160 related articles for article (PubMed ID: 36657711)
1. VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.
Shi HY; Xie MS; Guo YH; Yang CX; Gu JN; Qiao Q; Di RM; Qiu XB; Xu YJ; Yang YQ
Eur J Med Genet; 2023 Mar; 66(3):104705. PubMed ID: 36657711
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Detection and functional characterization of a novel
Qiao Q; Zhao CM; Yang CX; Gu JN; Guo YH; Zhang M; Li RG; Qiu XB; Xu YJ; Yang YQ
Clin Chem Lab Med; 2021 Apr; 59(5):955-963. PubMed ID: 33554560
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy.
Guo YH; Wang J; Guo XJ; Gao RF; Yang CX; Li L; Sun YM; Qiu XB; Xu YJ; Yang YQ
J Am Heart Assoc; 2022 Nov; 11(22):e027578. PubMed ID: 36346048
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy.
Di RM; Yang CX; Zhao CM; Yuan F; Qiao Q; Gu JN; Li XM; Xu YJ; Yang YQ
Eur J Med Genet; 2020 Apr; 63(4):103827. PubMed ID: 31857253
[TBL] [Abstract][Full Text] [Related]
9. Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy.
Xu YJ; Wang ZS; Yang CX; Di RM; Qiao Q; Li XM; Gu JN; Guo XJ; Yang YQ
J Cardiovasc Transl Res; 2019 Jun; 12(3):257-267. PubMed ID: 30536204
[TBL] [Abstract][Full Text] [Related]
10. CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.
Qiu XB; Qu XK; Li RG; Liu H; Xu YJ; Zhang M; Shi HY; Hou XM; Liu X; Yuan F; Sun YM; Wang J; Huang RT; Xue S; Yang YQ
Clin Chem Lab Med; 2017 Aug; 55(9):1417-1425. PubMed ID: 28099117
[TBL] [Abstract][Full Text] [Related]
11. Identification of
Gu JN; Yang CX; Ding YY; Qiao Q; Di RM; Sun YM; Wang J; Yang L; Xu YJ; Yang YQ
Diagnostics (Basel); 2023 Jan; 13(2):. PubMed ID: 36673052
[TBL] [Abstract][Full Text] [Related]
12. Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.
Xu JH; Gu JY; Guo YH; Zhang H; Qiu XB; Li RG; Shi HY; Liu H; Yang XX; Xu YJ; Qu XK; Yang YQ
Int Heart J; 2017 Aug; 58(4):521-529. PubMed ID: 28690296
[TBL] [Abstract][Full Text] [Related]
13. HAND2 loss-of-function mutation causes familial dilated cardiomyopathy.
Liu H; Xu YJ; Li RG; Wang ZS; Zhang M; Qu XK; Qiao Q; Li XM; Di RM; Qiu XB; Yang YQ
Eur J Med Genet; 2019 Sep; 62(9):103540. PubMed ID: 30217752
[TBL] [Abstract][Full Text] [Related]
14. HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy.
Zhou YM; Dai XY; Qiu XB; Yuan F; Li RG; Xu YJ; Qu XK; Huang RT; Xue S; Yang YQ
Clin Chem Lab Med; 2016 Jul; 54(7):1161-7. PubMed ID: 26581070
[TBL] [Abstract][Full Text] [Related]
15. A novel GATA4 loss-of-function mutation responsible for familial dilated cardiomyopathy.
Zhao L; Xu JH; Xu WJ; Yu H; Wang Q; Zheng HZ; Jiang WF; Jiang JF; Yang YQ
Int J Mol Med; 2014 Mar; 33(3):654-60. PubMed ID: 24366163
[TBL] [Abstract][Full Text] [Related]
16. TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy.
Zhang XL; Qiu XB; Yuan F; Wang J; Zhao CM; Li RG; Xu L; Xu YJ; Shi HY; Hou XM; Qu XK; Xu YW; Yang YQ
Biochem Biophys Res Commun; 2015 Mar; 459(1):166-71. PubMed ID: 25725155
[TBL] [Abstract][Full Text] [Related]
17. MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.
Yuan F; Qiu ZH; Wang XH; Sun YM; Wang J; Li RG; Liu H; Zhang M; Shi HY; Zhao L; Jiang WF; Liu X; Qiu XB; Qu XK; Yang YQ
Clin Chem Lab Med; 2018 Feb; 56(3):502-511. PubMed ID: 28902616
[TBL] [Abstract][Full Text] [Related]
18. SOX17 loss-of-function variation underlying familial congenital heart disease.
Zhao L; Jiang WF; Yang CX; Qiao Q; Xu YJ; Shi HY; Qiu XB; Wu SH; Yang YQ
Eur J Med Genet; 2021 May; 64(5):104211. PubMed ID: 33794346
[TBL] [Abstract][Full Text] [Related]
19. A novel TBX20 loss‑of‑function mutation contributes to adult‑onset dilated cardiomyopathy or congenital atrial septal defect.
Zhou YM; Dai XY; Huang RT; Xue S; Xu YJ; Qiu XB; Yang YQ
Mol Med Rep; 2016 Oct; 14(4):3307-14. PubMed ID: 27510170
[TBL] [Abstract][Full Text] [Related]
20. Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy.
Long PA; Larsen BT; Evans JM; Olson TM
J Am Heart Assoc; 2015 Dec; 4(12):. PubMed ID: 26656454
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
