Jing Y. Liu
Songjiang, China
Last Updated: 09/26/2026
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Found 27 publications
Loss-of-function variations in solute carrier family 38 member 6 are associated with essential tremor.
Journal: Signal transduction and targeted therapy
Published: December 12, 2024
GmNLP1 and GmNLP4 activate nitrate-induced CLE peptides NIC1a/b to mediate nitrate-regulated root nodulation.
Journal: The Plant journal : for cell and molecular biology
Published: January 04, 2024
Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsy.
Journal: Science China. Life sciences
Published: January 18, 2023
Norbisabolane-type sesquiterpenoid derivatives, benzofuran lignans and a phenolic glycoside from the roots of Glochidion wilsonii Hutch.
Journal: Phytochemistry
Published: June 29, 2022
The Pathology of Primary Familial Brain Calcification: Implications for Treatment.
Journal: Neuroscience bulletin
Published: May 21, 2022
Mechanisms of PiT2-loop7 Missense Mutations Induced Pi Dyshomeostasis.
Journal: Neuroscience bulletin
Published: February 12, 2022
Aligned Organization of Synapses and Mitochondria in Auditory Hair Cells.
Journal: Neuroscience bulletin
Published: July 15, 2021
A Novel SPAST Mutation Results in Spastin Accumulation and Defects in Microtubule Dynamics.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: June 24, 2021
Protein arginine methyltransferase 7 modulates neuronal excitability by interacting with NaV1.9.
Journal: Pain
Published: March 09, 2021
Severe brain calcification and migraine headache caused by SLC20A2 and PDGFRB heterozygous mutations in a five-year-old Chinese girl.
Journal: Molecular genetics & genomic medicine
Published: February 17, 2021
p.His16Arg of STXBP1 (MUNC18-1) Associated With Syntaxin 3B Causes Autosomal Dominant Congenital Nystagmus.
Journal: Frontiers in cell and developmental biology
Published: August 05, 2020
Last Updated: 09/26/2026