Detalhe da pesquisa
1.
Interleukin-15 in kidney disease and therapeutics.
Curr Opin Nephrol Hypertens
; 33(2): 174-180, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38164877
2.
ß-Arrestin pathway activation by selective ATR1 agonism promotes calcium influx in podocytes, leading to glomerular damage.
Clin Sci (Lond)
; 137(24): 1789-1804, 2023 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38051199
3.
Tobacco exposure in adults and children with proteinuric glomerulopathies: a NEPTUNE cohort study.
BMC Nephrol
; 24(1): 30, 2023 02 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36759756
4.
IL-1 receptor signaling in podocytes limits susceptibility to glomerular damage.
Am J Physiol Renal Physiol
; 322(2): F164-F174, 2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34894725
5.
The Human FSGS-Causing ANLN R431C Mutation Induces Dysregulated PI3K/AKT/mTOR/Rac1 Signaling in Podocytes.
J Am Soc Nephrol
; 29(8): 2110-2122, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30002222
6.
Losing their footing: Rac1 signaling causes podocyte detachment and FSGS.
Kidney Int
; 92(2): 283-285, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28709595
7.
Outscoring Current Classification Systems for Nephrotic Syndrome.
Am J Kidney Dis
; 79(6): 783-784, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35153081
8.
Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux.
Pediatr Nephrol
; 31(2): 247-53, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26408188
9.
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
J Am Soc Nephrol
; 26(4): 831-43, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25145932
10.
HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome.
J Am Soc Nephrol
; 26(7): 1701-10, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25349203
11.
Translating genetic findings in hereditary nephrotic syndrome: the missing loops.
Am J Physiol Renal Physiol
; 309(1): F24-8, 2015 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25810439
12.
Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS.
J Am Soc Nephrol
; 25(9): 1991-2002, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24676636
13.
Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity.
Am J Physiol Renal Physiol
; 306(12): F1442-50, 2014 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24740790
14.
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.
Kidney Int
; 86(6): 1253-9, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25229338
15.
TNXB mutations can cause vesicoureteral reflux.
J Am Soc Nephrol
; 24(8): 1313-22, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23620400
16.
Swollen Feet: Considering the Paradoxical Roles of Interleukins in Nephrotic Syndrome.
Biomedicines
; 12(4)2024 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-38672094
17.
Human mesenchymal stem cells exert potent antitumorigenic effects in a model of Kaposi's sarcoma.
J Exp Med
; 203(5): 1235-47, 2006 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16636132
18.
Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis.
Kidney Int
; 81(1): 94-9, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21866090
19.
Urinary Anomalies in 22q11.2 Deletion (DiGeorge syndrome): From Copy Number Variations to Single-Gene Determinants of Phenotype.
Am J Kidney Dis
; 70(1): 8-10, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28456345
20.
Hepatorenal correction in murine glycogen storage disease type I with a double-stranded adeno-associated virus vector.
Mol Ther
; 19(11): 1961-70, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21730973