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Efficacy of allergen-specific immunotherapy for peanut allergy: A meta-analysis of randomized controlled trials.
- Published in:
- Allergy & Asthma Proceedings, 2014, v. 35, n. 2, p. 171, doi. 10.2500/aap.2014.35.3730
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- Article
High-Frequency Exon Deletion of DNA Cross-Link Repair 1C Accounting for Severe Combined Immunodeficiency May Be Missed by Whole-Exome Sequencing.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.677748
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- Article
Intron retention by a novel intronic mutation in DKC1 gene caused recurrent still birth and early death in a Chinese family.
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- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 6, p. 1, doi. 10.1002/mgg3.1934
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- Article
Cellular Mechanisms Underlying B Cell Abnormalities in Patients With Gain-of-Function Mutations in the PIK3CD Gene.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.890073
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- Article
Rapid diagnosis of Talaromyces marneffei infection by metagenomic next-generation sequencing technology in a Chinese cohort of inborn errors of immunity.
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- Frontiers in Cellular & Infection Microbiology, 2022, v. 12, p. 01, doi. 10.3389/fcimb.2022.987692
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- Article
The three CYBA variants (rs4673, rs1049254 and rs1049255) are benign: new evidence from a patient with CGD.
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- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0492-6
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- Article
EDN1 Gene Variant is Associated with Neonatal Persistent Pulmonary Hypertension.
- Published in:
- Scientific Reports, 2016, p. 29877, doi. 10.1038/srep29877
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- Article
Clinical Characteristics and Immunogenetics of BCGosis/BCGitis in Chinese Children: A 6 Year Follow-Up Study.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094485
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- Article
The clinical, immunological and genetic features of 12 Chinese patients with STAT3 mutations.
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- Allergy, Asthma & Clinical Immunology, 2020, v. 16, n. 1, p. 1, doi. 10.1186/s13223-020-00462-w
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- Article
Efficacy of tocilizumab therapy in a patient with severe pancytopenia associated with a STAT3 gain-of-function mutation.
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- BMC Immunology, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12865-021-00411-1
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- Article
The histone methyltransferase Setd2 is indispensable for V(D)J recombination.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-11282-x
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- Article
PLCβ2 negatively regulates the inflammatory response to virus infection by inhibiting phosphoinositide-mediated activation of TAK1.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08524-3
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- Article
Chromosomal abnormalities related to fever of unknown origin in a Chinese pediatric cohort and literature review.
- Published in:
- 2022
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- Publication type:
- journal article
A Chinese DADA2 patient: report of two novel mutations and successful HSCT.
- Published in:
- Immunogenetics, 2019, v. 71, n. 4, p. 299, doi. 10.1007/s00251-018-01101-w
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- Article
Phenotypic and Immunological Characterization of Patients with Activated PI3Kδ Syndrome 1 Presenting with Autoimmunity.
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- Journal of Clinical Immunology, 2024, v. 44, n. 4, p. 1, doi. 10.1007/s10875-024-01705-w
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- Article
Nomogram for Predicting Early Mortality after Umbilical Cord Blood Transplantation in Children with Inborn Errors of Immunity.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 6, p. 1379, doi. 10.1007/s10875-023-01505-8
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- Article
Clinical and Genetic Characteristics of BCG Disease in Chinese Children: a Retrospective Study.
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- Journal of Clinical Immunology, 2023, v. 43, n. 4, p. 756, doi. 10.1007/s10875-022-01422-2
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- Article
Optical Genomic Mapping Identified a Heterozygous Structural Variant in NCF2 Related to Chronic Granulomatous Disease.
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- Journal of Clinical Immunology, 2022, v. 42, n. 8, p. 1614, doi. 10.1007/s10875-022-01331-4
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- Article
Variant Type X91<sup>+</sup> Chronic Granulomatous Disease: Clinical and Molecular Characterization in a Chinese Cohort.
