Dejun Zhang
MNR Key Laboratory Of Stratigraphy And Palaeontology
Beijing, 100037, China
Beijing, 100037, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 19 publications
Applying Flora Composition and Leaf Physiognomy to Reconstruct the Paleocommunity, Palaeoclimate, and Paleoenvironment of the Jehol Biota in Jilin, China.
Journal: Plants (Basel, Switzerland)
Published: October 28, 2025
Securing IoT Vision Systems: An Unsupervised Framework for Adversarial Example Detection Integrating Spatial Prototypes and Multidimensional Statistics.
Journal: Sensors (Basel, Switzerland)
Published: September 29, 2025
Research on Intrusion Detection Method Based on Transformer and CNN-BiLSTM in Internet of Things.
Journal: Sensors (Basel, Switzerland)
Published: March 24, 2025
Luteolin inhibits the JAK/STAT pathway to alleviate auditory cell apoptosis of acquired sensorineural hearing loss based on network pharmacology, molecular docking, molecular dynamics simulation, and experiments in vitro.
Journal: Toxicology and applied pharmacology
Published: November 15, 2023
Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles: A Universal and Dependable Noninvasive Prenatal Diagnosis Method Applied to Autosomal Recessive Nonsyndromic Hearing Loss in At-Risk Families.
Journal: The Journal of molecular diagnostics : JMD
Published: November 07, 2023
Exploration of a Novel Noninvasive Prenatal Testing Approach for Monogenic Disorders Based on Fetal Nucleated Red Blood Cells.
Journal: Clinical chemistry
Published: July 26, 2023
Molecular diagnose of a large hearing loss population from China by targeted genome sequencing.
Journal: Journal of human genetics
Published: February 22, 2022
Cochlear Implantation in a Patient with Neurofibromatosis Type 2 and an Intracochlear Schwannoma: A Case Report and Literature Review.
Journal: ORL; journal for oto-rhino-laryngology and its related specialties
Published: October 19, 2021
A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.
Journal: Annals of human genetics
Published: October 04, 2021
Gene4HL: An Integrated Genetic Database for Hearing Loss.
Journal: Frontiers in genetics
Published: September 09, 2021
Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis.
Journal: Frontiers in genetics
Published: May 10, 2021
Last Updated: 09/26/2026