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Min Liang

State Key Laboratory of Non-food Biomass Energy Technology

16H指数
47论文数
787被引数
收录论文 19
发表时间
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Dual defense mechanisms from a novel marine fungus Nigrograna chlamydospora sp. nov. B143: antifungal and anti-aflatoxigenic properties against Aspergillus flavus一种新型海洋真菌Nigrograna chlamydospora sp. nov. B143的双防御机制：对Aspergillus flavus的抗菌和抗黄曲霉毒素生成特性
errFrontiers in Microbiology
IF4.5
err2026-04-03
err0
errOAAI
errXO Xiaoyun Ou; QW Qiaozhen Wang; SH Shushi Huang; YL Youzhi Li; LY Ling Yang; YL Yuening Luo; SW Shaojie Wang; ML Min Liang; LP Lixia Pan; BL Bin Liu; DY Dengfeng Yang
err分享
err收藏
Interpretable Prediction of Late-Stage CKM Syndrome Association From Dietary Nutrients in Accelerated Aging Using SHAP and LIME利用SHAP和LIME解释加速衰老中饮食营养素对晚期CKM综合征关联的预测
errFood Science & Nutrition
IF3.8
err2026-02-17
err0
errOAAI
errTu, Hongxiang; Dai, Meijie; Zhu, Yanying; Liang, Min; Shen, Mo; Chen, Yuehui
err分享
err收藏
Impact of vestibular dysfunction on short - term auditory outcome in severe to profound unilateral idiopathic sudden sensorineural hearing loss: a retrospective analysis前庭功能障碍对重度至极重度特发性突发性感音神经性听力损失短期听觉预后的影响：一项回顾性分析
errACTA OTO-LARYNGOLOGICA
IF1
err2025-12-01
err0
PREAI
errHuang, Sihan; Zhu, Jingyi; Zhang, Jifang; Li, Shuna; Jin, Yulian; Zhang, Qing; Yang, Jun; Liang, Min
err分享
err收藏
Discovery and characterization of a novel alginate lyase PeAly15 and its truncated protein DUF4962 domain from Paenibacillus elgii HSFD1: Elucidation the molecular mechanism of endolytic mode解密一株解淀粉芽孢杆菌（Paenibacillus elgii HSFD1）的新型藻酸盐裂合酶PeAly15及其截短蛋白DUF4962结构域：阐明其内切裂解模式的分子机制
errINTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
IF8.5
err2025-05-01
err0
PREAI
errWei, Quanfeng; Li, Zhenhua; Liang, Min; Shen, Naikun; Pan, Lixia; Jiang, Mingguo; Yang, Dengfeng
err分享
err收藏
Mutation of CRYAB encoding a conserved mitochondrial chaperone and antiapoptotic protein causes hereditary optic atrophy
errJCI INSIGHT
IF6.1
err2024-11-19
err0
errOAAI
errWang, Chenghui; Zhang, Liyao; Nie, Zhipeng; Liang, Min; Liu, Hanqing; Yi, Qiuzi; Wang, Chunyan; Ai, Cheng; Zhang, Juanjuan; Gao, Yinglong; Ji, Yanchun; Guan, Min-Xin; Ai, Cheng; Zhang, Juanjuan; Gao, Yinglong; Ji, Yanchun; Guan, Min-Xin
err分享
err收藏
Mitochondrial tRNA variants in 811 Chinese probands with Leber?s hereditary optic neuropathy
errMitochondrion
IF4.5
err2022-07-01
err4
errOAAI
errJi, Yanchun; Zhang, Juanjuan; Liang, Min; Meng, Feilong; Zhang, Minglian; Mo, Jun Q.; Wang, Meng; Guan, Min-Xin
err分享
err收藏
Leber's hereditary optic neuropathy-associated ND6 14484T > C mutation caused pleiotropic effects on the complex I, RNA homeostasis, apoptosis and mitophagy
errHUMAN MOLECULAR GENETICS
IF3.2
err2022-05-14
err16
PREAI
errLiang, Min; Ji, Yanchun; Zhang, Liyao; Wang, Xuan; Hu, Cuifang; Zhang, Juanjuan; Zhu, Yiwei; Mo, Jun Q.; Guan, Min-Xin
err分享
err收藏
Mechanistic insights into mitochondrial tRNAAla 3′-end metabolism deficiency
errJOURNAL OF BIOLOGICAL CHEMISTRY
IF3.9
err2021-07-01
err21
errOAAI
errJi, Yanchun; Nie, Zhipeng; Meng, Feilong; Hu, Cuifang; Chen, Hui; Jin, Lihao; Chen, Mengquan; Zhang, Minglian; Zhang, Juanjuan; Liang, Min; Wang, Meng; Guan, Min-Xin
err分享
err收藏
Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy
errHUMAN MOLECULAR GENETICS
IF3.2
err2018-12-31
err39
PREAI
