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Transcriptomic, epigenomic, and spatial metabolomic cell profiling redefines regional human kidney anatomy.
Cell Metab. 2024 May 7;36(5):1105-1125.e10. doi: 10.1016/j.cmet.2024.02.015. Epub 2024 Mar 20.
Cell Metab. 2024.
PMID: 38513647
Free article.
Alport syndrome and Alport kidney diseases - elucidating the disease spectrum.
Puapatanakul P, Miner JH.
Puapatanakul P, et al.
Curr Opin Nephrol Hypertens. 2024 May 1;33(3):283-290. doi: 10.1097/MNH.0000000000000983. Epub 2024 Mar 13.
Curr Opin Nephrol Hypertens. 2024.
PMID: 38477333
Free PMC article.
Review.
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High resolution spatial profiling of kidney injury and repair using RNA hybridization-based in situ sequencing.
Wu H, Dixon EE, Xuanyuan Q, Guo J, Yoshimura Y, Debashish C, Niesnerova A, Xu H, Rouault M, Humphreys BD.
Wu H, et al.
Nat Commun. 2024 Feb 15;15(1):1396. doi: 10.1038/s41467-024-45752-8.
Nat Commun. 2024.
PMID: 38360882
Free PMC article.
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Tubular CPT1A deletion minimally affects aging and chronic kidney injury.
Hammoud S, Ivanova A, Osaki Y, Funk S, Yang H, Viquez O, Delgado R, Lu D, Phillips Mignemi M, Tonello J, Colon S, Lantier L, Wasserman DH, Humphreys BD, Koenitzer J, Kern J, de Caestecker M, Finkel T, Fogo A, Messias N, Lodhi IJ, Gewin LS.
Hammoud S, et al.
JCI Insight. 2024 Feb 22;9(6):e171961. doi: 10.1172/jci.insight.171961.
JCI Insight. 2024.
PMID: 38516886
Free PMC article.
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Quantitative assessment of glomerular basement membrane collagen IV α chains in paraffin sections from patients with focal segmental glomerulosclerosis and Alport gene variants.
Puapatanakul P, Isaranuwatchai S, Chanakul A, Surintrspanont J, Iampenkhae K, Kanjanabuch T, Suphapeetiporn K, Charu V, Suleiman HY, Praditpornsilpa K, Miner JH.
Puapatanakul P, et al.
Kidney Int. 2024 May;105(5):1049-1057. doi: 10.1016/j.kint.2024.01.036. Epub 2024 Feb 22.
Kidney Int. 2024.
PMID: 38401706
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Epigenetic reprogramming driving successful and failed repair in acute kidney injury.
Muto Y, Dixon EE, Yoshimura Y, Ledru N, Kirita Y, Wu H, Humphreys BD.
Muto Y, et al.
bioRxiv [Preprint]. 2024 Jan 23:2024.01.20.576421. doi: 10.1101/2024.01.20.576421.
bioRxiv. 2024.
PMID: 38328130
Free PMC article.
Preprint.
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A Case of Congenital Nephrotic Syndrome with Crescents Caused by a Novel Compound Heterozygous Pairing of NPHS1 Genetic Variants.
Goodman KN, Puapatanakul P, Barton KT, He M, Miner JH, Gaut JP.
Goodman KN, et al.
Case Rep Nephrol. 2024 Feb 27;2024:5121375. doi: 10.1155/2024/5121375. eCollection 2024.
Case Rep Nephrol. 2024.
PMID: 38444459
Free PMC article.
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