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Titlebook: Information and Communications Technologies; Second International Tammam A. T. Benmusa,Mohamed Samir Elbuni,Issmail Conference proceedings

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樓主: Twinge
51#
發(fā)表于 2025-3-30 08:37:04 | 只看該作者
Hanane Djellab,Amel Bouchemha,Fouzia Maamri,Farouk Boumehrez,Abdelhakim Sahourppropriate therapy. This textbook, the first of its kind, addresses all aspects of the disorder – from genetics, pathophysiology, and ongoing research,to clinical presentations, risk factors, and treatment..978-3-030-22096-9978-3-030-22094-5
52#
發(fā)表于 2025-3-30 15:06:09 | 只看該作者
53#
發(fā)表于 2025-3-30 18:18:05 | 只看該作者
54#
發(fā)表于 2025-3-30 23:18:21 | 只看該作者
Omar Bouagila Algaderi,Abdulkhalek M. Zatoutsponsible for the frequently fatal multiorgan system failure see in MAS. Whole-exome sequencing as well as targeted sequencing of pHLH-associated genes in patients with sJIA-associated MAS, demonstrated increased “burden” of rare protein altering variants affecting the cytolytic pathway compared to
55#
發(fā)表于 2025-3-31 01:47:22 | 只看該作者
56#
發(fā)表于 2025-3-31 07:22:55 | 只看該作者
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發(fā)表于 2025-3-31 10:46:48 | 只看該作者
58#
發(fā)表于 2025-3-31 13:26:25 | 只看該作者
Alharari Alsouri Alharari,Sami Saddek Bizzan,Abdulmoied Omar cancer stem cell (CSC), the CXCL8–CXCR1/2 signaling might be a key player in tumor development and metastasis. Agents targeting CXCR1/2 and CXCL8 antibodies have been discovered over past 20 years. Such inhibitors are anticipated to be effective in a variety of inflammatory disorders when used alon
59#
發(fā)表于 2025-3-31 18:29:35 | 只看該作者
ells, or astrocytes, which are able to present myelin antigens in the context of their MHC class II molecules. In this inflammatory microenvironment, T lymphocytes and other cells express cytokines and chemokines, which both promote and regulate the pathogenic process.
60#
發(fā)表于 2025-4-1 01:35:31 | 只看該作者
Petar Bisevac,Ana Toskovic,Mohamed Salb,Luka Jovanovic,Aleksandar Petrovic,Miodrag Zivkovic,Nebojsa ectively, these observations suggest that a significant number of autoreactive T cells ordinarily escape both negative selection in the thymus and clonal deletion in the periphery, and that their survival in the peripheral pool of mature T cells is not, in and of itself, predictive of autoimmune dis
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