BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

199 related articles for article (PubMed ID: 8437017)

  • 1. The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities.
    Bushby KM; Gardner-Medwin D; Nicholson LV; Johnson MA; Haggerty ID; Cleghorn NJ; Harris JB; Bhattacharya SS
    J Neurol; 1993 Feb; 240(2):105-12. PubMed ID: 8437017
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients.
    Nicholson LV; Johnson MA; Bushby KM; Gardner-Medwin D; Curtis A; Ginjaar IB; den Dunnen JT; Welch JL; Butler TJ; Bakker E
    J Med Genet; 1993 Sep; 30(9):737-44. PubMed ID: 8411068
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.
    Comi GP; Prelle A; Bresolin N; Moggio M; Bardoni A; Gallanti A; Vita G; Toscano A; Ferro MT; Bordoni A
    Brain; 1994 Feb; 117 ( Pt 1)():1-14. PubMed ID: 8149204
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy.
    Winnard AV; Klein CJ; Coovert DD; Prior T; Papp A; Snyder P; Bulman DE; Ray PN; McAndrew P; King W
    Hum Mol Genet; 1993 Jun; 2(6):737-44. PubMed ID: 8353493
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deletions in the 5' region of dystrophin and resulting phenotypes.
    Muntoni F; Gobbi P; Sewry C; Sherratt T; Taylor J; Sandhu SK; Abbs S; Roberts R; Hodgson SV; Bobrow M
    J Med Genet; 1994 Nov; 31(11):843-7. PubMed ID: 7853367
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec.
    Simard LR; Gingras F; Delvoye N; Vanasse M; Melançon SB; Labuda D
    Hum Genet; 1992 Jun; 89(4):419-24. PubMed ID: 1618490
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies.
    Claustres M; Tuffery S; Chevron MP; Jozelon MP; Martinez P; Echenne B; Demaille J
    Hum Genet; 1991 Dec; 88(2):179-84. PubMed ID: 1684565
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Additional dystrophin fragment in Becker muscular dystrophy may result from proteolytic cleavage at deletion junctions.
    Beggs AH; Hoffman EP; Kunkel LM
    Am J Med Genet; 1992 Oct; 44(3):378-81. PubMed ID: 1488990
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dystrophin expression in Duchenne patients with "in-frame" gene deletions.
    Nicholson LV; Bushby KM; Johnson MA; Gardner-Medwin D; Ginjaar IB
    Neuropediatrics; 1993 Apr; 24(2):93-7. PubMed ID: 8327067
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy.
    Yoshida K; Ikeda S; Nakamura A; Kagoshima M; Takeda S; Shoji S; Yanagisawa N
    Muscle Nerve; 1993 Nov; 16(11):1161-6. PubMed ID: 8413368
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?
    Vainzof M; Takata RI; Passos-Bueno MR; Pavanello RC; Zatz M
    Hum Mol Genet; 1993 Jan; 2(1):39-42. PubMed ID: 8490621
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Proximal dystrophin gene deletions and protein alterations in becker muscular dystrophy.
    Novaković I; Bojić D; Todorović S; Apostolski S; Luković L; Stefanović D; Milasin J
    Ann N Y Acad Sci; 2005 Jun; 1048():406-10. PubMed ID: 16154963
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin.
    Le Thiet Thanh ; Nguyen Thi Man ; Hori S; Sewry CA; Dubowitz V; Morris GE
    Am J Med Genet; 1995 Aug; 58(2):177-86. PubMed ID: 8533812
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R; Gluck E; Legum C; Shiloh Y
    Am J Med Genet; 1994 Feb; 49(4):369-73. PubMed ID: 8160727
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Duplication of dystrophin gene and dissimilar clinical phenotype in the same family.
    Toscano A; Vitiello L; Comi GP; Galvagni F; Miorin M; Prelle A; Fortunato F; Bardoni A; Mora M; Fiumara A
    Neuromuscul Disord; 1995 Nov; 5(6):475-81. PubMed ID: 8580729
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of deletions in the dystrophin gene in patients with Duchenne muscular dystrophy in the Bashkir Republic].
    Grinchuk OV; Khidiiatova IM; Kiselev AV; Magzhanov RV; Khusnutdinova EK
    Genetika; 1999 Apr; 35(4):551-5. PubMed ID: 10420280
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of dystrophin gene deletions in patients from the Mexican population with Duchenne/Becker muscular dystrophy.
    Coral-Vázquez R; Arenas D; Cisneros B; Peñaloza L; Kofman S; Salamanca F; Montañez C
    Arch Med Res; 1993; 24(1):1-6. PubMed ID: 8292871
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.
    Freund AA; Scola RH; Arndt RC; Lorenzoni PJ; Kay CK; Werneck LC
    Arq Neuropsiquiatr; 2007 Mar; 65(1):73-6. PubMed ID: 17420831
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A 400-kb tandem duplication within the dystrophin gene leads to severe Becker muscular dystrophy.
    Gold R; Kress W; Bettecken T; Reichmann H; Müller CR
    J Neurol; 1994 Mar; 241(5):331-4. PubMed ID: 8006687
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Additional dystrophin fragment in Becker muscular dystrophy patients: correlation with the pattern of DNA deletion.
    Vainzof M; Passos-Bueno MR; Rapaport D; Pavanello RC; Zatz M; Bulman DE
    Am J Med Genet; 1992 Oct; 44(3):382-4. PubMed ID: 1488991
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.