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 *

109 related articles for article (PubMed ID: 9097720)

  • 1. Alkaptonuria: from humans to moulds and back.
    Scazzocchio C
    Trends Genet; 1997 Apr; 13(4):125-7. PubMed ID: 9097720
    [No Abstract]   [Full Text] [Related]  

  • 2. Inborn error of metabolism.
    Konforti B
    Nat Struct Biol; 2000 Jul; 7(7):535-6. PubMed ID: 10876234
    [No Abstract]   [Full Text] [Related]  

  • 3. Alkaptonuria: such a long journey.
    Scriver CR
    Nat Genet; 1996 Sep; 14(1):5-6. PubMed ID: 8782808
    [No Abstract]   [Full Text] [Related]  

  • 4. Structural and functional analysis of mutations in alkaptonuria.
    Rodríguez JM; Timm DE; Titus GP; Beltrán-Valero De Bernabé D; Criado O; Mueller HA; Rodríguez De Córdoba S; Peñalva MA
    Hum Mol Genet; 2000 Sep; 9(15):2341-50. PubMed ID: 11001939
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Spectrophotometric determination of homogentisate using Aspergillus nidulans homogentisate dioxygenase.
    Fernández-Cañón JM; Peñalva MA
    Anal Biochem; 1997 Feb; 245(2):218-21. PubMed ID: 9056215
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sequence analysis of the homogentisate 1,2 dioxygenase gene in a family affected by alkaptonuria.
    Walter K; Gaa A; Schaefer HE
    J Med Genet; 1999 Aug; 36(8):645-6. PubMed ID: 10465119
    [No Abstract]   [Full Text] [Related]  

  • 7. Alkaptonuria in Italy: polymorphic haplotype background, mutational profile, and description of four novel mutations in the homogentisate 1,2-dioxygenase gene.
    Porfirio B; Chiarelli I; Graziano C; Mannoni A; Morrone A; Zammarchi E; De Bernabé DB; De Córdoba SR
    J Med Genet; 2000 Apr; 37(4):309-12. PubMed ID: 10819641
    [No Abstract]   [Full Text] [Related]  

  • 8. Fungal metabolic model for human type I hereditary tyrosinaemia.
    Fernández-Cañón JM; Peñalva MA
    Proc Natl Acad Sci U S A; 1995 Sep; 92(20):9132-6. PubMed ID: 7568087
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular characterization of a gene encoding a homogentisate dioxygenase from Aspergillus nidulans and identification of its human and plant homologues.
    Fernández-Cañón JM; Peñalva MA
    J Biol Chem; 1995 Sep; 270(36):21199-205. PubMed ID: 7673153
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular diagnosis of alkaptonuria mutation by analysis of homogentisate 1,2 dioxygenase mRNA from urine and blood.
    Ramos SM; Hernández M; Roces A; Larruga JM; González P; González AM; Pinto FM; Cabrera VM
    Am J Med Genet; 1998 Jun; 78(2):192-4. PubMed ID: 9674916
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular defects in alkaptonuria.
    Gehrig A; Schmidt SR; Müller CR; Srsen S; Srsnova K; Kress W
    Cytogenet Cell Genet; 1997; 76(1-2):14-6. PubMed ID: 9154114
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The molecular basis of alkaptonuria.
    Fernández-Cañón JM; Granadino B; Beltrán-Valero de Bernabé D; Renedo M; Fernández-Ruiz E; Peñalva MA; Rodríguez de Córdoba S
    Nat Genet; 1996 Sep; 14(1):19-24. PubMed ID: 8782815
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alkaptonuria in the Dominican Republic: identification of the founder AKU mutation and further evidence of mutation hot spots in the HGO gene.
    Goicoechea De Jorge E; Lorda I; Gallardo ME; Pérez B; Peréz De Ferrán C; Mendoza H; Rodríguez De Córdoba S
    J Med Genet; 2002 Jul; 39(7):E40. PubMed ID: 12114497
    [No Abstract]   [Full Text] [Related]  

  • 14. Crystal structure of human homogentisate dioxygenase.
    Titus GP; Mueller HA; Burgner J; Rodríguez De Córdoba S; Peñalva MA; Timm DE
    Nat Struct Biol; 2000 Jul; 7(7):542-6. PubMed ID: 10876237
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Are we ready to try to cure alkaptonuria?
    La Du BN
    Am J Hum Genet; 1998 Apr; 62(4):765-7. PubMed ID: 9529368
    [No Abstract]   [Full Text] [Related]  

  • 16. Novel mutations in the homogentisate-1,2-dioxygenase gene identified in Slovak patients with alkaptonuria.
    Zatková A; Polaková H; Micutková L; Zvarík M; Bosák V; Feráková E; Matusek J; Ferák V; Kádasi L
    J Med Genet; 2000 Jul; 37(7):539-42. PubMed ID: 10970188
    [No Abstract]   [Full Text] [Related]  

  • 17. [Alkaptonuria (homogentisic aciduria)].
    Takita H
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):328-31. PubMed ID: 9590059
    [No Abstract]   [Full Text] [Related]  

  • 18. Alkaptonuria: tracked down to chromosome 3.
    McKusick VA
    Genomics; 1994 Jan; 19(1):3-4. PubMed ID: 8188236
    [No Abstract]   [Full Text] [Related]  

  • 19. Cloning of the homogentisate 1,2-dioxygenase gene, the key enzyme of alkaptonuria in mouse.
    Schmidt SR; Gehrig A; Koehler MR; Schmid M; Müller CR; Kress W
    Mamm Genome; 1997 Mar; 8(3):168-71. PubMed ID: 9069115
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutational analysis of the HGO gene in Finnish alkaptonuria patients.
    Beltrán-Valero de Bernabé D; Peterson P; Luopajärvi K; Matintalo P; Alho A; Konttinen Y; Krohn K; Rodríguez de Córdoba S; Ranki A
    J Med Genet; 1999 Dec; 36(12):922-3. PubMed ID: 10594001
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.