BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 19375354)

  • 1. Ultrastructural pathology of the nuclear envelope in familial lamin A/C cardiomyopathy.
    Diercks GF; van Tintelen JP; Tio RA; Kerstjens-Frederikse WS; Pinto YM; Suurmeijer AJ
    Cardiovasc Pathol; 2010; 19(4):e135-6. PubMed ID: 19375354
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nesprin-1 and actin contribute to nuclear and cytoskeletal defects in lamin A/C-deficient cardiomyopathy.
    Nikolova-Krstevski V; Leimena C; Xiao XH; Kesteven S; Tan JC; Yeo LS; Yu ZY; Zhang Q; Carlton A; Head S; Shanahan C; Feneley MP; Fatkin D
    J Mol Cell Cardiol; 2011 Mar; 50(3):479-86. PubMed ID: 21156181
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation.
    Fidziańska A; Bilińska ZT; Tesson F; Wagner T; Walski M; Grzybowski J; Ruzyłło W; Hausmanowa-Petrusewicz I
    J Neurol Sci; 2008 Aug; 271(1-2):91-6. PubMed ID: 18502446
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
    Fatkin D; MacRae C; Sasaki T; Wolff MR; Porcu M; Frenneaux M; Atherton J; Vidaillet HJ; Spudich S; De Girolami U; Seidman JG; Seidman C; Muntoni F; Müehle G; Johnson W; McDonough B
    N Engl J Med; 1999 Dec; 341(23):1715-24. PubMed ID: 10580070
    [TBL] [Abstract][Full Text] [Related]  

  • 5. In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients.
    Sylvius N; Bilinska ZT; Veinot JP; Fidzianska A; Bolongo PM; Poon S; McKeown P; Davies RA; Chan KL; Tang AS; Dyack S; Grzybowski J; Ruzyllo W; McBride H; Tesson F
    J Med Genet; 2005 Aug; 42(8):639-47. PubMed ID: 16061563
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Expression of an LMNA-N195K variant of A-type lamins results in cardiac conduction defects and death in mice.
    Mounkes LC; Kozlov SV; Rottman JN; Stewart CL
    Hum Mol Genet; 2005 Aug; 14(15):2167-80. PubMed ID: 15972724
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the LMNA gene encoding lamin A/C.
    Genschel J; Schmidt HH
    Hum Mutat; 2000 Dec; 16(6):451-9. PubMed ID: 11102973
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.
    Jakobs PM; Hanson EL; Crispell KA; Toy W; Keegan H; Schilling K; Icenogle TB; Litt M; Hershberger RE
    J Card Fail; 2001 Sep; 7(3):249-56. PubMed ID: 11561226
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The laminopathies: a clinical review.
    Rankin J; Ellard S
    Clin Genet; 2006 Oct; 70(4):261-74. PubMed ID: 16965317
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption.
    Gupta P; Bilinska ZT; Sylvius N; Boudreau E; Veinot JP; Labib S; Bolongo PM; Hamza A; Jackson T; Ploski R; Walski M; Grzybowski J; Walczak E; Religa G; Fidzianska A; Tesson F
    Basic Res Cardiol; 2010 May; 105(3):365-77. PubMed ID: 20127487
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Dilated cardiomyopathy caused by LMNA mutations. Clinical and morphological studies.
    Bilińska ZT; Sylvius N; Grzybowski J; Fidziańska A; Michalak E; Walczak E; Walski M; Bieganowska K; Szymaniak E; Kuśmierczyk-Droszcz B; Lubiszewska B; Wagner T; Tesson F; Ruzyłło W
    Kardiol Pol; 2006 Aug; 64(8):812-9; discussion 820-1. PubMed ID: 16981056
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severe myocardial fibrosis caused by a deletion of the 5' end of the lamin A/C gene.
    van Tintelen JP; Tio RA; Kerstjens-Frederikse WS; van Berlo JH; Boven LG; Suurmeijer AJ; White SJ; den Dunnen JT; te Meerman GJ; Vos YJ; van der Hout AH; Osinga J; van den Berg MP; van Veldhuisen DJ; Buys CH; Hofstra RM; Pinto YM
    J Am Coll Cardiol; 2007 Jun; 49(25):2430-9. PubMed ID: 17599607
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation.
    Hershberger RE; Hanson EL; Jakobs PM; Keegan H; Coates K; Bousman S; Litt M
    Am Heart J; 2002 Dec; 144(6):1081-6. PubMed ID: 12486434
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effects of mechanical stress and carvedilol in lamin A/C-deficient dilated cardiomyopathy.
    Chandar S; Yeo LS; Leimena C; Tan JC; Xiao XH; Nikolova-Krstevski V; Yasuoka Y; Gardiner-Garden M; Wu J; Kesteven S; Karlsdotter L; Natarajan S; Carlton A; Rainer S; Feneley MP; Fatkin D
    Circ Res; 2010 Feb; 106(3):573-82. PubMed ID: 20019332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy.
    Perrot A; Hussein S; Ruppert V; Schmidt HH; Wehnert MS; Duong NT; Posch MG; Panek A; Dietz R; Kindermann I; Böhm M; Michalewska-Wludarczyk A; Richter A; Maisch B; Pankuweit S; Ozcelik C
    Basic Res Cardiol; 2009 Jan; 104(1):90-9. PubMed ID: 18795223
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice.
    Nikolova V; Leimena C; McMahon AC; Tan JC; Chandar S; Jogia D; Kesteven SH; Michalicek J; Otway R; Verheyen F; Rainer S; Stewart CL; Martin D; Feneley MP; Fatkin D
    J Clin Invest; 2004 Feb; 113(3):357-69. PubMed ID: 14755333
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Loss of lamin A/C expression revealed by immuno-electron microscopy in dilated cardiomyopathy with atrioventricular block caused by LMNA gene defects.
    Verga L; Concardi M; Pilotto A; Bellini O; Pasotti M; Repetto A; Tavazzi L; Arbustini E
    Virchows Arch; 2003 Nov; 443(5):664-71. PubMed ID: 12898247
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease.
    Wolf CM; Wang L; Alcalai R; Pizard A; Burgon PG; Ahmad F; Sherwood M; Branco DM; Wakimoto H; Fishman GI; See V; Stewart CL; Conner DA; Berul CI; Seidman CE; Seidman JG
    J Mol Cell Cardiol; 2008 Feb; 44(2):293-303. PubMed ID: 18182166
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
    Bonne G; Mercuri E; Muchir A; Urtizberea A; Bécane HM; Recan D; Merlini L; Wehnert M; Boor R; Reuner U; Vorgerd M; Wicklein EM; Eymard B; Duboc D; Penisson-Besnier I; Cuisset JM; Ferrer X; Desguerre I; Lacombe D; Bushby K; Pollitt C; Toniolo D; Fardeau M; Schwartz K; Muntoni F
    Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.