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Hong-Fu Li

Showing results (1-10 of 70) with videos related to

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Translational Neurodegeneration|February 5, 2016
Genotype-phenotype correlations of amyotrophic lateral sclerosisHong-Fu Li, Zhi-Ying Wu
Neuroscience Bulletin|June 27, 2007
N-methyl-D-aspartate receptors mediate diphosphorylation of extracellular signal-regulated kinases through Src family tyrosine kinases and Ca2+/calmodulin-dependent protein kinase II in rat hippocampus after cerebral ischemiaHui-Wen Wu, Hong-Fu Li, Jun Guo
Journal of Pain Research|December 11, 2019
Trigeminal Autonomic Cephalalgias Manifested As The Only Initial Symptom Of Ehlers-Danlos Syndrome Type IVMei-Jiao Chen, Hong-Fu Li, Shanying Mao
Neuroscience Bulletin|December 13, 2023
Paroxysmal Kinesigenic Dyskinesia: Genetics and Pathophysiological MechanismsJiao-Jiao Xu, Hong-Fu Li, Zhi-Ying Wu
BMC Neurology|September 21, 2016
Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencingCong Lu, Yi-Cen Zheng, Yi Dong, et al.
Neuroscience Bulletin|September 11, 2014
Paroxysmal kinesigenic dyskinesia and myotonia congenita in the same family: coexistence of a PRRT2 mutation and two CLCN1 mutationsHong-Fu Li, Wan-Jin Chen, Wang Ni, et al.
Clinical Genetics|September 1, 2022
Novel stop-gain RNF170 variation detected in a Chinese family with adolescent-onset hereditary spastic paraplegiaJing-Xin Fu, Qiao Wei, Yu-Lan Chen, et al.
Computational and Structural Biotechnology Journal|April 10, 2023
A multi-locus linear mixed model methodology for detecting small-effect QTLs for quantitative traits in MAGIC, NAM, and ROAM populationsGuo Li, Ya-Hui Zhou, Hong-Fu Li, et al.
Genomics, Proteomics & Bioinformatics|September 30, 2024
BLUPmrMLM: A Fast mrMLM Algorithm in Genome-wide Association StudiesHong-Fu Li, Jing-Tian Wang, Qiong Zhao, et al.
Neurology. Genetics|May 10, 2016
FTL mutation in a Chinese pedigree with neuroferritinopathyWang Ni, Hong-Fu Li, Yi-Cen Zheng, et al.
Pageof 7

Showing results (1-10 of 70) with videos related to

Sort By:
Pageof 7
Translational Neurodegeneration|February 5, 2016
Genotype-phenotype correlations of amyotrophic lateral sclerosisHong-Fu Li, Zhi-Ying Wu
Neuroscience Bulletin|June 27, 2007
N-methyl-D-aspartate receptors mediate diphosphorylation of extracellular signal-regulated kinases through Src family tyrosine kinases and Ca2+/calmodulin-dependent protein kinase II in rat hippocampus after cerebral ischemiaHui-Wen Wu, Hong-Fu Li, Jun Guo
Journal of Pain Research|December 11, 2019
Trigeminal Autonomic Cephalalgias Manifested As The Only Initial Symptom Of Ehlers-Danlos Syndrome Type IVMei-Jiao Chen, Hong-Fu Li, Shanying Mao
Neuroscience Bulletin|December 13, 2023
Paroxysmal Kinesigenic Dyskinesia: Genetics and Pathophysiological MechanismsJiao-Jiao Xu, Hong-Fu Li, Zhi-Ying Wu
BMC Neurology|September 21, 2016
Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencingCong Lu, Yi-Cen Zheng, Yi Dong, et al.
Neuroscience Bulletin|September 11, 2014
Paroxysmal kinesigenic dyskinesia and myotonia congenita in the same family: coexistence of a PRRT2 mutation and two CLCN1 mutationsHong-Fu Li, Wan-Jin Chen, Wang Ni, et al.
Clinical Genetics|September 1, 2022
Novel stop-gain RNF170 variation detected in a Chinese family with adolescent-onset hereditary spastic paraplegiaJing-Xin Fu, Qiao Wei, Yu-Lan Chen, et al.
Computational and Structural Biotechnology Journal|April 10, 2023
A multi-locus linear mixed model methodology for detecting small-effect QTLs for quantitative traits in MAGIC, NAM, and ROAM populationsGuo Li, Ya-Hui Zhou, Hong-Fu Li, et al.
Genomics, Proteomics & Bioinformatics|September 30, 2024
BLUPmrMLM: A Fast mrMLM Algorithm in Genome-wide Association StudiesHong-Fu Li, Jing-Tian Wang, Qiong Zhao, et al.
Neurology. Genetics|May 10, 2016
FTL mutation in a Chinese pedigree with neuroferritinopathyWang Ni, Hong-Fu Li, Yi-Cen Zheng, et al.
Pageof 7