欢迎您!
东篱公司
退出
申报数据库
申报指南
立项数据库
成果数据库
期刊论文
会议论文
著 作
专 利
项目获奖数据库
位置:
成果数据库
>
期刊
> 期刊详情页
Gene diagnosis and prenatal genetic diagnosis of a case of dystrophic epidermolysis bullosa family c
ISSN号:0926-9959
期刊名称:J Eur Acad Dermatol Venereol
时间:2015.8.20
页码:0-0
相关项目:马拉色菌及其变应原致敏FLG突变小鼠的机制
作者:
Cheng R|Liang J|Li M|Yao Z|
同期刊论文项目
马拉色菌及其变应原致敏FLG突变小鼠的机制
期刊论文 16
同项目期刊论文
Interactions between FLG mutations and allergens in atopic dermatitis.
Mutations analysis in filaggrin gene in northern China patients with atopic dermatitis
Genotype-phenotype correlation of xeroderma pigmentosum in a Chinese Han population.
Mutations in POFUT1, encoding protein O-fucosyltransferase 1, cause generalized Dowling-Degos diseas
Mutations analysis in filaggrin gene in northern China patients with atopic dermatitis.
Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a
Prevalent and rare mutations in IL-36RN gene in Chinese patients with generalized pustular psoriasis
A novel mutation in the COL7A1 gene results in a unique phenotype of epidermolysis bullosa prurigino
Analyses of FLG mutation frequency and filaggrin expression in isolatedichthyosis vulgaris (IV) and
A recurrent mutation in the APCDD1 gene responsible for hereditary hypotrichosis simplex in a large
Common FLG mutation K4671X not associated with atopic dermatitis in Han Chinese in a family associat
Lidocaine inhibits staphylococcal enterotoxin-stimulated activation of peripheral blood mononuclear
Effects of lidocaine on regulatory T cells in atopic dermatitis.