BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 23071165)

  • 1. Nuclear lamins: functions and clinical implications.
    Cortelli P; Terlizzi R; Capellari S; Benarroch E
    Neurology; 2012 Oct; 79(16):1726-31. PubMed ID: 23071165
    [No Abstract]   [Full Text] [Related]  

  • 2. Expression and localization of nuclear proteins in autosomal-dominant Emery-Dreifuss muscular dystrophy with LMNA R377H mutation.
    Reichart B; Klafke R; Dreger C; Krüger E; Motsch I; Ewald A; Schäfer J; Reichmann H; Müller CR; Dabauvalle MC
    BMC Cell Biol; 2004 Mar; 5():12. PubMed ID: 15053843
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Lamins A and C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy.
    Motsch I; Kaluarachchi M; Emerson LJ; Brown CA; Brown SC; Dabauvalle MC; Ellis JA
    Eur J Cell Biol; 2005 Sep; 84(9):765-81. PubMed ID: 16218190
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Both lamin A and lamin C mutations cause lamina instability as well as loss of internal nuclear lamin organization.
    Broers JL; Kuijpers HJ; Ostlund C; Worman HJ; Endert J; Ramaekers FC
    Exp Cell Res; 2005 Apr; 304(2):582-92. PubMed ID: 15748902
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Nesprin-1 and -2 are involved in the pathogenesis of Emery Dreifuss muscular dystrophy and are critical for nuclear envelope integrity.
    Zhang Q; Bethmann C; Worth NF; Davies JD; Wasner C; Feuer A; Ragnauth CD; Yi Q; Mellad JA; Warren DT; Wheeler MA; Ellis JA; Skepper JN; Vorgerd M; Schlotter-Weigel B; Weissberg PL; Roberts RG; Wehnert M; Shanahan CM
    Hum Mol Genet; 2007 Dec; 16(23):2816-33. PubMed ID: 17761684
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Dysfunction of lamin A triggers a DNA damage response and cellular senescence.
    Lees-Miller SP
    DNA Repair (Amst); 2006 Feb; 5(2):286-9. PubMed ID: 16344005
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phosphorylation of lamins determine their structural properties and signaling functions.
    Torvaldson E; Kochin V; Eriksson JE
    Nucleus; 2015; 6(3):166-71. PubMed ID: 25793944
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lamin A/C assembly defects in Emery-Dreifuss muscular dystrophy can be regulated by culture medium composition.
    Holt I; Nguyen TM; Wehnert M; Morris GE
    Neuromuscul Disord; 2006 Jun; 16(6):368-73. PubMed ID: 16697197
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The nuclear lamins and the nuclear envelope.
    Rzepecki R
    Cell Mol Biol Lett; 2002; 7(4):1019-35. PubMed ID: 12511969
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The nuclear envelope, muscular dystrophy and gene expression.
    Wilson KL
    Trends Cell Biol; 2000 Apr; 10(4):125-9. PubMed ID: 10740265
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery-Dreifuss muscular dystrophy.
    Walter MC; Witt TN; Weigel BS; Reilich P; Richard P; Pongratz D; Bonne G; Wehnert MS; Lochmüller H
    Neuromuscul Disord; 2005 Jan; 15(1):40-4. PubMed ID: 15639119
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice.
    Puckelwartz MJ; Kessler E; Zhang Y; Hodzic D; Randles KN; Morris G; Earley JU; Hadhazy M; Holaska JM; Mewborn SK; Pytel P; McNally EM
    Hum Mol Genet; 2009 Feb; 18(4):607-20. PubMed ID: 19008300
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery-Dreifuss muscular dystrophy.
    Wang Y; Herron AJ; Worman HJ
    Hum Mol Genet; 2006 Aug; 15(16):2479-89. PubMed ID: 16825283
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differentiation of C2C12 myoblasts expressing lamin A mutated at a site responsible for Emery-Dreifuss muscular dystrophy is improved by inhibition of the MEK-ERK pathway and stimulation of the PI3-kinase pathway.
    Favreau C; Delbarre E; Courvalin JC; Buendia B
    Exp Cell Res; 2008 Apr; 314(6):1392-405. PubMed ID: 18294630
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nuclear envelope proteins in health and diseases.
    Bonne G
    Semin Cell Dev Biol; 2014 May; 29():93-4. PubMed ID: 24755165
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 14.