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Ke Wang

Researcher at Capital Medical University

Publications -  53
Citations -  528

Ke Wang is an academic researcher from Capital Medical University. The author has contributed to research in topics: Medicine & Chordoma. The author has an hindex of 13, co-authored 45 publications receiving 409 citations.

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Clinical features and surgical outcomes of patients with skull base chordoma: a retrospective analysis of 238 patients.

TL;DR: Marginal resection, or gross-total resection when possible, should be performed in patients with primary chordomas to achieve better long-term survival, and both tumor location and bone invasion demonstrated clinical value.
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Decreased autophagy in rat heart induced by anti-β1-adrenergic receptor autoantibodies contributes to the decline in mitochondrial membrane potential.

TL;DR: Results suggested that β1-AABs exerted significant decreased ΔΨm, which may contribute to cardiac dysfunction, most likely by decreasing cardiac autophagy in vivo, and myocardial radionuclide imaging technology may be needed to assess the risk in developing cardiac dysfunction for the people who have β1 -AABs in their blood.
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Cardiac Specific Overexpression of Mitochondrial Omi/HtrA2 Induces Myocardial Apoptosis and Cardiac Dysfunction

TL;DR: In vitro and in vivo overexpression of mitochondrial Omi/HtrA2 induces cardiac apoptosis and dysfunction, and strategies to directly inhibit Omi or its cytosolic translocation from mitochondria may protect against heart injury.
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Variations in the protein level of Omi/HtrA2 in the heart of aged rats may contribute to the increased susceptibility of cardiomyocytes to ischemia/reperfusion injury and cell death

TL;DR: It is demonstrated that increased expression and leakage of Omi/HtrA2 enhanced MI/R injury in aging hearts via degrading XIAP and promoting myocardial apoptosis.
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Factors for tumor progression in patients with skull base chordoma.

TL;DR: The nomogram appears useful for risk stratification of tumor progression in primary cases, and it will be necessary to identify the rapid‐growth histopathological subtype as an independent predictor of rapid progression.