Junfeng Wu

发表

Clinical characteristics and mutation analysis of X-linked severe combined immunodeficiency in China

Xiaodong Zhao, Zhi‐Yong Zhang, Cui Zhang, 2013, World Journal of Pediatrics.

T-cell receptor diversity is selectively skewed in T-cell populations of patients with Wiskott-Aldrich syndrome.

Xiaodong Zhao, Wenwei Tu, Xiaodong Zhao, 2015, The Journal of allergy and clinical immunology.

N-WASP Is Essential for the Negative Regulation of B Cell Receptor Signaling

A. Upadhyaya, S. Snapper, Chaohong Liu, 2013, PLoS biology.

Loss of Function Mutation in ELF4 Causes Autoinflammatory and Immunodeficiency Disease in Human.

F. You, Lili Cao, Xiaodong Zhao, 2022, Journal of clinical immunology.

Abatacept is effective in Chinese patients with LRBA and CTLA4 deficiency

Xiaodong Zhao, Mo Wang, Junfeng Wu, 2020, Genes & diseases.

Abnormalities of follicular helper T-cell number and function in Wiskott-Aldrich syndrome.

Chaohong Liu, Xiaodong Zhao, Junfeng Wu, 2016, Blood.

Effects of N-linked glycosylation of the fusion protein on replication of human metapneumovirus in vitro and in mouse lungs.

Xiaodong Zhao, Ping Liu, Junfeng Wu, 2011, The Journal of general virology.

Novel DOCK8 gene mutations lead to absence of protein expression in patients with hyper-IgE syndrome

Chaohong Liu, Liping Jiang, Xiaodong Zhao, 2015, Immunologic Research.

Clinical, immunologic, and genetic characteristics of RAG mutations in 15 Chinese patients with SCID and Omenn syndrome

Jing Liu, Chaohong Liu, Liping Jiang, 2016, Immunologic research.

Molecular and Phenotypic Characterization of Nine Patients with STAT1 GOF Mutations in China

Xiaodong Zhao, Qin Zhao, Junfeng Wu, 2019, Journal of Clinical Immunology.

Loss of Function Mutation in ELF4 Causes Autoinflammatory and Immunodeficiency Disease in Human

L. Cao, F. You, J. Wu, 2021, Journal of Clinical Immunology.

Molecular and immunological characterization of DNA ligase IV deficiency.

Xiaodong Zhao, Junfeng Wu, Y. An, 2016, Clinical immunology.

WASp Deficiency Selectively Affects the TCR Diversity of Different Memory T Cell Subsets in WAS Chimeric Mice

Xiaodong Zhao, Qin Zhao, Junfeng Wu, 2022, Frontiers in immunology.

Clinical, immunologic, and genetic characteristics of RAG mutations in 15 Chinese patients with SCID and Omenn syndrome

Jing Liu, Chaohong Liu, Xiaodong Zhao, 2015, Immunologic Research.

In vivo reversion of an inherited mutation in a Chinese patient with Wiskott-Aldrich syndrome.

W. Liu, Xiaodong Zhao, Mo Wang, 2015, Human immunology.

Novel DOCK8 gene mutations lead to absence of protein expression in patients with hyper-IgE syndrome

Chaohong Liu, Xiaodong Zhao, Dao-qi Wu, 2015, Immunologic Research.

Multicentric Carpo-Tarsal Osteolysis Syndrome Mimicking Juvenile Idiopathic Arthritis: Two Case Reports and Review of the Literature

Junfeng Wu, Xuemei Tang, Y. An, 2021, Frontiers in Pediatrics.

A Multicenter Cohort Study of Immune Dysregulation Disorders Caused by ELF4 Variants in China

Xiaodong Zhao, Junfeng Wu, Lina Zhou, 2023, Journal of Clinical Immunology.