Xianqin Zhang

20PUBLICATIONS
14CO-AUTHORS
HaematologyMolecular targetsNeonatologyNeurology and neuromuscular diseasesGene mapping
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Publications (20)

|Jul 29, 2026
Cyclosporine Stabilized the Hemoglobin Level in Children With Novel Compound Heterozygous Mutations in the LIG1 Gene: A Single Case Report.

|Jun 04, 2026
tubb5 knockout in zebrafish causes neurodevelopmental defects via notch pathways.

|Oct 10, 2025
Novel Compound Heterozygous Mutation in the KCNJ1 Gene Causes Bartter Syndrome.

Linglu Xiao, Yanqin Ying, Weimin Jia

|Jun 06, 2025
Knockout of bcas3 gene causes neurodevelopment defects in zebrafish.

|Oct 30, 2024
Novel splicing mutations in PATL2 and WEE2 cause oocyte degradation and fertilization failure.

Zhenxing Liu, Lixia Zhu, Hui He

|Apr 11, 2024
A Mettl16/m6A/mybl2b/Igf2bp1 axis ensures cell cycle progression of embryonic hematopoietic stem and progenitor cells.

Yunqiao Han, Kui Sun, Shanshan Yu

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Frequent Collaborators

1 joint publications

Yunqiao Han

1 joint publications

Kui Sun

1 joint publications

Liyan Dai

1 joint publications

Chaolin Jiang