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- Journal of Clinical Immunology, 2022, v. 42, n. 7, p. 1564, doi. 10.1007/s10875-022-01324-3
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- Article
Low-Dose Pioglitazone does not Increase ROS Production in Chronic Granulomatous Disease Patients with Severe Infection.
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- Journal of Clinical Immunology, 2020, v. 40, n. 1, p. 131, doi. 10.1007/s10875-019-00719-z
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- Article
Current Status of the Management of Mendelian Susceptibility to Mycobacterial Disease in Mainland China.
- Published in:
- Journal of Clinical Immunology, 2019, v. 39, n. 6, p. 600, doi. 10.1007/s10875-019-00672-x
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- Article
Report of a Chinese Cohort with Leukocyte Adhesion Deficiency-I and Four Novel Mutations.
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- Journal of Clinical Immunology, 2019, v. 39, n. 3, p. 309, doi. 10.1007/s10875-019-00617-4
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- Article
Novel Heterogeneous Mutation of TNFAIP3 in a Chinese Patient with Behçet-Like Phenotype and Persistent EBV Viremia.
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- Journal of Clinical Immunology, 2019, v. 39, n. 2, p. 188, doi. 10.1007/s10875-019-00604-9
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- Article
Report of a Chinese Cohort with Activated Phosphoinositide 3-Kinase δ Syndrome.
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 8, p. 854, doi. 10.1007/s10875-018-0568-x
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- Article
A Cohort of 169 Chronic Granulomatous Disease Patients Exposed to BCG Vaccination: a Retrospective Study from a Single Center in Shanghai, China (2004-2017).
- Published in:
- Journal of Clinical Immunology, 2018, v. 38, n. 3, p. 260, doi. 10.1007/s10875-018-0486-y
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- Publication type:
- Article
LIG4 syndrome: clinical and molecular characterization in a Chinese cohort.
- Published in:
- 2020
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- Publication type:
- journal article
Endothelial cells promote neural stem cell proliferation and differentiation associated with VEGF activated Notch and Pten signaling.
- Published in:
- Developmental Dynamics, 2010, v. 239, n. 9, p. 2345, doi. 10.1002/dvdy.22377
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- Article
The TRIM37 variants in Mulibrey nanism patients paralyze follicular helper T cell differentiation.
- Published in:
- Cell Discovery, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41421-023-00561-z
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- Article
Screening for primary immunodeficiency diseases by next‐generation sequencing in early life.
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- Clinical & Translational Immunology, 2020, v. 9, n. 5, p. 1, doi. 10.1002/cti2.1138
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- Article
Severe G6PD deficiency leads to recurrent infections and defects in ROS production: Case report and literature review.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.1035673
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- Article
Further Delineation of the Spectrum of XMEN Disease in Six Chinese Pediatric Patients.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.768000
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- Publication type:
- Article
CARD11 regulates the thymic Treg development in an NF-kB-independent manner.
- Published in:
- Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1364957
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- Article
Effects of hypothermia on NSE and S-100 protein levels in CSF in neonates following hypoxic/ischaemic brain damage.
- Published in:
- Acta Paediatrica, 2012, v. 101, n. 8, p. e316, doi. 10.1111/j.1651-2227.2012.02679.x
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- Article
Novel Compound Heterozygous Variants in the FAS Gene Lead to Fetal Onset of Autoimmune Lymphoproliferative Syndrome (ALPS).
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- Journal of Clinical Immunology, 2024, v. 45, n. 1, p. 1, doi. 10.1007/s10875-024-01812-8
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- Publication type:
- Article
Novel Mutation in the Moesin (MSN) Gene Leads to Immunodeficiency with Epstein–Barr Virus (EBV) Infection and Dermatomyositis-Like Symptoms.
- Published in:
- Journal of Clinical Immunology, 2024, v. 44, n. 7, p. 1, doi. 10.1007/s10875-024-01755-0
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- Publication type:
- Article