We analyzed the steroid sulfatase (STS) gene in nine Japanese patients with X-linked ichthyosis (XLI) by a polymerase chain reaction technique and subsequent DNA sequencing. Eight of nine patients showed complete deletion of the STS gene. In a patient of XLI exhibiting a normal amplifying pattern with predicted sizes of the STS gene, a novel mutation was found resulting in the appearance of a stop codon in exon 7 of the STS gene. This suggests that exon 7 or an area in its downstream region is important for STS activity
We have isolated several cDNA clones from a lambda gt11 expression library by screening with antibod...
Abstract Background X-linked ichthyosis (XLI) is a recessive keratinization condition caused by defi...
X-linked ichthyosis (XLI) is a relatively common keratinization disorder which is caused, in the vas...
We analyzed the steroid sulfatase (STS) gene in nine Japanese patients with X-linked ichthyosis (XLI...
X-linked ichthyosis (XLI) is an inborn error of metabolism caused by steroid sulfatase (STS) deficie...
X-linked ichthyosis is caused by steroid sulfatase deficiency which results from abnormalities in it...
X-linked ichthyosis is an inherited disorder due to steroid sulfatase deficiency. It is clinically c...
X-linked ichthyosis is an inherited disease due to steroid sulfatase deficiency. Onset is at birth o...
目的 检测一个中国汉族人X-性连锁鱼鳞病家系的类固醇硫酸酯酶(STS)基因突变情况.方法 收集1个X-性连锁鱼鳞病家系的临床资料,提取外周血DNA,通过PCR扩增外周血基因组DNA类固醇硫酸酯酶基因的...
We report on a Sardinian pedigree with congenital ichthyosis associated with normal levels of steroi...
Scaling in patients with recessive X-linked ichthyosis is caused by lack of activity of the enzyme s...
Deletions are the most common molecular defect in steroid sulfatase (STS) deficiency. We describe th...
Steroid sulfatase (STS) deficiency is the biochemical defect of X-linked ichthyosis (XLI), one of th...
AbstractX-linked ichthyosis is an inherited genetic disorder of the skin that results from steroid s...
Introduction: Ichthyosis is a disorder of keratinization characterized by diffuse uniform and persis...
We have isolated several cDNA clones from a lambda gt11 expression library by screening with antibod...
Abstract Background X-linked ichthyosis (XLI) is a recessive keratinization condition caused by defi...
X-linked ichthyosis (XLI) is a relatively common keratinization disorder which is caused, in the vas...
We analyzed the steroid sulfatase (STS) gene in nine Japanese patients with X-linked ichthyosis (XLI...
X-linked ichthyosis (XLI) is an inborn error of metabolism caused by steroid sulfatase (STS) deficie...
X-linked ichthyosis is caused by steroid sulfatase deficiency which results from abnormalities in it...
X-linked ichthyosis is an inherited disorder due to steroid sulfatase deficiency. It is clinically c...
X-linked ichthyosis is an inherited disease due to steroid sulfatase deficiency. Onset is at birth o...
目的 检测一个中国汉族人X-性连锁鱼鳞病家系的类固醇硫酸酯酶(STS)基因突变情况.方法 收集1个X-性连锁鱼鳞病家系的临床资料,提取外周血DNA,通过PCR扩增外周血基因组DNA类固醇硫酸酯酶基因的...
We report on a Sardinian pedigree with congenital ichthyosis associated with normal levels of steroi...
Scaling in patients with recessive X-linked ichthyosis is caused by lack of activity of the enzyme s...
Deletions are the most common molecular defect in steroid sulfatase (STS) deficiency. We describe th...
Steroid sulfatase (STS) deficiency is the biochemical defect of X-linked ichthyosis (XLI), one of th...
AbstractX-linked ichthyosis is an inherited genetic disorder of the skin that results from steroid s...
Introduction: Ichthyosis is a disorder of keratinization characterized by diffuse uniform and persis...
We have isolated several cDNA clones from a lambda gt11 expression library by screening with antibod...
Abstract Background X-linked ichthyosis (XLI) is a recessive keratinization condition caused by defi...
X-linked ichthyosis (XLI) is a relatively common keratinization disorder which is caused, in the vas...