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                             15 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 B cell activating factor levels are linked to distinct B cell markers in multiple sclerosis and following B cell depletion and repopulation Asplund Högelin, Klara

258 C p.
artikel
2 Challenges for gene editing in common variable immunodeficiency disorders: Current and future prospects Ameratunga, Rohan

258 C p.
artikel
3 Chlorophyll a and novel synthetic derivatives alleviate atopic dermatitis by suppressing Th2 cell differentiation via IL-4 receptor modulation Kang, Koon Mook

258 C p.
artikel
4 Comment on Narsale et al. Th2 cell clonal expansion at diagnosis in human type 1 diabetes. Clin Immunol. 2023 Oct 29 Pinheiro, Marcelo Maia

258 C p.
artikel
5 Editorial Board
258 C p.
artikel
6 Fas lpr gene dosage tunes the extent of lymphoproliferation and T cell differentiation in lupus Bohat, Ritu

258 C p.
artikel
7 Fibroblasts in immune-mediated inflammatory diseases: The soil of inflammation Zhou, Yifan

258 C p.
artikel
8 Huanglian Jiedu Wan intervened with “Shi-Re Shanghuo” syndrome through regulating immune balance mediated by biomarker succinate Luo, Keke

258 C p.
artikel
9 Lactobacillus rhamnosus (LR) ameliorates pulmonary and extrapulmonary acute respiratory distress syndrome (ARDS) via targeting neutrophils Sapra, Leena

258 C p.
artikel
10 Natural supplements in antiphospholipid syndrome: A case for further study Kello, Nina

258 C p.
artikel
11 Oxidative stress is involved in immunosuppression and macrophage regulation in glioblastoma Liang, Xisong

258 C p.
artikel
12 Porphyromonas gingivalis with collagen immunization induces ACPA-positive rheumatoid arthritis in C3H mice Yang, Chao

258 C p.
artikel
13 Recent advances in the involvement of epigenetics in the pathogenesis of systemic lupus erythematosus Zhou, Hong-Yan

258 C p.
artikel
14 Tissue-resident memory T cells exhibit phenotypically and functionally heterogeneous in human physiological and pathological nasal mucosa Yu, Sifei

258 C p.
artikel
15 Two cases of pediatric primary immunodeficiency caused by a familial moesin(MSN)gene mutation Li, Muquan

258 C p.
artikel
                             15 gevonden resultaten
 
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