These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 14764915)

  • 21. 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]  

  • 22. Nck adaptor proteins link nephrin to the actin cytoskeleton of kidney podocytes.
    Jones N; Blasutig IM; Eremina V; Ruston JM; Bladt F; Li H; Huang H; Larose L; Li SS; Takano T; Quaggin SE; Pawson T
    Nature; 2006 Apr; 440(7085):818-23. PubMed ID: 16525419
    [TBL] [Abstract][Full Text] [Related]  

  • 23. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
    Guaragna MS; Cleto TL; Souza ML; Lutaif AC; de Castro LC; Penido MG; Maciel-Guerra AT; Belangero VM; Guerra-Junior G; De Mello MP
    Nephrology (Carlton); 2016 Sep; 21(9):753-7. PubMed ID: 26560236
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Congenital nephrotic syndrome].
    Hattori M
    Nihon Rinsho; 2004 Oct; 62(10):1861-6. PubMed ID: 15500131
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Structure and function of the glomerular filtration barrier].
    Musiał K; Zwolińska D
    Pol Merkur Lekarski; 2005 Mar; 18(105):317-20. PubMed ID: 15997642
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Nephrin-signature molecule of the glomerular podocyte?
    Welsh GI; Saleem MA
    J Pathol; 2010 Feb; 220(3):328-37. PubMed ID: 19950250
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community.
    Frishberg Y; Ben-Neriah Z; Suvanto M; Rinat C; Männikkö M; Feinstein S; Becker-Cohen R; Jalanko H; Zlotogora J; Kestilä M
    Genet Med; 2007 Mar; 9(3):180-4. PubMed ID: 17413422
    [TBL] [Abstract][Full Text] [Related]  

  • 28. WT1 activates a glomerular-specific enhancer identified from the human nephrin gene.
    Guo G; Morrison DJ; Licht JD; Quaggin SE
    J Am Soc Nephrol; 2004 Nov; 15(11):2851-6. PubMed ID: 15504938
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Nephrin is expressed in the pancreatic beta cells.
    Palmén T; Ahola H; Palgi J; Aaltonen P; Luimula P; Wang S; Jaakkola I; Knip M; Otonkoski T; Holthöfer H
    Diabetologia; 2001 Oct; 44(10):1274-80. PubMed ID: 11692176
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.
    Heeringa SF; Vlangos CN; Chernin G; Hinkes B; Gbadegesin R; Liu J; Hoskins BE; Ozaltin F; Hildebrandt F;
    Nephrol Dial Transplant; 2008 Nov; 23(11):3527-33. PubMed ID: 18503012
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Role of nephrin in cell junction formation in human nephrogenesis.
    Ruotsalainen V; Patrakka J; Tissari P; Reponen P; Hess M; Kestilä M; Holmberg C; Salonen R; Heikinheimo M; Wartiovaara J; Tryggvason K; Jalanko H
    Am J Pathol; 2000 Dec; 157(6):1905-16. PubMed ID: 11106563
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Nephrotic plasma alters slit diaphragm-dependent signaling and translocates nephrin, Podocin, and CD2 associated protein in cultured human podocytes.
    Coward RJ; Foster RR; Patton D; Ni L; Lennon R; Bates DO; Harper SJ; Mathieson PW; Saleem MA
    J Am Soc Nephrol; 2005 Mar; 16(3):629-37. PubMed ID: 15659563
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome.
    Kestilä M; Lenkkeri U; Männikkö M; Lamerdin J; McCready P; Putaala H; Ruotsalainen V; Morita T; Nissinen M; Herva R; Kashtan CE; Peltonen L; Holmberg C; Olsen A; Tryggvason K
    Mol Cell; 1998 Mar; 1(4):575-82. PubMed ID: 9660941
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Alternatively spliced nephrin in experimental glomerular disease of the rat.
    Luimula P; Aaltonen P; Ahola H; Palmen T; Holthöfer H
    Pediatr Res; 2000 Dec; 48(6):759-62. PubMed ID: 11102543
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Nephrin--a unique structural and signaling protein of the kidney filter.
    Patrakka J; Tryggvason K
    Trends Mol Med; 2007 Sep; 13(9):396-403. PubMed ID: 17766183
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Nephrin mRNA regulation by protein kinase C.
    Wang SX; Menè P; Holthöfer H
    J Nephrol; 2001; 14(2):98-103. PubMed ID: 11411021
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The podocyte protein nephrin is required for cardiac vessel formation.
    Wagner N; Morrison H; Pagnotta S; Michiels JF; Schwab Y; Tryggvason K; Schedl A; Wagner KD
    Hum Mol Genet; 2011 Jun; 20(11):2182-94. PubMed ID: 21402589
    [TBL] [Abstract][Full Text] [Related]  

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

  • 39. Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.
    Lenkkeri U; Männikkö M; McCready P; Lamerdin J; Gribouval O; Niaudet PM; Antignac C K; Kashtan CE; Homberg C; Olsen A; Kestilä M; Tryggvason K
    Am J Hum Genet; 1999 Jan; 64(1):51-61. PubMed ID: 9915943
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Nephrin in experimental glomerular disease.
    Luimula P; Ahola H; Wang SX; Solin ML; Aaltonen P; Tikkanen I; Kerjaschki D; Holthöfer H
    Kidney Int; 2000 Oct; 58(4):1461-8. PubMed ID: 11012881
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.