日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?

三代家族成员出现细胞免疫缺陷、肢体远端异常和泌尿生殖系统畸形:一种新的常染色体显性遗传综合征?

Edery, P; Le Deist, F; Briard, M L; Debré, M; Munnich, A; Griscelli, C; Fischer, A; Lyonnet, S

Diversity, functionality, and stability of the T cell repertoire derived in vivo from a single human T cell precursor

源自单个人类T细胞前体的体内T细胞库的多样性、功能性和稳定性

Bousso, P; Wahn, V; Douagi, I; Horneff, G; Pannetier, C; Le Deist, F; Zepp, F; Niehues, T; Kourilsky, P; Fischer, A; de Saint Basile, G

Cytomegalovirus infection in infants with autoimmune lymphoproliferative syndrome (ALPS)

患有自身免疫性淋巴增生综合征(ALPS)的婴儿的巨细胞病毒感染

Arkwright, P D; Rieux-Laucat, F; Le Deist, F; Stevens, R F; Angus, B; Cant, A J

Consequences of Fas-mediated human dendritic cell apoptosis induced by measles virus.

麻疹病毒诱导的 Fas 介导的人类树突状细胞凋亡的后果

Servet-Delprat C, Vidalain P O, Azocar O, Le Deist F, Fischer A, Rabourdin-Combe C

Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneity

家族性噬血细胞性淋巴组织细胞增生症与 10q21-22 的关联及异质性证据

Dufourcq-Lagelouse, R; Jabado, N; Le Deist, F; Stéphan, J L; Souillet, G; Bruin, M; Vilmer, E; Schneider, M; Janka, G; Fischer, A; de Saint Basile, G

Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome

奥门综合征患者外周血和组织浸润淋巴细胞中人类T细胞库高度受限

Rieux-Laucat, F; Bahadoran, P; Brousse, N; Selz, F; Fischer, A; Le Deist, F; De Villartay, J P

Defect in IgV gene somatic hypermutation in common variable immuno-deficiency syndrome

常见变异型免疫缺陷综合征中IgV基因体细胞高频突变的缺陷

Levy, Y; Gupta, N; Le Deist, F; Garcia, C; Fischer, A; Weill, J C; Reynaud, C A

Numbers of T cell receptor (TCR) alpha beta+ but not of TcR gamma delta+ intraepithelial lymphocytes correlate with the grade of villous atrophy in coeliac patients on a long term normal diet

长期正常饮食的乳糜泻患者绒毛萎缩程度与上皮内淋巴细胞中T细胞受体(TCR)αβ+细胞的数量相关,而与TCRγδ+细胞的数量无关。

Kutlu, T; Brousse, N; Rambaud, C; Le Deist, F; Schmitz, J; Cerf-Bensussan, N

Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency

人类常染色体隐性遗传性重症联合免疫缺陷中粒细胞巨噬细胞集落形成单位和皮肤成纤维细胞的放射敏感性增加

Cavazzana-Calvo, M; Le Deist, F; De Saint Basile, G; Papadopoulo, D; De Villartay, J P; Fischer, A