BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

306 related articles for article (PubMed ID: 16481888)

  • 1. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review.
    Franceschini N; North KE; Kopp JB; McKenzie L; Winkler C
    Genet Med; 2006 Feb; 8(2):63-75. PubMed ID: 16481888
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling.
    Rood IM; Deegens JKJ; Lugtenberg D; Bongers EMHF; Wetzels JFM
    Am J Kidney Dis; 2019 Mar; 73(3):400-403. PubMed ID: 30241959
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.
    Koziell A; Grech V; Hussain S; Lee G; Lenkkeri U; Tryggvason K; Scambler P
    Hum Mol Genet; 2002 Feb; 11(4):379-88. PubMed ID: 11854170
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The mutation-dependent pathogenicity of NPHS2 p.R229Q: A guide for clinical assessment.
    Mikó Á; K Menyhárd D; Kaposi A; Antignac C; Tory K
    Hum Mutat; 2018 Dec; 39(12):1854-1860. PubMed ID: 30260545
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Broadening the spectrum of diseases related to podocin mutations.
    Caridi G; Bertelli R; Di Duca M; Dagnino M; Emma F; Onetti Muda A; Scolari F; Miglietti N; Mazzucco G; Murer L; Carrea A; Massella L; Rizzoni G; Perfumo F; Ghiggeri GM
    J Am Soc Nephrol; 2003 May; 14(5):1278-86. PubMed ID: 12707396
    [TBL] [Abstract][Full Text] [Related]  

  • 10. WT-1 and NPHS2 mutation analysis in patients with non-familial steroid-resistant focal-segmental glomerulosclerosis.
    Löwik MM; Levtchenko EN; Monnens LA; van den Heuvel LP
    Clin Nephrol; 2003 Feb; 59(2):143-6. PubMed ID: 12608558
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. The podocin V260E mutation predicts steroid resistant nephrotic syndrome in black South African children with focal segmental glomerulosclerosis.
    Govender MA; Fabian J; Gottlich E; Levy C; Moonsamy G; Maher H; Winkler CA; Ramsay M
    Commun Biol; 2019; 2():416. PubMed ID: 31754646
    [TBL] [Abstract][Full Text] [Related]  

  • 14. NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children.
    Maruyama K; Iijima K; Ikeda M; Kitamura A; Tsukaguchi H; Yoshiya K; Hoshii S; Wada N; Uemura O; Satomura K; Honda M; Yoshikawa N
    Pediatr Nephrol; 2003 May; 18(5):412-6. PubMed ID: 12687458
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Late onset of familial nephrotic syndrome associated with a compound heterozygous mutation of the podocin-encoding gene.
    Ardiles LG; Carrasco AE; Carpio JD; Mezzano SA
    Nephrology (Carlton); 2005 Dec; 10(6):553-6. PubMed ID: 16354237
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome.
    Oleggini R; Bertelli R; Di Donato A; Di Duca M; Caridi G; Sanna-Cherchi S; Scolari F; Murer L; Allegri L; Coppo R; Emma F; Camussi G; Perfumo F; Ghiggeri GM
    Gene Expr; 2006; 13(1):59-66. PubMed ID: 16572591
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Mutations in NPHS2 in familial steroid-resistant nephrotic syndrome in Southern Chinese Han ethnic group].
    Fu R; Chen XM; Wang QH; Chen SP; Yu ZH; Ye LY; Ren RN; Huang J; Wang CF
    Zhonghua Er Ke Za Zhi; 2008 Aug; 46(8):591-6. PubMed ID: 19099831
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosis.
    Benetti E; Caridi G; Centi S; Vella MD; Ghiggeri GM; Artifoni L; Murer L
    Saudi J Kidney Dis Transpl; 2014 Jul; 25(4):854-7. PubMed ID: 24969201
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.