errJi, Yanchun; Zhang, Juanjuan; Yu, Jialing; Wang, Ying; Lu, Yuanyuan; Liang, Min; Li, Qiang; Jin, Xiaofen; Wei, Yinsheng; Meng, Feilong; Gao, Yinglong; Cang, Xiaohui; Tong, Yi; Liu, Xiaoling; Zhang, Minglian; Jiang, Peifang; Zhu, Tao; Mo, Jun Qin; Huang, Taosheng; Jiang, Pingping; Guan, Min-Xin
err分享
err收藏
Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation
errHUMAN MOLECULAR GENETICS
IF3.2
err2016-07-17
err35
errOAAI
errJiang, Pingping; Liang, Min; Zhang, Chaofan; Zhao, Xiaoxu; He, Qiufen; Cui, Limei; Liu, Xiaoling; Sun, Yan-Hong; Fu, Qun; Ji, Yanchun; Bai, Yidong; Huang, Taosheng; Guan, Min-Xin
err分享
err收藏
Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2016-05-13
err40
errOAAI
errJi, Yanchun; Liang, Min; Zhang, Juanjuan; Zhu, Ling; Zhang, Zengjun; Fu, Runing; Liu, Xiaoling; Zhang, Minglian; Fu, Qun; Zhao, Fuxin; Tong, Yi; Sun, Yanhong; Jiang, Pingping; Guan, Min-Xin
err分享
err收藏
The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation
errHUMAN MOLECULAR GENETICS
IF3.2
err2015-12-08
err99
errOAAI
errJiang, Pingping; Jin, Xiaofen; Peng, Yanyan; Wang, Meng; Liu, Hao; Liu, Xiaoling; Zhang, Zengjun; Ji, Yanchun; Zhang, Juanjuan; Liang, Min; Zhao, Fuxin; Sun, Yan-Hong; Zhang, Minglian; Zhou, Xiangtian; Chen, Ye; Mo, Jun Qin; Huang, Taosheng; Qu, Jia; Guan, Min-Xin
err分享
err收藏
Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2015-07-25
err50
errOAAI
errJiang, Pingping; Liang, Min; Zhang, Juanjuan; Gao, Yinglong; He, Zheyun; Yu, Han; Zhao, Fuxin; Ji, Yanchun; Liu, Xiaoling; Zhang, Minglian; Fu, Qun; Tong, Yi; Sun, Yanhong; Zhou, Xiangtian; Huang, Taosheng; Qu, Jia; Guan, Min-Xin
err分享
err收藏
Frequency and Spectrum of Mitochondrial ND6 Mutations in 1218 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2014-03-06
err45
PREAI
errLiang, Min; Jiang, Pingping; Li, Feng; Zhang, Juanjuan; Ji, Yanchun; He, Yiqun; Xu, Meifen; Zhu, Jinping; Meng, Xiangjuan; Zhao, Fuxin; Tong, Yi; Liu, Xiaoling; Sun, Yanhong; Zhou, Xiangtian; Mo, Jun Qin; Qu, Jia; Guan, Min-Xin
err分享
err收藏
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families
errMitochondrion
IF4.5
err2013-11-01
err22
PREAI
errZhang, Juanjuan; Zhao, Fuxin; Fu, Qun; Liang, Min; Tong, Yi; Liu, Xiaoling; Lin, Bei; Mi, Hui; Zhang, Minglian; Wei, Qi-Ping; Xue, Ling; Jiang, Pingping; Zhou, Xiangtian; Mo, Jun Qin; Huang, Taosheng; Qu, Jia; Guan, Min-Xin
err分享
err收藏
Leber's Hereditary Optic Neuropathy Is Associated with the T3866C Mutation in Mitochondrial ND1 Gene in Three Han Chinese Families
errINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
IF4.7
err2012-07-09
err41
errOAAI
errZhou, Xiangtian; Qian, Yaping; Zhang, Juanjuan; Tong, Yi; Jiang, Pingping; Liang, Min; Dai, Xianning; Zhou, Huihui; Zhao, Fuxin; Ji, Yanchun; Mo, Jun Qin; Qu, Jia; Guan, Min-Xin
err分享
err收藏
The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation
errMitochondrion
IF4.5
err2011-11-01
err26
PREAI
errQian, Yaping; Zhou, Xiangtian; Liang, Min; Qu, Jia; Guan, Min-Xin
err分享
err收藏
Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation
errMOLECULAR GENETICS AND METABOLISM
IF3.5
err2010-10-01
err42
PREAI
errZhang, Minglian; Zhou, Xiangtian; Li, Chengwu; Zhao, Fuxin; Zhang, Juanjuan; Yuan, Meixia; Sun, Yan-Hong; Wang, Jingzheng; Tong, Yi; Liang, Min; Yang, Li; Cai, Wanshi; Wang, Lifei; Qu, Jia; Guan, Min-Xin
err分享
err收藏
MCVS - Software for simulation of the motion, impact, control of space system with variable structure
errCOMPUTERS & STRUCTURES
IF4.8
err1997-12-01
err0
PREAI
errLiang, M; Hong, JZ
err分享
err收藏

研究方向

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