Shuju Zhang
Changsha, China
Last Updated: 09/26/2026
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Found 13 publications
An agentic system for rare disease diagnosis with traceable reasoning.
Journal: Nature
Published: June 30, 2025
Clinical and genetic analysis of a child with Spondyloocular syndrome due to compound heterozygous variants of XYLT2 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 11, 2024
The Investigation of Nfκb Inhibitors to Block Cell Proliferation in OSCC Cells Lines.
Journal: Current medicinal chemistry
Published: February 09, 2024
Genetic analysis of novel pathogenic gene HROB in a family with primary ovarian insufficiency.
Journal: Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences
Published: December 18, 2023
Sex differences exist in adult heart group 2 innate lymphoid cells.
Journal: BMC immunology
Published: June 16, 2022
Case Report: A de novo Variant of CRYGC Gene Associated With Congenital Cataract and Microphthalmia.
Case Report: A de novo Variant of CRYGC Gene Associated With Congenital Cataract and Microphthalmia.
Journal: Frontiers in genetics
Published: January 31, 2022
Docosahexaenoic acid supplementation represses the early immune response against murine cytomegalovirus but enhances NK cell effector function.
Journal: BMC immunology
Published: November 07, 2021
Identification of nafamostat mesylate as a selective stimulator of NK cell IFN-γ production via metabolism-related compound library screening.
Journal: Immunologic research
Published: September 23, 2021
Screening for Active Compounds Targeting Human Natural Killer Cell Activation Identifying Daphnetin as an Enhancer for IFN-γ Production and Direct Cytotoxicity.
Journal: Frontiers in immunology
Published: March 15, 2021
Conditional knockout of Tsc1 in RORγt-expressing cells induces brain damage and early death in mice.
Conditional knockout of Tsc1 in RORγt-expressing cells induces brain damage and early death in mice.
Journal: Journal of neuroinflammation
Published: January 15, 2021
Capillary Malformation-Arteriovenous Malformation Combined Alagille Syndrome in a Patient With Double Gene Variations of RASA1 and NOTCH2.
Journal: Frontiers in genetics
Published: August 19, 2019
Last Updated: 09/26/2026