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 *

137 related articles for article (PubMed ID: 9199582)

  • 1. Up-regulation of the brain and Purkinje-cell forms of dystrophin transcripts, in Becker muscular dystrophy.
    Nakamura A; Ikeda S; Yazaki M; Yoshida K; Kobayashi O; Yanagisawa N; Takeda S
    Am J Hum Genet; 1997 Jun; 60(6):1555-8. PubMed ID: 9199582
    [No Abstract]   [Full Text] [Related]  

  • 2. Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp21 muscular dystrophy patients (Duchenne and Becker type).
    Mongini T; Doriguzzi C; Palmucci L; Chiadò-Piat L
    Eur J Clin Invest; 1996 Apr; 26(4):322-4. PubMed ID: 8732491
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dystrophin-related protein in Becker muscular dystrophy.
    Higuchi I; Niiyama T; Fukunaga H; Nakamura K; Nakagawa M; Osame M
    Intern Med; 1994 Jun; 33(6):334-6. PubMed ID: 7919618
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Muscular dystrophies detected by immunophenotyping and genotype analysis (mRNA and DNA)].
    Lukás Z; Vojtísková M; Fajkusová L; Bednarík J; Kadanka Z; Hájek J; Hermanová M; Vohánka S; Vytopil M
    Cesk Patol; 2001 Nov; 37(4):137-45. PubMed ID: 11813630
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The frequency of patients with dystrophin abnormalities in a limb-girdle patient population.
    Arikawa E; Hoffman EP; Kaido M; Nonaka I; Sugita H; Arahata K
    Neurology; 1991 Sep; 41(9):1491-6. PubMed ID: 1842672
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy.
    Hattori N; Kaido M; Nishigaki T; Inui K; Fujimura H; Nishimura T; Naka T; Hazama T
    Neuromuscul Disord; 1999 Jun; 9(4):220-6. PubMed ID: 10399748
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Muscular dystrophy, mental retardation and cardiomyopathy not associated with dystrophin deficiency.
    Villanova M; Malandrini A; Biancotti R; Löfgren A; Mongini T; Six J; Salvestroni R; Parrotta E; Van Broeckhoven C; Paolozzi C; Guazzi G
    Neuromuscul Disord; 1996 May; 6(3):167-72. PubMed ID: 8784804
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dystrophin, its gene, and the dystrophinopathies.
    Roberts RG
    Adv Genet; 1995; 33():177-231. PubMed ID: 7484453
    [No Abstract]   [Full Text] [Related]  

  • 9. Asymptomatic Becker muscular dystrophy: expression of dystrophin and dystrophin-related protein.
    Tachi N; Wakai S; Watanabe Y; Ohya K; Chiba S
    Pediatr Neurol; 1993; 9(3):207-9. PubMed ID: 8352853
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cardiac dystrophin abnormalities in Becker muscular dystrophy assessed by endomyocardial biopsy.
    Maeda M; Nakao S; Miyazato H; Setoguchi M; Arima S; Higuchi I; Osame M; Taira A; Nomoto K; Toda H
    Am Heart J; 1995 Apr; 129(4):702-7. PubMed ID: 7900621
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation.
    Patria SY; Alimsardjono H; Nishio H; Takeshima Y; Nakamura H; Matsuo M
    Proc Assoc Am Physicians; 1996 Jul; 108(4):308-14. PubMed ID: 8863344
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Dystrophin and dystrophin-associated proteins. Their evaluation at the neuromuscular pathology laboratory].
    Navarro C
    Rev Neurol; 1999 Jan 16-31; 28(2):154-8. PubMed ID: 10101784
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects.
    Mizuno Y; Nonaka I; Hirai S; Ozawa E
    J Neurol Sci; 1993 Oct; 119(1):43-52. PubMed ID: 8246010
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Somatic mosaicism of a point mutation in the dystrophin gene in a patient presenting with an asymmetrical muscle weakness and contractures.
    Helderman-van den Enden AT; Ginjaar HB; Kneppers AL; Bakker E; Breuning MH; de Visser M
    Neuromuscul Disord; 2003 May; 13(4):317-21. PubMed ID: 12868501
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Immunopathology and molecular genetics of dystrophinopathies.
    Brown SC; Torelli S; Jimenez C; Muntoni F; Sewry CA
    Suppl Clin Neurophysiol; 2004; 57():313-21. PubMed ID: 16106629
    [No Abstract]   [Full Text] [Related]  

  • 17. Limb-girdle muscular dystrophy.
    Mathews KD; Moore SA
    Curr Neurol Neurosci Rep; 2003 Jan; 3(1):78-85. PubMed ID: 12507416
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An unusual variant of Becker muscular dystrophy.
    de Visser M; Bakker E; Defesche JC; Bolhuis PA; van Ommen GJ
    Ann Neurol; 1990 May; 27(5):578-81. PubMed ID: 2193611
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel dystrophin mutations revealed by analysis of dystrophin mRNA: alternative splicing suppresses the phenotypic effect of a nonsense mutation.
    Fajkusová L; Lukás Z; Tvrdíková M; Kuhrová V; Hájek J; Fajkus J
    Neuromuscul Disord; 2001 Mar; 11(2):133-8. PubMed ID: 11257468
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Utrophin: a potential replacement for dystrophin?
    Tinsley JM; Davies KE
    Neuromuscul Disord; 1993; 3(5-6):537-9. PubMed ID: 8186707
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.