562 related articles for article (PubMed ID: 16050398)
1. Molecular basis of steroid-resistant nephrotic syndrome.
Antignac C
Nefrologia; 2005; 25 Suppl 2():25-8. PubMed ID: 16050398
[TBL] [Abstract][Full Text] [Related]
2. Genetic basis of nephrotic syndrome--review.
Obeidová H; Merta M; Reiterová J; Maixnerová D; Stekrová J; Rysavá R; Tesar V
Prague Med Rep; 2006; 107(1):5-16. PubMed ID: 16752799
[TBL] [Abstract][Full Text] [Related]
3. [Heterozygotic mutation in NPHS2 gene as a cause of familial steroid resistant nephrotic syndrome in two siblings--case report].
Drozdz D; Pietrzyk JA; Wierzchowska-Słowiaczek E; Sancewicz-Pach K; Antignac C; Miezyński W
Przegl Lek; 2006; 63 Suppl 3():85-6. PubMed ID: 16898497
[TBL] [Abstract][Full Text] [Related]
4. The genetic basis of FSGS and steroid-resistant nephrosis.
Pollak MR
Semin Nephrol; 2003 Mar; 23(2):141-6. PubMed ID: 12704574
[TBL] [Abstract][Full Text] [Related]
5. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.
Boute N; Gribouval O; Roselli S; Benessy F; Lee H; Fuchshuber A; Dahan K; Gubler MC; Niaudet P; Antignac C
Nat Genet; 2000 Apr; 24(4):349-54. PubMed ID: 10742096
[TBL] [Abstract][Full Text] [Related]
6. In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation.
Zhang SY; Marlier A; Gribouval O; Gilbert T; Heidet L; Antignac C; Gubler MC
Kidney Int; 2004 Sep; 66(3):945-54. PubMed ID: 15327385
[TBL] [Abstract][Full Text] [Related]
7. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.
Sako M; Nakanishi K; Obana M; Yata N; Hoshii S; Takahashi S; Wada N; Takahashi Y; Kaku Y; Satomura K; Ikeda M; Honda M; Iijima K; Yoshikawa N
Kidney Int; 2005 Apr; 67(4):1248-55. PubMed ID: 15780077
[TBL] [Abstract][Full Text] [Related]
8. Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern.
Suvanto M; Patrakka J; Jahnukainen T; Sjöström PM; Nuutinen M; Arikoski P; Kataja J; Kestilä M; Jalanko H
Clin Exp Nephrol; 2017 Aug; 21(4):677-684. PubMed ID: 27573339
[TBL] [Abstract][Full Text] [Related]
9. Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis.
Löwik M; Levtchenko E; Westra D; Groenen P; Steenbergen E; Weening J; Lilien M; Monnens L; van den Heuvel L
Nephrol Dial Transplant; 2008 Oct; 23(10):3146-51. PubMed ID: 18443213
[TBL] [Abstract][Full Text] [Related]
10. [Structure and function of the glomerular filtration barrier].
Musiał K; Zwolińska D
Pol Merkur Lekarski; 2005 Mar; 18(105):317-20. PubMed ID: 15997642
[TBL] [Abstract][Full Text] [Related]
11. The heart of children with steroid-resistant nephrotic syndrome: is it all podocin?
Frishberg Y; Feinstein S; Rinat C; Becker-Cohen R; Lerer I; Raas-Rothschild A; Ferber B; Nir A
J Am Soc Nephrol; 2006 Jan; 17(1):227-31. PubMed ID: 16291839
[TBL] [Abstract][Full Text] [Related]
12. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
Hinkes BG; Mucha B; Vlangos CN; Gbadegesin R; Liu J; Hasselbacher K; Hangan D; Ozaltin F; Zenker M; Hildebrandt F;
Pediatrics; 2007 Apr; 119(4):e907-19. PubMed ID: 17371932
[TBL] [Abstract][Full Text] [Related]
13. [A genetic viewpoint of focal glomerular sclerosis: fom genes to glomerular pathophysiology [corrected]].
Aucella F; Bisceglia L; Stallone C
G Ital Nefrol; 2003; 20(4):356-67. PubMed ID: 14523896
[TBL] [Abstract][Full Text] [Related]
14. Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains.
Huber TB; Simons M; Hartleben B; Sernetz L; Schmidts M; Gundlach E; Saleem MA; Walz G; Benzing T
Hum Mol Genet; 2003 Dec; 12(24):3397-405. PubMed ID: 14570703
[TBL] [Abstract][Full Text] [Related]
15. NPHS2 mutations in children with steroid-resistant nephrotic syndrome.
Otukesh H; Ghazanfari B; Fereshtehnejad SM; Bakhshayesh M; Hashemi M; Hoseini R; Chalian M; Salami A; Mehdipor L; Rahiminia A
Iran J Kidney Dis; 2009 Apr; 3(2):99-102. PubMed ID: 19395786
[TBL] [Abstract][Full Text] [Related]
16. A novel NPHS2 gene mutation in Turkish children with familial steroid-resistant nephrotic syndrome.
Ozer EA; Aksu N; Erdogan H; Yavascan O; Kara O; Gribouval O; Gubler MC; Antignac C
Nephrology (Carlton); 2004 Oct; 9(5):310-2. PubMed ID: 15504144
[TBL] [Abstract][Full Text] [Related]
17. Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome.
Santín S; Bullich G; Tazón-Vega B; García-Maset R; Giménez I; Silva I; Ruíz P; Ballarín J; Torra R; Ars E
Clin J Am Soc Nephrol; 2011 May; 6(5):1139-48. PubMed ID: 21415313
[TBL] [Abstract][Full Text] [Related]
18. Nephrotic plasma alters slit diaphragm-dependent signaling and translocates nephrin, Podocin, and CD2 associated protein in cultured human podocytes.
Coward RJ; Foster RR; Patton D; Ni L; Lennon R; Bates DO; Harper SJ; Mathieson PW; Saleem MA
J Am Soc Nephrol; 2005 Mar; 16(3):629-37. PubMed ID: 15659563
[TBL] [Abstract][Full Text] [Related]
19. Analysis of recessive CD2AP and ACTN4 mutations in steroid-resistant nephrotic syndrome.
Benoit G; Machuca E; Nevo F; Gribouval O; Lepage D; Antignac C
Pediatr Nephrol; 2010 Mar; 25(3):445-51. PubMed ID: 19956976
[TBL] [Abstract][Full Text] [Related]
20. The relationship among nephrin, podocin, CD2AP, and alpha-actinin might not be a true 'interaction' in podocyte.
Fan Q; Xing Y; Ding J; Guan N; Zhang J
Kidney Int; 2006 Apr; 69(7):1207-15. PubMed ID: 16501493
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
