BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

177 related articles for article (PubMed ID: 8151635)

  • 1. Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats.
    Goldman A; Ramsay M; Jenkins T
    J Med Genet; 1994 Jan; 31(1):37-40. PubMed ID: 8151635
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ethnicity and myotonic dystrophy: a possible explanation for its absence in sub-Saharan Africa.
    Goldman A; Ramsay M; Jenkins T
    Ann Hum Genet; 1996 Jan; 60(1):57-65. PubMed ID: 8835099
    [TBL] [Abstract][Full Text] [Related]  

  • 3. New founder haplotypes at the myotonic dystrophy locus in southern Africa.
    Goldman A; Ramsay M; Jenkins T
    Am J Hum Genet; 1995 Jun; 56(6):1373-8. PubMed ID: 7762560
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats.
    Mor-Cohen R; Magal N; Gadoth N; Achiron A; Shohat T; Shohat M
    Isr J Med Sci; 1997 Mar; 33(3):190-3. PubMed ID: 9313789
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonin gene.
    Mor-Cohen R; Magal N; Gadoth N; Shohat T; Shohat M
    Am J Med Genet; 1997 Aug; 71(2):156-9. PubMed ID: 9217214
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CTG repeats distribution and Alu insertion polymorphism at myotonic dystrophy (DM) gene in Amhara and Oromo populations of Ethiopia.
    Gennarelli M; Pavoni M; Cruciani F; De Stefano G; Dallapiccola B; Novelli G
    Hum Genet; 1999; 105(1-2):165-7. PubMed ID: 10480373
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in Thailand.
    Theerasasawat S; Papsing C; Pulkes T
    J Clin Neurosci; 2010 Dec; 17(12):1520-2. PubMed ID: 20801043
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo myotonic dystrophy mutation in a Nigerian kindred.
    Krahe R; Eckhart M; Ogunniyi AO; Osuntokun BO; Siciliano MJ; Ashizawa T
    Am J Hum Genet; 1995 May; 56(5):1067-74. PubMed ID: 7726160
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations.
    Rubinsztein DC; Leggo J; Amos W; Barton DE; Ferguson-Smith MA
    Hum Mol Genet; 1994 Nov; 3(11):2031-5. PubMed ID: 7874122
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations.
    Davies J; Yamagata H; Shelbourne P; Buxton J; Ogihara T; Nokelainen P; Nakagawa M; Williamson R; Johnson K; Miki T
    J Med Genet; 1992 Nov; 29(11):766-9. PubMed ID: 1453423
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy.
    Ashizawa T; Monckton DG; Vaishnav S; Patel BJ; Voskova A; Caskey CT
    Genomics; 1996 Aug; 36(1):47-53. PubMed ID: 8812415
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distribution of CTG repeats at the DMPK gene in myotonic dystrophy patients and healthy individuals from the Mexican population.
    Magaña JJ; Cortés-Reynosa P; Escobar-Cedillo R; Gómez R; Leyva-García N; Cisneros B
    Mol Biol Rep; 2011 Feb; 38(2):1341-6. PubMed ID: 20635151
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular analysis of the CTG trinucleotide repeat in South African myotonic dystrophy families--implications for diagnosis and counselling.
    Goldman A; Ramsay M; Jenkins T
    S Afr Med J; 1995 Nov; 85(11):1161-4. PubMed ID: 8597005
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of CTG repeat length variation in the
    Ambrose KK; Ishak T; Lian LH; Goh KJ; Wong KT; Ahmad-Annuar A; Thong MK
    BMJ Open; 2017 Mar; 7(3):e010711. PubMed ID: 28363916
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene.
    Mahadevan M; Tsilfidis C; Sabourin L; Shutler G; Amemiya C; Jansen G; Neville C; Narang M; Barceló J; O'Hoy K
    Science; 1992 Mar; 255(5049):1253-5. PubMed ID: 1546325
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A molecular protocol for diagnosing myotonic dystrophy.
    Guida M; Marger RS; Papp AC; Snyder PJ; Sedra MS; Kissel JT; Mendell JR; Prior TW
    Clin Chem; 1995 Jan; 41(1):69-72. PubMed ID: 7813083
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variation of CTG-repeat number of the DMPK gene in muscle tissue.
    Ansved T; Edström L; Grandell U; Hedberg B; Anvret M
    Neuromuscul Disord; 1997 May; 7(3):152-5. PubMed ID: 9185177
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Somatic instability of CTG repeat in myotonic dystrophy.
    Ashizawa T; Dubel JR; Harati Y
    Neurology; 1993 Dec; 43(12):2674-8. PubMed ID: 8255475
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Myotonic dystrophy CTG repeats in an Italian population sample: evaluation of the polymorphism for forensic applications.
    D'Apote L; Pelotti S; Bini C; Rimondi S; Ceccardi S; Ferri G; Pappalardo G
    Am J Forensic Med Pathol; 2000 Mar; 21(1):86-9. PubMed ID: 10739235
    [TBL] [Abstract][Full Text] [Related]  

  • 20. DMPK-associated myotonic dystrophy and CTG repeats in Alabama African Americans.
    Acton RT; Rivers CA; Watson B; Oh SJ
    Clin Genet; 2007 Nov; 72(5):448-53. PubMed ID: 17877752
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.