BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

228 related articles for article (PubMed ID: 24072153)

  • 1. 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]  

  • 2. NPHS2 R229Q polymorphism in steroid resistant nephrotic syndrome: is it responsive to immunosuppressive therapy?
    Mishra OP; Kakani N; Singh AK; Narayan G; Abhinay A; Prasad R; Batra VV
    J Trop Pediatr; 2014 Jun; 60(3):231-7. PubMed ID: 24519673
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. NPHS2 gene in steroid-resistant nephrotic syndrome: prevalence, clinical course, and mutational spectrum in South-West Iranian children.
    Basiratnia M; Yavarian M; Torabinezhad S; Erjaee A
    Iran J Kidney Dis; 2013 Sep; 7(5):357-62. PubMed ID: 24072147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. 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]  

  • 9. 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]  

  • 10. [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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. NPHS2 variation in Chinese southern infants with late steroid-resistant nephrotic syndrome.
    Dai Y; Yang H; Gao P; Liu WD
    Ren Fail; 2014 Oct; 36(9):1395-8. PubMed ID: 25112471
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 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. 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]  

  • 20. Association Between
    Zhou Q; Weng Q; Zhang X; Liu Y; Tong J; Hao X; Shi H; Shen P; Ren H; Xie J; Chen N
    Front Med (Lausanne); 2022; 9():937122. PubMed ID: 35935761
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.