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Daniel W. Chan

Researcher at Hong Kong Polytechnic University

Publications -  707
Citations -  47988

Daniel W. Chan is an academic researcher from Hong Kong Polytechnic University. The author has contributed to research in topics: Cancer & Prostate cancer. The author has an hindex of 106, co-authored 663 publications receiving 41915 citations. Previous affiliations of Daniel W. Chan include Merck & Co. & Charité.

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Influence of radical prostatectomy on serum hormone levels

TL;DR: It is suggested that the sexual dysfunction associated with radical prostatectomy cannot be explained by androgen deficiency alone and that the normal prostate and/or prostate neoplasm could secrete a substance or substances that give negative feedback control to pituitary gonadotropin secretion.
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Abnormal type I collagen metabolism by cultured fibroblasts in lethal perinatal osteogenesis imperfecta

TL;DR: Cultured skin fibroblasts from seven consecutive cases of lethal perinatal osteogenesis imperfecta (OI) expressed defects of type I collagen metabolism, and it is postulated that the greater modification of these chains was due to structural defects of the alpha-chains leading to delayed helix formation.

Integrated Proteogenomic Characterization of Human High-Grade Serous Ovarian Cancer

TL;DR: In this article, a detailed analysis of the molecular components and underlying mechanisms associated with ovarian cancer was provided, such as how different copy-number alterna-tions in the Proteome, the proteins associated with chromosomal instability, the sets of signalingpathways that diverse genome rearrangements converge on, and the ones associated with short overall survival.
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Genetic polymorphisms associated with intervertebral disc degeneration

TL;DR: Of the 20 genes analyzed, polymorphisms in vitamin D receptor, aggrecan, Type IX collagen, asporin, MMP3, IL1, and IL6 show the most promise as functional variants.
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Genetics of disc degeneration

TL;DR: The evidence for genetic disposition, the genes or biological processes that are implicated, and the need to consolidate resources and clarify phenotype definition to take advantage of the new technologies in genetic analysis to enhance the understanding of this condition are reviewed.