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 *

103 related articles for article (PubMed ID: 3346018)

  • 1. Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD gene.
    Pernelle JJ; Chafey P; Chelly J; Wahrmann JP; Kaplan JC; Tomé F; Fardeau M
    Hum Genet; 1988 Mar; 78(3):285. PubMed ID: 3346018
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nebulin and titin expression in Duchenne muscular dystrophy appears normal.
    Fürst D; Nave R; Osborn M; Weber K; Bardosi A; Archidiacono N; Ferro M; Romano V; Romeo G
    FEBS Lett; 1987 Nov; 224(1):49-53. PubMed ID: 3678494
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Immunocytochemical study of nebulin in Duchenne muscular dystrophy.
    Bonilla E; Miranda AF; Prelle A; Salviati G; Betto R; Zeviani M; Schon EA; DiMauro S; Rowland LP
    Neurology; 1988 Oct; 38(10):1600-3. PubMed ID: 3419605
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Is nebulin the defective gene product in Duchenne muscular dystrophy?
    Wood DS; Zeviani M; Prelle A; Bonilla E; Salviati G; Miranda AF; DiMauro S; Rowland LP
    N Engl J Med; 1987 Jan; 316(2):107-8. PubMed ID: 3785354
    [No Abstract]   [Full Text] [Related]  

  • 5. Immunological identification of a high molecular weight protein as a candidate for the product of the Duchenne muscular dystrophy gene.
    Kao L; Krstenansky J; Mendell J; Rammohan KW; Gruenstein E
    Proc Natl Acad Sci U S A; 1988 Jun; 85(12):4491-5. PubMed ID: 3288996
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Conservation of the Duchenne muscular dystrophy gene in mice and humans.
    Hoffman EP; Monaco AP; Feener CC; Kunkel LM
    Science; 1987 Oct; 238(4825):347-50. PubMed ID: 3659917
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dystrophin: the protein product of the Duchenne muscular dystrophy locus.
    Hoffman EP; Brown RH; Kunkel LM
    Cell; 1987 Dec; 51(6):919-28. PubMed ID: 3319190
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].
    Baiget M; del Río E; Gallano P
    Neurologia; 1989 Oct; 4(8):268-76. PubMed ID: 2576910
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.
    Smith TJ; Forrest SM; Cross GS; Davies KE
    Nucleic Acids Res; 1987 Dec; 15(23):9761-9. PubMed ID: 3697082
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular analysis of Duchenne and Becker muscular dystrophies.
    Love DR; Forrest SM; Smith TJ; England S; Flint T; Davies KE; Speer A
    Br Med Bull; 1989 Jul; 45(3):659-80. PubMed ID: 2688822
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Transcription of the dystrophin gene in Duchenne muscular dystrophy muscle.
    Muntoni F; Strong PN
    FEBS Lett; 1989 Jul; 252(1-2):95-8. PubMed ID: 2668030
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy.
    Chen JD; Denton MJ; Morgan G; Pearn JH; Mackinlay AG
    Am J Hum Genet; 1988 May; 42(5):777-80. PubMed ID: 3358426
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic abnormalities in Duchenne and Becker dystrophies: clinical correlations.
    Medori R; Brooke MH; Waterston RH
    Neurology; 1989 Apr; 39(4):461-5. PubMed ID: 2648185
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
    Kunkel LM; Hejtmancik JF; Caskey CT; Speer A; Monaco AP; Middlesworth W; Colletti CA; Bertelson C; Müller U; Bresnan M; Shapiro F; Tantravahi U; Speer J; Latt SA; Bartlett R; Pericak-Vance MA; Roses AD; Thompson MW; Ray PN; Worton RG; Fischbeck KH; Gallano P; Coulon M; Duros C; Boue J; Junien C; Chelly J; Hamard G; Jeanpierre M; Lambert M; Kaplan JC; Emery A; Dorkins H; McGlade S; Davies KE; Boehm C; Arveiler B; Lemaire C; Morgan GJ; Denton MJ; Amos J; Bobrow M; Benham F; Boswinkel E; Cole C; Dubowitz V; Hart K; Hodgson S; Johnson L; Walker A; Roncuzzi L; Ferlini A; Nobile C; Romeo G; Wilcox DE; Affara NA; Ferguson-Smith MA; Lindolf M; Kaariainen H; de la Chapelle A; Ionasescu V; Searby C; Ionasescu R; Bakker E; van Ommen GJ; Pearson PL; Greenberg CR; Hamerton JL; Wrogemann K; Doherty RA; Polakowska R; Hyser C; Quirk S; Thomas N; Harper JF; Darras BT; Francke U
    Nature; 1986 Jul 3-9; 322(6074):73-7. PubMed ID: 3014348
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A normal male with an inherited deletion of one exon within the DMD gene.
    Nordenskjöld M; Nicholson L; Edström L; Anvret M; Eiserman M; Slater C; Stolpe L
    Hum Genet; 1990 Jan; 84(2):207-9. PubMed ID: 2404853
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.