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: 8990023)

  • 1. CTG trinucleotide repeat lengths in myotonic dystrophy alleles of patients with senile cataracts.
    Aves SJ; Tongue N; Findlay KL; Rich WJ; West SP
    Hum Mutat; 1997; 9(1):95-6. PubMed ID: 8990023
    [No Abstract]   [Full Text] [Related]  

  • 2. [Detection for trinucleotide repeats in myotonic dystrophy type 1].
    Li Y; Da YW
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Feb; 29(1):16-8. PubMed ID: 22311484
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Expansion and mutation rate in CTG repeats in the myotonic dystrophy gene].
    Khidiiatova IM; Fatkhlislamova RI; Magzhanov RV; Popova SN; Slominskiĭ PA; Limborskaia SA; Khusnutdinova EK
    Genetika; 2000 Oct; 36(10):1410-3. PubMed ID: 11094756
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CTG amplification in the DM1PK gene is not associated with idiopathic male subfertility.
    Kunej T; Teran N; Zorn B; Peterlin B
    Hum Reprod; 2004 Sep; 19(9):2084-7. PubMed ID: 15284213
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions.
    Arsenault ME; Prévost C; Lescault A; Laberge C; Puymirat J; Mathieu J
    Neurology; 2006 Apr; 66(8):1248-50. PubMed ID: 16636244
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Intergenerational contraction of the CTG repeats in 2 families with myotonic dystrophy type 1.
    Puymirat J; Giguère Y; Mathieu J; Bouchard JP
    Neurology; 2009 Dec; 73(24):2126-7. PubMed ID: 20018643
    [No Abstract]   [Full Text] [Related]  

  • 8. 250 CTG repeats in DMPK is a threshold for correlation of expansion size and age at onset of juvenile-adult DM1.
    Savić D; Rakocvic-Stojanovic V; Keckarevic D; Culjkovic B; Stojkovic O; Mladenovic J; Todorovic S; Apostolski S; Romac S
    Hum Mutat; 2002 Feb; 19(2):131-9. PubMed ID: 11793472
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Instability of myotonic dystrophy CTG trinucleotide repeat].
    Ashizawa T
    Rinsho Shinkeigaku; 1997 Dec; 37(12):1151. PubMed ID: 9577674
    [No Abstract]   [Full Text] [Related]  

  • 10. An expanded CTG trinucleotide repeat causes trans RNA interference: a new hypothesis for the pathogenesis of myotonic dystrophy.
    Sasagawa N; Takahashi N; Suzuki K; Ishiura S
    Biochem Biophys Res Commun; 1999 Oct; 264(1):76-80. PubMed ID: 10527844
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Cataract as an only clinical manifestation of myotonic dystrophy--a new example of somatic instability of CTG repeats expansion in myotonin protein kinase gene].
    Saito Y; Sato K; Kawai M
    Rinsho Shinkeigaku; 1997 Aug; 37(8):714-6. PubMed ID: 9404152
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Allelic polymorphism and analysis of haplotypes of the muscle protein kinase genes and haplotype analysis in residents of northwestern Russia and patients with myotonic dystrophy].
    Malysheva OV; Ivashchenko TE; Vasil'eva TN; Saĭkova LA; Baranov VS
    Genetika; 1998 Feb; 34(2):295-9. PubMed ID: 9589858
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Analysis of expansion of the triplet repeat (CTG)n in myotonic dystrophy patients from Bashkir].
    Slominskiĭ PA; Popova SN; Fatkhlislamova RI; Akhmadeeva LR; Magzhanov RV; Khusnutdinova EK; Limborskaia SA
    Genetika; 2000 Jun; 36(6):844-8. PubMed ID: 10923268
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan: implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1.
    Pan H; Lin HM; Ku WY; Li TC; Li SY; Lin CC; Hsiao KM
    Eur J Hum Genet; 2001 Aug; 9(8):638-41. PubMed ID: 11528511
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DNA analysis in a suspected individual with myotonic dystrophy family history and her abortus.
    Bi X; Xie H; Zheng H; Ding S; Zhang S; Wang Y; Xu Z; Ren D
    Chin Med J (Engl); 2002 Nov; 115(11):1628-31. PubMed ID: 12609075
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of polymorphism of CTG repetitive sequences in the gene of myotonic dystrophy in human populations of the Volga-Ural region].
    Fatkhlislamova RI; Khidiatova IM; Khusnutdinova EK; Popova SN; Slominskiĭ PA; Limborskaia SA
    Genetika; 1999 Jul; 35(7):988-93. PubMed ID: 10519076
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1.
    Abbruzzese C; Costanzi Porrini S; Mariani B; Gould FK; McAbney JP; Monckton DG; Ashizawa T; Giacanelli M
    Ann Neurol; 2002 Oct; 52(4):435-41. PubMed ID: 12325072
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [DNA analysis of a pedigree with myotonic dystrophy in Songjiang county, Shanghai].
    Xie H; Zheng H; Zheng S; Deng B; Xu J; Cui Y; Wang Y; Xu Z; Ren D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct; 17(5):319-22. PubMed ID: 11024209
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A pedigree with myotonic dystrophy: non-CTG, non-CCTG repeat expansion].
    Zhao XP; Xie HJ; Zheng HM; Yu ZL; Cui Y; Ding SJ; Ren DM; Tang GM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):459-62. PubMed ID: 15476170
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The correlation of CTG repeat length with material and social deprivation in myotonic dystrophy.
    Laberge L; Veillette S; Mathieu J; Auclair J; Perron M
    Clin Genet; 2007 Jan; 71(1):59-66. PubMed ID: 17204048
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.