BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

258 related articles for article (PubMed ID: 30241959)

  • 1. 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]  

  • 2. 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]  

  • 3. [NPHS2 Mutation analysis study in children with steroid-resistant nephrotic syndrome].
    Azocar M; Vega Á; Farfán M; Cano F
    Rev Chil Pediatr; 2016; 87(1):31-6. PubMed ID: 26455708
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
    Dhandapani MC; Venkatesan V; Rengaswamy NB; Gowrishankar K; Ekambaram S; Sengutavan P; Perumal V
    Clin Exp Nephrol; 2017 Feb; 21(1):127-133. PubMed ID: 26820844
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa.
    Nandlal L; Winkler CA; Bhimma R; Cho S; Nelson GW; Haripershad S; Naicker T
    Eur J Pediatr; 2022 Oct; 181(10):3595-3606. PubMed ID: 35920919
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
    Weber S; Gribouval O; Esquivel EL; Morinière V; Tête MJ; Legendre C; Niaudet P; Antignac C
    Kidney Int; 2004 Aug; 66(2):571-9. PubMed ID: 15253708
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome.
    Megremis S; Mitsioni A; Mitsioni AG; Fylaktou I; Kitsiou-Tzelli S; Stefanidis CJ; Kanavakis E; Traeger-Synodinos J
    Genet Test Mol Biomarkers; 2009 Apr; 13(2):249-56. PubMed ID: 19371226
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. WT1 and NPHS2 gene mutation analysis and clinical management of steroid-resistant nephrotic syndrome.
    Ramanathan AS; Vijayan M; Rajagopal S; Rajendiran P; Senguttuvan P
    Mol Cell Biochem; 2017 Feb; 426(1-2):177-181. PubMed ID: 27885584
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome.
    Chernin G; Heeringa SF; Gbadegesin R; Liu J; Hinkes BG; Vlangos CN; Vega-Warner V; Hildebrandt F
    Pediatr Nephrol; 2008 Sep; 23(9):1455-60. PubMed ID: 18543005
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 13.