BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

377 related articles for article (PubMed ID: 12704574)

  • 21. Focal segmental glomerulosclerosis: recent advances.
    Pollak MR
    Curr Opin Nephrol Hypertens; 2008 Mar; 17(2):138-42. PubMed ID: 18277145
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Animal models of FSGS: lessons for pathogenesis and treatment.
    Fogo AB
    Semin Nephrol; 2003 Mar; 23(2):161-71. PubMed ID: 12704576
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis.
    Komatsuda A; Wakui H; Maki N; Kigawa A; Goto H; Ohtani H; Hamai K; Oyama Y; Makoto H; Sawada K; Imai H
    Ren Fail; 2003 Jan; 25(1):87-93. PubMed ID: 12617336
    [TBL] [Abstract][Full Text] [Related]  

  • 24. TRPC6 and FSGS: the latest TRP channelopathy.
    Mukerji N; Damodaran TV; Winn MP
    Biochim Biophys Acta; 2007 Aug; 1772(8):859-68. PubMed ID: 17459670
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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; 12(24):3397-405. PubMed ID: 14570703
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Steroid-resistant idiopathic childhood nephrosis: overdiagnosed and undertreated.
    Ehrich JH; Geerlings C; Zivicnjak M; Franke D; Geerlings H; Gellermann J
    Nephrol Dial Transplant; 2007 Aug; 22(8):2183-93. PubMed ID: 17504846
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
    Trautmann A; Bodria M; Ozaltin F; Gheisari A; Melk A; Azocar M; Anarat A; Caliskan S; Emma F; Gellermann J; Oh J; Baskin E; Ksiazek J; Remuzzi G; Erdogan O; Akman S; Dusek J; Davitaia T; Özkaya O; Papachristou F; Firszt-Adamczyk A; Urasinski T; Testa S; Krmar RT; Hyla-Klekot L; Pasini A; Özcakar ZB; Sallay P; Cakar N; Galanti M; Terzic J; Aoun B; Caldas Afonso A; Szymanik-Grzelak H; Lipska BS; Schnaidt S; Schaefer F;
    Clin J Am Soc Nephrol; 2015 Apr; 10(4):592-600. PubMed ID: 25635037
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical features and mutational survey of NPHS2 (podocin) in Japanese children with focal segmental glomerulosclerosis who underwent renal transplantation.
    Furue T; Hattori M; Tsukaguchi H; Kitamura A; Oomori T; Ogino D; Nakakura H; Ashida A; Miura K; Hisano M; Takahashi K; Chikamoto H; Akioka Y; Sakano T
    Pediatr Transplant; 2008 May; 12(3):341-6. PubMed ID: 18208440
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Urinary cytokines and steroid responsiveness in idiopathic nephrotic syndrome of childhood.
    Woroniecki RP; Shatat IF; Supe K; Du Z; Kaskel FJ
    Am J Nephrol; 2008; 28(1):83-90. PubMed ID: 17914249
    [TBL] [Abstract][Full Text] [Related]  

  • 30. CD80, suPAR and nephrotic syndrome in a case of NPHS2 mutation.
    Cara-Fuentes G; Araya C; Wei C; Rivard C; Ishimoto T; Reiser J; Johnson RJ; Garin EH
    Nefrologia; 2013; 33(5):727-31. PubMed ID: 24089165
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.
    Caridi G; Bertelli R; Carrea A; Di Duca M; Catarsi P; Artero M; Carraro M; Zennaro C; Candiano G; Musante L; Seri M; Ginevri F; Perfumo F; Ghiggeri GM
    J Am Soc Nephrol; 2001 Dec; 12(12):2742-2746. PubMed ID: 11729243
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [New findings on the pathogenesis of nephrotic syndrome (review article)].
    Tesar V; Zima T; Kalousová M
    Sb Lek; 2002; 103(3):379-95. PubMed ID: 12688182
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Podocyte proteins in Galloway-Mowat syndrome.
    Srivastava T; Whiting JM; Garola RE; Dasouki MJ; Ruotsalainen V; Tryggvason K; Hamed R; Alon US
    Pediatr Nephrol; 2001 Dec; 16(12):1022-9. PubMed ID: 11793093
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism.
    Choi HJ; Lee BH; Cho HY; Moon KC; Ha IS; Nagata M; Choi Y; Cheong HI
    Am J Kidney Dis; 2008 May; 51(5):834-8. PubMed ID: 18436095
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Direct effect of plasma permeability factors from patients with idiopatic FSGS on nephrin and podocin expression in human podocytes.
    Doublier S; Musante L; Lupia E; Candiano G; Spatola T; Caridi G; Zennaro C; Carraro M; Ghiggeri GM; Camussi G
    Int J Mol Med; 2005 Jul; 16(1):49-58. PubMed ID: 15942677
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Functional analysis of promoter mutations in the ACTN4 and SYNPO genes in focal segmental glomerulosclerosis.
    Dai S; Wang Z; Pan X; Wang W; Chen X; Ren H; Hao C; Han B; Chen N
    Nephrol Dial Transplant; 2010 Mar; 25(3):824-35. PubMed ID: 19666657
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 19.