BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

504 related articles for article (PubMed ID: 11854170)

  • 1. 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]  

  • 2. No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations.
    Schultheiss M; Ruf RG; Mucha BE; Wiggins R; Fuchshuber A; Lichtenberger A; Hildebrandt F
    Pediatr Nephrol; 2004 Dec; 19(12):1340-8. PubMed ID: 15338398
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.
    Machuca E; Benoit G; Nevo F; Tête MJ; Gribouval O; Pawtowski A; Brandström P; Loirat C; Niaudet P; Gubler MC; Antignac C
    J Am Soc Nephrol; 2010 Jul; 21(7):1209-17. PubMed ID: 20507940
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
    Abid A; Khaliq S; Shahid S; Lanewala A; Mubarak M; Hashmi S; Kazi J; Masood T; Hafeez F; Naqvi SA; Rizvi SA; Mehdi SQ
    Gene; 2012 Jul; 502(2):133-7. PubMed ID: 22565185
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect.
    Thomas MM; Ahmed HM; El-Dessouky SH; Ramadan A; Botrous OE; Abdel-Hamid MS
    Mol Genet Genomics; 2022 May; 297(3):689-698. PubMed ID: 35278126
    [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 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. 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]  

  • 14. 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]  

  • 15. The Role of p.Ser1105Ser (in
    Thi Kim Lien N; Van Dem P; Thu Huong N; Minh Dien T; Thi Thu Thuy T; Van Tung N; Huy Hoang N; Thi Quynh Huong N
    Medicina (Kaunas); 2019 Apr; 55(4):. PubMed ID: 31013750
    [No Abstract]   [Full Text] [Related]  

  • 16. Genetic forms of nephrotic syndrome.
    Niaudet P
    Pediatr Nephrol; 2004 Dec; 19(12):1313-8. PubMed ID: 15503167
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.
    Berdeli A; Mir S; Yavascan O; Serdaroglu E; Bak M; Aksu N; Oner A; Anarat A; Donmez O; Yildiz N; Sever L; Tabel Y; Dusunsel R; Sonmez F; Cakar N
    Pediatr Nephrol; 2007 Dec; 22(12):2031-40. PubMed ID: 17899208
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 26.