Retrospective analysis of patients with severe combined immunodeficiency and alternative diagnostic criteria: A 20-year single centre experience [0.03%]
重症联合免疫缺陷病的回顾性分析及替代诊断标准：单中心20年经验
Sevim Busra Korkmaz,Mehmet Ali Karaselek,Selma Erol Aytekin et al.
Sevim Busra Korkmaz et al.
Severe combined immunodeficiency (SCID) is an inborn errors of immunity (IEI) disorder characterized by impairment in the development and function of lymphocytes and could be fatal if not treated with hematopoietic stem cell transplant in t...
Interleukin-21 receptor gene polymorphism (rs2285452 A/G) is associated with susceptibility to Behçet's disease [0.03%]
白细胞介素21受体基因多态性（rs2285452A/G）与贝赫切特病易感性的关联研究
Rajaa Lahmar,Elyes Chabchoub,Ramzi Zemni et al.
Rajaa Lahmar et al.
Behçet's disease (BD) is a chronic auto inflammatory disorder of unknown aetiology. Recently, the dysregulation of interleukin-21 receptor (IL-21R) has been incriminated in different autoimmune and auto-inflammatory diseases, such as syste...
Genetic landscape of human platelet antigen variants in the Indian population analysed from 1029 whole genomes [0.03%]
基于印度人群1029个全基因组测序的血小板相关人类同种异型基因遗传图谱分析
Mercy Rophina,Rahul C Bhoyar,Mohamed Imran et al.
Mercy Rophina et al.
Genetic variants in human platelet antigens (HPAs) considered allo- or auto antigens are associated with various disorders, including neonatal alloimmune thrombocytopenia, platelet transfusion refractoriness and post-transfusion purpura. Al...
Nomenclature for factors of the HLA system, update January, February and March 2023 [0.03%]
2023年1—3月HLA系统因素命名法更新
Steven G E Marsh;WHO Nomenclature Committee for Factors of the HLA System
Steven G E Marsh;WHO Nomenclature Committee for Factors of the HLA System
Solute carrier family 11 member 1 genetic polymorphisms rs17235409 and rs3731865 associate with susceptibility to extremity post-traumatic osteomyelitis in a Chinese Han population [0.03%]
溶质载体家族11成员1基因多态性rs17235409和rs3731865与中国汉族人群肢体战伤后骨髓炎易感性的关联研究
Nan Jiang,Yong-Cong Zhong,Qing-Rong Lin et al.
Nan Jiang et al.
Genetic variations in the solute carrier family 11 member 1 (SLC11A1) gene have been implicated in developing inflammatory disorders. However, it is still unclear whether such polymorphisms contribute to the pathogenesis of post-traumatic o...
Investigation of the relationship between IL17A, IL17F and ILR1N polymorphisms and COVID-19 severity: The predictive role of IL17A rs2275913 polymorphism in the clinical course of COVID-19 [0.03%]
IL17A、IL17F和ILR1N多态性与COVID-19严重程度的关系研究：IL17A rs2275913多态性在COVID-19临床病程中的预测作用
Gunes Cakmak Genc,Sevim Karakas Celik,Busra Yilmaz et al.
Gunes Cakmak Genc et al.
Coronavirus disease 2019 (COVID-19) is an infectious respiratory disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Although the mortality rate of the disease has been relatively under control as of 2022, more t...
Research progress of B subfamily of leucocyte immunoglobulin-like receptors in inflammation [0.03%]
B类白细胞免疫球蛋白样受体家族在炎症反应中的研究进展
Mengting Zhang,Jun Yang,Jing Zhang et al.
Mengting Zhang et al.
Leucocyte immunoglobulin-like receptors subfamily B (LILRB) belongs to the type I transmembrane glycoproteins, which is the immunosuppressive receptor. LILRBs are widely expressed in bone marrow cells, hematopoietic stem cells, nerve cells ...
Killer cell immunoglobulin-like receptor three domains long cytoplasmic tail 1 gene *007 may modulate disease progression of human immunodeficiency virus-1 infection in the Japanese population [0.03%]
杀细胞免疫球蛋白样受体三域长胞内尾1基因*007可能调节人类免疫缺陷病毒1型感染者疾病的进展：一项日本人群研究
Taeko K Naruse,Makiko Konishi-Takemura,Risa Yanagida et al.
Taeko K Naruse et al.
One of the KIR allele, KIR3DL1*007, was associated with the progression to acquired immunodeficiency syndrome and not with the susceptibility to HIV-1 infection in the Japanese and Indian populations, implying that KIR3DL1*007-positive NK c...
Interleukin 17A and 17F polymorphisms and asthma susceptibility: Correspondence [0.03%]
关于白细胞介素17A和17F的多态性与哮喘易感性的相关性 correspondence
Amnuay Kleebayoon,Viroj Wiwanitkit
Amnuay Kleebayoon
IL-17A and IL-17F polymorphisms and asthma risk: A meta-analysis [0.03%]
基于Meta分析的IL-17A和IL-17F多态性与哮喘易感性的关系研究
Young Ho Lee
Young Ho Lee