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J

Jolán E. Walter

University of South Florida
H指数:44
被引数:6,786

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Synergistic interaction between the macrophage polarizing signals IL-4 and IFNγ is controlled by the STAT6/STAT1/IRF1 axis

巨噬细胞极化信号IL-4和IFNγ之间的协同作用由STAT6/STAT1/IRF1轴调控

2026-08-260
OAAI
Bronchiectasis, Low IgG Levels and Lack of Vaccination are Risk Factors for Covid-19 Hospitalization in X-linked Agammaglobulinemia – A Retrospective Multicenter Study

支气管扩张、低IgG水平和疫苗接种缺失是X连锁无丙种球蛋白血症患者发生新冠住院的风险因素——一项回顾性多中心研究

2025-11-150
OAAI
The ClinGen Severe Combined Immunodeficiency Disease Variant Curation Expert Panel: Specifications for classification of variants in ADA, DCLRE1C, IL2RG, IL7R, JAK3, RAG1, and RAG2

ClinGen严重联合免疫缺陷病变异注释专家小组:ADA、DCLRE1C、IL2RG、IL7R、JAK3、RAG1和RAG2变异分类规范

2025-10-140
PRE
Simultaneous STING and lymphotoxin-β receptor activation induces B cell responses in tertiary lymphoid structures to potentiate antitumor immunity

同时激活STING和淋巴毒素-β受体在三级淋巴组织中诱导B细胞反应以增强抗肿瘤免疫

2025-09-020
OAAI
Case Report: A novel CXCR4 variant (p.S341Y) in a family with a pathogenic NFKB1 variant and variable clinical manifestations

病例报告:在一个携带致病性NFKB1变异且临床表型多样的家族中发现一种新型CXCR4变异(p.S341Y)。

2025-08-200
OA
The c.64 + 2 T > A Founder Variant Hits Home: Report on 14 Patients Expands the Phenotypic Landscape of Inherited ARPC1B Deficiency — a Comparative Analysis

c.64 + 2 T > A始祖变异敲响警钟:14例患者的报告扩展了遗传性ARPC1B缺乏症的表型景观——一项比较分析

2025-07-160
PRE
Multi-Year Registry Study of Elapegademase Treatment in Patients With Adenosine Deaminase Severe Combined Immunodeficiency (ADA-SCID) Requiring Enzyme Replacement Therapy

多中心研究:接受酶替代疗法治疗的腺苷脱氨酶严重联合免疫缺陷(ADA-SCID)患者中elapegademase治疗的多年登记研究

2025-03-270
OA
Efficacy, Safety, Tolerability, and Serum IgG Trough Levels of Hyaluronidase-Facilitated Subcutaneous Immunoglobulin 10% in US Pediatric Patients with Primary Immunodeficiency Diseases

有效性、安全性、耐受性及血清IgG谷浓度:10%透明质酸酶辅助皮下免疫球蛋白在美国原发性免疫缺陷病儿科患者中的应用

2025-03-140
OA
Multiomics dissection of human RAG deficiency reveals distinctive patterns of immune dysregulation but a common inflammatory signature

多组学分析揭示人类RAG缺陷症表现出独特的免疫失调模式,但具有共同的炎症特征

2025-01-010
OA
A novel transmembrane CXCR4 variant that expands the WHIM genotype-phenotype paradigm
2024-07-122
OAAI