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Jing-Yu Liu

Showing results (121-130 of 130) with videos related to

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Brain : a Journal of Neurology|December 19, 2019
Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcificationZhidong Cen, You Chen, Si Chen, et al.
Developmental Cell|August 29, 2023
Maternal and embryonic signals cause functional differentiation of luminal epithelial cells and receptivity establishmentHai-Quan Wang, Yang Liu, Dong Li, et al.
Journal of Medical Genetics|September 9, 2018
Long-read sequencing identified intronic repeat expansions in <i>SAMD12</i> from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsySheng Zeng, Mei-Yun Zhang, Xue-Jing Wang, et al.
Nature Genetics|February 14, 2012
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasisCheng Wang, Yulei Li, Lei Shi, et al.
Parkinsonism & Related Disorders|April 21, 2019
Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from ChinaSi Chen, Zhidong Cen, Feng Fu, et al.
Brain : a Journal of Neurology|December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorQi-Ying Sun, Qian Xu, Yun Tian, et al.
Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Nature|October 14, 2014
Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammationXianqin Zhang, Dusan Bogunovic, Béatrice Payelle-Brogard, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2018
Coding mutations in <i>NUS1</i> contribute to Parkinson's diseaseJi-Feng Guo, Lu Zhang, Kai Li, et al.
Nature Genetics|March 8, 2011
Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han populationFan Wang, Cheng-Qi Xu, Qing He, et al.
Pageof 13

Showing results (121-130 of 130) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 130 results.
Brain : a Journal of Neurology|December 19, 2019
Biallelic loss-of-function mutations in JAM2 cause primary familial brain calcificationZhidong Cen, You Chen, Si Chen, et al.
Developmental Cell|August 29, 2023
Maternal and embryonic signals cause functional differentiation of luminal epithelial cells and receptivity establishmentHai-Quan Wang, Yang Liu, Dong Li, et al.
Journal of Medical Genetics|September 9, 2018
Long-read sequencing identified intronic repeat expansions in <i>SAMD12</i> from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsySheng Zeng, Mei-Yun Zhang, Xue-Jing Wang, et al.
Nature Genetics|February 14, 2012
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasisCheng Wang, Yulei Li, Lei Shi, et al.
Parkinsonism & Related Disorders|April 21, 2019
Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from ChinaSi Chen, Zhidong Cen, Feng Fu, et al.
Brain : a Journal of Neurology|December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorQi-Ying Sun, Qian Xu, Yun Tian, et al.
Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Nature|October 14, 2014
Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammationXianqin Zhang, Dusan Bogunovic, Béatrice Payelle-Brogard, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 24, 2018
Coding mutations in <i>NUS1</i> contribute to Parkinson's diseaseJi-Feng Guo, Lu Zhang, Kai Li, et al.
Nature Genetics|March 8, 2011
Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han populationFan Wang, Cheng-Qi Xu, Qing He, et al.
Pageof 13