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 *

382 related articles for article (PubMed ID: 17217858)

  • 21. Alteration of performance in a mouse model of Emery-Dreifuss muscular dystrophy caused by A-type lamins gene mutation.
    Thomasson R; Vignier N; Peccate C; Mougenot N; Noirez P; Muchir A
    Hum Mol Genet; 2019 Jul; 28(13):2237-2244. PubMed ID: 31220270
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy.
    Morris GE; Manilal S
    Hum Mol Genet; 1999; 8(10):1847-51. PubMed ID: 10469836
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Expression of emerin and lamins in muscle of patients with different forms of Emery-Dreifuss muscular dystrophy.
    Niebroj-Dobosz I; Fidzianska A; Hausmanowa-Petrusewicz I
    Acta Myol; 2003 Sep; 22(2):52-7. PubMed ID: 14959564
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Emerin in health and disease.
    Koch AJ; Holaska JM
    Semin Cell Dev Biol; 2014 May; 29():95-106. PubMed ID: 24365856
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Muscle cell differentiation and development pathway defects in Emery-Dreifuss muscular dystrophy.
    Storey EC; Holt I; Morris GE; Fuller HR
    Neuromuscul Disord; 2020 Jun; 30(6):443-456. PubMed ID: 32522500
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy.
    Brown CA; Lanning RW; McKinney KQ; Salvino AR; Cherniske E; Crowe CA; Darras BT; Gominak S; Greenberg CR; Grosmann C; Heydemann P; Mendell JR; Pober BR; Sasaki T; Shapiro F; Simpson DA; Suchowersky O; Spence JE
    Am J Med Genet; 2001 Sep; 102(4):359-67. PubMed ID: 11503164
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.
    Park YE; Hayashi YK; Goto K; Komaki H; Hayashi Y; Inuzuka T; Noguchi S; Nonaka I; Nishino I
    Neuromuscul Disord; 2009 Jan; 19(1):29-36. PubMed ID: 19070492
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy.
    Favreau C; Dubosclard E; Ostlund C; Vigouroux C; Capeau J; Wehnert M; Higuet D; Worman HJ; Courvalin JC; Buendia B
    Exp Cell Res; 2003 Jan; 282(1):14-23. PubMed ID: 12490190
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Emery-Dreifuss muscular dystrophy.
    Helbling-Leclerc A; Bonne G; Schwartz K
    Eur J Hum Genet; 2002 Mar; 10(3):157-61. PubMed ID: 11973618
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Nuclear envelope defects associated with LMNA mutations cause dilated cardiomyopathy and Emery-Dreifuss muscular dystrophy.
    Raharjo WH; Enarson P; Sullivan T; Stewart CL; Burke B
    J Cell Sci; 2001 Dec; 114(Pt 24):4447-57. PubMed ID: 11792810
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Dysfunctional lamins as mediators of oxidative stress in Emery-Dreifuss muscular dystrophy.
    Niebroj-Dobosz I; Sokołowska B; Madej-Pilarczyk A; Marchel M; Hausmanowa-Petrusewicz I
    Folia Neuropathol; 2017; 55(3):193-198. PubMed ID: 28984111
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Increased solubility of lamins and redistribution of lamin C in X-linked Emery-Dreifuss muscular dystrophy fibroblasts.
    Markiewicz E; Venables R; Mauricio-Alvarez-Reyes ; Quinlan R; Dorobek M; Hausmanowa-Petrucewicz I; Hutchison C
    J Struct Biol; 2002; 140(1-3):241-53. PubMed ID: 12490172
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Structural analysis of emerin, an inner nuclear membrane protein mutated in X-linked Emery-Dreifuss muscular dystrophy.
    Wolff N; Gilquin B; Courchay K; Callebaut I; Worman HJ; Zinn-Justin S
    FEBS Lett; 2001 Jul; 501(2-3):171-6. PubMed ID: 11470279
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Emery-Dreifuss muscular dystrophy at the nuclear envelope: 10 years on.
    Ellis JA
    Cell Mol Life Sci; 2006 Dec; 63(23):2702-9. PubMed ID: 17013557
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology.
    Maraldi NM; Lattanzi G; Sabatelli P; Ognibene A; Columbaro M; Capanni C; Rutigliano C; Mattioli E; Squarzoni S
    Eur J Histochem; 2003; 47(1):3-16. PubMed ID: 12685553
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene].
    Onishi Y; Higuchi J; Ogawa T; Namekawa A; Hayashi H; Odakura H; Goto K; Hayashi YK
    Rinsho Shinkeigaku; 2002 Feb; 42(2):140-4. PubMed ID: 12424964
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy.
    Bonne G; Di Barletta MR; Varnous S; Bécane HM; Hammouda EH; Merlini L; Muntoni F; Greenberg CR; Gary F; Urtizberea JA; Duboc D; Fardeau M; Toniolo D; Schwartz K
    Nat Genet; 1999 Mar; 21(3):285-8. PubMed ID: 10080180
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The cell cycle dependent mislocalisation of emerin may contribute to the Emery-Dreifuss muscular dystrophy phenotype.
    Fairley EA; Riddell A; Ellis JA; Kendrick-Jones J
    J Cell Sci; 2002 Jan; 115(Pt 2):341-54. PubMed ID: 11839786
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Emery-Dreifuss dystrophy: a 4-year follow-up on a laminopathy of special interest.
    Hausmanowa-Petrusewicz I; Madej-Pilarczyk A; Marchel M; Opolski G
    Neurol Neurochir Pol; 2009; 43(5):415-20. PubMed ID: 20054742
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Emery-Dreifuss muscular dystrophy - a 40 year retrospective.
    Emery AE
    Neuromuscul Disord; 2000 Jun; 10(4-5):228-32. PubMed ID: 10838246
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.