Detalhe da pesquisa
1.
[Gene editing for the treatment of primary immunodeficiency disease].
Zhongguo Dang Dai Er Ke Za Zhi
; 23(7): 743-748, 2021 Jul.
Artigo
Chinês
| MEDLINE | ID: mdl-34266535
2.
Dynamics of NK, CD8 and Tfh cell mediated the production of cytokines and antiviral antibodies in Chinese patients with moderate COVID-19.
J Cell Mol Med
; 24(24): 14270-14279, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33145962
3.
Wiskott-Aldrich syndrome protein may be critical for CD8+ T cell function following MCMV infection.
Cell Immunol
; 338: 43-50, 2019 04.
Artigo
Inglês
| MEDLINE | ID: mdl-30981413
4.
The influence of living donor SHROOM3 and ABCB1 genetic variants on renal function after kidney transplantation.
Pharmacogenet Genomics
; 27(1): 19-26, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27779570
5.
[Genotype of Thalassemia in Han Chinese and Tibetans in Sichuan Province,China.]
Sichuan Da Xue Xue Bao Yi Xue Ban
; 47(6): 941-944, 2016 Nov.
Artigo
Chinês
| MEDLINE | ID: mdl-28598129
6.
Clinical and molecular characteristics of Chinese patients with X-linked lymphoproliferative syndrome type 1.
Pediatr Blood Cancer
; 61(11): 2043-7, 2014 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-25044636
7.
[MonoMAC syndrome].
Zhongguo Dang Dai Er Ke Za Zhi
; 16(8): 869-73, 2014 Aug.
Artigo
Chinês
| MEDLINE | ID: mdl-25140787
8.
Vitamin D supplementation reduced blood inflammatory cytokines expression and improved graft function in kidney transplant recipients.
Front Immunol
; 14: 1152295, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37483634
9.
Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome.
Pediatr Allergy Immunol
; 22(5): 482-7, 2011 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-21771083
10.
Assessment of serum Tim-3 and Gal-9 levels in predicting the risk of infection after kidney transplantation.
Int Immunopharmacol
; 75: 105803, 2019 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-31401383
11.
Enhanced IL-6/phosphorylated STAT3 signaling is related to the imbalance of circulating T follicular helper/T follicular regulatory cells in patients with rheumatoid arthritis.
Arthritis Res Ther
; 20(1): 200, 2018 08 29.
Artigo
Inglês
| MEDLINE | ID: mdl-30157931
12.
Donor ABCB1 3435 C>T genetic polymorphisms influence early renal function in kidney transplant recipients treated with tacrolimus.
Pharmacogenomics
; 17(3): 249-57, 2016 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-26784512
13.
Clinical, molecular, and T cell subset analyses in a small cohort of Chinese patients with hyper-IgM syndrome type 1.
Hum Immunol
; 75(7): 633-40, 2014 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-24768948
14.
[Expression and significance of interleukin-6, interferon-inducible protein-10 and interleukin-17 in serum and synovial fluid of patients with juvenile idiopathic arthritis].
Zhonghua Er Ke Za Zhi
; 51(6): 472-6, 2013 Jun.
Artigo
Chinês
| MEDLINE | ID: mdl-24120067
15.
Distribution, clinical features and molecular analysis of primary immunodeficiency diseases in Chinese children: a single-center study from 2005 to 2011.
Pediatr Infect Dis J
; 32(10): 1127-34, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23673420
16.
[Screening for cytotoxic defects with flow cytometric detection of CD107α on natural killer cells and cytotoxic lymphocyte cells].
Zhonghua Er Ke Za Zhi
; 50(5): 386-91, 2012 May.
Artigo
Chinês
| MEDLINE | ID: mdl-22883044
17.
[Genetic and proteinic analysis of a Chinese boy with X-linked lymphoproliferative disease and his maternal relatives].
Zhonghua Er Ke Za Zhi
; 49(6): 416-20, 2011 Jun.
Artigo
Chinês
| MEDLINE | ID: mdl-21924052
18.
[A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child].
Zhonghua Er Ke Za Zhi
; 47(11): 824-8, 2009 Nov.
Artigo
Chinês
| MEDLINE | ID: mdl-20078992
19.
[A compound heterozygosity mutation in the interleukin-7 receptor-alpha gene resulted in severe combined immunodeficiency in a Chinese patient].
Zhonghua Er Ke Za Zhi
; 47(9): 691-5, 2009 Sep.
Artigo
Chinês
| MEDLINE | ID: mdl-20021794