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A novel hypomorphic ζ-chain-associated protein tyrosine kinase 70 kDa mutation with normal CD8+ T cells count

Chinese medical journal, 2020-07, Vol.133 (14), p.1759-1760

2020

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When WAS Gene Diagnosis Is Needed: Seeking Clues Through Comparison Between Patients With Wiskott-Aldrich Syndrome and Idiopathic Thrombocytopenic Purpura

Frontiers in immunology, 2019-07, Vol.10, p.1549-1549

2019

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Effect of Low-Frequency Electrical Stimulation Combined with Tonifying Kidney and Blood Pills on Uterine Rejuvenation after Abortion

Evidence-based complementary and alternative medicine, 2022-10, Vol.2022, p.1-10

2022

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Serum IP-10 is useful for identifying renal and overall disease activity in pediatric systemic lupus erythematosus

Pediatric nephrology (Berlin, West), 2018-05, Vol.33 (5), p.837-845

2018

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Genome-Wide ChIP-seq and RNA-seq Analyses of STAT3 Target Genes in TLRs Activated Human Peripheral Blood B Cells

Frontiers in immunology, 2022-03, Vol.13, p.821457-821457

2022

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Role of SOCS3 in enhanced acute-phase protein genes by neonatal macrophages in response to IL-6

Journal of microbiology, immunology and infection, 2021-04, Vol.54 (2), p.206-212

2021

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A Novel Mutation of Notch homolog protein 2 gene in a Chinese Family with Hajdu-Cheney Syndrome

Chinese medical journal, 2017-12, Vol.130 (23), p.2883-2884

2017

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Phenomic Analysis of Chronic Granulomatous Disease Reveals More Severe Integumentary Infections in X-Linked Compared With Autosomal Recessive Chronic Granulomatous Disease

Frontiers in immunology, 2022-01, Vol.12, p.803763

2022

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Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency

Frontiers in immunology, 2017-07, Vol.8, p.808-808

2017

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Clinical, Laboratory, and Molecular Characteristics and Remission Status in Children With Severe Congenital and Non-congenital Neutropenia

Frontiers in pediatrics, 2018-10, Vol.6, p.305-305

2018

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Role of Zc3h12a in enhanced IL-6 production by newborn mononuclear cells in response to lipopolysaccharide

Pediatrics and neonatology, 2018-06, Vol.59 (3), p.288-295

2018

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Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia: Report from Shanghai, China (2000-2015)

Medicine (Baltimore), 2016-08, Vol.95 (32), p.e4544-e4544

2016

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Measurement of solution properties and molecular weight of hydroxyethyl starches using multi-angle laser light scattering: An interlaboratory comparison

Journal of pharmaceutical and biomedical analysis, 2022-09, Vol.219, p.114905-114905, Article 114905

2022

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Immunoregulatory effect of human β-defensin 1 on neonatal cord blood monocyte-derived dendritic cells and T cells

Molecular immunology, 2019-05, Vol.109, p.99-107

2019

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Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

Medicine (Baltimore), 2010-11, Vol.89 (6), p.381-402

2010

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Variable clinical phenotypes of X-Linked lymphoproliferative syndrome in China: Report of five cases with three novel mutations and review of the literature

Human immunology, 2016-08, Vol.77 (8), p.658-666

2016

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DNA induction of MDM2 promotes proliferation of human renal mesangial cells and alters peripheral B cells subsets in pediatric systemic lupus erythematosus

Molecular immunology, 2018-02, Vol.94, p.166-175

2018

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Correction to: Better recognition, diagnosis and management of non‐IgE‐mediated cow's milk allergy in infancy: iMAP—an international interpretation of the MAP (Milk Allergy in Primary Care) guideline

Clinical and translational allergy, 2018-01, Vol.8 (1), p.4-n/a, Article 4

2018

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Sunitinib Induces NK-κB-dependent NKG2D Ligand Expression in Nasopharyngeal Carcinoma and Hepatoma Cells

