Found: 25
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ISL1 loss-of-function mutation contributes to congenital heart defects.
- Published in:
- Heart & Vessels, 2019, v. 34, n. 4, p. 658, doi. 10.1007/s00380-018-1289-z
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- Article
ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy.
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- Heart & Vessels, 2018, v. 33, n. 7, p. 722, doi. 10.1007/s00380-017-1110-4
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Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy.
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- Clinical Chemistry & Laboratory Medicine, 2021, v. 59, n. 5, p. 955, doi. 10.1515/cclm-2020-1318
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- Article
MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.
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- Clinical Chemistry & Laboratory Medicine, 2018, v. 56, n. 3, p. 502, doi. 10.1515/cclm-2017-0461
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- Article
CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.
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- Clinical Chemistry & Laboratory Medicine, 2017, v. 55, n. 9, p. 1417, doi. 10.1515/cclm-2016-0612
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- Article
HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy.
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- Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 7, p. 1161, doi. 10.1515/cclm-2015-0766
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- Article
A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
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- G3: Genes | Genomes | Genetics, 2016, v. 6, n. 4, p. 987, doi. 10.1534/g3.115.026518
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KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.
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- Genes, 2021, v. 12, n. 3, p. 408, doi. 10.3390/genes12030408
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- Article
A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.
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- Pediatric Cardiology, 2015, v. 36, n. 7, p. 1400, doi. 10.1007/s00246-015-1173-x
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- Article
A Novel NKX2.6 Mutation Associated with Congenital Ventricular Septal Defect.
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- Pediatric Cardiology, 2015, v. 36, n. 3, p. 646, doi. 10.1007/s00246-014-1060-x
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- Article
Impact of prior permanent pacemaker on long-term clinical outcomes of patients undergoing percutaneous coronary intervention.
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- Clinical Cardiology, 2017, v. 40, n. 4, p. 205, doi. 10.1002/clc.22645
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- Article
Microbiota in Gut, Oral Cavity, and Mitral Valves Are Associated With Rheumatic Heart Disease.
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- Frontiers in Cellular & Infection Microbiology, 2021, v. 11, p. N.PAG, doi. 10.3389/fcimb.2021.643092
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- Article
NR2F2 loss-of-function mutation is responsible for congenital bicuspid aortic valve.
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- International Journal of Molecular Medicine, 2019, v. 43, n. 4, p. 1839
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- Article
A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.
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- International Journal of Molecular Medicine, 2015, v. 35, n. 2, p. 478, doi. 10.3892/ijmm.2014.2029
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- Article
NKX2-6 mutation predisposes to familial atrial fibrillation.
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- International Journal of Molecular Medicine, 2014, v. 34, n. 6, p. 1581, doi. 10.3892/ijmm.2014.1971
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- Article
GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy.
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- International Journal of Molecular Medicine, 2014, v. 34, n. 5, p. 1315, doi. 10.3892/ijmm.2014.1896
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- Article
GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve.
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- International Journal of Molecular Medicine, 2014, v. 33, n. 5, p. 1219, doi. 10.3892/ijmm.2014.1700
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- Article
THE VALUE OF TREADMILL EXERCISE TEST PARAMETERS TO PREDICT THE MARATHON PERFORMANCE OF YOUNG AND MIDDLE-AGED RECREATIONAL ATHLETES IN CHINA.
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- Journal of Mechanics in Medicine & Biology, 2020, v. 20, n. 8, p. N.PAG, doi. 10.1142/S0219519420500578
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- Article
Novel GATA6 Mutations Associated with Congenital Ventricular Septal Defect or Tetralogy of Fallot.
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- DNA & Cell Biology, 2012, v. 31, n. 11, p. 1610, doi. 10.1089/dna.2012.1814
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- Article
GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot.
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- Human Mutation, 2013, v. 34, n. 12, p. 1662, doi. 10.1002/humu.22434
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Novel Germline GJA5/Connexin40 Mutations Associated with Lone Atrial Fibrillation Impair Gap Junctional Intercellular Communication.
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- Human Mutation, 2013, v. 34, n. 4, p. 603, doi. 10.1002/humu.22278
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- Article
Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block.
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- Molecular Medicine Reports, 2017, v. 15, n. 4, p. 2247, doi. 10.3892/mmr.2017.6249
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- Article
TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.
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- Molecular Medicine Reports, 2016, v. 13, n. 5, p. 4349, doi. 10.3892/mmr.2016.5043
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Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathy.
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- Molecular Medicine Reports, 2015, v. 12, n. 3, p. 3718, doi. 10.3892/mmr.2015.3843
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- Article
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.
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- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0124409
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- Article