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 *

155 related articles for article (PubMed ID: 28810563)

  • 21. [From gene to disease; altered RNA processing as a cause of myotonic dystrophy type 1].
    de Die-Smulders CE; Faber CG; Smeets HJ
    Ned Tijdschr Geneeskd; 2005 Sep; 149(37):2043-6. PubMed ID: 16184945
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Myotonic dystrophies: clinical presentation, pathogenesis, diagnostics and therapy].
    Finsterer J; Rudnik-Schöneborn S
    Fortschr Neurol Psychiatr; 2015 Jan; 83(1):9-17. PubMed ID: 25602187
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Targeting DMPK with Antisense Oligonucleotide Improves Muscle Strength in Myotonic Dystrophy Type 1 Mice.
    Jauvin D; Chrétien J; Pandey SK; Martineau L; Revillod L; Bassez G; Lachon A; MacLeod AR; Gourdon G; Wheeler TM; Thornton CA; Bennett CF; Puymirat J
    Mol Ther Nucleic Acids; 2017 Jun; 7():465-474. PubMed ID: 28624222
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Myotonic dystrophy protein kinase (DMPK) gene expression in lymphocytes of patients with myotonic dystrophy.
    Depardon F; Cisneros B; Alonso-Vilatela E; Montañez C
    Arch Med Res; 2001; 32(2):123-8. PubMed ID: 11343809
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studies.
    Meola G; Sansone V; Radice S; Skradski S; Ptacek L
    Neuromuscul Disord; 1996 May; 6(3):143-50. PubMed ID: 8784800
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Localization of DM-PK in normal and myotonic dystrophy muscles].
    Tachi N; Ohya K
    Nihon Rinsho; 1997 Dec; 55(12):3210-3. PubMed ID: 9436438
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Myotonic dystrophy type 1 patient-derived iPSCs for the investigation of CTG repeat instability.
    Ueki J; Nakamori M; Nakamura M; Nishikawa M; Yoshida Y; Tanaka A; Morizane A; Kamon M; Araki T; Takahashi MP; Watanabe A; Inagaki N; Sakurai H
    Sci Rep; 2017 Feb; 7():42522. PubMed ID: 28211918
    [TBL] [Abstract][Full Text] [Related]  

  • 30. CTG-repeat length in distal and proximal leg muscles of symptomatic and non-symptomatic patients with myotonic dystrophy: relation to muscle strength and degree of histopathological abnormalities.
    Hedberg B; Anvret M; Ansved T
    Eur J Neurol; 1999 May; 6(3):341-6. PubMed ID: 10210916
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Somatic mosaicism of p(CTG)n expansion in a case of myotonic dystrophy with parotid tumor].
    Ogata K; Takahashi A; Oguchi N; Ishitoya J; Fuse S; Shimpo T
    Rinsho Shinkeigaku; 1998 Aug; 38(8):736-8. PubMed ID: 9916519
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy.
    Winchester CL; Ferrier RK; Sermoni A; Clark BJ; Johnson KJ
    Hum Mol Genet; 1999 Mar; 8(3):481-92. PubMed ID: 9949207
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Muscle wasting in myotonic dystrophies: a model of premature aging.
    Mateos-Aierdi AJ; Goicoechea M; Aiastui A; Fernández-Torrón R; Garcia-Puga M; Matheu A; López de Munain A
    Front Aging Neurosci; 2015; 7():125. PubMed ID: 26217220
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.
    Seznec H; Agbulut O; Sergeant N; Savouret C; Ghestem A; Tabti N; Willer JC; Ourth L; Duros C; Brisson E; Fouquet C; Butler-Browne G; Delacourte A; Junien C; Gourdon G
    Hum Mol Genet; 2001 Nov; 10(23):2717-26. PubMed ID: 11726559
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Idiopathic ventricular fibrillation and the V1764fsX1786 frameshift mutation of the SCN5A gene in a myotonic dystrophy type 1 patient.
    Shimoyama T; Hayashi H; Suzuki F; Nishiyama Y; Miyamoto Y; Aiba T; Shimizu W; Kimura K
    J Clin Neurosci; 2020 Apr; 74():242-244. PubMed ID: 32063450
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Novel heat pulse extension-PCR-based method for detection of large CTG-repeat expansions in myotonic dystrophy type 1.
    Orpana AK; Ho TH; Alagrund K; Ridanpää M; Aittomäki K; Stenman J
    J Mol Diagn; 2013 Jan; 15(1):110-5. PubMed ID: 23159592
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts.
    Sarkar PS; Appukuttan B; Han J; Ito Y; Ai C; Tsai W; Chai Y; Stout JT; Reddy S
    Nat Genet; 2000 May; 25(1):110-4. PubMed ID: 10802668
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Mechanisms of skeletal muscle wasting in a mouse model for myotonic dystrophy type 1.
    Morriss GR; Rajapakshe K; Huang S; Coarfa C; Cooper TA
    Hum Mol Genet; 2018 Aug; 27(16):2789-2804. PubMed ID: 29771332
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.