Journal of immunotherapy (1997), 2017-06, Vol.40 (5), p.164-174

2017

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Effects of Epstein-Barr virus on the development of dendritic cells derived from cord blood monocytes: an essential role for apoptosis

The Brazilian journal of infectious diseases, 2012-01, Vol.16 (1), p.19-26

2012

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Identification of sociodemographic and clinical factors associated with the levels of human β-defensin-1 and human β-defensin-2 in the human milk of Han Chinese

British journal of nutrition, 2014-03, Vol.111 (5), p.867-874

2014

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A novel point mutation in CD18 causing leukocyte adhesion deficiency in a Chinese patient

Chinese medical journal, 2010-05, Vol.123 (10), p.1278-1282

2010

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Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity

Frontiers in immunology, 2022-07, Vol.13, p.883446-883446

2022

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Clinical features and follow-up of Chinese patients with symptomatic hypogammaglobulinemia in infancy

Chinese medical journal, 2009-08, Vol.122 (16), p.1877-1883

2009

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Antimicrobial activity of human β-defensins against lactic acid bacteria

Natural product research, 2015-11, Vol.29 (22), p.2164-2166

2015

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A novel hypomorphic ζ-chain-associated protein tyrosine kinase 70 kDa mutation with normal CD8+ T cells count

When WAS Gene Diagnosis Is Needed: Seeking Clues Through Comparison Between Patients With Wiskott-Aldrich Syndrome and Idiopathic Thrombocytopenic Purpura

Effect of Low-Frequency Electrical Stimulation Combined with Tonifying Kidney and Blood Pills on Uterine Rejuvenation after Abortion

Serum IP-10 is useful for identifying renal and overall disease activity in pediatric systemic lupus erythematosus

Genome-Wide ChIP-seq and RNA-seq Analyses of STAT3 Target Genes in TLRs Activated Human Peripheral Blood B Cells

Role of SOCS3 in enhanced acute-phase protein genes by neonatal macrophages in response to IL-6

A Novel Mutation of Notch homolog protein 2 gene in a Chinese Family with Hajdu-Cheney Syndrome

Phenomic Analysis of Chronic Granulomatous Disease Reveals More Severe Integumentary Infections in X-Linked Compared With Autosomal Recessive Chronic Granulomatous Disease

Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency

Clinical, Laboratory, and Molecular Characteristics and Remission Status in Children With Severe Congenital and Non-congenital Neutropenia

Role of Zc3h12a in enhanced IL-6 production by newborn mononuclear cells in response to lipopolysaccharide

Clinical characteristics and genetic profiles of 174 patients with X-linked agammaglobulinemia: Report from Shanghai, China (2000-2015)

Measurement of solution properties and molecular weight of hydroxyethyl starches using multi-angle laser light scattering: An interlaboratory comparison

Immunoregulatory effect of human β-defensin 1 on neonatal cord blood monocyte-derived dendritic cells and T cells

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

Variable clinical phenotypes of X-Linked lymphoproliferative syndrome in China: Report of five cases with three novel mutations and review of the literature

DNA induction of MDM2 promotes proliferation of human renal mesangial cells and alters peripheral B cells subsets in pediatric systemic lupus erythematosus

Correction to: Better recognition, diagnosis and management of non‐IgE‐mediated cow's milk allergy in infancy: iMAP—an international interpretation of the MAP (Milk Allergy in Primary Care) guideline

Sunitinib Induces NK-κB-dependent NKG2D Ligand Expression in Nasopharyngeal Carcinoma and Hepatoma Cells

Effects of Epstein-Barr virus on the development of dendritic cells derived from cord blood monocytes: an essential role for apoptosis

Identification of sociodemographic and clinical factors associated with the levels of human β-defensin-1 and human β-defensin-2 in the human milk of Han Chinese

A novel point mutation in CD18 causing leukocyte adhesion deficiency in a Chinese patient

Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity

Clinical features and follow-up of Chinese patients with symptomatic hypogammaglobulinemia in infancy

Antimicrobial activity of human β-defensins against lactic acid bacteria

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