Detalhe da pesquisa
1.
A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.
J Am Soc Nephrol
; 26(4): 831-43, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25145932
2.
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
Inglês
| MEDLINE | ID: mdl-25349203
3.
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
Inglês
| MEDLINE | ID: mdl-24676636
4.
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
Inglês
| MEDLINE | ID: mdl-24740790
5.
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.
Kidney Int
; 86(6): 1253-9, 2014 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-25229338
6.
TNXB mutations can cause vesicoureteral reflux.
J Am Soc Nephrol
; 24(8): 1313-22, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23620400
7.
A hybrid CFHR3-1 gene causes familial C3 glomerulopathy.
J Am Soc Nephrol
; 23(7): 1155-60, 2012 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-22626820
8.
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
Inglês
| MEDLINE | ID: mdl-21866090
9.
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
Inglês
| MEDLINE | ID: mdl-21730973
10.
Screening for NPHS2 mutations may help predict FSGS recurrence after transplantation.
J Am Soc Nephrol
; 22(3): 579-85, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-21355056
11.
TRPC6 enhances angiotensin II-induced albuminuria.
J Am Soc Nephrol
; 22(3): 526-35, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-21258036
12.
A new locus for familial FSGS on chromosome 2p.
J Am Soc Nephrol
; 21(8): 1390-7, 2010 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-20616172
13.
2007 Young Investigator Award: TRP'ing into a new era for glomerular disease.
J Am Soc Nephrol
; 19(6): 1071-5, 2008 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-18434567
14.
TRPC6 and FSGS: the latest TRP channelopathy.
Biochim Biophys Acta
; 1772(8): 859-68, 2007 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-17459670
15.
TORCing up the importance of calcium signaling.
J Am Soc Nephrol
; 22(8): 1391-3, 2011 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-21757772
16.
Focal and segmental glomerulosclerosis: varying biologic mechanisms underlie a final histopathologic end point.
Semin Nephrol
; 26(2): 89-94, 2006 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-16530601
17.
Association of genetic polymorphisms with risk of renal injury after coronary bypass graft surgery.
Am J Kidney Dis
; 45(3): 519-30, 2005 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-15754274
18.
Gq signaling causes glomerular injury by activating TRPC6.
J Clin Invest
; 125(5): 1913-26, 2015 May.
Artigo
Inglês
| MEDLINE | ID: mdl-25844902
19.
Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation.
Clin Kidney J
; 8(5): 538-42, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26413278
20.
Genetic testing in nephrotic syndrome--challenges and opportunities.
Nat Rev Nephrol
; 9(3): 179-84, 2013 03.
Artigo
Inglês
| MEDLINE | ID: mdl-23321566