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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2022 | 4 |
2024 | 3 |
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7 results
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Page 1
Alport syndrome and Alport kidney diseases - elucidating the disease spectrum.
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.
Comparative analysis of dCas9-VP64 variants and multiplexed guide RNAs mediating CRISPR activation.
Omachi K, Miner JH.
Omachi K, et al.
PLoS One. 2022 Jun 28;17(6):e0270008. doi: 10.1371/journal.pone.0270008. eCollection 2022.
PLoS One. 2022.
PMID: 35763517
Free PMC article.
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A COL4A4-G394S Variant and Impaired Collagen IV Trimerization in a Patient with Mild Alport Syndrome.
Kohler J, Omachi K, Charu V, Miner JH, Bhalla V.
Kohler J, et al.
Kidney360. 2022 Oct 26;3(11):1899-1908. doi: 10.34067/KID.0005472022. eCollection 2022 Nov 24.
Kidney360. 2022.
PMID: 36514391
Free PMC article.
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An ex vivo culture model of kidney podocyte injury reveals mechanosensitive, synaptopodin-templating, sarcomere-like structures.
Jiang S, Alisafaei F, Huang YY, Hong Y, Peng X, Qu C, Puapatanakul P, Jain S, Miner JH, Genin GM, Suleiman HY.
Jiang S, et al.
Sci Adv. 2022 Sep 2;8(35):eabn6027. doi: 10.1126/sciadv.abn6027. Epub 2022 Aug 31.
Sci Adv. 2022.
PMID: 36044576
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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NanoLuc reporters identify COL4A5 nonsense mutations susceptible to drug-induced stop codon readthrough.
Omachi K, Kai H, Roberge M, Miner JH.
Omachi K, et al.
iScience. 2022 Feb 8;25(3):103891. doi: 10.1016/j.isci.2022.103891. eCollection 2022 Mar 18.
iScience. 2022.
PMID: 35243249
Free PMC article.
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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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