BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1036 related articles for article (PubMed ID: 16265841)

  • 1. Myotonic dystrophies.
    Huang CC; Kuo HC
    Chang Gung Med J; 2005 Aug; 28(8):517-26. PubMed ID: 16265841
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.
    Le Ber I; Martinez M; Campion D; Laquerrière A; Bétard C; Bassez G; Girard C; Saugier-Veber P; Raux G; Sergeant N; Magnier P; Maisonobe T; Eymard B; Duyckaerts C; Delacourte A; Frebourg T; Hannequin D
    Brain; 2004 Sep; 127(Pt 9):1979-92. PubMed ID: 15215218
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population.
    Vallo L; Bonifazi E; Borgiani P; Novelli G; Botta A
    Mol Cell Probes; 2005 Feb; 19(1):71-4. PubMed ID: 15652222
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Congenital myotonic dystrophy: variability in muscle involvement and histopathological process.
    Kuo HC; Huang CC; Chu CC; Wai YY; Hsiao KM; Chu NS
    Acta Neurol Taiwan; 2006 Mar; 15(1):13-20. PubMed ID: 16599279
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. DM2 CCTG*CAGG repeats are crossover hotspots that are more prone to expansions than the DM1 CTG*CAG repeats in Escherichia coli.
    Dere R; Wells RD
    J Mol Biol; 2006 Jun; 360(1):21-36. PubMed ID: 16753177
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. Correlation among subcortical white matter lesions, intelligence and CTG repeat expansion in classic myotonic dystrophy type 1.
    Kuo HC; Hsieh YC; Wang HM; Chuang WL; Huang CC
    Acta Neurol Scand; 2008 Feb; 117(2):101-7. PubMed ID: 18184345
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Molecular pathways to myotonic dystrophy].
    Ishiura S
    Nihon Rinsho; 2005 Mar; 63(3):515-21. PubMed ID: 15773354
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Upgrading molecular diagnostics of myotonic dystrophies: multiplexing for simultaneous characterization of the DMPK and ZNF9 repeat motifs.
    Radvansky J; Ficek A; Kadasi L
    Mol Cell Probes; 2011 Aug; 25(4):182-5. PubMed ID: 21550396
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions.
    Hamshere MG; Harley H; Harper P; Brook JD; Brookfield JF
    J Med Genet; 1999 Jan; 36(1):59-61. PubMed ID: 9950368
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Instability in the transmission of the myotonic dystrophy CTG repeat in human oocytes and preimplantation embryos.
    Dean NL; Tan SL; Ao A
    Fertil Steril; 2006 Jul; 86(1):98-105. PubMed ID: 16716318
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans.
    Kim SY; Kim JY; Kim GP; Sung JJ; Lim KS; Lee KW; Chae JH; Hong YH; Seong MW; Park SS
    Korean J Lab Med; 2008 Dec; 28(6):483-92. PubMed ID: 19127114
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Myotonic dystrophy type 1 (DM1): a triplet repeat expansion disorder.
    Kumar A; Agarwal S; Agarwal D; Phadke SR
    Gene; 2013 Jun; 522(2):226-30. PubMed ID: 23570879
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Effect of triplet repeat expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy.
    Frisch R; Singleton KR; Moses PA; Gonzalez IL; Carango P; Marks HG; Funanage VL
    Mol Genet Metab; 2001; 74(1-2):281-91. PubMed ID: 11592825
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Myotonic dystrophy].
    Nanba E
    Nihon Rinsho; 2005 Mar; 63(3):429-33. PubMed ID: 15773341
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RNA pathogenesis of the myotonic dystrophies.
    Day JW; Ranum LP
    Neuromuscul Disord; 2005 Jan; 15(1):5-16. PubMed ID: 15639115
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1.
    Sistiaga A; Urreta I; Jodar M; Cobo AM; Emparanza J; Otaegui D; Poza JJ; Merino JJ; Imaz H; Martí-Massó JF; López de Munain A
    Psychol Med; 2010 Mar; 40(3):487-95. PubMed ID: 19627641
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 52.