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 *

135 related articles for article (PubMed ID: 11379877)

  • 21. [DNA diagnosis in myotonic dystrophy].
    Tachi N
    Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Distribution and evolution of CTG repeats at the myotonin protein kinase gene in human populations.
    Deka R; Majumder PP; Shriver MD; Stivers DN; Zhong Y; Yu LM; Barrantes R; Yin SJ; Miki T; Hundrieser J; Bunker CH; McGarvey ST; Sakallah S; Ferrell RE; Chakraborty R
    Genome Res; 1996 Feb; 6(2):142-54. PubMed ID: 8919693
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. CTG repeat number at the myotonic dystrophy locus in healthy Kuwaiti individuals: possible explanation of why myotonic dystrophy is rare in Kuwait.
    Alfadhli S; Elshafey AE; Bastaki L; Al-Awadi S
    Arch Neurol; 2004 Jun; 61(6):895-8. PubMed ID: 15210527
    [TBL] [Abstract][Full Text] [Related]  

  • 26. French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion.
    Lavedan C; Hofmann-Radvanyi H; Boileau C; Bonaïti-Pellié C; Savoy D; Shelbourne P; Duros C; Rabes JP; Dehaupas I; Luce S
    J Med Genet; 1994 Jan; 31(1):33-6. PubMed ID: 8151634
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Relative stability of a minimal CTG repeat expansion in a large kindred with myotonic dystrophy.
    Simmons Z; Thornton CA; Seltzer WK; Richards CS
    Neurology; 1998 May; 50(5):1501-4. PubMed ID: 9596022
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Instability of normal (CTG)n alleles in the DM kinase gene.
    Dow DJ; Rubinsztein DC; Yates JR; Barton DE; Ferguson-Smith MA
    J Med Genet; 1997 Oct; 34(10):871-3. PubMed ID: 9350827
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Convergent myotonic dystrophy (DM) haplotypes: potential inconsistencies in human disease gene localization.
    Whiting EJ; Tsilfidis C; Surh L; MacKenzie AE; Korneluk RG
    Eur J Hum Genet; 1995; 3(3):195-202. PubMed ID: 7583045
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins.
    Tishkoff SA; Pakstis AJ; Stoneking M; Kidd JR; Destro-Bisol G; Sanjantila A; Lu RB; Deinard AS; Sirugo G; Jenkins T; Kidd KK; Clark AG
    Am J Hum Genet; 2000 Oct; 67(4):901-25. PubMed ID: 10986042
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese population.
    Yamagata H; Nakagawa M; Johnson K; Miki T
    J Hum Genet; 1998; 43(4):246-9. PubMed ID: 9852676
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation.
    Yamagata H; Miki T; Nakagawa M; Johnson K; Deka R; Ogihara T
    Hum Genet; 1996 Feb; 97(2):145-7. PubMed ID: 8566943
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Characteristics of myotonic dystrophy in Istria: molecular genetic approach. Part II: Analysis of genetic polymorphisms.
    Medica I; Logar N; Peterlin B
    Coll Antropol; 2000 Dec; 24(2):287-94. PubMed ID: 11216395
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy.
    López de Munain A; Cobo AM; Sáenz A; Blanco A; Poza JJ; Martorell L; Martí-Massó JF; Baiget M
    Genet Epidemiol; 1996; 13(5):483-7. PubMed ID: 8905394
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prevalence of myotonic dystrophy in Israeli Jewish communities: inter-community variation and founder premutations.
    Segel R; Silverstein S; Lerer I; Kahana E; Meir R; Sagi M; Zilber N; Korczyn AD; Shapira Y; Argov Z; Abeliovich D
    Am J Med Genet A; 2003 Jun; 119A(3):273-8. PubMed ID: 12784291
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission.
    O'Hoy KL; Tsilfidis C; Mahadevan MS; Neville CE; Barceló J; Hunter AG; Korneluk RG
    Science; 1993 Feb; 259(5096):809-12. PubMed ID: 8094260
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Ancestral Origin of the First Indian Families with Myotonic Dystrophy Type 2.
    Damen M; Schijvenaars M; Schimmel-Naber M; Groothuismink J; Coenen M; Tieleman A
    J Neuromuscul Dis; 2021; 8(4):715-722. PubMed ID: 34024776
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCR.
    Cheng S; Barceló JM; Korneluk RG
    Hum Mutat; 1996; 7(4):304-10. PubMed ID: 8723679
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Dynamic balance of segregation distortion and selection maintains normal allele sizes at the myotonic dystrophy locus.
    Polański A; Chakraborty R; Kimmel M; Deka R
    Math Biosci; 1998 Jan; 147(1):93-112. PubMed ID: 9401353
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.