Ling Su
Guangzhou Medical University
7 Papers
30 Citations
Ling Su is an academic researcher from Guangzhou Medical University. The author has contributed to research in topics: PHEX & Gene mutation. The author has an hindex of 3, co-authored 7 publications.
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Papers
The EGFR-P38 MAPK axis up-regulates PD-L1 through miR-675-5p and down-regulates HLA-ABC via hexokinase-2 in hepatocellular carcinoma cells
Zongcai Liu,Fen Ning,Yanna Cai,Huiying Sheng,Ruidan Zheng,Xi Yin,Zhikun Lu,Ling Su,Xiaodan Chen,Chunhua Zeng,Haifang Wang,Li Liu +11 more
TL;DR: In this paper, the authors investigated the impact of EGFR signaling on PD-L1 and human leukocyte antigen class-I (HLA-I) expression in HCC cells and its underlying mechanisms.
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Two homozygous mutations in the exon 5 of BCKDHB gene that may cause the classic form of maple syrup urine disease
TL;DR: The novel homozygous mutation p.Asp173Tyr and the founder homozygus p.Arg168His may be responsible for the clinical presentation of the two CMSUD patients, facilitating the future genetic counselling and prenatal diagnosis.
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Clinical features, BTD gene mutations, and their functional studies of eight symptomatic patients with biotinidase deficiency from Southern China.
Zongcai Liu,Xiaoyuan Zhao,Huiying Sheng,Yanna Cai,Xi Yin,Xiaodan Chen,Ling Su,Zhikun Lu,Chunhua Zeng,Xiuzhen Li,Li Liu +10 more
TL;DR: The clinical features, BTD gene mutations and their functional studies of eight symptomatic children with BTD deficiency from southern China, for the first time, will be helpful in establishing the definitive diagnosis of B TD deficiency at the gene level, offering appropriate genetic counseling, and providing clues to structure/function relationships of the enzyme.
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Clinical and molecular characteristics in 15 patients with androgen receptor gene mutations from South China.
TL;DR: A wide range of spectrum of AIS (from partial AIS to complete AIS) caused by AR mutations in South China population is presented, suggesting that further study with larger data set need to be performed to elucidate the differences of the phenotypes in this study.
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Clinical and biochemical characteristics of patients with ornithine transcarbamylase deficiency.
Minzhi Peng,Xiuzhen Li,Huifen Mei,Huiying Sheng,Xi Yin,Minyan Jiang,Yanna Cai,Ling Su,Yunting Lin,Yongxian Shao,Li Liu +10 more
TL;DR: Unique profiles were observed in each group of OTCD patients, indicating specific physiological changes that happened to them, as indicated by significantly lower levels of protein consumption indicators, including essential AAs, 1-methylhistidine, acylcarnitines et al., but high levels of ammonia.
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