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Laurent Abel

Hôpital Necker-Enfants Malades
H指数:131
被引数:6.0万

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Correction to: Rare Pathogenic Variants in Mitochondrial and Inflammation-Associated Genes May Lead to Inflammatory Cardiomyopathy in Chagas Disease

更正:线粒体和炎症相关基因中的罕见致病性变异可能导致恰加斯病中的炎症性心肌病

2026-08-150
OA
Human LFA-1 governs T cell immune surveillance of the skin

人LFA-1调控T细胞对皮肤的免疫监视

2026-02-270
PRE
A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity

显性人类IFNAR1缺乏症的常见形式会损害ifn-α 和-ω,但不会损害ifn-β 依赖性免疫

2024-12-160
OAAI
ACK1 and BRK non-receptor tyrosine kinase deficiencies are associated with familial systemic lupus and involved in efferocytosis
2024-11-210
OAAI
Auto-Abs neutralizing type I IFNs in patients with severe Powassan, Usutu, or Ross River virus disease
2024-11-010
OAAI
Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERIC-mediated monocyte activation

白细胞CBL杂合性丧失患者的自身炎症是由组成型ERIC介导的单核细胞激活引起的

2024-10-150
PRE
IL-7-dependent and -independent lineages of IL-7R-dependent human T cells
2024-10-010
OAAI
Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases

色素失禁是胸腺发育不良,I型ifn自身抗体和病毒性疾病的基础

2024-10-011
OAAI
Autoantibodies neutralizing type I IFNs underlie severe tick-borne encephalitis in ∼10% of patients
2024-09-243
OAAI
Gain-of-function human UNC93B1 variants cause systemic lupus erythematosus and chilblain lupus
2024-06-1310
OAAI
Helper T cell immunity in humans with inherited CD4 deficiency
2024-04-013
OAAI
Neutralizing IFN-γ autoantibodies are rare and in HLA-DRB1*15:02 or 16:02 individuals

中和性ifn-γ 自身抗体在HLA-DRB1 * 15:02或16:02个体中很少见

2024-03-120
OAAI
The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants
Science
IF45.8
2024-01-010
OA
Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

Auto-abs中和I型干扰素患者的疫苗突破性低氧新型冠状病毒肺炎肺炎

2023-12-2243
OAAI
Genome-wide detection of human intronic AG-gain variants located between splicing branchpoints and canonical splice acceptor sites

位于剪接分支点和典型剪接受体位点之间的人类内含子AG增益变体的全基因组检测

2023-11-065
OAAI