Detalhe da pesquisa
1.
Autosomal dominant tubulointerstitial kidney disease-UMOD is the most frequent non polycystic genetic kidney disease.
BMC Nephrol
; 19(1): 301, 2018 10 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-30376835
2.
Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis.
Nephrol Dial Transplant
; 31(6): 961-70, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26346198
3.
From juvenile hyperuricaemia to dysfunctional uromodulin: an ongoing metamorphosis.
Pediatr Nephrol
; 31(11): 2035-42, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26872483
4.
Hemizygous loss of function mutations in CLCN5 causing end-stage kidney disease without Dent disease phenotype.
Clin Kidney J
; 16(1): 192-194, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36726441
5.
A Role for Genetic Modifiers in Tubulointerstitial Kidney Diseases.
Genes (Basel)
; 14(8)2023 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37628633
6.
A genotype-to-phenotype approach suggests under-reporting of single nucleotide variants in nephrocystin-1 (NPHP1) related disease (UK 100,000 Genomes Project).
Sci Rep
; 13(1): 9369, 2023 06 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37296294
7.
Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations.
Kidney Int Rep
; 5(9): 1472-1485, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32954071
8.
Statins prevent oxidized low-density lipoprotein- and lysophosphatidylcholine-induced proliferation of human endothelial cells.
Vascul Pharmacol
; 41(2): 67-73, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15196477
9.
Cerivastatin activates endothelial calcium-activated potassium channels and thereby modulates endothelial nitric oxide production and cell proliferation.
J Am Soc Nephrol
; 15(4): 868-75, 2004 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15034088