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Journal Abstract Search

109 related items for PubMed ID: 8007602

  • 1. Exclusion of eight genes as mutated loci in congenital nephrotic syndrome of the Finnish type.
    Kestilä M, Männikkö M, Holmberg C, Korpela K, Savolainen ER, Peltonen L, Tryggvason K.
    Kidney Int; 1994 Apr; 45(4):986-90. PubMed ID: 8007602
    [Abstract] [Full Text] [Related]

  • 2. Noncollagenous matrix components of glomeruli in congenital nephrotic syndrome of the Finnish type: evidence of abnormal splitting of nidogen?
    Ljungberg P, Haltia A, Kuusela P, Jalanko H, Holmberg C, Holthöfer H.
    Exp Nephrol; 1996 Apr; 4(5):286-94. PubMed ID: 8931984
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  • 3. Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.
    Kestilä M, Männikkö M, Holmberg C, Gyapay G, Weissenbach J, Savolainen ER, Peltonen L, Tryggvason K.
    Am J Hum Genet; 1994 May; 54(5):757-64. PubMed ID: 8178817
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  • 4. Congenital nephrotic syndrome of the Finnish type is not associated with the Pax-2 gene despite the promising transgenic animal model.
    Kestilä M, Männikkö M, Holmberg C, Tryggvason K, Peltonen L.
    Genomics; 1994 Feb; 19(3):570-2. PubMed ID: 8188301
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  • 8. Interactions of basement membrane components.
    Woodley DT, Rao CN, Hassell JR, Liotta LA, Martin GR, Kleinman HK.
    Biochim Biophys Acta; 1983 Dec 27; 761(3):278-83. PubMed ID: 6228259
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  • 9. Effects of methylprednisolone on glomerular and medullary mRNA levels for extracellular matrices in puromycin aminonucleoside nephrosis.
    Nakamura T, Ebihara I, Fukui M, Tomino Y, Koide H.
    Kidney Int; 1991 Nov 27; 40(5):874-81. PubMed ID: 1762292
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  • 10. Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysis.
    Männikkö M, Kestilä M, Lenkkeri U, Alakurtti H, Holmberg C, Leisti J, Salonen R, Aula P, Mustonen A, Peltonen L, Tryggvason K.
    Kidney Int; 1997 Mar 27; 51(3):868-72. PubMed ID: 9067923
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  • 11. Localization of binding sites for laminin, heparan sulfate proteoglycan and fibronectin on basement membrane (type IV) collagen.
    Laurie GW, Bing JT, Kleinman HK, Hassell JR, Aumailley M, Martin GR, Feldmann RJ.
    J Mol Biol; 1986 May 05; 189(1):205-16. PubMed ID: 2946868
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  • 12. Extracellular matrix component mRNA expression in glomeruli in experimental focal glomerulosclerosis.
    Ebihara I, Suzuki S, Nakamura T, Fukui M, Yaguchi Y, Tomino Y, Koide H.
    J Am Soc Nephrol; 1993 Jan 05; 3(7):1387-97. PubMed ID: 8439650
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  • 13. [Changes in the expression of basement membrane and type I collagen gene in focal glomerular sclerosis (FGS)].
    Nakamura T.
    Nihon Jinzo Gakkai Shi; 1990 Nov 05; 32(11):1253-61. PubMed ID: 2082058
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  • 14. Formation of a supramolecular complex is involved in the reconstitution of basement membrane components.
    Kleinman HK, McGarvey ML, Hassell JR, Martin GR.
    Biochemistry; 1983 Oct 11; 22(21):4969-74. PubMed ID: 6227336
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  • 15. The incubation of laminin, collagen IV, and heparan sulfate proteoglycan at 35 degrees C yields basement membrane-like structures.
    Grant DS, Leblond CP, Kleinman HK, Inoue S, Hassell JR.
    J Cell Biol; 1989 Apr 11; 108(4):1567-74. PubMed ID: 2522456
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  • 16. Pathobiochemical aspects of diabetic nephropathy.
    Schleicher E, Nerlich A, Gerbitz KD.
    Klin Wochenschr; 1988 Sep 15; 66(18):873-82. PubMed ID: 2972877
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  • 17. Heparan sulfate proteoglycan is present in basement membrane as a double-tracked structure.
    Inoue S, Grant D, Leblond CP.
    J Histochem Cytochem; 1989 May 15; 37(5):597-602. PubMed ID: 2522961
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  • 18. Alterations in proteoglycan metabolism in the nephrotic syndrome induced by the aminonucleoside of puromycin.
    Klein DJ, Dehnel PJ, Oegema TR, Brown DM.
    Lab Invest; 1984 May 15; 50(5):543-51. PubMed ID: 6232422
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  • 19. Localization of laminin, type IV collagen, fibronectin, and heparan sulfate proteoglycan in chick retinal pigment epithelium basement membrane during embryonic development.
    Turksen K, Aubin JE, Sodek J, Kalnins VI.
    J Histochem Cytochem; 1985 Jul 15; 33(7):665-71. PubMed ID: 3159787
    [Abstract] [Full Text] [Related]

  • 20. Haplotype analysis of congenital nephrotic syndrome of the Finnish type in non-Finnish families.
    Männikkö M, Lenkkeri U, Kashtan CE, Kestilä M, Holmberg C, Tryggvason K.
    J Am Soc Nephrol; 1996 Dec 15; 7(12):2700-3. PubMed ID: 8989752
    [Abstract] [Full Text] [Related]

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