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Loss of Endothelial Hypoxia Inducible Factor-Prolyl Hydroxylase 2 Induces Cardiac Hypertrophy and Fibrosis.
- Published in:
- 2021
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- Publication type:
- journal article
Guide to forensic pathology practice for death cases related to coronavirus disease 2019 (COVID-19) (Trial draft).
- Published in:
- Forensic Sciences Research, 2020, v. 5, n. 1, p. 1, doi. 10.1080/20961790.2020.1744400
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- Publication type:
- Article
The forensic pathological analysis of sport-related sudden cardiac death in Southern China.
- Published in:
- Forensic Sciences Research, 2020, v. 5, n. 1, p. 47, doi. 10.1080/20961790.2017.1319785
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- Publication type:
- Article
Brugada syndrome: a fatal disease with complex genetic etiologies – still a long way to go.
- Published in:
- Forensic Sciences Research, 2017, v. 2, n. 3, p. 115, doi. 10.1080/20961790.2017.1333203
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- Publication type:
- Article
RAF1 mutation leading to hypertrophic cardiomyopathy in a Chinese family with a history of sudden cardiac death: A diagnostic insight into Noonan syndrome.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2290
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- Publication type:
- Article
Vinculin variant M94I identified in sudden unexplained nocturnal death syndrome decreases cardiac sodium current.
- Published in:
- Scientific Reports, 2017, p. 42953, doi. 10.1038/srep42953
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- Publication type:
- Article
Investigation of the Application of miR10b and miR135b in the Identification of Semen Stains.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0137067
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- Publication type:
- Article
Ursolic Acid Simultaneously Targets Multiple Signaling Pathways to Suppress Proliferation and Induce Apoptosis in Colon Cancer Cells
- Published in:
- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0063872
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- Publication type:
- Article
Analysis of false-positive results of diatom test in the diagnosis of drowning—would not be an impediment.
- Published in:
- International Journal of Legal Medicine, 2019, v. 133, n. 6, p. 1819, doi. 10.1007/s00414-019-02021-4
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- Publication type:
- Article
Genetic diagnosis of acute aortic dissection in South China Han population using next-generation sequencing.
- Published in:
- International Journal of Legal Medicine, 2018, v. 132, n. 5, p. 1273, doi. 10.1007/s00414-018-1890-9
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- Publication type:
- Article
Molecular pathological study on LRRC10 in sudden unexplained nocturnal death syndrome in the Chinese Han population.
- Published in:
- International Journal of Legal Medicine, 2017, v. 131, n. 3, p. 621, doi. 10.1007/s00414-016-1516-z
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- Publication type:
- Article
Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population.
- Published in:
- International Journal of Legal Medicine, 2017, v. 131, n. 1, p. 53, doi. 10.1007/s00414-016-1397-1
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- Publication type:
- Article
Identification of rare variants of DSP gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population.
- Published in:
- International Journal of Legal Medicine, 2016, v. 130, n. 2, p. 317, doi. 10.1007/s00414-015-1275-2
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- Publication type:
- Article
Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in the southern Chinese Han population.
- Published in:
- International Journal of Legal Medicine, 2014, v. 128, n. 6, p. 933, doi. 10.1007/s00414-014-0973-5
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- Publication type:
- Article
Analysis of linkage and linkage disequilibrium for syntenic STRs on 12 chromosomes.
- Published in:
- International Journal of Legal Medicine, 2014, v. 128, n. 5, p. 735, doi. 10.1007/s00414-014-1032-y
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- Publication type:
- Article
Involvement of Mechanosensitive Channel Piezo1 in Renal Fibrosis.
- Published in:
- FASEB Journal, 2021, v. 35, p. N.PAG, doi. 10.1096/fasebj.2021.35.S1.01718
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- Publication type:
- Article
Sudden Unexplained Nocturnal Death Syndrome: The Hundred Years' Enigma.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population.
- Published in:
- Journal of the American Heart Association, 2018, v. 7, n. 1, p. 1, doi. 10.1161/jaha.117.006320
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- Publication type:
- Article
An East Asian Common Variant Vinculin P.Asp841His Was Associated With Sudden Unexplained Nocturnal Death Syndrome in the Chinese Han Population.
- Published in:
- 2017
- By:
- Publication type:
- journal article
SCN5A Rare Variants in Familial Dilated Cardiomyopathy Decrease Peak Sodium Current Depending on the Common Polymorphism H558R and Common Splice Variant Q1077del.
- Published in:
- CTS: Clinical & Translational Science, 2010, v. 3, n. 6, p. 287, doi. 10.1111/j.1752-8062.2010.00249.x
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- Publication type:
- Article
Characteristics of Mechanical Asphyxia: A Retrospective Epidemiological Study in Two Developed Cities in China.
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- Journal of Forensic Science & Medicine, 2023, v. 9, n. 1, p. 57, doi. 10.4103/jfsm.jfsm_45_22
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- Publication type:
- Article
Sudden Cardiac Death and Cardiac Sodium Channel Diseases.
- Published in:
- Journal of Forensic Science & Medicine, 2022, v. 8, n. 4, p. 179, doi. 10.4103/jfsm.jfsm_123_22
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- Publication type:
- Article
HCN4 Gene Variations in Sudden Unexplained Nocturnal Death Syndrome in the Southern Han Chinese Population,.
- Published in:
- Journal of Forensic Sciences, 2019, v. 64, n. 4, p. 1112, doi. 10.1111/1556-4029.13958
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- Publication type:
- Article
The Diagnostic Value of Quantitative Assessment of Diatom Test for Drowning: An Analysis of 128 Water-related Death Cases using Microwave Digestion-Vacuum Filtration-Automated Scanning Electron Microscopy.
- Published in:
- Journal of Forensic Sciences, 2017, v. 62, n. 6, p. 1638, doi. 10.1111/1556-4029.13455
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- Publication type:
- Article
Molecular Autopsy of Desmosomal Protein Plakophilin-2 in Sudden Unexplained Nocturnal Death Syndrome.
- Published in:
- Journal of Forensic Sciences, 2016, v. 61, n. 3, p. 687, doi. 10.1111/1556-4029.13027
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- Publication type:
- Article