Wu JF - Search Results

1

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

Zhang C, Zhang ZY, Wu JF, Tang XM, Yang XQ, Jiang LP, Zhao XD. Zhang C, et al. Among authors: wu jf. World J Pediatr. 2013 Feb;9(1):42-7. doi: 10.1007/s12519-011-0330-4. Epub 2011 Nov 21. World J Pediatr. 2013. PMID: 22105576

2

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

Zhang J, Dou Y, Wu J, She W, Luo L, Zhao Y, Liu P, Zhao X. Zhang J, et al. J Gen Virol. 2011 Jul;92(Pt 7):1666-1675. doi: 10.1099/vir.0.030049-0. Epub 2011 Mar 30. J Gen Virol. 2011. PMID: 21450943

3

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

Wu J, Liu D, Tu W, Song W, Zhao X. Wu J, et al. J Allergy Clin Immunol. 2015 Jan;135(1):209-16. doi: 10.1016/j.jaci.2014.06.025. Epub 2014 Aug 1. J Allergy Clin Immunol. 2015. PMID: 25091438

4

[Clinical characteristics and treatment responses of X-linked thrombocytopenia].

Zhang X, Liu D, Luo G, Du H, Wu J, Zou L, Zhao X. Zhang X, et al. Zhonghua Er Ke Za Zhi. 2014 Dec;52(12):890-5. Zhonghua Er Ke Za Zhi. 2014. PMID: 25619343 Chinese.

5

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

Xie JW, Zhang ZY, Wu JF, Liu DW, Liu W, Zhao Y, Jiang LP, Tang XM, Wang M, Zhao XD. Xie JW, et al. Among authors: wu jf. Hum Immunol. 2015 Jun;76(6):406-13. doi: 10.1016/j.humimm.2015.04.001. Epub 2015 Apr 8. Hum Immunol. 2015. PMID: 25862925

6

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

Bai X, Liu J, Zhang Z, Liu C, Zhang Y, Tang W, Dai R, Wu J, Tang X, Zhang Y, Ding Y, Jiang L, Zhao X. Bai X, et al. Immunol Res. 2016 Apr;64(2):497-507. doi: 10.1007/s12026-015-8723-4. Immunol Res. 2016. PMID: 26476733

7

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

Qin T, An Y, Liu C, Wu J, Dai R, Liu D, Li X, Jiang L, Wu D, Tang X, Song W, Wang T, Zhao X. Qin T, et al. Immunol Res. 2016 Feb;64(1):260-71. doi: 10.1007/s12026-015-8745-y. Immunol Res. 2016. PMID: 26659092

8

Molecular and immunological characterization of DNA ligase IV deficiency.

Jiang J, Tang W, An Y, Tang M, Wu J, Qin T, Zhao X. Jiang J, et al. Clin Immunol. 2016 Feb;163:75-83. doi: 10.1016/j.clim.2015.12.016. Epub 2016 Jan 4. Clin Immunol. 2016. PMID: 26762768

9

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

Zhang X, Dai R, Li W, Zhao H, Zhang Y, Zhou L, Du H, Luo G, Wu J, Niu L, An Y, Zhang Z, Ding Y, Song W, Liu C, Zhao X. Zhang X, et al. Blood. 2016 Jun 23;127(25):3180-91. doi: 10.1182/blood-2015-06-652636. Epub 2016 May 11. Blood. 2016. PMID: 27170596 Free PMC article.

10

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

Chen X, Xu Q, Li X, Wang L, Yang L, Chen Z, Zeng T, Xue X, Xu T, Wang Y, Jia Y, Zhao Q, Wu J, Liang F, Tang X, Yang J, An Y, Zhao X. Chen X, et al. J Clin Immunol. 2020 Jan;40(1):82-95. doi: 10.1007/s10875-019-00688-3. Epub 2019 Nov 4. J Clin Immunol. 2020. PMID: 31686315

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