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 *

151 related articles for article (PubMed ID: 22587749)

  • 1. Severe dilated cardiomyopathy in a patient with myotonic dystrophy type 2 and homozygous repeat expansion in ZNF9.
    Lee TM; Maurer MS; Karbassi I; Braastad C; Batish SD; Chung WK
    Congest Heart Fail; 2012; 18(3):183-6. PubMed ID: 22587749
    [No Abstract]   [Full Text] [Related]  

  • 2. Myotonic dystrophy type 2 is rare in the Japanese population.
    Matsuura T; Minami N; Arahata H; Ohno K; Abe K; Hayashi YK; Nishino I
    J Hum Genet; 2012 Mar; 57(3):219-20. PubMed ID: 22258159
    [No Abstract]   [Full Text] [Related]  

  • 3. Mutant (CCTG)n expansion causes abnormal expression of zinc finger protein 9 (ZNF9) in myotonic dystrophy type 2.
    Raheem O; Olufemi SE; Bachinski LL; Vihola A; Sirito M; Holmlund-Hampf J; Haapasalo H; Li YP; Udd B; Krahe R
    Am J Pathol; 2010 Dec; 177(6):3025-36. PubMed ID: 20971734
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An expansion in the ZNF9 gene causes PROMM in a previously described family with an incidental CLCN1 mutation.
    Lamont PJ; Jacob RL; Mastaglia FL; Laing NG
    J Neurol Neurosurg Psychiatry; 2004 Feb; 75(2):343. PubMed ID: 14742629
    [No Abstract]   [Full Text] [Related]  

  • 5. The unstable CCTG repeat responsible for myotonic dystrophy type 2 originates from an AluSx element insertion into an early primate genome.
    Kurosaki T; Ueda S; Ishida T; Abe K; Ohno K; Matsuura T
    PLoS One; 2012; 7(6):e38379. PubMed ID: 22723857
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Improvement of the diagnostic procedure in proximal myotonic myopathy/myotonic dystrophy type 2.
    Jakubiczka S; Vielhaber S; Kress W; Küpferling P; Reuner U; Kunath B; Wieacker P
    Neurogenetics; 2004 Feb; 5(1):55-9. PubMed ID: 14666402
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical and genetic analysis of a family with PROMM.
    Grewal RP; Zhang S; Ma W; Rosenberg M; Krahe R
    J Clin Neurosci; 2004 Aug; 11(6):603-5. PubMed ID: 15261229
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2.
    Kamsteeg EJ; Kress W; Catalli C; Hertz JM; Witsch-Baumgartner M; Buckley MF; van Engelen BG; Schwartz M; Scheffer H
    Eur J Hum Genet; 2012 Dec; 20(12):1203-8. PubMed ID: 22643181
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Myotonic dystrophy type 2 and related myotonic disorders.
    Meola G; Moxley RT
    J Neurol; 2004 Oct; 251(10):1173-82. PubMed ID: 15503094
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene.
    Sun C; Van Ghelue M; Tranebjærg L; Thyssen F; Nilssen Ø; Torbergsen T
    Clin Genet; 2011 Dec; 80(6):574-80. PubMed ID: 21204798
    [TBL] [Abstract][Full Text] [Related]  

  • 12. RNA Foci, CUGBP1, and ZNF9 are the primary targets of the mutant CUG and CCUG repeats expanded in myotonic dystrophies type 1 and type 2.
    Jones K; Jin B; Iakova P; Huichalaf C; Sarkar P; Schneider-Gold C; Schoser B; Meola G; Shyu AB; Timchenko N; Timchenko L
    Am J Pathol; 2011 Nov; 179(5):2475-89. PubMed ID: 21889481
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Myotonic syndromes.
    Mankodi A; Thornton CA
    Curr Opin Neurol; 2002 Oct; 15(5):545-52. PubMed ID: 12351998
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype.
    Coenen MJ; Tieleman AA; Schijvenaars MM; Leferink M; Ranum LP; Scheffer H; van Engelen BG
    Eur J Hum Genet; 2011 May; 19(5):567-70. PubMed ID: 21224892
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Haploinsuffciency for Znf9 in Znf9+/- mice is associated with multiorgan abnormalities resembling myotonic dystrophy.
    Chen W; Wang Y; Abe Y; Cheney L; Udd B; Li YP
    J Mol Biol; 2007 Apr; 368(1):8-17. PubMed ID: 17335846
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2).
    Botta A; Caldarola S; Vallo L; Bonifazi E; Fruci D; Gullotta F; Massa R; Novelli G; Loreni F
    Biochim Biophys Acta; 2006 Mar; 1762(3):329-34. PubMed ID: 16376058
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2.
    Ranum LP; Day JW
    Curr Neurol Neurosci Rep; 2002 Sep; 2(5):465-70. PubMed ID: 12169228
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinically probable multiple system atrophy with predominant parkinsonism associated with myotonic dystrophy type 2.
    Lim SY; Wadia P; Wenning GK; Lang AE
    Mov Disord; 2009 Jul; 24(9):1407-9. PubMed ID: 19441131
    [No Abstract]   [Full Text] [Related]  

  • 19. ZNF9 activation of IRES-mediated translation of the human ODC mRNA is decreased in myotonic dystrophy type 2.
    Sammons MA; Antons AK; Bendjennat M; Udd B; Krahe R; Link AJ
    PLoS One; 2010 Feb; 5(2):e9301. PubMed ID: 20174632
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.