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1 . Academic Journal
Both gain- and loss-of-function variants of KCNA1 are associated with paroxysmal kinesignic dyskinesia
저자
by
Sun, Wan-Bing
;
Fu, Jing-Xin
;
Chen, Yu-Lan
;
Li, Hong-Fu
;
Wu, Zhi-Ying
, et al.
소스
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Journal of Genetics and Genomics
March 2024
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7 . Academic Journal
Green synthesis of silver nanoparticles using Phlebopus portentosus polysaccharide and their antioxidant, antidiabetic, anticancer, and antimicrobial activities
저자
by
Li, Hong-Fu
;
Pan, Zhang-Chao
;
Chen, Jiao-Man
;
Zeng, Lei-Xia
;
Xie, Hui-Jing
, et al.
소스
In
International Journal of Biological Macromolecules
January 2024 254 Part 1
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7 . Academic Journal
Pathogenicity classification of SOD1 variants of uncertain significance by in vitro aggregation propensity
저자
by
Chen, Lu-Xi
;
Xu, Hai-Feng
;
Lin, Hui-Xia
;
Yang, Xin-Xia
;
Li, Hong-Fu
, et al.
소스
In
Neurobiology of Aging
March 2023 123:182-190
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7 . Academic Journal
A multi-locus linear mixed model methodology for detecting small-effect QTLs for quantitative traits in MAGIC, NAM, and ROAM populations
저자
by
Li, Guo
;
Zhou, Ya-Hui
;
Li, Hong-Fu
;
Zhang, Yuan-Ming
.
소스
In
Computational and Structural Biotechnology Journal
2023 21:2241-2252
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6 . Academic Journal
Associations between neuroanatomical abnormality and motor symptoms in paroxysmal kinesigenic dyskinesia
저자
by
Li, Hong-Fu
;
Yang, Liqin
;
Yin, Dazhi
;
Chen, Wan-Jin
;
Liu, Gong-Lu
, et al.
소스
In
Parkinsonism and Related Disorders
May 2019 62:134-140
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7 . Academic Journal
Novel PLA2G6 mutations and clinical heterogeneity in Chinese cases with phospholipase A2-associated neurodegeneration
저자
by
Chen, Yi-Jun
;
Chen, Yu-Chao
;
Dong, Hai-Lin
;
Li, Li-Xi
;
Ni, Wang
, et al.
소스
In
Parkinsonism and Related Disorders
April 2018 49:88-94
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7 . Academic Journal
Systematic screening and characterization of prototype constituents and metabolites of total astragalosides using HPLC-ESI-IT-TOF-MSn after oral administration to rats
저자
by
Li, Hong-Fu
;
Xu, Feng
;
Yang, Ping
;
Liu, Guang-Xue
;
Shang, Ming-Ying
, et al.
소스
In
Journal of Pharmaceutical and Biomedical Analysis
5 August 2017 142:102-112
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7 . Academic Journal
Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype.
저자
by
Wei, Qiao
;
Yu, Hao
;
Wang, Pei‐Shan
;
Xie, Juan‐Juan
;
Dong, Hai‐Lin
, et al.
소스
CNS Neuroscience & Therapeutics
. Nov2023, p1. 8p. 3 Illustrations, 1 Chart.
Open Access (Wiley)
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7 . Academic Journal
A novel PCYT2 mutation identified in a Chinese consanguineous family with hereditary spastic paraplegia
저자
by
Wei, Qiao
;
Luo, Wen-Jiao
;
Yu, Hao
;
Wang, Pei-Shan
;
Dong, Hai-Lin
, et al.
소스
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Journal of Genetics and Genomics
20 August 2021 48(8):751-754
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7 . Report
Charge resolution in the isochronous mass spectrometry and the mass of $^{51}$Co
저자
by
Zhou, Xu
;
Wang, Meng
;
Zhang, Yu-Hu
;
Xu, Hu-Shan
;
Yuan, You-Jin
, et al.
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Open Access (Arxiv)
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