444 related articles for article (PubMed ID: 17416352)
21. Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy.
Gerull B; Gramlich M; Atherton J; McNabb M; Trombitás K; Sasse-Klaassen S; Seidman JG; Seidman C; Granzier H; Labeit S; Frenneaux M; Thierfelder L
Nat Genet; 2002 Feb; 30(2):201-4. PubMed ID: 11788824
[TBL] [Abstract][Full Text] [Related]
22. Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome.
Ruppert V; Nolte D; Aschenbrenner T; Pankuweit S; Funck R; Maisch B
Biochem Biophys Res Commun; 2004 May; 318(2):535-43. PubMed ID: 15120634
[TBL] [Abstract][Full Text] [Related]
23. Familial dilated cardiomyopathy with troponin T K210del mutation.
Martins E; Silva-Cardoso J; Alves C; Pereira H; Soares B; Damasceno A; Abreu-Lima C; Amorim A; Rocha-Gonçalves F
Rev Port Cardiol; 2006 Mar; 25(3):295-300. PubMed ID: 16789403
[TBL] [Abstract][Full Text] [Related]
24. Prevalence of desmin mutations in dilated cardiomyopathy.
Taylor MR; Slavov D; Ku L; Di Lenarda A; Sinagra G; Carniel E; Haubold K; Boucek MM; Ferguson D; Graw SL; Zhu X; Cavanaugh J; Sucharov CC; Long CS; Bristow MR; Lavori P; Mestroni L; ;
Circulation; 2007 Mar; 115(10):1244-51. PubMed ID: 17325244
[TBL] [Abstract][Full Text] [Related]
25. Characterization of recombinant and natural forms of the human LIM domain-containing protein FHL2.
El Mourabit H; Müller S; Tunggal L; Paulsson M; Aumailley M
Protein Expr Purif; 2003 Nov; 32(1):95-103. PubMed ID: 14680945
[TBL] [Abstract][Full Text] [Related]
26. Sarcomeric protein mutations in dilated cardiomyopathy.
Chang AN; Potter JD
Heart Fail Rev; 2005 Sep; 10(3):225-35. PubMed ID: 16416045
[TBL] [Abstract][Full Text] [Related]
27. Evaluation of 15 candidate genes for dilated cardiomyopathy in the Newfoundland dog.
Wiersma AC; Stabej P; Leegwater PA; Van Oost BA; Ollier WE; Dukes-McEwan J
J Hered; 2008; 99(1):73-80. PubMed ID: 17998275
[TBL] [Abstract][Full Text] [Related]
28. Characterization of the canine desmin (DES) gene and evaluation as a candidate gene for dilated cardiomyopathy in the Dobermann.
Stabej P; Imholz S; Versteeg SA; Zijlstra C; Stokhof AA; Domanjko-Petric A; Leegwater PA; van Oost BA
Gene; 2004 Oct; 340(2):241-9. PubMed ID: 15475165
[TBL] [Abstract][Full Text] [Related]
29. [Familial dilated cardiomyopathy: current status and clinical benefits of basic research].
Castro Beiras A; Monserrat L; Hermida M
Rev Esp Cardiol; 2003; 56 Suppl 1():7-12. PubMed ID: 15626357
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. 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]
32. A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.
Yuan F; Qiu XB; Li RG; Qu XK; Wang J; Xu YJ; Liu X; Fang WY; Yang YQ; Liao DN
Int J Mol Med; 2015 Feb; 35(2):478-86. PubMed ID: 25503402
[TBL] [Abstract][Full Text] [Related]
33. Dilated cardiomyopathy mutant tropomyosin mice develop cardiac dysfunction with significantly decreased fractional shortening and myofilament calcium sensitivity.
Rajan S; Ahmed RP; Jagatheesan G; Petrashevskaya N; Boivin GP; Urboniene D; Arteaga GM; Wolska BM; Solaro RJ; Liggett SB; Wieczorek DF
Circ Res; 2007 Jul; 101(2):205-14. PubMed ID: 17556658
[TBL] [Abstract][Full Text] [Related]
34. Identification of a missense mutation in the melusin-encoding ITGB1BP2 gene in a patient with dilated cardiomyopathy.
Ruppert V; Meyer T; Richter A; Maisch B; Pankuweit S;
Gene; 2013 Jan; 512(2):206-10. PubMed ID: 23124043
[TBL] [Abstract][Full Text] [Related]
35. Evaluation of the titin-cap gene (TCAP) as candidate for dilated cardiomyopathy in Irish wolfhounds.
Philipp U; Vollmar A; Distl O
Anim Biotechnol; 2008; 19(4):231-6. PubMed ID: 18855248
[TBL] [Abstract][Full Text] [Related]
36. Characterization of human FHL2 transcript variants and gene expression regulation in hepatocellular carcinoma.
Ng CF; Zhou WJ; Ng PK; Li MS; Ng YK; Lai PB; Tsui SK
Gene; 2011 Jul; 481(1):41-7. PubMed ID: 21540083
[TBL] [Abstract][Full Text] [Related]
37. A mutation in the glutamate-rich region of RNA-binding motif protein 20 causes dilated cardiomyopathy through missplicing of titin and impaired Frank-Starling mechanism.
Beqqali A; Bollen IA; Rasmussen TB; van den Hoogenhof MM; van Deutekom HW; Schafer S; Haas J; Meder B; Sørensen KE; van Oort RJ; Mogensen J; Hubner N; Creemers EE; van der Velden J; Pinto YM
Cardiovasc Res; 2016 Oct; 112(1):452-63. PubMed ID: 27496873
[TBL] [Abstract][Full Text] [Related]
38. Cardiomyopathy in zebrafish due to mutation in an alternatively spliced exon of titin.
Xu X; Meiler SE; Zhong TP; Mohideen M; Crossley DA; Burggren WW; Fishman MC
Nat Genet; 2002 Feb; 30(2):205-9. PubMed ID: 11788825
[TBL] [Abstract][Full Text] [Related]
39. [Dilated cardiomyopathy: etiology, clinical criteria for diagnosis and screening of the familial form].
Startari U; Taylor MR; Sinagra G; Di Lenarda A; Mestroni L
Ital Heart J Suppl; 2002 Apr; 3(4):378-85. PubMed ID: 12025380
[TBL] [Abstract][Full Text] [Related]
40. Modulation of aryl hydrocarbon receptor activity by four and a half LIM domain 2.
Kollara A; Brown TJ
Int J Biochem Cell Biol; 2009 May; 41(5):1182-8. PubMed ID: 19015043
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
