106 related articles for article (PubMed ID: 11180602)
1. A R644C mutation within lamin A extends the mutations causing dilated cardiomyopathy.
Genschel J; Bochow B; Kuepferling S; Ewert R; Hetzer R; Lochs H; Schmidt H
Hum Mutat; 2001 Feb; 17(2):154. PubMed ID: 11180602
[No Abstract] [Full Text] [Related]
2. 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]
3. Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype.
Charniot JC; Pascal C; Bouchier C; Sébillon P; Salama J; Duboscq-Bidot L; Peuchmaurd M; Desnos M; Artigou JY; Komajda M
Hum Mutat; 2003 May; 21(5):473-81. PubMed ID: 12673789
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin.
Holt I; Clements L; Manilal S; Brown SC; Morris GE
Eur J Hum Genet; 2001 Mar; 9(3):204-8. PubMed ID: 11313760
[TBL] [Abstract][Full Text] [Related]
7. [Diseases associated with lamin A/C gene defects: what the clinical cardiologist ought to know].
Pasotti M; Repetto A; Pisani A; Arbustini E
Ital Heart J Suppl; 2004 Feb; 5(2):98-111. PubMed ID: 15080529
[TBL] [Abstract][Full Text] [Related]
8. Gene symbol: LMNA. Disease: Cardiomyopathy, dilated, with conduction defect 1.
Arbustini Eloisa AE; Pilotto A; Pasotti M; Grasso M; Diegoli M; Campana C; Gavazzi A; Alessandra R; Tavazzi L
Hum Genet; 2005 Jul; 117(2-3):298. PubMed ID: 16156025
[No Abstract] [Full Text] [Related]
9. Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy.
Taylor MR; Slavov D; Gajewski A; Vlcek S; Ku L; Fain PR; Carniel E; Di Lenarda A; Sinagra G; Boucek MM; Cavanaugh J; Graw SL; Ruegg P; Feiger J; Zhu X; Ferguson DA; Bristow MR; Gotzmann J; Foisner R; Mestroni L;
Hum Mutat; 2005 Dec; 26(6):566-74. PubMed ID: 16247757
[TBL] [Abstract][Full Text] [Related]
10. [Mutations of the lamin A/C gene causing familial partial lipodystrophy: significance for the development of hyperlipidemia and insulin resistant diabetes mellitus].
Genschel J; Lochs H; Schmidt HH
Z Gastroenterol; 2000 Apr; 38(4):341-3. PubMed ID: 10820868
[No Abstract] [Full Text] [Related]
11. 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]
12. Expanded spectrum of gene causing both hypertrophic cardiomyopathy and dilated cardiomyopathy.
Morimoto S
Circ Res; 2009 Aug; 105(4):313-5. PubMed ID: 19679850
[No Abstract] [Full Text] [Related]
13. Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement.
Schmidt HH; Lochs H
Circulation; 2001 Jan; 103(4):E20. PubMed ID: 11157732
[No Abstract] [Full Text] [Related]
14. 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]
15. Lamin A/C and cardiac diseases.
Sylvius N; Tesson F
Curr Opin Cardiol; 2006 May; 21(3):159-65. PubMed ID: 16601451
[TBL] [Abstract][Full Text] [Related]
16. Gene symbol: LMNA.
Arbustini E; Pasotti M; Pilotto A; Diegoli M; Brega A; Disabella E; Grasso M; Marziliano N
Hum Genet; 2007 Feb; 120(6):910. PubMed ID: 17438628
[No Abstract] [Full Text] [Related]
17. 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]
18. 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]
19. Gene symbol: CMD1A. Disease: Dilated cardiomyopathy associated with conduction system disease.
Arbustini EA; Pasotti M; Pilotto A; Repetto A; Grasso M; Diegoli M
Hum Genet; 2005 Jul; 117(2-3):295. PubMed ID: 16156018
[No Abstract] [Full Text] [Related]
20. The role of Lamin A/C mutations in Danish patients with idiopathic dilated cardiomyopathy.
Møller DV; Pham TT; Gustafsson F; Hedley P; Ersbøll MK; Bundgaard H; Andersen CB; Torp-Pedersen C; Køber L; Christiansen M
Eur J Heart Fail; 2009 Nov; 11(11):1031-5. PubMed ID: 19875404
[No Abstract] [Full Text] [Related]
[Next] [New Search]
