Zhihao Xing
No. 7019 Yitian Rd
Shenzhen, China
Shenzhen, China
Last Updated: 09/26/2026
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Found 13 publications
SPP1+ Macrophages Involved in Juvenile Xanthogranuloma via PPARG Signaling Pathway.
Journal: Journal of inflammation research
Published: March 01, 2026
Comparison of the time to detection (TTD) of different blood culture systems and antibiotic adsorption capacity of different pediatric blood culture bottles of BD and bioMérieux.
Journal: Microbiology spectrum
Published: November 21, 2025
Divergent Sensitization Kinetics to Indoor Allergens in Children: Early Dust Mite Surges vs Delayed Cat Dander Peaks During COVID-19 Lockdowns.
Journal: Journal of asthma and allergy
Published: July 28, 2025
Systematic identification and validation of ceRNA-driven regulatory mechanisms in pediatric β-Thalassemia major.
Journal: Annals of hematology
Published: October 31, 2024
Rapid and one-tube detection of human metapneumovirus using the RT-RPA and CRISPR/Cas12a.
Journal: Journal of virological methods
Published: April 29, 2024
Integrating DNA/RNA microbe detection and host response for accurate diagnosis, treatment and prognosis of childhood infectious meningitis and encephalitis.
Journal: Journal of translational medicine
Published: July 18, 2023
Contributions of ARID5B, IKZF1, PIP4K2A, and GATA3 Gene Polymorphisms to Childhood Acute Lymphoblastic Leukemia in a Chinese Population.
Journal: Journal of pediatric hematology/oncology
Published: December 23, 2021
Comparison and development of a metagenomic next-generation sequencing protocol for combined detection of DNA and RNA pathogens in cerebrospinal fluid.
Journal: BMC infectious diseases
Published: August 24, 2021
Overexpression of BIRC6 driven by EGF-JNK-HECTD1 signaling is a potential therapeutic target for triple-negative breast cancer.
Journal: Molecular therapy. Nucleic acids
Published: June 08, 2021
A prediction model for risk factors of testicular atrophy after orchiopexy in children with undescended testis.
Journal: Translational pediatrics
Published: May 20, 2021
Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature.
Journal: BMC medical genomics
Published: December 16, 2020
Last Updated: 09/26/2026