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 *

158 related articles for article (PubMed ID: 1388424)

  • 1. Phenotypic Duchenne muscular dystrophy with C-terminal domain.
    Higuchi I; Fukunaga H; Usuki F; Moritoyo T; Osame M
    Pediatr Neurol; 1992; 8(4):310-2. PubMed ID: 1388424
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dystrophin or a "related protein" in Duchenne muscular dystrophy?
    Nicholson LV; Johnson MA; Davison K; O'Donnell E; Falkous G; Barron M; Harris JB
    Acta Neurol Scand; 1992 Jul; 86(1):8-14. PubMed ID: 1519480
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Duchenne muscular dystrophy in a girl identified by dystrophin deficiency.
    Maytal J; Shanske AL; Fox JE; Lipper S; Eviatar L
    Neuropediatrics; 1991 Aug; 22(3):163-5. PubMed ID: 1944823
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophy.
    Hoffman EP; Garcia CA; Chamberlain JS; Angelini C; Lupski JR; Fenwick R
    Ann Neurol; 1991 Oct; 30(4):605-10. PubMed ID: 1789686
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deletion analysis for Duchenne (and Becker) muscular dystrophy.
    Kimber RD; Hyland VJ; Haan EA; Mulley JC
    Aust Paediatr J; 1989 Oct; 25(5):292-5. PubMed ID: 2590130
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Becker-type muscular dystrophy. Report of a family with one postmortem study.
    Martin JJ; Leroy J; Ceuterick C; Lübke U; Van Buggenhout E; Van Vuchelen J; Van Broeckhoven C
    Clin Neurol Neurosurg; 1992; 94 Suppl():S123-6. PubMed ID: 1320486
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
    Miranda AF; Francke U; Bonilla E; Martucci G; Schmidt B; Salviati G; Rubin M
    Am J Med Genet; 1989 Feb; 32(2):268-73. PubMed ID: 2648829
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Skewed inactivation of an X chromosome deleted at the dystrophin gene in an asymptomatic mother and her affected daughter.
    Tihy F; Vogt N; Recan D; Malfoy B; Leturcq F; Coquet M; Serville F; Fontan D; Guillard JM; Kaplan JC
    Hum Genet; 1994 May; 93(5):563-7. PubMed ID: 8168835
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Multiplex PCR excludes Duchenne muscular dystrophy in a twin pregnancy.
    Wadelius C; Annéran G; Dahl N; Holmgren G; Gustavson KH
    Clin Genet; 1991 Apr; 39(4):314-6. PubMed ID: 2070552
    [No Abstract]   [Full Text] [Related]  

  • 12. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus.
    Towbin JA; Hejtmancik JF; Brink P; Gelb B; Zhu XM; Chamberlain JS; McCabe ER; Swift M
    Circulation; 1993 Jun; 87(6):1854-65. PubMed ID: 8504498
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Screening Duchenne and Becker muscular dystrophy patients for deletions in 30 exons of the dystrophin gene by three-multiplex PCR.
    Covone AE; Caroli F; Romeo G
    Am J Hum Genet; 1992 Sep; 51(3):675-7. PubMed ID: 1496997
    [No Abstract]   [Full Text] [Related]  

  • 14. Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophy.
    Bushby KM; Cleghorn NJ; Curtis A; Haggerty ID; Nicholson LV; Johnson MA; Harris JB; Bhattacharya SS
    Hum Genet; 1991 Dec; 88(2):195-9. PubMed ID: 1757094
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Amino-terminal deletion of 53% of dystrophin results in an intermediate Duchenne-Becker muscular dystrophy phenotype.
    Takeshima Y; Nishio H; Narita N; Wada H; Ishikawa Y; Ishikawa Y; Minami R; Nakamura H; Matsuo M
    Neurology; 1994 Sep; 44(9):1648-51. PubMed ID: 7936290
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy.
    Nicholson LV; Johnson MA; Gardner-Medwin D; Bhattacharya S; Harris JB
    Acta Neuropathol; 1990; 80(3):239-50. PubMed ID: 2205076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.
    Beggs AH; Neumann PE; Arahata K; Arikawa E; Nonaka I; Anderson MS; Kunkel LM
    Proc Natl Acad Sci U S A; 1992 Jan; 89(2):623-7. PubMed ID: 1731332
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophin.
    Matsumura K; Burghes AH; Mora M; Tomé FM; Morandi L; Cornello F; Leturcq F; Jeanpierre M; Kaplan JC; Reinert P
    J Clin Invest; 1994 Jan; 93(1):99-105. PubMed ID: 8282827
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An unusual case of Duchenne muscular dystrophy.
    Topaloğlu H; Dinçer P; Göğüş S; Ayter S; Topçu M
    Brain Dev; 1993; 15(4):313-5. PubMed ID: 8250158
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prediction of dystrophin phenotype by DNA analysis in Duchenne/Becker muscular dystrophy.
    Specht LA; Beggs AH; Korf B; Kunkel LM; Shapiro F
    Pediatr Neurol; 1992; 8(6):432-6. PubMed ID: 1476571
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.