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Journal Abstract Search

807 related items for PubMed ID: 10742096

  • 1. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.
    Boute N, Gribouval O, Roselli S, Benessy F, Lee H, Fuchshuber A, Dahan K, Gubler MC, Niaudet P, Antignac C.
    Nat Genet; 2000 Apr; 24(4):349-54. PubMed ID: 10742096
    [Abstract] [Full Text] [Related]

  • 2. [Characterization of the NPH2 gene, coding for the glomerular protein podocin, implicated in a familial form of cortico-resistant nephrotic syndrome transmitted as an autosomal recessive].
    Boute N, Roselli S, Gribouval O, Niaudet P, Gubler MC, Antignac C.
    Nephrologie; 2002 Apr; 23(1):35-6. PubMed ID: 11908478
    [No Abstract] [Full Text] [Related]

  • 3. Molecular basis of steroid-resistant nephrotic syndrome.
    Antignac C.
    Nefrologia; 2005 Apr; 25 Suppl 2():25-8. PubMed ID: 16050398
    [Abstract] [Full Text] [Related]

  • 4. [A novel mutation of NPHS2 identified in a Chinese family with steroid-resistant nephrotic syndrome].
    Yu ZH, Ding J, Guan N, Shi Y, Zhang JJ, Huang JP, Yao Y, Yang JY.
    Zhonghua Er Ke Za Zhi; 2004 Feb; 42(2):108-12. PubMed ID: 15059485
    [Abstract] [Full Text] [Related]

  • 5. Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains.
    Huber TB, Simons M, Hartleben B, Sernetz L, Schmidts M, Gundlach E, Saleem MA, Walz G, Benzing T.
    Hum Mol Genet; 2003 Dec 15; 12(24):3397-405. PubMed ID: 14570703
    [Abstract] [Full Text] [Related]

  • 6. [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 Dec 15; 63 Suppl 3():85-6. PubMed ID: 16898497
    [Abstract] [Full Text] [Related]

  • 7. Genetic basis of nephrotic syndrome--review.
    Obeidová H, Merta M, Reiterová J, Maixnerová D, Stekrová J, Rysavá R, Tesar V.
    Prague Med Rep; 2006 Dec 15; 107(1):5-16. PubMed ID: 16752799
    [Abstract] [Full Text] [Related]

  • 8. Podocin localizes in the kidney to the slit diaphragm area.
    Roselli S, Gribouval O, Boute N, Sich M, Benessy F, Attié T, Gubler MC, Antignac C.
    Am J Pathol; 2002 Jan 15; 160(1):131-9. PubMed ID: 11786407
    [Abstract] [Full Text] [Related]

  • 9. NPHS2 mutations in children with steroid-resistant nephrotic syndrome.
    Otukesh H, Ghazanfari B, Fereshtehnejad SM, Bakhshayesh M, Hashemi M, Hoseini R, Chalian M, Salami A, Mehdipor L, Rahiminia A.
    Iran J Kidney Dis; 2009 Apr 15; 3(2):99-102. PubMed ID: 19395786
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 18(5):412-6. PubMed ID: 12687458
    [Abstract] [Full Text] [Related]

  • 11. [A genetic viewpoint of focal glomerular sclerosis: fom genes to glomerular pathophysiology [corrected]].
    Aucella F, Bisceglia L, Stallone C.
    G Ital Nefrol; 2003 May 15; 20(4):356-67. PubMed ID: 14523896
    [Abstract] [Full Text] [Related]

  • 12. The heart of children with steroid-resistant nephrotic syndrome: is it all podocin?
    Frishberg Y, Feinstein S, Rinat C, Becker-Cohen R, Lerer I, Raas-Rothschild A, Ferber B, Nir A.
    J Am Soc Nephrol; 2006 Jan 15; 17(1):227-31. PubMed ID: 16291839
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 23(10):3146-51. PubMed ID: 18443213
    [Abstract] [Full Text] [Related]

  • 14. 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 15; 10(6):553-6. PubMed ID: 16354237
    [Abstract] [Full Text] [Related]

  • 15. NPHS2 mutations in adult patients with primary focal segmental glomerulosclerosis.
    Monteiro EJ, Pereira AC, Pereira AB, Krieger JE, Mastroianni-Kirsztajn G.
    J Nephrol; 2006 Dec 15; 19(3):366-71. PubMed ID: 16874699
    [Abstract] [Full Text] [Related]

  • 16. Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome.
    Karle SM, Uetz B, Ronner V, Glaeser L, Hildebrandt F, Fuchshuber A.
    J Am Soc Nephrol; 2002 Feb 15; 13(2):388-393. PubMed ID: 11805166
    [Abstract] [Full Text] [Related]

  • 17. 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, Arbeitsgemeinschaft für Paediatrische Nephrologie Study Group.
    Pediatrics; 2007 Apr 15; 119(4):e907-19. PubMed ID: 17371932
    [Abstract] [Full Text] [Related]

  • 18. Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children.
    Yu Z, Ding J, Huang J, Yao Y, Xiao H, Zhang J, Liu J, Yang J.
    Nephrol Dial Transplant; 2005 May 15; 20(5):902-8. PubMed ID: 15769810
    [Abstract] [Full Text] [Related]

  • 19. NPHS2 mutation analysis and primary nephrotic syndrome in southern Indians.
    Jaffer A, Unnisa W, Raju DS, Jahan P.
    Nephrology (Carlton); 2014 Jul 15; 19(7):398-403. PubMed ID: 24674236
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 11(4):379-88. PubMed ID: 11854170
    [Abstract] [Full Text] [Related]

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