BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 7780062)

  • 1. Autosomal recessive Alport syndrome: mutation in the COL4A3 gene in a woman with Alport syndrome and posttransplant antiglomerular basement membrane nephritis.
    Ding J; Stitzel J; Berry P; Hawkins E; Kashtan CE
    J Am Soc Nephrol; 1995 Mar; 5(9):1714-7. PubMed ID: 7780062
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A COL4A3 gene mutation and post-transplant anti-alpha 3(IV) collagen alloantibodies in Alport syndrome.
    Kalluri R; van den Heuvel LP; Smeets HJ; Schroder CH; Lemmink HH; Boutaud A; Neilson EG; Hudson BG
    Kidney Int; 1995 Apr; 47(4):1199-204. PubMed ID: 7783419
    [TBL] [Abstract][Full Text] [Related]  

  • 3. COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome.
    Buzza M; Wang YY; Dagher H; Babon JJ; Cotton RG; Powell H; Dowling J; Savige J
    Kidney Int; 2001 Aug; 60(2):480-3. PubMed ID: 11473630
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The pathogenesis of Alport syndrome involves type IV collagen molecules containing the alpha 3(IV) chain: evidence from anti-GBM nephritis after renal transplantation.
    Hudson BG; Kalluri R; Gunwar S; Weber M; Ballester F; Hudson JK; Noelken ME; Sarras M; Richardson WR; Saus J
    Kidney Int; 1992 Jul; 42(1):179-87. PubMed ID: 1635348
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes.
    Kashtan CE
    Medicine (Baltimore); 1999 Sep; 78(5):338-60. PubMed ID: 10499074
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.
    Imafuku A; Nozu K; Sawa N; Hasegawa E; Hiramatsu R; Kawada M; Hoshino J; Tanaka K; Ishii Y; Takaichi K; Fujii T; Ohashi K; Iijima K; Ubara Y
    Nephrology (Carlton); 2018 Oct; 23(10):940-947. PubMed ID: 28704582
    [TBL] [Abstract][Full Text] [Related]  

  • 7. COL4A5 deletions in three patients with Alport syndrome and posttransplant antiglomerular basement membrane nephritis.
    Ding J; Zhou J; Tryggvason K; Kashtan CE
    J Am Soc Nephrol; 1994 Aug; 5(2):161-8. PubMed ID: 7993995
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Alport syndrome or progressive hereditary nephritis with hearing loss].
    Gubler MC; Heidet L; Antignac C
    Nephrol Ther; 2007 Jun; 3(3):113-20. PubMed ID: 17540313
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal dominant Alport syndrome linked to the type IV collage alpha 3 and alpha 4 genes (COL4A3 and COL4A4).
    Jefferson JA; Lemmink HH; Hughes AE; Hill CM; Smeets HJ; Doherty CC; Maxwell AP
    Nephrol Dial Transplant; 1997 Aug; 12(8):1595-9. PubMed ID: 9269635
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation in alpha 5(IV) collagen chain gene in nonfamilial hematuria.
    Kitagawa K; Nakanishi K; Iijima K; Nishio H; Sado Y; Sano K; Nakamura H; Yoshikawa N
    J Am Soc Nephrol; 1995 Aug; 6(2):264-8. PubMed ID: 7579094
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Targets of alloantibodies in Alport anti-glomerular basement membrane disease after renal transplantation.
    Brainwood D; Kashtan C; Gubler MC; Turner AN
    Kidney Int; 1998 Mar; 53(3):762-6. PubMed ID: 9507224
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Successful renal transplantation in a family with a novel mutation in COL4A3 gene and autosomal recessive Alport syndrome.
    Girimaji N; Murugan Sm S; Nada R; Sharma A; Rathi M; Kohli HS; Gupta KL; Ramachandran R
    Nephrology (Carlton); 2020 Jun; 25(6):497-501. PubMed ID: 31925849
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Distribution of familial nephritis antigen in normal tissue and renal basement membranes of patients with homozygous and heterozygous Alport familial nephritis. Relationship of familial nephritis and Goodpasture antigens to novel collagen chains and type IV collagen.
    Kleppel MM; Kashtan C; Santi PA; Wieslander J; Michael AF
    Lab Invest; 1989 Sep; 61(3):278-89. PubMed ID: 2671490
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel mutation of COL4A3 presents a different contribution to Alport syndrome and thin basement membrane nephropathy.
    Hou P; Chen Y; Ding J; Li G; Zhang H
    Am J Nephrol; 2007; 27(5):538-44. PubMed ID: 17726307
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome.
    Heidet L; Arrondel C; Forestier L; Cohen-Solal L; Mollet G; Gutierrez B; Stavrou C; Gubler MC; Antignac C
    J Am Soc Nephrol; 2001 Jan; 12(1):97-106. PubMed ID: 11134255
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Loss of alpha3/alpha4(IV) collagen from the glomerular basement membrane induces a strain-dependent isoform switch to alpha5alpha6(IV) collagen associated with longer renal survival in Col4a3-/- Alport mice.
    Kang JS; Wang XP; Miner JH; Morello R; Sado Y; Abrahamson DR; Borza DB
    J Am Soc Nephrol; 2006 Jul; 17(7):1962-9. PubMed ID: 16769745
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Thin basement membrane nephropathy.
    Savige J; Rana K; Tonna S; Buzza M; Dagher H; Wang YY
    Kidney Int; 2003 Oct; 64(4):1169-78. PubMed ID: 12969134
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Autosomal Recessive Alport Syndrome Unveiled by Pregnancy.
    Drury ER; Stillman IE; Pollak MR; Denker BM
    Nephron; 2019; 143(4):288-292. PubMed ID: 31408864
    [TBL] [Abstract][Full Text] [Related]  

  • 20. COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome.
    Longo I; Porcedda P; Mari F; Giachino D; Meloni I; Deplano C; Brusco A; Bosio M; Massella L; Lavoratti G; Roccatello D; Frascá G; Mazzucco G; Muda AO; Conti M; Fasciolo F; Arrondel C; Heidet L; Renieri A; De Marchi M
    Kidney Int; 2002 Jun; 61(6):1947-56. PubMed ID: 12028435
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.