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To explore any association between AV and FLG LoF mutations in a cohort of genotyped patients of Bangladeshi ancestry with atopic eczema (AE) in East London. METHODS. A retrospective notes review was performed on 245 patients who had been genotyped for FLG LoF mutations and undergone clinical ...
Infantile eczema linked to cat ownership in children with gene mutation Two loss-of-function mutations of FLG, RS01X and 2282de14, now have been shown to be responsible for a lack of filaggrin in the upper epidermis among approximately 10% of Europeans, he said. Filaggrin mutation blamed for...
(or ichthyosis bullosa of Siemens) (Kremer et al., 1994; Steijlen et al., 1994), a congenital skin disease characterized by dry skin and barrier loss (Traupe et al., 1986) and recently found to be differentially expressed in patients with vesicular hand eczema (Voorberg et al., 2021)...
上海交通大学 博士学位论文 FLG基因功能缺失突变及其疾病相关性研究 姓名:***申请学位级别:博士 专业:皮肤病与性病学 指导教师:**荣 201205 上海交通大学博士学位论文 FLG基因功能缺失突变及其疾病相关性研究 摘要 目的:分析中间丝相关蛋白基I因(Filaggrin,FLG)功能缺失突变与特应性 皮炎(atopicdermatitis,AD)和单纯...
To explore any association between AV and FLG LoF mutations in a cohort of genotyped patients of Bangladeshi ancestry with atopic eczema (AE) in East London. METHODS. A retrospective notes review was performed on 245 patients who had been genotyped for FLG LoF mutations and undergone clinical ...