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Yu Qiang Nie

Researcher at Guangzhou Medical University

Publications -  19
Citations -  403

Yu Qiang Nie is an academic researcher from Guangzhou Medical University. The author has contributed to research in topics: Medicine & DNA methylation. The author has an hindex of 9, co-authored 12 publications receiving 308 citations.

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Association of Fusobacterium nucleatum infection with colorectal cancer in Chinese patients

TL;DR: F. nucleatum was enriched in CRC tissues and associated with CRC development and metastasis and its association with CRC invasiveness in Chinese patients was observed.
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Natural course of nonalcoholic fatty liver disease in southern China: A prospective cohort study

TL;DR: This study aimed to perform a prospective cohort study to investigate NAFLD in a Chinese population, the natural course of which has not been well documented.
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Association between metabolic syndrome and the development of non-alcoholic fatty liver disease.

TL;DR: The diagnosis and the number of components of MS were prospectively associated with the risk of developing non-alcoholic fatty liver disease, suggesting a beneficial effect of intervention at the very early stage of MS on the prevention of NAFLD.
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Overexpression of activated leukocute cell adhesion molecule in gastric cancer is associated with advanced stages and poor prognosis and miR-9 deregulation.

TL;DR: The results of the current study indicated that membranous ALCAM expression and high serum sALCAM levels are independent prognostic markers of poor survival for patients with GC, and that the overexpression of A LCAM may be due to the downregulation of miR‑9.
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Fatty liver mediated by peroxisome proliferator-activated receptor-α DNA methylation can be reversed by a methylation inhibitor and curcumin

TL;DR: The studies in vitro and in vivo aimed to investigate the influence of DNA methylation of peroxisome proliferator activated receptor‐α (PPAR‐α) gene in non‐alcoholic fatty liver disease (NAFLD) pathogenesis and to observe whether theDNA methylation inhibitor 5‐Aza‐2'‐deoxycytidine and the herbal medicine curcumin might reverse the effect both in vivo and in vitro.