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Modified N-linked glycosylation status predicts trafficking defective human Piezo1 channel mutations.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02528-w
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- Publication type:
- Article
Analysis of protein sequence and interaction data for candidate disease gene prediction.
- Published in:
- Nucleic Acids Research, 2006, v. 34, n. 19, p. e130, doi. 10.1093/nar/gkl707
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- Publication type:
- Article
RhoA/ROCK Signaling and Pleiotropic α<sub>1A</sub>-Adrenergic Receptor Regulation of Cardiac Contractility.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099024
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- Article
Complexity of Murine Cardiomyocyte miRNA Biogenesis, Sequence Variant Expression and Function.
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- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0030933
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- Publication type:
- Article
Investigation of Association between PFO Complicated by Cryptogenic Stroke and a Common Variant of the Cardiac Transcription Factor GATA4.
- Published in:
- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0020711
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- Publication type:
- Article
Decreased Bone Formation and Osteopenia in Lamin A/C-Deficient Mice.
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- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0019313
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- Publication type:
- Article
Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent.
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- NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00211-x
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- Article
Non‐ischaemic dilated cardiomyopathy: recognising the genetic links.
- Published in:
- Internal Medicine Journal, 2023, v. 53, n. 2, p. 178, doi. 10.1111/imj.15921
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- Publication type:
- Article
Electrophysiologic Characteristics of Accessory Atrioventricular Connections in an Inherited Form of Wolff-Parkinson-White Syndrome.
- Published in:
- Journal of Cardiovascular Electrophysiology, 1999, v. 10, n. 5, p. 629, doi. 10.1111/j.1540-8167.1999.tb00239.x
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- Publication type:
- Article
Regulation of murine cardiac contractility by activation of α1A-adrenergic receptor-operated Ca2+ entry.
- Published in:
- Cardiovascular Research, 2011, v. 91, n. 2, p. 310, doi. 10.1093/cvr/cvr081
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- Publication type:
- Article
Gentrepid V2.0: a web server for candidate disease gene prediction.
- Published in:
- BMC Bioinformatics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2105-14-249
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- Publication type:
- Article
Comparison of automated candidate gene prediction systems using genes implicated in type 2 diabetes by genome-wide association studies.
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- BMC Bioinformatics, 2009, v. 10, p. 1, doi. 10.1186/1471-2105-10-S1-S69
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- Publication type:
- Article
Titin-related Cardiomyopathy: Is it a Distinct Disease?
- Published in:
- Current Cardiology Reports, 2022, v. 24, n. 9, p. 1069, doi. 10.1007/s11886-022-01726-0
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- Publication type:
- Article
A heterozygous variant in the human cardiac miR-133 gene, MIR133A2, alters miRNA duplex processing and strand abundance.
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- BMC Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2156-14-18
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- Publication type:
- Article
Familial dilated cardiomyopathy: Current challenges and future directions.
- Published in:
- Global Cardiology Science & Practice, 2012, v. 2012, n. 1, p. 1, doi. 10.5339/gcsp.2012.8
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- Publication type:
- Article
Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across species.
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- Journal of Cell Biology, 2011, v. 193, n. 7, p. 1181, doi. 10.1083/jcb.201006114
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- Article
Variants of Uncertain Significance and "Missing Pathogenicity".
- Published in:
- 2020
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- Publication type:
- Editorial
Genetic testing in cardiovascular disease.
- Published in:
- Medical Journal of Australia, 2024, v. 220, n. 8, p. 428, doi. 10.5694/mja2.52278
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- Publication type:
- Article
Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations.
- Published in:
- Congenital Heart Disease, 2012, v. 7, n. 2, p. 151, doi. 10.1111/j.1747-0803.2011.00573.x
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- Publication type:
- Article
Loss of Cited2 causes congenital heart disease by perturbing left–right patterning of the body axis.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 6, p. 1097, doi. 10.1093/hmg/ddq554
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- Publication type:
- Article
α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 20, p. 4007, doi. 10.1093/hmg/ddq315
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- Publication type:
- Article
Mutation of HAIRY-AND-ENHANCER-OF-SPLIT-7 in humans causes spondylocostal dysostosis.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 23, p. 3761, doi. 10.1093/hmg/ddn272
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- Publication type:
- Article
Loss of Sec-1 Family Domain-Containing 1 (scfd1) Causes Severe Cardiac Defects and Endoplasmic Reticulum Stress in Zebrafish.
- Published in:
- Journal of Cardiovascular Development & Disease (JCDD), 2023, v. 10, n. 10, p. 408, doi. 10.3390/jcdd10100408
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- Publication type:
- Article