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John A. Rudd

Researcher at The Chinese University of Hong Kong

Publications -  150
Citations -  3822

John A. Rudd is an academic researcher from The Chinese University of Hong Kong. The author has contributed to research in topics: Ondansetron & Receptor. The author has an hindex of 36, co-authored 142 publications receiving 3387 citations. Previous affiliations of John A. Rudd include University of Bradford & University of Applied Sciences, Kaiserslautern.

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Journal ArticleDOI

The miR-124 regulates the expression of BACE1/β-secretase correlated with cell death in Alzheimer's disease.

TL;DR: Findings suggest that miR-124 may work as a basilic regulating factor to alleviate cell death in the process of AD by targeting BACE1, play an essential role in the control of Bace1 gene expression, and might be considered as a novel therapeutic target in treating AD.
Journal ArticleDOI

Study of the anti-proliferative effects and synergy of phthalides from Angelica sinensis on colon cancer cells.

TL;DR: The three phthalides might have anti-cancer potential, yet the phthalide, in combination with other ingredients in Angelica sinensis extract, display significant synergy leading to a stronger anti-tumor effect.
Journal ArticleDOI

Cytotoxic acylphloroglucinol derivatives from the twigs of Garcinia cowa.

TL;DR: The compounds isolated were evaluated for their cytotoxicity against two cancer cell lines and against normal colon cells, and the results demonstrated their selective toxicity toward the cancer cells.
Journal ArticleDOI

Anti-emetic activity of ghrelin in ferrets exposed to the cytotoxic anti-cancer agent cisplatin.

TL;DR: An ability of ghrelin to reduce emesis is consistent with a role in modulating gastro-intestinal functions and identifies a novel approach to the treatment of emesis.
Book ChapterDOI

The Role of Tachykinins and the Tachykinin NK1 Receptor in Nausea and Emesis

TL;DR: The spectrum of antiemetic effects against stimuli acting via both peripheral and centrally acting emetic stimuli, a requirement for brain penetration and blockade of emesis by microinjection of antagonists into the brain stem all support a central site of action with the nucleus tractus solitarius and the vicinity of the Botzinger complex being the favoured locations although definitive studies are awaited.