Found: 12
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Mapping Chromatin Occupancy of Ppp1r1b-lncRNA Genome-Wide Using Chromatin Isolation by RNA Purification (ChIRP)-seq.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 24, p. 2805, doi. 10.3390/cells12242805
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- Publication type:
- Article
Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in LMOD2 Gene Causing Infantile Dilated Cardiomyopathy.
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- Cells (2073-4409), 2023, v. 12, n. 11, p. 1455, doi. 10.3390/cells12111455
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- Publication type:
- Article
Echocardiographic markers of pulmonary hemodynamics and right ventricular hypertrophy in rat models of pulmonary hypertension.
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- Pulmonary Circulation, 2020, v. 10, n. 2, p. 1, doi. 10.1177/2045894020910976
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- Publication type:
- Article
A novel murine model of atrial fibrillation by diphtheria toxin-induced injury.
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- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.977735
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- Publication type:
- Article
Post-Transcriptional Modification by Alternative Splicing and Pathogenic Splicing Variants in Cardiovascular Development and Congenital Heart Defects.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 2, p. 1555, doi. 10.3390/ijms24021555
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- Publication type:
- Article
High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 10, p. 5469, doi. 10.3390/ijms25105469
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- Article
p38 Mitogen-activated protein kinase regulates chamber-specific perinatal growth in heart.
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- 2020
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- Publication type:
- journal article
Gene-environment regulation of chamber-specific maturation during hypoxemic perinatal circulatory transition.
- Published in:
- Journal of Molecular Medicine, 2020, v. 98, n. 7, p. 1009, doi. 10.1007/s00109-020-01933-8
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- Publication type:
- Article
COVID-19: molecular diagnostics overview.
- Published in:
- Journal of Molecular Medicine, 2020, v. 98, n. 7, p. 947, doi. 10.1007/s00109-020-01931-w
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- Publication type:
- Article
Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot.
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- Journal of Molecular Medicine, 2019, v. 97, n. 12, p. 1711, doi. 10.1007/s00109-019-01857-y
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- Publication type:
- Article
Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara syndrome and unique neuropathologic findings.
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- Epilepsia (Series 4), 2013, v. 54, n. 5, p. e81, doi. 10.1111/epi.12137
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- Publication type:
- Article
Network-basedanalysis reveals thepotential involvement of proteasome subunit alpha-2 in tetralogy of Fallot.
- Published in:
- Physiology & Pharmacology, 2020, v. 24, n. 4, p. 298, doi. 10.32598/ppj.24.4.90
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- Publication type:
- Article