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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 research & therapy, 2018-08, Vol.20 (1), p.200-200, Article 200

2018

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Dynamics of NK, CD8 and Tfh cell mediated the production of cytokines and antiviral antibodies in Chinese patients with moderate COVID‐19

Journal of cellular and molecular medicine, 2020-12, Vol.24 (24), p.14270-14279

2020

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Vitamin D supplementation reduced blood inflammatory cytokines expression and improved graft function in kidney transplant recipients

Frontiers in immunology, 2023-07, Vol.14, p.1152295-1152295

2023

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Donor ABCB1 3435 C>T genetic polymorphisms influence early renal function in kidney transplant recipients treated with tacrolimus

Pharmacogenomics, 2016-02, Vol.17 (3), p.249-257

2016

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Clinical and molecular characteristics of Chinese patients with X-linked lymphoproliferative syndrome type 1

Pediatric blood & cancer, 2014-11, Vol.61 (11), p.2043-2047

2014

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Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome

Pediatric allergy and immunology, 2011-08, Vol.22 (5), p.482-487

2011

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Retrospective study of 98 patients with X-linked agammaglobulinemia complicated with arthritis

Clinical rheumatology, 2022-06, Vol.41 (6), p.1889-1897

2022

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The influence of living donor SHROOM3 and ABCB1 genetic variants on renal function after kidney transplantation

Pharmacogenetics and genomics, 2017-01, Vol.27 (1), p.19-26

2017

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Wiskott-Aldrich syndrome protein may be critical for CD8+ T cell function following MCMV infection

Cellular immunology, 2019-04, Vol.338, p.43-50

2019

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Clinical, molecular, and T cell subset analyses in a small cohort of Chinese patients with hyper-IgM syndrome type 1

Human immunology, 2014-07, Vol.75 (7), p.633-640

2014

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Distribution, Clinical Features and Molecular Analysis of Primary Immunodeficiency Diseases in Chinese Children: A Single-center Study From 2005 to 2011

The Pediatric infectious disease journal, 2013-10, Vol.32 (10), p.1127-1134

2013

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Genotype of Thalassemia in Han Chinese and Tibetans in Sichuan Province,China.

Sichuan da xue xue bao. Journal of Sichuan University. Yi xue ban, 2016-11, Vol.47 (6), p.941-944

2016

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Screening for cytotoxic defects with flow cytometric detection of CD107α on natural killer cells and cytotoxic lymphocyte cells

Zhonghua er ke za zhi, 2012-05, Vol.50 (5), p.386

2012

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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, 2013-06, Vol.51 (6), p.472

2013

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Genetic and proteinic analysis of a Chinese boy with X-linked lymphoproliferative disease and his maternal relatives

Zhonghua er ke za zhi, 2011-06, Vol.49 (6), p.416

2011

Volltextzugriff (PDF)

A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child

Zhonghua er ke za zhi, 2009-11, Vol.47 (11), p.824

2009

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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, 2009-09, Vol.47 (9), p.691

2009

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Gene editing for the treatment of primary immunodeficiency disease

Zhongguo dang dai er ke za zhi, 2021-07, Vol.23 (7), p.743-748

2021

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A sensitive and compact mercury analyzer by integrating dielectric barrier discharge induced cold vapor generation and optical emission spectrometry

Chinese chemical letters, 2017-02, Vol.28 (2), p.189-196

2017

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Remote ischemic preconditioning protects liver ischemia-reperfusion injury by regulating eNOS-NO pathway and liver microRNA expressions in fatty liver rats

Hepatobiliary & pancreatic diseases international, 2017-08, Vol.16 (4), p.387-394

2017

Volltextzugriff (PDF)

基因编辑治疗原发性免疫缺陷病

中国当代儿科杂志, 2021-07, Vol.23 (7), p.743-748

2021

Volltextzugriff (PDF)

Assessment of serum Tim-3 and Gal-9 levels in predicting the risk of infection after kidney transplantation

International immunopharmacology, 2019-10, Vol.75, p.105803-105803, Article 105803

2019

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A Unitary-UCA-Root-MUSIC Algorithm Based on MSWF

Applied mechanics and materials, 2014-08, Vol.610, p.339-344

2014

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Donor

Pharmacogenomics, 2016-02, Vol.17 (3), p.249-257

2016

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MonoMAC syndrome

Zhongguo dang dai er ke za zhi, 2014-08, Vol.16 (8), p.869

2014

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1 – 25 von 4.937

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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

Dynamics of NK, CD8 and Tfh cell mediated the production of cytokines and antiviral antibodies in Chinese patients with moderate COVID‐19

Vitamin D supplementation reduced blood inflammatory cytokines expression and improved graft function in kidney transplant recipients

Donor ABCB1 3435 C>T genetic polymorphisms influence early renal function in kidney transplant recipients treated with tacrolimus

Clinical and molecular characteristics of Chinese patients with X-linked lymphoproliferative syndrome type 1

Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome

Retrospective study of 98 patients with X-linked agammaglobulinemia complicated with arthritis

The influence of living donor SHROOM3 and ABCB1 genetic variants on renal function after kidney transplantation

Wiskott-Aldrich syndrome protein may be critical for CD8+ T cell function following MCMV infection

Clinical, molecular, and T cell subset analyses in a small cohort of Chinese patients with hyper-IgM syndrome type 1

Distribution, Clinical Features and Molecular Analysis of Primary Immunodeficiency Diseases in Chinese Children: A Single-center Study From 2005 to 2011

Genotype of Thalassemia in Han Chinese and Tibetans in Sichuan Province,China.

Screening for cytotoxic defects with flow cytometric detection of CD107α on natural killer cells and cytotoxic lymphocyte cells

Expression and significance of interleukin-6, interferon-inducible protein-10 and interleukin-17 in serum and synovial fluid of patients with juvenile idiopathic arthritis

Genetic and proteinic analysis of a Chinese boy with X-linked lymphoproliferative disease and his maternal relatives

A novel missense mutation of FOXP3 causes immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in a Chinese child

A compound heterozygosity mutation in the interleukin-7 receptor-alpha gene resulted in severe combined immunodeficiency in a Chinese patient

Gene editing for the treatment of primary immunodeficiency disease

A sensitive and compact mercury analyzer by integrating dielectric barrier discharge induced cold vapor generation and optical emission spectrometry

Remote ischemic preconditioning protects liver ischemia-reperfusion injury by regulating eNOS-NO pathway and liver microRNA expressions in fatty liver rats

基因编辑治疗原发性免疫缺陷病

Assessment of serum Tim-3 and Gal-9 levels in predicting the risk of infection after kidney transplantation

A Unitary-UCA-Root-MUSIC Algorithm Based on MSWF

Donor

MonoMAC syndrome

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