Zhuo Li

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Venues

International journal of molecular sciences

Molecular genetics & genomic medicine

Oral diseases

Biology

Central South University

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Central South University Jan 01 2001

China

Assistant Professor :: Center for Medical Genetics

Publications

Hua Teng, Siyi Chen, Fang Liu, Yanling Teng, Yunlong Li, Desheng Liang, Lingqian Wu, Zhuo Li
O-Sialoglycoprotein Endopeptidase Deficiency Impairs Proteostasis and Induces Autophagy in Human Embryonic Stem Cells. International journal of molecular sciences 25 (14) (2024)
Hua Teng, Siyi Chen, Fang Liu, Yanling Teng, Yunlong Li, Desheng Liang, Lingqian Wu, Zhuo Li
O-Sialoglycoprotein Endopeptidase Deficiency Impairs Proteostasis and Induces Autophagy in Human Embryonic Stem Cells. International journal of molecular sciences 25 (14) (2024)
Hua Teng, Siyi Chen, Fang Liu, Yanling Teng, Yunlong Li, Desheng Liang, Lingqian Wu, Zhuo Li
O-Sialoglycoprotein Endopeptidase Deficiency Impairs Proteostasis and Induces Autophagy in Human Embryonic Stem Cells. International journal of molecular sciences 25 (14) (2024)
Hua Teng, Siyi Chen, Fang Liu, Yanling Teng, Yunlong Li, Desheng Liang, Lingqian Wu, Zhuo Li
O-Sialoglycoprotein Endopeptidase Deficiency Impairs Proteostasis and Induces Autophagy in Human Embryonic Stem Cells. International journal of molecular sciences 25 (14) (2024)
Menglin Li, Zhuo Li, Miaomiao Chen, Zhiqing Hu, Miaojin Zhou, Lingqian Wu, Chunhua Zhang, Desheng Liang
Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism. International journal of molecular sciences 24 (1) (2023)
Menglin Li, Zhuo Li, Miaomiao Chen, Zhiqing Hu, Miaojin Zhou, Lingqian Wu, Chunhua Zhang, Desheng Liang
Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism. International journal of molecular sciences 24 (1) (2023)
Menglin Li, Zhuo Li, Miaomiao Chen, Zhiqing Hu, Miaojin Zhou, Lingqian Wu, Chunhua Zhang, Desheng Liang
Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism. International journal of molecular sciences 24 (1) (2023)
Qin Xing, Qimin Zhou, Hongyan Li, Zhongjie Wang, Shun Li, Jiayu Wu, Huimin Zhu, Desheng Liang, Zhuo Li, Lingqian Wu
Identification of six novel mutations in EDA from 20 hypohidrotic ectodermal dysplasia families. Oral diseases (2023)
Menglin Li, Zhuo Li, Miaomiao Chen, Zhiqing Hu, Miaojin Zhou, Lingqian Wu, Chunhua Zhang, Desheng Liang
Novel Missense Variants in PAX8 and NKX2-1 Cause Congenital Hypothyroidism. International journal of molecular sciences 24 (1) (2023)
Hongyan Li, Fang Liu, Hanzhe Kuang, Hua Teng, Siyi Chen, Sijing Zeng, Qimin Zhou, Zhaokai Li, Desheng Liang, Zhuo Li, Lingqian Wu
WDR73 Depletion Destabilizes PIP4K2C Activity and Impairs Focal Adhesion Formation in Galloway-Mowat Syndrome. Biology 11 (10) (2022)
Xuefei Li, Zhuo Li, Miao Yang, Yan Luo, Li Hu, Zhi Xiao, Aji Huang, Juan Huang
Two tSNPs in BRIP1 are associated with breast cancer during TDT analysis. Molecular genetics & genomic medicine 9 (2) (2021)
Jing Liu, Qin Liu, Shuting Yang, Na Ma, Jialun Pang, Ying Peng, Hui Xi, Zhengjun Jia, Yingchun Luo, Meiping Jiang, Yanling Teng, Wenxian Yu, Zhuo Li, Hua Wang
Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review. Molecular genetics & genomic medicine 9 (8) (2021)
Jianyan Pan, Chunhua Zhang, Yanling Teng, Sijing Zeng, Siyi Chen, Desheng Liang, Zhuo Li, Lingqian Wu
Detection of Spinal Muscular Atrophy Using a Duplexed Real-Time PCR Approach With Locked Nucleic Acid-Modified Primers. Annals of laboratory medicine 41 (1) (2020)
Jing Liu, Pengsiyuan Lin, Jialun Pang, Zhengjun Jia, Ying Peng, Hui Xi, Lingqian Wu, Zhuo Li, Hua Wang
Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome. Molecular genetics & genomic medicine 8 (8) (2020)
Siyuan Linpeng, Jing Liu, Jianyan Pan, Yingxi Cao, Yanling Teng, Desheng Liang, Zhuo Li, Lingqian Wu
Diagnosis of Joubert Syndrome 10 in a Fetus with Suspected Dandy-Walker Variant by WES: A Novel Splicing Mutation in OFD1. BioMed research international 2018 (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Zhuo Li