BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 9556046)

  • 1. Prenatal diagnosis of Menkes disease.
    Kaler SG; Tümer Z
    Prenat Diagn; 1998 Mar; 18(3):287-9. PubMed ID: 9556046
    [No Abstract]   [Full Text] [Related]  

  • 2. [Menkes' disease and brain dysfunction].
    Aoki T; Yamaguchi Y; Omura I; Watanabe A; Shimizu N
    No To Shinkei; 2001 May; 53(5):427-35. PubMed ID: 11424353
    [No Abstract]   [Full Text] [Related]  

  • 3. Menkes disease: recent advances and new aspects.
    Tümer Z; Horn N
    J Med Genet; 1997 Apr; 34(4):265-74. PubMed ID: 9138147
    [No Abstract]   [Full Text] [Related]  

  • 4. Fibroblast silver loading for the diagnosis of Menkes disease.
    Verheijen FW; Beerens CE; Havelaar AC; Kleijer WJ; Mancini GM
    J Med Genet; 1998 Oct; 35(10):849-51. PubMed ID: 9783711
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical utility gene card for: Menkes disease.
    Tümer Z; Klomp L
    Eur J Hum Genet; 2011 Oct; 19(10):. PubMed ID: 21487442
    [No Abstract]   [Full Text] [Related]  

  • 6. Copper transport and its alterations in Menkes and Wilson diseases.
    DiDonato M; Sarkar B
    Biochim Biophys Acta; 1997 Feb; 1360(1):3-16. PubMed ID: 9061035
    [No Abstract]   [Full Text] [Related]  

  • 7. Menkes disease mutations and response to early copper histidine treatment.
    Kaler SG
    Nat Genet; 1996 May; 13(1):21-2. PubMed ID: 8673098
    [No Abstract]   [Full Text] [Related]  

  • 8. RFLVs in mottled dappled alleles.
    Reed V; Boyd Y
    Nat Genet; 1994 Sep; 8(1):11-2. PubMed ID: 7726911
    [No Abstract]   [Full Text] [Related]  

  • 9. An Ile/Val polymorphism at codon 1464 of the ATP7A gene.
    Ogawa A; Yamamoto S; Takayanagi M; Kogo T; Kanazawa M; Kohno Y
    J Hum Genet; 1999; 44(6):423-4. PubMed ID: 10570920
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnostic conundrum involving a novel ATP7A duplication.
    Schoonveld C; Donsante A; del Gaudio D; Waggoner D; Das S; Kaler SG
    Clin Genet; 2013 Jul; 84(1):97-8. PubMed ID: 23151012
    [No Abstract]   [Full Text] [Related]  

  • 11. A green light glows on copper disorders research.
    Rinaldi A
    Trends Biochem Sci; 2001 Feb; 26(2):92. PubMed ID: 11166565
    [No Abstract]   [Full Text] [Related]  

  • 12. Identification of four novel mutations in classical Menkes disease and successful prenatal DNA diagnosis.
    Hahn S; Cho K; Ryu K; Kim J; Pai K; Kim M; Park H; Yoo O
    Mol Genet Metab; 2001 May; 73(1):86-90. PubMed ID: 11350187
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Menkes and Wilson diseases.
    Monaco AP; Chelly J
    Adv Genet; 1995; 33():233-53. PubMed ID: 7484454
    [No Abstract]   [Full Text] [Related]  

  • 14. Deletion of the promoter region in the Atp7a gene of the mottled dappled mouse.
    Levinson B; Packman S; Gitschier J
    Nat Genet; 1997 Jul; 16(3):224-5. PubMed ID: 9207785
    [No Abstract]   [Full Text] [Related]  

  • 15. Molecular genetic mutation analysis in Menkes-disease with prenatal diagnosis.
    László A; Endreffy E; Tümer Z; Horn N; Szabó J
    Ideggyogy Sz; 2010 Jan; 63(1-2):48-51. PubMed ID: 20420124
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A copper treatable Menkes disease mutation associated with defective trafficking of a functional Menkes copper ATPase.
    Kim BE; Smith K; Petris MJ
    J Med Genet; 2003 Apr; 40(4):290-5. PubMed ID: 12676902
    [No Abstract]   [Full Text] [Related]  

  • 17. Late-onset treatment in Menkes disease: is there a correlation between genotype and response to therapy?
    Olivares JL; Bueno I; Gallati S; Ramos FJ
    Clin Genet; 2006 Apr; 69(4):363-6. PubMed ID: 16630173
    [No Abstract]   [Full Text] [Related]  

  • 18. Two highly polymorphic CA repeats in the Menkes gene (ATP7A).
    Begy CR; Dierick HA; Innis JW; Glover TW
    Hum Genet; 1995 Sep; 96(3):355-6. PubMed ID: 7649557
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes disease.
    Ogawa A; Yamamoto S; Takayanagi M; Kogo T; Kanazawa M; Kohno Y
    J Hum Genet; 1999; 44(3):206-9. PubMed ID: 10319589
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice.
    Mercer JF; Grimes A; Ambrosini L; Lockhart P; Paynter JA; Dierick H; Glover TW
    Nat Genet; 1994 Apr; 6(4):374-8. PubMed ID: 8054977
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.