BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 18823551)

  • 1. NPHS2 variation in focal and segmental glomerulosclerosis.
    Tonna SJ; Needham A; Polu K; Uscinski A; Appel GB; Falk RJ; Katz A; Al-Waheeb S; Kaplan BS; Jerums G; Savige J; Harmon J; Zhang K; Curhan GC; Pollak MR
    BMC Nephrol; 2008 Sep; 9():13. PubMed ID: 18823551
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prevalence of the
    de Almeida R; da Silva WC; Garbin HI; Itaquy TP; Dos Santos Pereira F; Garcia CD; Keitel E; Sales Luiz Vianna F; Veronese FV
    Clin Nephrol; 2020 Oct; 94(4):187-196. PubMed ID: 32691731
    [TBL] [Abstract][Full Text] [Related]  

  • 3. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele.
    Tsukaguchi H; Sudhakar A; Le TC; Nguyen T; Yao J; Schwimmer JA; Schachter AD; Poch E; Abreu PF; Appel GB; Pereira AB; Kalluri R; Pollak MR
    J Clin Invest; 2002 Dec; 110(11):1659-66. PubMed ID: 12464671
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recessive NPHS2 (Podocin) mutations are rare in adult-onset idiopathic focal segmental glomerulosclerosis.
    He N; Zahirieh A; Mei Y; Lee B; Senthilnathan S; Wong B; Mucha B; Hildebrandt F; Cole DE; Cattran D; Pei Y
    Clin J Am Soc Nephrol; 2007 Jan; 2(1):31-7. PubMed ID: 17699384
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome.
    Santín S; Tazón-Vega B; Silva I; Cobo MÁ; Giménez I; Ruíz P; García-Maset R; Ballarín J; Torra R; Ars E;
    Clin J Am Soc Nephrol; 2011 Feb; 6(2):344-54. PubMed ID: 20947785
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.
    Laurin LP; Lu M; Mottl AK; Blyth ER; Poulton CJ; Weck KE
    Nephrol Dial Transplant; 2014 Nov; 29(11):2062-9. PubMed ID: 24500309
    [TBL] [Abstract][Full Text] [Related]  

  • 7. NPHS2 homozygous p.R229Q variant: potential modifier instead of causal effect in focal segmental glomerulosclerosis.
    Kerti A; Csohány R; Wagner L; Jávorszky E; Maka E; Tory K
    Pediatr Nephrol; 2013 Oct; 28(10):2061-4. PubMed ID: 23800802
    [TBL] [Abstract][Full Text] [Related]  

  • 8. R229Q polymorphism of NPHS2 gene in patients with late-onset steroid-resistance nephrotic syndrome: a preliminary study.
    Fotouhi N; Ardalan M; Jabbarpour Bonyadi M; Abdolmohammadi R; Kamalifar A; Nasri H; Einollahi B
    Iran J Kidney Dis; 2013 Sep; 7(5):399-403. PubMed ID: 24072153
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The p.R229Q variant of the NPHS2 (podocin) gene in focal segmental glomerulosclerosis and steroid-resistant nephrotic syndrome: a meta-analysis.
    Lu L; Wan H; Yin Y; Feng WJ; Wang M; Zou YC; Huang B; Wang DT; Shi Y; Zhao Y; Wei LB
    Int Urol Nephrol; 2014 Jul; 46(7):1383-93. PubMed ID: 24715228
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin.
    Bertelli R; Ginevri F; Caridi G; Dagnino M; Sandrini S; Di Duca M; Emma F; Sanna-Cherchi S; Scolari F; Neri TM; Murer L; Massella L; Basile G; Rizzoni G; Perfumo F; Ghiggeri GM
    Am J Kidney Dis; 2003 Jun; 41(6):1314-21. PubMed ID: 12776285
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular analysis of NPHS2 and ACTN4 genes in a series of 33 Italian patients affected by adult-onset nonfamilial focal segmental glomerulosclerosis.
    Aucella F; De Bonis P; Gatta G; Muscarella LA; Vigilante M; di Giorgio G; D'Errico M; Zelante L; Stallone C; Bisceglia L
    Nephron Clin Pract; 2005; 99(2):c31-6. PubMed ID: 15627790
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Clinical features and mutational survey of NPHS2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation.
    Furue T; Hattori M; Tsukaguchi H; Kitamura A; Oomori T; Ogino D; Nakakura H; Ashida A; Miura K; Hisano M; Takahashi K; Chikamoto H; Akioka Y; Sakano T
    Pediatr Transplant; 2008 May; 12(3):341-6. PubMed ID: 18208440
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant.
    Machuca E; Hummel A; Nevo F; Dantal J; Martinez F; Al-Sabban E; Baudouin V; Abel L; Grünfeld JP; Antignac C
    Kidney Int; 2009 Apr; 75(7):727-35. PubMed ID: 19145239
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome.
    Reiterová J; Safránková H; Obeidová L; Stěkrová J; Maixnerová D; Merta M; Tesař V
    Folia Biol (Praha); 2012; 58(2):64-8. PubMed ID: 22578956
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The R229Q mutation in NPHS2 may predispose to proteinuria in thin-basement-membrane nephropathy.
    Tonna S; Wang YY; Wilson D; Rigby L; Tabone T; Cotton R; Savige J
    Pediatr Nephrol; 2008 Dec; 23(12):2201-7. PubMed ID: 18726620
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.
    Bińczak-Kuleta A; Rubik J; Litwin M; Ryder M; Lewandowska K; Taryma-Leśniak O; Clark JS; Grenda R; Ciechanowicz A
    Bosn J Basic Med Sci; 2014 May; 14(2):89-93. PubMed ID: 24856380
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Recurrence of proteinuria 10 years post-transplant in NPHS2-associated focal segmental glomerulosclerosis after conversion from cyclosporin A to sirolimus.
    Höcker B; Knüppel T; Waldherr R; Schaefer F; Weber S; Tönshoff B
    Pediatr Nephrol; 2006 Oct; 21(10):1476-9. PubMed ID: 16721582
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NPHS2 variation in sporadic focal segmental glomerulosclerosis.
    McKenzie LM; Hendrickson SL; Briggs WA; Dart RA; Korbet SM; Mokrzycki MH; Kimmel PL; Ahuja TS; Berns JS; Simon EE; Smith MC; Trachtman H; Michel DM; Schelling JR; Cho M; Zhou YC; Binns-Roemer E; Kirk GD; Kopp JB; Winkler CA
    J Am Soc Nephrol; 2007 Nov; 18(11):2987-95. PubMed ID: 17942957
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Co-Inheritance of Functional Podocin Variants with Heterozygous Collagen IV Mutations Predisposes to Renal Failure.
    Stefanou C; Pieri M; Savva I; Georgiou G; Pierides A; Voskarides K; Deltas C
    Nephron; 2015; 130(3):200-12. PubMed ID: 26138234
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.