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 *

356 related articles for article (PubMed ID: 2648829)

  • 1. 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]  

  • 2. 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]  

  • 3. Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.
    Bonilla E; Schmidt B; Samitt CE; Miranda AF; Hays AP; de Oliveira AB; Chang HW; Servidei S; Ricci E; Younger DS
    Am J Pathol; 1988 Dec; 133(3):440-5. PubMed ID: 3059802
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
    Darras BT; Koenig M; Kunkel LM; Francke U
    Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Membrane changes in Duchenne/Becker muscular dystrophy: lectin binding and localization of dystrophin].
    Voit T; Patel K; Sewry CA; Strong PN; Dubowitz V; Dunn MJ
    Monatsschr Kinderheilkd; 1989 Jan; 137(1):20-7. PubMed ID: 2646527
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dystrophin as a diagnostic marker in Duchenne and Becker muscular dystrophy. Correlation of immunofluorescence and western blot.
    Voit T; Stuettgen P; Cremer M; Goebel HH
    Neuropediatrics; 1991 Aug; 22(3):152-62. PubMed ID: 1944822
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X-linked dystrophies: from gene localization to gene therapy.
    Chamberlain JS
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):610-4. PubMed ID: 1392134
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Localization of dystrophin in cultures of human muscle.
    Ecob-Prince MS; Hill MA; Brown AE
    Muscle Nerve; 1989 Jul; 12(7):594-7. PubMed ID: 2674706
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Immunocytochemical study of dystrophin in muscle cultures from patients with Duchenne muscular dystrophy and unaffected control patients.
    Miranda AF; Bonilla E; Martucci G; Moraes CT; Hays AP; Dimauro S
    Am J Pathol; 1988 Sep; 132(3):410-6. PubMed ID: 3046367
    [TBL] [Abstract][Full Text] [Related]  

  • 10. ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy.
    Fitzgerald KM; Cibis GW; Gettel AH; Rinaldi R; Harris DJ; White RA
    J Med Genet; 1999 Apr; 36(4):316-22. PubMed ID: 10227401
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle.
    Zubrzycka-Gaarn EE; Bulman DE; Karpati G; Burghes AH; Belfall B; Klamut HJ; Talbot J; Hodges RS; Ray PN; Worton RG
    Nature; 1988 Jun; 333(6172):466-9. PubMed ID: 3287171
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy.
    Lupski JR; Garcia CA; Zoghbi HY; Hoffman EP; Fenwick RG
    Am J Med Genet; 1991 Sep; 40(3):354-64. PubMed ID: 1683155
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.
    Wood S; Shukin RJ; McGillivray BC; Ray PN; Worton RG
    Am J Med Genet; 1988 Feb; 29(2):419-23. PubMed ID: 2895584
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
    Ligon AH; Kashork CD; Richards CS; Shaffer LG
    Eur J Hum Genet; 2000 Apr; 8(4):293-8. PubMed ID: 10854113
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy.
    Shomrat R; Driks N; Legum C; Shiloh Y
    Am J Med Genet; 1992 Feb; 42(3):281-7. PubMed ID: 1536162
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Observations on the pathogenesis of Duchenne muscular dystrophy in the light of recent progress in molecular genetics.
    Kakulas BA
    Aust Paediatr J; 1988; 24 Suppl 1():4-8. PubMed ID: 3060072
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of a point mutation and germinal mosaicism in a Duchenne muscular dystrophy family.
    Wilton SD; Chandler DC; Kakulas BA; Laing NG
    Hum Mutat; 1994; 3(2):133-40. PubMed ID: 8199594
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy.
    Kimura S; Sugino S; Ohtani Y; Matsukura M; Nishino I; Ikezawa M; Sakata A; Kondo Y; Yoshioka K; Huard J; Nonaka I; Miike T
    Ann Neurol; 1998 Dec; 44(6):967-71. PubMed ID: 9851444
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies.
    Vainzof M; Pavanello RC; Pavanello-Filho I; Rapaport D; Passos-Bueno MR; Zubrzycka-Gaarn EE; Bulman DE; Zatz M
    Am J Med Genet; 1991 Apr; 39(1):38-41. PubMed ID: 1867262
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diagnosis and carrier detection in a Duchenne muscular dystrophy family by multiplex polymerase chain reaction and microsatellite analysis.
    Jongpiputvanich S; Norapucsunton T; Mutirangura A
    J Med Assoc Thai; 1996 Dec; 79 Suppl 1():S15-21. PubMed ID: 9071063
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.