SARS-CoV-2-Induced Immunosuppression: A Molecular Mimicry Syndrome [0.03%]
SARS-CoV-2诱导的免疫抑制：一种分子模拟综合征
Darja Kanduc
Darja Kanduc
Background Contrary to immunological expectations, decay of adaptive responses against severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) characterizes recovered patients compared with patients who had a severe disease course or d...
Role of PAX7 Gene rs766325 and rs4920520 Polymorphisms in the Etiology of Non-syndromic Cleft Lip and Palate: A Genetic Study [0.03%]
PAX7基因多态性在非综合征唇腭裂致病因素中的作用遗传学研究
Mahamad Irfanulla Khan,Prashanth Cs,Narasimhamurty Srinath
Mahamad Irfanulla Khan
Non-syndromic cleft lip and palate (NSCLP) is one of the most common birth defects in humans with an overall prevalence of ∼1 in 700 live births around the world. The etiology of NSCLP is complex involving multiple genes, environmental fac...
Pitfalls of PCR-RFLP in Detecting SARS-CoV-2 D614G Mutation [0.03%]
PCR-RFLP检测SARS-CoV-2 D614G突变的局限性分析
Kok-Siong Poon,Karen Mei-Ling Tan
Kok-Siong Poon
Mannose-Binding Lectin 2 Gene Polymorphism during Pandemic: COVID-19 Family [0.03%]
突发疫情期间的甘露聚糖结合凝集素2基因多态性：COVID-19家系研究
Tufan Tukek,Sacide Pehlivan,Yasemin Oyaci et al.
Tufan Tukek et al.
Mannose-binding lectin 2 (MBL2) is a serine protease which is believed to be an important factor in the inherited immune system. In this article, we present a coronavirus disease 2019 (COVID-19) family of five patients: a 56-year-old father...
Efficacy and Safety of Hypomethylating Agents in Chronic Myelomonocytic Leukemia: A Single-Arm Meta-analysis [0.03%]
低甲基化药物治疗慢性粒单细胞白血病疗效和安全性的单臂 meta 分析
Xinhui Zheng,Liwei Lv,Xiangjun Li et al.
Xinhui Zheng et al.
Background Chronic myelomonocytic leukemia (CMML) is a myeloid neoplasm with features of the myelodysplastic syndromes (MDSs) and myeloproliferative neoplasm presenting with peripheral blood monocytosis and an inherent risk for transformati...
A Computational Data Mining Strategy to Identify the Common Genetic Markers of Temporomandibular Joint Disorders and Osteoarthritis [0.03%]
用于识别颞下颌关节病和骨关节炎的共有遗传标志物的计算数据挖掘策略
Vijayashree Priyadharsini Jayaseelan,Paramasivam Arumugam
Vijayashree Priyadharsini Jayaseelan
Statement of Problem Prosthodontic planning in patients with temporomandibular joint disorders (TMDs) is a challenge for the clinicians. Purpose A differential biomarker identification could aid in developing methods for early detection and...
Comparison of Bioinformatics Approaches for Fetal Microdeletions and Monogenic Variations Estimation in Non-invasive Prenatal Testing [0.03%]
无创产前检测中生物信息学方法评估胎儿拷贝数微缺失和单基因变异的比较研究
Lizzy Teleboshe Paul,Mahmut Cerkez Ergoren
Lizzy Teleboshe Paul
Prenatal testing provides crucial information about the health status of fetuses as well as recommending better treatment. For the past decades, prenatal testing using chorionic villus sampling and amniocentesis were the two majorly used fo...
Genotype-Phenotype Correlations for Putative Haploinsufficient Genes in Deletions of 6q26-q27: Report of Eight Patients and Review of Literature [0.03%]
六号染色体短臂末端缺失中假定的单剂量基因的基因型表型相关性：八名患者报告及文献复习
Xiaolei Xie,Hongyan Chai,Autumn DiAdamo et al.
Xiaolei Xie et al.
Background Cytogenomic analyses have been used to detect pathogenic copy number variants. Patients with deletions at 6q26-q27 present variable clinical features. We reported clinical and cytogenomic findings of eight unrelated patients with...
Aliya A Rizvi,Mohammad Abbas,Sushma Verma et al.
Aliya A Rizvi et al.
Diabetes has become a pandemic as the number of diabetic people continues to rise globally. Being a heterogeneous disease, it has different manifestations and associated complications in different individuals like diabetic nephropathy, neur...