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 *

98 related articles for article (PubMed ID: 7421876)

  • 21. Canine and feline models of human inherited muscle diseases.
    Shelton GD; Engvall E
    Neuromuscul Disord; 2005 Feb; 15(2):127-38. PubMed ID: 15694134
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Phenytoin, methysergide, and penicillamine in hereditary muscular dystrophy of the chicken.
    Entrikin RK; Patterson GT; Wilson BW
    Exp Neurol; 1981 Apr; 72(1):82-90. PubMed ID: 7202629
    [No Abstract]   [Full Text] [Related]  

  • 23. Aberrant glycosylation of alpha-dystroglycan causes defective binding of laminin in the muscle of chicken muscular dystrophy.
    Saito F; Blank M; Schröder J; Manya H; Shimizu T; Campbell KP; Endo T; Mizutani M; Kröger S; Matsumura K
    FEBS Lett; 2005 Apr; 579(11):2359-63. PubMed ID: 15848172
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Experimental animal information file: effect of bestatin in muscular dystrophy in mice].
    Kawamata J
    Gan To Kagaku Ryoho; 1983 Nov; 10(11):2425-6. PubMed ID: 6639104
    [No Abstract]   [Full Text] [Related]  

  • 25. Ringo, a Golden Retriever Muscular Dystrophy (GRMD) dog with absent dystrophin but normal strength.
    Ambrósio CE; Valadares MC; Zucconi E; Cabral R; Pearson PL; Gaiad TP; Canovas M; Vainzof M; Miglino MA; Zatz M
    Neuromuscul Disord; 2008 Nov; 18(11):892-3. PubMed ID: 18667316
    [No Abstract]   [Full Text] [Related]  

  • 26. [Hereditary defect of muscle cell membranes].
    Zdrodovskaia EP; Lotosh EA; Podlesnaia AI
    Biofizika; 1968; 13(3):572-4. PubMed ID: 5747593
    [No Abstract]   [Full Text] [Related]  

  • 27. Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.
    Arimura T; Helbling-Leclerc A; Massart C; Varnous S; Niel F; Lacène E; Fromes Y; Toussaint M; Mura AM; Keller DI; Amthor H; Isnard R; Malissen M; Schwartz K; Bonne G
    Hum Mol Genet; 2005 Jan; 14(1):155-69. PubMed ID: 15548545
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A rapid PCR method for genotyping the Large(myd) mouse, a model of glycosylation-deficient congenital muscular dystrophy.
    Browning CA; Grewal PK; Moore CJ; Hewitt JE
    Neuromuscul Disord; 2005 May; 15(5):331-5. PubMed ID: 15833424
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Baclofen, procainamide, verapamil, and prenylamine in hereditary muscular dystrophy of the chicken.
    Entrikin RK; Patterson GT; Wilson BW
    Exp Neurol; 1981 Oct; 74(1):86-92. PubMed ID: 7286127
    [No Abstract]   [Full Text] [Related]  

  • 30. Dominant-negative inhibition of Ca2+ influx via TRPV2 ameliorates muscular dystrophy in animal models.
    Iwata Y; Katanosaka Y; Arai Y; Shigekawa M; Wakabayashi S
    Hum Mol Genet; 2009 Mar; 18(5):824-34. PubMed ID: 19050039
    [TBL] [Abstract][Full Text] [Related]  

  • 31. By-passing the nonsense mutation in the 4 CV mouse model of muscular dystrophy by induced exon skipping.
    Mitrpant C; Fletcher S; Iversen PL; Wilton SD
    J Gene Med; 2009 Jan; 11(1):46-56. PubMed ID: 19006096
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Duchenne Boulogne myopathy and free radicals; potential value of lazaroids in the treatment of this disease].
    Poindron P; Metzinger L; Warter JM
    C R Seances Soc Biol Fil; 1995; 189(6):1199-217. PubMed ID: 8763042
    [No Abstract]   [Full Text] [Related]  

  • 33. Strength and endurance in the therapeutic evaluation of prednisolone-treated MDX mice.
    Hudecki MS; Pollina CM; Granchelli JA; Daly MK; Byrnes T; Wang JC; Hsiao JC
    Res Commun Chem Pathol Pharmacol; 1993 Jan; 79(1):45-60. PubMed ID: 8434132
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Avian muscular dystrophy: use of proper "controls".
    Entrikin RK
    Muscle Nerve; 1984 May; 7(4):337-8. PubMed ID: 6727918
    [No Abstract]   [Full Text] [Related]  

  • 35. Sustained whole-body functional rescue in congestive heart failure and muscular dystrophy hamsters by systemic gene transfer.
    Zhu T; Zhou L; Mori S; Wang Z; McTiernan CF; Qiao C; Chen C; Wang DW; Li J; Xiao X
    Circulation; 2005 Oct; 112(17):2650-9. PubMed ID: 16230483
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Correction of genetic disease by making sense from nonsense.
    Kaufman RJ
    J Clin Invest; 1999 Aug; 104(4):367-8. PubMed ID: 10449426
    [No Abstract]   [Full Text] [Related]  

  • 37. Synaptic plasticity in the dy2J mouse model of laminin alpha2-deficient congenital muscular dystrophy.
    Anderson JL; Head SI; Morley JW
    Brain Res; 2005 Apr; 1042(1):23-8. PubMed ID: 15823249
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Muscular dystrophy syndrome in the Cornish chicken.
    Wagner WD; Peterson RA
    Am J Vet Res; 1970 Feb; 31(2):331-8. PubMed ID: 5414876
    [No Abstract]   [Full Text] [Related]  

  • 39. Expression of full-length utrophin prevents muscular dystrophy in mdx mice.
    Tinsley J; Deconinck N; Fisher R; Kahn D; Phelps S; Gillis JM; Davies K
    Nat Med; 1998 Dec; 4(12):1441-4. PubMed ID: 9846586
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel cell-penetrating alpha-keto-amide calpain inhibitors as potential treatment for muscular dystrophy.
    Lescop C; Herzner H; Siendt H; Bolliger R; Henneböhle M; Weyermann P; Briguet A; Courdier-Fruh I; Erb M; Foster M; Meier T; Magyar JP; von Sprecher A
    Bioorg Med Chem Lett; 2005 Dec; 15(23):5176-81. PubMed ID: 16185867
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.