161 related articles for article (PubMed ID: 30794913)
1. The R9H phospholamban mutation is associated with highly penetrant dilated cardiomyopathy and sudden death in a spontaneous canine model.
Yost O; Friedenberg SG; Jesty SA; Olby NJ; Meurs KM
Gene; 2019 May; 697():118-122. PubMed ID: 30794913
[TBL] [Abstract][Full Text] [Related]
2. A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death.
Meurs KM; Friedenberg SG; Kolb J; Saripalli C; Tonino P; Woodruff K; Olby NJ; Keene BW; Adin DB; Yost OL; DeFrancesco TC; Lahmers S; Tou S; Shelton GD; Granzier H
Hum Genet; 2019 May; 138(5):515-524. PubMed ID: 30715562
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Genetic deletion of arginine 14 in phospholamban causes dilated cardiomyopathy with attenuated electrocardiographic R amplitudes.
Posch MG; Perrot A; Geier C; Boldt LH; Schmidt G; Lehmkuhl HB; Hetzer R; Dietz R; Gutberlet M; Haverkamp W; Ozcelik C
Heart Rhythm; 2009 Apr; 6(4):480-6. PubMed ID: 19324307
[TBL] [Abstract][Full Text] [Related]
5. Evaluation of the phospholamban gene in purebred large-breed dogs with dilated cardiomyopathy.
Stabej P; Leegwater PA; Stokhof AA; Domanjko-Petric A; van Oost BA
Am J Vet Res; 2005 Mar; 66(3):432-6. PubMed ID: 15822587
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Next-generation sequencing identifies a homozygous mutation in ACADVL associated with pediatric familial dilated cardiomyopathy.
Carlus SJ; Almuzaini IS; Karthikeyan M; Loganathan L; Al-Harbi GS; Abdallah AM; Al-Harbi KM
Eur Rev Med Pharmacol Sci; 2019 Feb; 23(4):1710-1721. PubMed ID: 30840296
[TBL] [Abstract][Full Text] [Related]
8. Familial Dilated Cardiomyopathy and Sudden Cardiac Arrest: New Association with a
Rico Y; Ramis MF; Massot M; Torres-Juan L; Pons J; Fortuny E; Ripoll-Vera T; González R; Peral V; Rossello X; Heine Suñer D
Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946838
[TBL] [Abstract][Full Text] [Related]
9. Mutation analysis of the phospholamban gene in 315 South Africans with dilated, hypertrophic, peripartum and arrhythmogenic right ventricular cardiomyopathies.
Fish M; Shaboodien G; Kraus S; Sliwa K; Seidman CE; Burke MA; Crotti L; Schwartz PJ; Mayosi BM
Sci Rep; 2016 Feb; 6():22235. PubMed ID: 26917049
[TBL] [Abstract][Full Text] [Related]
10. [Association between phospholamban gene mutation and dilated cardiomyopathy in the Chengdu area].
Chen XY; Rao L; Zhou B; Zhang L; Chen H; Wang YP; Wang B
Sichuan Da Xue Xue Bao Yi Xue Ban; 2005 Sep; 36(5):683-5. PubMed ID: 16235537
[TBL] [Abstract][Full Text] [Related]
11. GATA5 loss-of-function mutation in familial dilated cardiomyopathy.
Zhang XL; Dai N; Tang K; Chen YQ; Chen W; Wang J; Zhao CM; Yuan F; Qiu XB; Qu XK; Yang YQ; Xu YW
Int J Mol Med; 2015 Mar; 35(3):763-70. PubMed ID: 25543888
[TBL] [Abstract][Full Text] [Related]
12. A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death.
Pérez-Serra A; Toro R; Campuzano O; Sarquella-Brugada G; Berne P; Iglesias A; Mangas A; Brugada J; Brugada R
J Card Fail; 2015 Mar; 21(3):217-25. PubMed ID: 25498755
[TBL] [Abstract][Full Text] [Related]
13. A missense mutation in the CHRM2 gene is associated with familial dilated cardiomyopathy.
Zhang L; Hu A; Yuan H; Cui L; Miao G; Yang X; Wang L; Liu J; Liu X; Wang S; Zhang Z; Liu L; Zhao R; Shen Y
Circ Res; 2008 Jun; 102(11):1426-32. PubMed ID: 18451336
[TBL] [Abstract][Full Text] [Related]
14. Exome Sequencing Identifies a Novel DES Mutation (R227C) in a Chinese Dilated Cardiomyopathy Family.
Yu R; Liu L; Chen C; Shen JM
Cardiology; 2017; 137(2):78-82. PubMed ID: 28171858
[TBL] [Abstract][Full Text] [Related]
15. A novel splicing variant in FLNC gene responsible for a highly penetrant familial dilated cardiomyopathy in an extended Iranian family.
Nozari A; Aghaei-Moghadam E; Zeinaloo A; Mollazadeh R; Majnoon MT; Alavi A; Ghasemi Firouzabadi S; Mohammadzadeh A; Banihashemi S; Nikzaban M; Najmabadi H; Behjati F
Gene; 2018 Jun; 659():160-167. PubMed ID: 29551499
[TBL] [Abstract][Full Text] [Related]
16. Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
Fernlund E; Österberg AW; Kuchinskaya E; Gustafsson M; Jansson K; Gunnarsson C
Pediatr Cardiol; 2017 Aug; 38(6):1262-1268. PubMed ID: 28669108
[TBL] [Abstract][Full Text] [Related]
17. ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy.
Sun YM; Wang J; Xu YJ; Wang XH; Yuan F; Liu H; Li RG; Zhang M; Li YJ; Shi HY; Zhao L; Qiu XB; Qu XK; Yang YQ
Heart Vessels; 2018 Jul; 33(7):722-732. PubMed ID: 29445930
[TBL] [Abstract][Full Text] [Related]
18. Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience.
van Spaendonck-Zwarts KY; van Rijsingen IA; van den Berg MP; Lekanne Deprez RH; Post JG; van Mil AM; Asselbergs FW; Christiaans I; van Langen IM; Wilde AA; de Boer RA; Jongbloed JD; Pinto YM; van Tintelen JP
Eur J Heart Fail; 2013 Jun; 15(6):628-36. PubMed ID: 23349452
[TBL] [Abstract][Full Text] [Related]
19. TBX20 loss-of-function mutation associated with familial dilated cardiomyopathy.
Zhao CM; Bing-Sun ; Song HM; Wang J; Xu WJ; Jiang JF; Qiu XB; Yuan F; Xu JH; Yang YQ
Clin Chem Lab Med; 2016 Feb; 54(2):325-32. PubMed ID: 26118961
[TBL] [Abstract][Full Text] [Related]
20. An
Furrow E; Tate N; Minor K; Martinson S; Larrabee S; Anttila M; Sleeper M; Henthorn P
Genes (Basel); 2023 Apr; 14(5):. PubMed ID: 37239348
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]