in the kidney.
Bailey MA, Hillman KA, Unwin RJ. Bailey MA, et al. Among authors: hillman ka. J Auton Nerv Syst. 2000 Jul 3;81(1-3):264-70. doi: 10.1016/s0165-1838(00)00125-9. J Auton Nerv Syst. 2000. PMID: 10869730 Review.
Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.
Lennon R, Stuart HM, Bierzynska A, Randles MJ, Kerr B, Hillman KA, Batra G, Campbell J, Storey H, Flinter FA, Koziell A, Welsh GI, Saleem MA, Webb NJ, Woolf AS. Lennon R, et al. Among authors: hillman ka. Pediatr Nephrol. 2015 Sep;30(9):1459-65. doi: 10.1007/s00467-015-3067-9. Epub 2015 Mar 5. Pediatr Nephrol. 2015. PMID: 25739341 Free PMC article.
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