Hui-ying Sheng
9 Jinsui Road
Guangzhou, China
Guangzhou, China
Last Updated: 09/26/2026
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Found 8 publications
Clinical and biochemical characteristics of patients with ornithine transcarbamylase deficiency.
Journal: Clinical biochemistry
Published: April 19, 2020
Simultaneous quantification of 48 plasma amino acids by liquid chromatography-tandem mass spectrometry to investigate urea cycle disorders.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: August 11, 2018
Epidermal growth factor and tumor necrosis factor α cooperatively promote the motility of hepatocellular carcinoma cell lines via synergistic induction of fibronectin by NF-κB/p65.
Journal: Biochimica et biophysica acta. General subjects
Published: June 16, 2017
Identification of a novel pathogenic mutation in PDHA1 gene for pyruvate dehydrogenase complex deficiency
Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: August 20, 2015
A novel ABCD1 gene mutation in a Chinese patient with X-linked adrenoleukodystrophy.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: November 22, 2013
Gene mutations and clinical manifestations in children with glycogen storage disease type Ib
Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: August 23, 2013
Wolman disease with novel mutation of LIPA gene in a Chinese infant
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: November 20, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026