Detalles de la búsqueda
1.
Myocardial tissue-specific Dnmt1 knockout in rats protects against pathological injury induced by Adriamycin.
Lab Invest
; 100(7): 974-985, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32051532
2.
Familial hypertrophic cardiomyopathy caused by a de novo Gly716Arg mutation of the ß-myosin heavy chain.
Cardiol Young
; 27(3): 467-472, 2017 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-27161882
3.
Cardiac-specific Trim44 knockout in rat attenuates isoproterenol-induced cardiac remodeling via inhibition of AKT/mTOR pathway.
Dis Model Mech
; 16(5)2023 05 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35855640
4.
Different clinical characteristics and outcomes of hypertrophic cardiomyopathy with and without hypertension: seeking the truth.
J Geriatr Cardiol
; 20(2): 109-120, 2023 Feb 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-36910243
5.
Using machine learning to aid treatment decision and risk assessment for severe three-vessel coronary artery disease.
J Geriatr Cardiol
; 19(5): 367-376, 2022 May 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-35722036
6.
[Comparison of clinical characteristics of Chinese patients with apical hypertrophic cardiomyopathy and typical hypertrophic cardiomyopathy].
Zhonghua Xin Xue Guan Bing Za Zhi
; 39(3): 228-32, 2011 Mar.
Artículo
en Zh
| MEDLINE | ID: mdl-21609527
7.
[The genotype-phenotype correlation of the MYH7 gene c.1273G > a mutation in familial hypertrophic cardiomyopathy].
Yi Chuan
; 31(5): 485-8, 2009 May.
Artículo
en Zh
| MEDLINE | ID: mdl-19586842
8.
[A novel hot-spot mutation S236G in the cardiac myosin binding protein C gene in Chinese patient with hypertrophic cardiomyopathy].
Zhonghua Xin Xue Guan Bing Za Zhi
; 37(12): 1078-80, 2009 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-20193176
9.
Han Chinese family with early-onset Parkinson's disease carries novel compound heterozygous mutations in the PARK2 gene.
Brain Behav
; 9(9): e01372, 2019 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-31386307
10.
[Genetic heterogeneity of myosin heavy chain 7 gene G823E mutation in familial hypertrophic cardiomyopathy in Chinese].
Zhonghua Yi Xue Za Zhi
; 88(44): 3120-2, 2008 Dec 02.
Artículo
en Zh
| MEDLINE | ID: mdl-19159593
11.
[The genotype-phenotype correlation of MYH7 gene G15391A mutation and MYBPC3 gene G12101A mutation in familial hypertrophic cardiomyopathy].
Zhonghua Xin Xue Guan Bing Za Zhi
; 36(12): 1059-62, 2008 Dec.
Artículo
en Zh
| MEDLINE | ID: mdl-19134269
12.
[Family hypertrophic cardiomyopathy caused by a 14035c > t mutation in cardiac troponin T gene].
Zhonghua Yi Xue Za Zhi
; 87(6): 371-4, 2007 Feb 06.
Artículo
en Zh
| MEDLINE | ID: mdl-17456375
13.
[Clinical features of dilated cardiomyopathy-like hypertrophic cardiomyopathy caused by a 13261 G > A mutation in cardiac myosin-binding protein C gene].
Zhonghua Xin Xue Guan Bing Za Zhi
; 35(1): 17-20, 2007 Jan.
Artículo
en Zh
| MEDLINE | ID: mdl-17386157
14.
[Familiar hypertrophic cardiomyopathy caused by a IVS15-1G > A mutation in cardiac myosin-binding protein C gene].
Zhonghua Xin Xue Guan Bing Za Zhi
; 34(8): 699-702, 2006 Aug.
Artículo
en Zh
| MEDLINE | ID: mdl-17081393
15.
[A novel LMNA gene mutation E82K associated with familial dilated cardiomyopathy].
Zhonghua Xin Xue Guan Bing Za Zhi
; 33(10): 875-9, 2005 Oct.
Artículo
en Zh
| MEDLINE | ID: mdl-16266469
16.
Myocardial bridging as a common phenotype of hypertrophic cardiomyopathy has no effect on prognosis.
Am J Med Sci
; 347(6): 429-33, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24270076
17.
Screening of pathogenic genes in Chinese patients with arrhythmogenic right ventricular cardiomyopathy.
Chin Med J (Engl)
; 126(22): 4238-41, 2013 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-24238504
18.
Methylation of FOXP3 in regulatory T cells is related to the severity of coronary artery disease.
Atherosclerosis
; 228(2): 346-52, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23566804
Resultados
1 -
18
de 18
1
Próxima >
>>