BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 1757963)

  • 1. Becker muscular dystrophy patient with a large intragenic dystrophin deletion: implications for functional minigenes and gene therapy.
    Love DR; Flint TJ; Genet SA; Middleton-Price HR; Davies KE
    J Med Genet; 1991 Dec; 28(12):860-4. PubMed ID: 1757963
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Very mild muscular dystrophy associated with the deletion of 46% of dystrophin.
    England SB; Nicholson LV; Johnson MA; Forrest SM; Love DR; Zubrzycka-Gaarn EE; Bulman DE; Harris JB; Davies KE
    Nature; 1990 Jan; 343(6254):180-2. PubMed ID: 2404210
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Molecular pathology of Duchenne and Becker muscular dystrophy].
    Gilgenkrantz H; Chelly J; Récan D; Chafey P; Kaplan JC
    C R Seances Soc Biol Fil; 1992; 186(4):349-53. PubMed ID: 1301222
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Somatic mosaicism for a deletion of the dystrophin gene in a carrier of Becker muscular dystrophy.
    Voit T; Neuen-Jacob E; Mahler V; Jauch A; Cremer M
    Eur J Pediatr; 1992 Feb; 151(2):112-6. PubMed ID: 1537352
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies.
    Chelly J; Gilgenkrantz H; Lambert M; Hamard G; Chafey P; Récan D; Katz P; de la Chapelle A; Koenig M; Ginjaar IB
    Cell; 1990 Dec; 63(6):1239-48. PubMed ID: 2261642
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy.
    Arahata K; Beggs AH; Honda H; Ito S; Ishiura S; Tsukahara T; Ishiguro T; Eguchi C; Orimo S; Arikawa E
    J Neurol Sci; 1991 Feb; 101(2):148-56. PubMed ID: 2033400
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection.
    Asano J; Tomatsu S; Sukegawa K; Ikedo Y; Minami R; Iida M; Nishimura M; Nakagawa M; Ohshiro M; Orii T
    Clin Genet; 1991 Jun; 39(6):419-24. PubMed ID: 1863988
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.
    Malhotra SB; Hart KA; Klamut HJ; Thomas NS; Bodrug SE; Burghes AH; Bobrow M; Harper PS; Thompson MW; Ray PN
    Science; 1988 Nov; 242(4879):755-9. PubMed ID: 3055295
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Splicing mutations in DMD/BMD detected by RT-PCR/PTT: detection of a 19AA insertion in the cysteine rich domain of dystrophin compatible with BMD.
    Roest PA; Bout M; van der Tuijn AC; Ginjaar IB; Bakker E; Hogervorst FB; van Ommen GJ; den Dunnen JT
    J Med Genet; 1996 Nov; 33(11):935-9. PubMed ID: 8950674
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
    Gangopadhyay SB; Sherratt TG; Heckmatt JZ; Dubowitz V; Miller G; Shokeir M; Ray PN; Strong PN; Worton RG
    Am J Hum Genet; 1992 Sep; 51(3):562-70. PubMed ID: 1496988
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Southern blot and PCR analyses of dystrophin gene deletions in Japanese patients with Duchenne muscular dystrophy.
    Nakajima T; Matsuo M; Nakamura H; Fujiwara Y
    Kobe J Med Sci; 1991 Feb; 37(1):21-33. PubMed ID: 1921260
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patients.
    Chaturvedi LS; Mukherjee M; Srivastava S; Mittal RD; Mittal B
    Exp Mol Med; 2001 Dec; 33(4):251-6. PubMed ID: 11795488
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of deletions in the dystrophin gene giving mild phenotypes.
    Love DR; Flint TJ; Marsden RF; Bloomfield JF; Daniels RJ; Forrest SM; Gabrielli O; Giorgi P; Novelli G; Davies KE
    Am J Med Genet; 1990 Sep; 37(1):136-42. PubMed ID: 2240031
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genotypic diagnosis of Duchenne and Becker muscular dystrophies].
    Tuffery-Giraud S; Chambert S; Demaille J; Claustres M
    Ann Biol Clin (Paris); 1999; 57(4):417-26. PubMed ID: 10432364
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Half the dystrophin gene is apparently enough for a mild clinical course: confirmation of its potential use for gene therapy.
    Passos-Bueno MR; Vainzof M; Marie SK; Zatz M
    Hum Mol Genet; 1994 Jun; 3(6):919-22. PubMed ID: 7951237
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular genetic and immunological analysis of dystrophin of a young patient with X-linked muscular dystrophy.
    Ikeya K; Saito K; Hayashi K; Tanaka H; Hagiwara Y; Yoshida M; Yamauchi A; Fukuyama Y; Ishiguro T; Eguchi C
    Am J Med Genet; 1992 Jun; 43(3):580-7. PubMed ID: 1605252
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis.
    Gold R; Kress W; Meurers B; Meng G; Reichmann H; Müller CR
    Muscle Nerve; 1992 Feb; 15(2):214-8. PubMed ID: 1549142
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of carriers of Duchenne/Becker muscular dystrophy by a novel method based on detection of junction fragments in the dystrophin gene.
    Yamagishi H; Kato S; Hiraishi Y; Ishihara T; Hata J; Matsuo N; Takano T
    J Med Genet; 1996 Dec; 33(12):1027-31. PubMed ID: 9004137
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.