Shiyue Du
Hubei Key Laboratory Of Embryonic Stem Cell Research
Shiyan, 442000, China
Shiyan, 442000, China
Last Updated: 09/26/2026
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Found 8 publications
Testis-specific gene C3ORF22/BC048671 is dispensable for spermiogenesis and male fertility.
Journal: Reproductive biology
Published: July 08, 2025
Functional characterization of novel NPRL3 mutations identified in three families with focal epilepsy.
Journal: Science China. Life sciences
Published: January 18, 2023
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
A Novel CDH1 Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate.
Journal: Genetic testing and molecular biomarkers
Published: October 23, 2019
A PRRT2 variant in a Chinese family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures results in loss of interaction with STX1B.
Journal: Epilepsia
Published: September 07, 2017
PiT2 regulates neuronal outgrowth through interaction with microtubule-associated protein 1B.
Journal: Scientific reports
Published: February 27, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026