Found: 13
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Analysis of the Gene Expression Profile of Curcumin-Treated Kidney on Endotoxin-Induced Renal Inflammation.
- Published in:
- Inflammation, 2013, v. 36, n. 1, p. 80, doi. 10.1007/s10753-012-9522-x
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- Article
Cover.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1459
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- Article
Clinical and genetic analysis of lipoprotein glomerulopathy patients caused by APOE mutations.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1281
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- Article
Role of the retinoic acid receptor-α in HIV-associated nephropathy.
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- Kidney International, 2011, v. 79, n. 6, p. 624, doi. 10.1038/ki.2010.470
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- Article
A systems approach identifies HIPK2 as a key regulator of kidney fibrosis.
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- Nature Medicine, 2012, v. 18, n. 4, p. 580, doi. 10.1038/nm.2685
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- Article
A Rare Genetic Defect of MBL2 Increased the Risk for Progression of IgA Nephropathy.
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- Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.00537
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- Article
Develop and Validate a Risk Score in Predicting Renal Failure in Focal Segmental Glomerulosclerosis.
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- Kidney Diseases, 2023, v. 9, n. 4, p. 285, doi. 10.1159/000529773
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- Article
Proteasome inhibitor MG132 inhibits the process of renal interstitial fibrosis.
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- Experimental & Therapeutic Medicine, 2019, v. 17, n. 4, p. 2953
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- Article
A Validation Study Comparing Risk Prediction Models of IgA Nephropathy.
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- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.753901
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- Article
Uromodulin and progression of IgA nephropathy.
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- Clinical Kidney Journal, 2024, v. 17, n. 8, p. 1, doi. 10.1093/ckj/sfae209
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- Article
Mutation in XPO5 causes adult-onset autosomal dominant familial focal segmental glomerulosclerosis.
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- Human Genomics, 2022, v. 16, n. 1, p. 1, doi. 10.1186/s40246-022-00430-y
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- Article
Glomerular Transcriptome Profiles in Focal Glomerulosclerosis: New Genes and Pathways for Steroid Resistance.
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- 2020
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- Publication type:
- journal article
New risk score for predicting steroid resistance in patients with focal segmental glomerulosclerosis or minimal change disease.
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- Clinical Proteomics, 2020, v. 17, n. 1, p. 1, doi. 10.1186/s12014-020-09282-x
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- Publication type:
- Article