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 *

92 related articles for article (PubMed ID: 20929834)

  • 1. Genetics. Exposing a DUX tale.
    Mahadevan MS
    Science; 2010 Sep; 329(5999):1607-8. PubMed ID: 20929834
    [No Abstract]   [Full Text] [Related]  

  • 2. A unifying genetic model for facioscapulohumeral muscular dystrophy.
    Lemmers RJ; van der Vliet PJ; Klooster R; Sacconi S; Camaño P; Dauwerse JG; Snider L; Straasheijm KR; van Ommen GJ; Padberg GW; Miller DG; Tapscott SJ; Tawil R; Frants RR; van der Maarel SM
    Science; 2010 Sep; 329(5999):1650-3. PubMed ID: 20724583
    [TBL] [Abstract][Full Text] [Related]  

  • 3. FSHD: a repeat contraction disease finally ready to expand (our understanding of its pathogenesis).
    Pearson CE
    PLoS Genet; 2010 Oct; 6(10):e1001180. PubMed ID: 21060814
    [No Abstract]   [Full Text] [Related]  

  • 4. The D4Z4 repeat-mediated pathogenesis of facioscapulohumeral muscular dystrophy.
    van der Maarel SM; Frants RR
    Am J Hum Genet; 2005 Mar; 76(3):375-86. PubMed ID: 15674778
    [No Abstract]   [Full Text] [Related]  

  • 5. Pearls in the junk: dissecting the molecular pathogenesis of facioscapulohumeral muscular dystrophy.
    Dmitriev P; Lipinski M; Vassetzky YS
    Neuromuscul Disord; 2009 Jan; 19(1):17-20. PubMed ID: 18974002
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy.
    van Overveld PG; Lemmers RJ; Sandkuijl LA; Enthoven L; Winokur ST; Bakels F; Padberg GW; van Ommen GJ; Frants RR; van der Maarel SM
    Nat Genet; 2003 Dec; 35(4):315-7. PubMed ID: 14634647
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Facioscapulohumeral muscular dystrophy].
    Nakagawa M; Higuchi I
    Ryoikibetsu Shokogun Shirizu; 2001; (35):39-45. PubMed ID: 11555966
    [No Abstract]   [Full Text] [Related]  

  • 8. [Genetics and epigenetics of facio-scapulohumeral progressive (Landouzy-Dejerine) muscular dystrophy].
    Petrov A; Laoudj D; Vasetskiĭ E
    Genetika; 2003 Feb; 39(2):202-6. PubMed ID: 12669415
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.
    Lemmers RJ; de Kievit P; Sandkuijl L; Padberg GW; van Ommen GJ; Frants RR; van der Maarel SM
    Nat Genet; 2002 Oct; 32(2):235-6. PubMed ID: 12355084
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recurrent somatic mosaicism for D4Z4 contractions in a family with facioscapulohumeral muscular dystrophy.
    Buzhov BT; Lemmers RJ; Tournev I; van der Wielen MJ; Ishpekova B; Petkov R; Petrova J; Frants RR; Padberg GW; van der Maarel SM
    Neuromuscul Disord; 2005 Jul; 15(7):471-5. PubMed ID: 15935668
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Facioscapulohumeral muscular dystrophy: molecular pathological advances and future directions.
    Statland JM; Tawil R
    Curr Opin Neurol; 2011 Oct; 24(5):423-8. PubMed ID: 21734574
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy.
    Broucqsault N; Morere J; Gaillard MC; Dumonceaux J; Torrents J; Salort-Campana E; Maues De Paula A; Bartoli M; Fernandez C; Chesnais AL; Ferreboeuf M; Sarda L; Dufour H; Desnuelle C; Attarian S; Levy N; Nguyen K; Magdinier F; Roche S
    Hum Mol Genet; 2013 Oct; 22(20):4206-14. PubMed ID: 23777630
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pushing the genetic frontier with facioscapulohumeral muscular dystrophy.
    Greenberg SA; Padberg GW
    Neurology; 2007 Feb; 68(8):544-5. PubMed ID: 17310022
    [No Abstract]   [Full Text] [Related]  

  • 14. [Facioscapulohumeral muscular dystrophy].
    Wilbers J; Frants RR; van Engelen BG; Padberg GW; van der Maarel SM
    Ned Tijdschr Tandheelkd; 2010 Jan; 117(1):11-4. PubMed ID: 20180344
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy].
    Pikó H; Molnár MJ; Herczegfalvi A; Mayer P; Karcagi V
    Orv Hetil; 2011 Sep; 152(39):1576-85. PubMed ID: 21920844
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Facioscapulohumeral muscular dystrophy.
    Sacconi S; Salviati L; Desnuelle C
    Biochim Biophys Acta; 2015 Apr; 1852(4):607-14. PubMed ID: 24882751
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular combing reveals allelic combinations in facioscapulohumeral dystrophy.
    Nguyen K; Walrafen P; Bernard R; Attarian S; Chaix C; Vovan C; Renard E; Dufrane N; Pouget J; Vannier A; Bensimon A; Lévy N
    Ann Neurol; 2011 Oct; 70(4):627-33. PubMed ID: 22028222
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Facioscapulohumeral muscular dystrophy and limb-girdle muscular dystrophy: "double trouble" overlapping syndrome?
    Simeoni S; Russo V; Gigli GL; Scalise A
    J Neurol Sci; 2015 Jan; 348(1-2):292-3. PubMed ID: 25528007
    [No Abstract]   [Full Text] [Related]  

  • 19. Genomic analysis of facioscapulohumeral muscular dystrophy.
    Clapp J; Bolland DJ; Hewitt JE
    Brief Funct Genomic Proteomic; 2003 Oct; 2(3):213-23. PubMed ID: 15239924
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A functional role for 4qA/B in the structural rearrangement of the 4q35 region and in the regulation of FRG1 and ANT1 in facioscapulohumeral dystrophy.
    Pirozhkova I; Petrov A; Dmitriev P; Laoudj D; Lipinski M; Vassetzky Y
    PLoS One; 2008; 3(10):e3389. PubMed ID: 18852887
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.