BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 10074584)

  • 1. Molecular genetic and immunohistochemical study of autosomal recessive Alport's syndrome.
    Nomura S; Naito I; Fukushima T; Tokura T; Kataoka N; Tanaka I; Tanaka H; Osawa G
    Am J Kidney Dis; 1998 Jun; 31(6):E4. PubMed ID: 10074584
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary abnormalities of renal basement membranes.
    Savige J
    Pathology; 1991 Oct; 23(4):350-5. PubMed ID: 1686082
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Renal pathology and ultrastructural findings in Alport's syndrome.
    Noël LH
    Ren Fail; 2000 Nov; 22(6):751-8. PubMed ID: 11104162
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution.
    Gubler MC; Knebelmann B; Beziau A; Broyer M; Pirson Y; Haddoum F; Kleppel MM; Antignac C
    Kidney Int; 1995 Apr; 47(4):1142-7. PubMed ID: 7783412
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Alport's syndrome: apropos of 2 families].
    Grünfeld JP
    Nephrologie; 2000; 21(6):295-8. PubMed ID: 11117109
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel model of autosomal dominant Alport syndrome in Dalmatian dogs.
    Hood JC; Huxtable C; Naito I; Smith C; Sinclair R; Savige J
    Nephrol Dial Transplant; 2002 Dec; 17(12):2094-8. PubMed ID: 12454218
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group.
    Frascà GM; Onetti-Muda A; Mari F; Longo I; Scala E; Pescucci C; Roccatello D; Alpa M; Coppo R; Li Volti G; Feriozzi S; Bergesio F; Schena FP; Renieri A;
    Nephrol Dial Transplant; 2005 Mar; 20(3):545-51. PubMed ID: 15618242
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Expression of alpha (IV) chains in Alport's syndrome and its correlation with ultrastructural and genetic data.
    Mazzucco G; Barsotti P; Onetti Muda A; Fortunato M; Faraggiana T; De Marchi M; Monga G
    Contrib Nephrol; 1997; 122():129-31. PubMed ID: 9399054
    [No Abstract]   [Full Text] [Related]  

  • 9. Autosomal dominant Alport's syndrome: study of a large Tunisian family.
    Kharrat M; Makni S; Makni K; Kammoun K; Charfeddine K; Azaeiz H; Jarraya F; Ben Hmida M; Gubler MC; Ayadi H; Hachicha J
    Saudi J Kidney Dis Transpl; 2006 Sep; 17(3):320-5. PubMed ID: 16970251
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Siblings with Alport's syndrome showing unique staining patterns for alpha5(IV) and alpha6(IV) chains of collagen type IV.
    Tsuji T; Fujigaki Y; Sakakima M; Sado Y; Hishida A
    Clin Exp Nephrol; 2010 Jun; 14(3):283-7. PubMed ID: 20213338
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ultrastructural appearance of renal and other basement membranes in the Bull terrier model of autosomal dominant hereditary nephritis.
    Hood JC; Savige J; Seymour AE; Dowling J; Martinello P; Colville D; Sinclair R; Naito I; Jennings G; Huxtable C
    Am J Kidney Dis; 2000 Aug; 36(2):378-91. PubMed ID: 10922317
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Autosomal recessive Alport's syndrome and benign familial hematuria are collagen type IV diseases.
    Tazón Vega B; Badenas C; Ars E; Lens X; Milà M; Darnell A; Torra R
    Am J Kidney Dis; 2003 Nov; 42(5):952-9. PubMed ID: 14582039
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndrome.
    Turco AE; Bresin E; Rossetti S; Peterlin B; Morandi R; Pignatti PF
    Am J Kidney Dis; 1997 Aug; 30(2):174-9. PubMed ID: 9261027
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Glomerular expression of type IV collagen chains in normal and X-linked Alport syndrome kidneys.
    Heidet L; Cai Y; Guicharnaud L; Antignac C; Gubler MC
    Am J Pathol; 2000 Jun; 156(6):1901-10. PubMed ID: 10854213
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Ultrastructural and immunohistochemical findings in Alport's syndrome: a study of 108 patients from 97 Italian families with particular emphasis on COL4A5 gene mutation correlations.
    Mazzucco G; Barsotti P; Muda AO; Fortunato M; Mihatsch M; Torri-Tarelli L; Renieri A; Faraggiana T; De Marchi M; Monga G
    J Am Soc Nephrol; 1998 Jun; 9(6):1023-31. PubMed ID: 9621285
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Type IV collagen of the glomerular basement membrane. Evidence that the chain specificity of network assembly is encoded by the noncollagenous NC1 domains.
    Boutaud A; Borza DB; Bondar O; Gunwar S; Netzer KO; Singh N; Ninomiya Y; Sado Y; Noelken ME; Hudson BG
    J Biol Chem; 2000 Sep; 275(39):30716-24. PubMed ID: 10896941
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A model of autosomal recessive Alport syndrome in English cocker spaniel dogs.
    Lees GE; Helman RG; Kashtan CE; Michael AF; Homco LD; Millichamp NJ; Ninomiya Y; Sado Y; Naito I; Kim Y
    Kidney Int; 1998 Sep; 54(3):706-19. PubMed ID: 9734596
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.