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Interactions between Intestinal Microflora/Probiotics and the Immune System

BioMed research international, 2019, Vol.2019, p.6764919-8

2019

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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, 2017-08, Vol.7 (1), p.26-n/a, Article 26

2017

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Clinical Manifestation of Hyper IgE Syndrome Including Otitis Media

Current allergy and asthma reports, 2018-10, Vol.18 (10), p.51-7, Article 51

2018

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Clinical Features and Genetic Analysis of 48 Patients with Chronic Granulomatous Disease in a Single Center Study from Shanghai, China (2005–2015): New Studies and a Literature Review

Journal of Immunology Research, 2017-01, Vol.2017, p.8745254-17

2017

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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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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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Clinical Features and Genetic Analysis of 20 Chinese Patients with X-Linked Hyper-IgM Syndrome

Journal of Immunology Research, 2014-01, Vol.2014, p.683160-12

2014

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T-cell Defects in a Patient with NFKBIA Gene Mutation

Journal of clinical immunology, 2024-06, Vol.44 (5), p.110, Article 110

2024

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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.803763-803763

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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Systemic Vasculitis and High IgE Level in a Patient with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2019-04, Vol.In Press (In Press)

2019

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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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Dynamic change, influencing factors, and clinical impact of cellular components in human breast milk

Pediatric research, 2023-05, Vol.93 (6), p.1765-1771

2023

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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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Molecular Diagnosis of Severe Combined Immunodeficiency—Identification of IL2RG, JAK3, IL7R, DCLRE1C, RAG1, and RAG2 Mutations in a Cohort of Chinese and Southeast Asian Children

Journal of clinical immunology, 2011-04, Vol.31 (2), p.281-296

2011

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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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Clinical Manifestations and Genetic Analysis of 17 Patients with Autosomal Dominant Hyper-IgE Syndrome in Mainland China: New Reports and a Literature Review

Journal of clinical immunology, 2017-02, Vol.37 (2), p.166-179

2017

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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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Exploring dynamic change and influencing factors of TGF-β1 and MUC1 in human breast milk, and their association with infantile diseases

Translational pediatrics, 2023-06, Vol.12 (6), p.1139-1147

2023

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Interactions between Intestinal Microflora/Probiotics and the Immune System

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 Manifestation of Hyper IgE Syndrome Including Otitis Media

Clinical Features and Genetic Analysis of 48 Patients with Chronic Granulomatous Disease in a Single Center Study from Shanghai, China (2005–2015): New Studies and a Literature Review

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

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

Clinical Features and Genetic Analysis of 20 Chinese Patients with X-Linked Hyper-IgM Syndrome

T-cell Defects in a Patient with NFKBIA Gene Mutation

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

Systemic Vasculitis and High IgE Level in a Patient with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency

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

Dynamic change, influencing factors, and clinical impact of cellular components in human breast milk

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)

Molecular Diagnosis of Severe Combined Immunodeficiency—Identification of IL2RG, JAK3, IL7R, DCLRE1C, RAG1, and RAG2 Mutations in a Cohort of Chinese and Southeast Asian Children

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

Clinical Manifestations and Genetic Analysis of 17 Patients with Autosomal Dominant Hyper-IgE Syndrome in Mainland China: New Reports and a Literature Review

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

Exploring dynamic change and influencing factors of TGF-β1 and MUC1 in human breast milk, and their association with infantile diseases

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