Found: 7
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A novel mutation KCNQ1p.Thr312del is responsible for long QT syndrome type 1.
- Published in:
- Heart & Vessels, 2019, v. 34, n. 1, p. 177, doi. 10.1007/s00380-018-1223-4
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- Publication type:
- Article
Semaphorin 3a transfection into the left stellate ganglion reduces susceptibility to ventricular arrhythmias after myocardial infarction in rats.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Psychometric Properties of the Teachers' Sense of Efficacy Scale for Chinese Special Education Teachers.
- Published in:
- Journal of Psychoeducational Assessment, 2021, v. 39, n. 2, p. 212, doi. 10.1177/0734282920946143
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- Publication type:
- Article
[Retracted] Chelerythrine chloride induces apoptosis in renal cancer HEK‑293 and SW‑839 cell lines.
- Published in:
- 2024
- By:
- Publication type:
- Correction Notice
Impact of phosphomimetic and non-phosphorylatable mutations of phospholemman on L-type calcium channels gating in HEK 293T cells.
- Published in:
- Journal of Cellular & Molecular Medicine, 2015, v. 19, n. 3, p. 642, doi. 10.1111/jcmm.12484
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- Publication type:
- Article
Common variants in SCN10A gene associated with Brugada syndrome.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 2, p. 157, doi. 10.1093/hmg/ddab217
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- Publication type:
- Article
Research of Yuanhu Zhitong prescription based on strategy of integrative pharmacology.
- Published in:
- China Journal of Chinese Materia Medica, 2015, v. 40, n. 6, p. 1048, doi. 10.4268/cjcmm20150612
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- Publication type:
- Article