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Functional Characterization of a Spectrum of Novel Romano-Ward Syndrome KCNQ1 Variants.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 2, p. 1350, doi. 10.3390/ijms24021350
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- Article
Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients.
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- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0472-x
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- Article
The Mitochondrial Genome of the Venomous Cone Snail Conus consors.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051528
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- Article
Cardiac Gene Defects Can Cause Sudden Cardiac Death in Young People.
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- Deutsches Ärzteblatt International, 2009, v. 106, n. 4, p. 4
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- Article
Variant interpretation in molecular autopsy: a useful dilemma.
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- International Journal of Legal Medicine, 2022, v. 136, n. 2, p. 475, doi. 10.1007/s00414-021-02764-z
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- Article
Post-mortem genetic investigation of cardiac disease–associated genes in sudden infant death syndrome (SIDS) cases.
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- International Journal of Legal Medicine, 2021, v. 135, n. 1, p. 207, doi. 10.1007/s00414-020-02394-x
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- Article
Changes in gene expression patterns in postmortem human myocardial infarction.
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- International Journal of Legal Medicine, 2020, v. 134, n. 5, p. 1753, doi. 10.1007/s00414-020-02311-2
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- Article
Increased inducible nitric oxide synthase (iNOS) expression in human myocardial infarction.
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- International Journal of Legal Medicine, 2020, v. 134, n. 2, p. 575, doi. 10.1007/s00414-019-02051-y
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- Article
Influence of genetic modifiers on sudden cardiac death cases.
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- International Journal of Legal Medicine, 2018, v. 132, n. 2, p. 379, doi. 10.1007/s00414-017-1739-7
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- Article
Cardiac channelopathy causing sudden death as revealed by molecular autopsy.
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- International Journal of Legal Medicine, 2013, v. 127, n. 1, p. 145, doi. 10.1007/s00414-012-0679-5
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- Article
Biological Activities of Ethanolic Extracts from Deep-Sea Antarctic Marine Sponges.
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- Marine Drugs, 2013, v. 11, n. 4, p. 1126, doi. 10.3390/md11041126
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- Article
Characterization of an N-terminal Na<sub>v</sub>1.5 channel variant – a potential risk factor for arrhythmias and sudden death?
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- BMC Medical Genetics, 2020, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12881-020-01170-3
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- Article
Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function.
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- Pflügers Archiv: European Journal of Physiology, 2016, v. 468, n. 10, p. 1663, doi. 10.1007/s00424-016-1870-1
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- Article
Biological Activities of Aqueous and Organic Extracts from Tropical Marine Sponges.
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- Marine Drugs, 2010, v. 8, n. 5, p. 1550, doi. 10.3390/md8051550
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- Article
Venomous Secretions from Marine Snails of the Terebridae Family Target Acetylcholine Receptors.
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- Toxins, 2013, v. 5, n. 5, p. 1043, doi. 10.3390/toxins5051043
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- Article
Telemedical monitoring in patients with inborn cardiac disease – experience of a tertiary care centre.
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- Mammalian Genome, 2023, v. 34, n. 2, p. 323, doi. 10.1007/s00335-022-09972-x
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- Article
"Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders".
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- BMC Cardiovascular Disorders, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12872-024-04065-w
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- Article
The Evolution of a αD-Conopeptides Targeting Neuronal Nicotinic Acetylcholine Receptors.
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- Acta Chimica Slovenica, 2011, v. 58, n. 4, p. 730
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- Article
Potassium channel TASK-5 forms functional heterodimers with TASK-1 and TASK-3 to break its silence.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51288-8
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- Article