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 *

99 related articles for article (PubMed ID: 2248149)

  • 41. Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies.
    Matsumura K; Campbell KP
    Muscle Nerve; 1994 Jan; 17(1):2-15. PubMed ID: 8264699
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Molecular markers for myoblast transplantation in GRMD.
    Bartlett RJ; Sharp NJ; Hung WY; Kornegay JN; Roses AD
    Adv Exp Med Biol; 1990; 280():273-8. PubMed ID: 1978966
    [No Abstract]   [Full Text] [Related]  

  • 43. [Manifesting carriers of Duchenne muscular dystrophy over two generations].
    Itagaki Y; Saida K; Nishitani H; Matsuo M; Nishio H
    Rinsho Shinkeigaku; 1993 Apr; 33(4):377-81. PubMed ID: 8103723
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Investigation of a female manifesting Becker muscular dystrophy.
    Glass IA; Nicholson LV; Watkiss E; Johnson MA; Roberts RG; Abbs S; Brittain-Jones S; Boddie HG
    J Med Genet; 1992 Aug; 29(8):578-82. PubMed ID: 1518025
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [Spinal form of Ullrich's disease in monozygotic twins].
    Aver'ianov IuN; Il'ina NA; Mazaeva IV; Berezova NIu
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982; 82(3):51-4. PubMed ID: 7200707
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Transferring myoblasts in Duchenne dystrophy.
    Dubowitz V
    BMJ; 1992 Oct; 305(6858):844-5. PubMed ID: 1422391
    [No Abstract]   [Full Text] [Related]  

  • 47. Muscular dystrophies: diseases of the dystrophin-glycoprotein complex.
    Worton R
    Science; 1995 Nov; 270(5237):755-6. PubMed ID: 7481760
    [No Abstract]   [Full Text] [Related]  

  • 48. Human myoblast transplantation between immunohistocompatible donors and recipients produces immune reactions.
    Huard J; Roy R; Bouchard JP; Malouin F; Richards CL; Tremblay JP
    Transplant Proc; 1992 Dec; 24(6):3049-51. PubMed ID: 1466052
    [No Abstract]   [Full Text] [Related]  

  • 49. A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriers.
    Vainzof M; Passos-Bueno MR; Pavanello RC; Schreiber R; Zatz M
    J Med Genet; 1992 Jul; 29(7):476-9. PubMed ID: 1640426
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Clinical diagnosis of Duchenne muscular dystrophy using anti-dystrophin antibodies].
    Arahata K
    No To Shinkei; 1991 May; 43(5):411-9. PubMed ID: 1910928
    [No Abstract]   [Full Text] [Related]  

  • 51. Fetal dystrophin to diagnose carrier status.
    Ginjaar IB; Soffers S; Moorman AF; Nicholson LV; Morris GE; Bakker E; van Haeringen A; van Ommen GJ
    Lancet; 1991 Jul; 338(8761):258-9. PubMed ID: 1676813
    [No Abstract]   [Full Text] [Related]  

  • 52. [Dystrophin gene expression in patients with Duchenne muscular dystrophy after myoblast transplantation].
    Shishkin SS; Terekhov SM; Krokhina TB; Shakhovskaia NI; Podobedova AN; Linnaia GF; Tarasov VI; Ovchinnikov VI; Krakhmaleva IN; Zakharov SF; Ershova ES; Limborskaia SA; Pogoda TV; Zotikov EA; Kut'ina RM; Tarksh MA; Sukhorukov VS; Gerasimova NL
    Genetika; 2001 Aug; 37(8):1104-11. PubMed ID: 11642111
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins.
    Gomez MR; Engel AG; Dewald G; Peterson HA
    Neurology; 1977 Jun; 27(6):537-41. PubMed ID: 559260
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Can muscular dystrophy be treated?].
    Somer H
    Duodecim; 1992; 108(6):575-7. PubMed ID: 1366117
    [No Abstract]   [Full Text] [Related]  

  • 55. The muscular dystrophies.
    Dubowitz V
    Postgrad Med J; 1992 Jul; 68(801):500-6. PubMed ID: 1437944
    [No Abstract]   [Full Text] [Related]  

  • 56. Successful transplantation of genetically corrected DMD myoblasts following ex vivo transduction with the dystrophin minigene.
    Moisset PA; Skuk D; Asselin I; Goulet M; Roy B; Karpati G; Tremblay JP
    Biochem Biophys Res Commun; 1998 Jun; 247(1):94-9. PubMed ID: 9636661
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Chromosome 4q DNA rearrangement in monozygotic twins discordant for facioscapulohumeral muscular dystrophy.
    Tawil R; Storvick D; Weiffenbach B; Altherr MR; Feasby TE; Griggs RC
    Hum Mutat; 1993; 2(6):492-4. PubMed ID: 8111417
    [No Abstract]   [Full Text] [Related]  

  • 58. Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
    Prior TW; Papp AC; Snyder PJ; Mendell JR
    Muscle Nerve; 1992 Aug; 15(8):960-3. PubMed ID: 1353862
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [Duchenne muscular dystrophy].
    Ishiura S; Sugita H
    No To Shinkei; 1991 May; 43(5):405-9. PubMed ID: 1910927
    [No Abstract]   [Full Text] [Related]  

  • 60. [Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations].
    Gold R; Kress W; Meurers B; Müller CR; Reichmann H
    Nervenarzt; 1991 Jun; 62(6):360-8. PubMed ID: 1876220
    [No Abstract]   [Full Text] [Related]  

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