Desheng Liang (D Liang)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2013-2024
Publications (10 Years): 17

Top Venues

International journal of molecular sciences

Biology

Annals of laboratory medicine

BioMed research international

Central South University

Central South University (PHD)

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

Affiliation History

Central South University

China

Professor :: Center for Medical Genetics

Education History

Central South University

China

PHD :: Center for Medical Genetics

Publications

Rou Xiao, Yan Chen, Zhiqing Hu, Qiyu Tang, Peiyun Wang, Miaojin Zhou, Lingqian Wu, Desheng Liang
Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia A. International journal of molecular sciences 25 (7) (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)
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)
Rou Xiao, Yan Chen, Zhiqing Hu, Qiyu Tang, Peiyun Wang, Miaojin Zhou, Lingqian Wu, Desheng Liang
Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia A. International journal of molecular sciences 25 (7) (2024)
Rou Xiao, Yan Chen, Zhiqing Hu, Qiyu Tang, Peiyun Wang, Miaojin Zhou, Lingqian Wu, Desheng Liang
Identification of the Efficient Enhancer Elements in FVIII-Padua for Gene Therapy Study of Hemophilia A. International journal of molecular sciences 25 (7) (2024)
Qiyu Tang, Zhiqing Hu, Junya Zhao, Tao Zhou, Shuqing Tang, Peiyun Wang, Rou Xiao, Yan Chen, Lingqian Wu, Miaojin Zhou, Desheng Liang
CRISPR-Mediated In Situ Introduction or Integration of F9-Padua in Human iPSCs for Gene Therapy of Hemophilia B. International journal of molecular sciences 24 (10) (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)
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)
Zhiqing Hu, Zhuo Li, Yong Wu, Junya Zhao, Lingqian Wu, Miaojin Zhou, Desheng Liang
Targeted B-domain deletion restores F8 function in human endothelial cells and mice. Signal transduction and targeted therapy 7 (1) (2022)
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)
Yiti Zhang, Baitao Zeng, Ao Gu, Qinyu Kang, Mingri Zhao, Guangnan Peng, Miaojin Zhou, Wanxi Liu, Min Liu, Lingjie Ding, Desheng Liang, Xionghao Liu, Mujun Liu
Damaged DNA Is an Early Event of Neurodegeneration in Induced Pluripotent Stem Cell-Derived Motoneurons with UBQLN2 P497H Mutation. International journal of molecular sciences 23 (19) (2022)
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)
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)
K Xia, H Guo, Z Hu, G Xun, L Zuo, Y Peng, K Wang, Y He, Z Xiong, L Sun, Q Pan, Z Long, X Zou, X Li, W Li, X Xu, L Lu, Y Liu, Y Hu, D Tian, L Long, J Ou, Y Liu, X Li, L Zhang, Y Pan, J Chen, H Peng, Q Liu, X Luo, W Su, L Wu, Desheng Liang, H Dai, X Yan, Y Feng, B Tang, J Li, Z Miedzybrodzka, J Xia, Z Zhang, X Luo, X Zhang, D St Clair, J Zhao, F Zhang
Common genetic variants on 1p13.2 associate with risk of autism. Molecular psychiatry 19 (11) (2013)

Desheng Liang.css-eqlu8i{font-size:small;padding-left:4px;} (D Liang)

Publication Activity (10 Years)

Top Topics

Top Venues

Desheng Liang (D Liang)