Art

J-GLOBAL ID：201702288499479181   Reference number：17A0680950

Novel and emerging therapies in the treatment of recessive dystrophic epidermolysis bullosa

劣性栄養障害性表皮水疱症の治療における新規と新興の治療

Author (2)： Rashidghamat Ellie (St. John’s Institute of Dermatology, King’s College London) ,  McGrath John A. (St. John’s Institute of Dermatology, King’s College London)
Material： Intractable & Rare Diseases Research  (IRDR)
Volume： 6  Issue： 1  Page： 6-20(J-STAGE)  Publication year： 2017 
JST Material Number： F1228A  ISSN： 2186-3644  CODEN： IRDRA3  Document type： Article
Article type： 文献レビュー  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： *hereditary disease ,...
Semi thesaurus term： *COL7A1 gene ,...

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Author keywords (5)： Epidermolysis bullosa ,  treatment ,  protein ,  cell ,  gene

JST classification (1)： Treatment for skin diseases in general  (GF05010P)

Reference (144)：

• 1. Fine JD, Bruckner-Tuderman L, Eady RA, et al. Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification. J Am Acad Dermatol. 2014; 70:1103-1126.
• 2. Hsu CK, Wang SP, Lee JY, McGrath JA. Treatment of hereditary epidermolysis bullosa: Updates and future prospects. Am J Clin Dermatol. 2014; 15:1-6.
• 3. Sakai LY, Keene DR, Morris NP, Burgeson RE. Type VII collagen is a major structural component of anchoring fibrils. J Cell Biol. 1986; 103:1577-1586.
• 4. Shimizu H, McGrath JA, Christiano AM, Nishikawa T, Uitto J. Molecular basis of recessive dystrophic epidermolysis bullosa: Genotype/phenotype correlation in a case of moderate clinical severity. J Invest Dermatol. 1996; 106:119-124.
• 5. Dang N, Murrell DF. Mutation analysis and characterization of COL7A1 mutations in dystrophic epidermolysis bullosa. Exp Dermatol. 2008; 17:553-568.

Terms in the title (2)： 劣性栄養障害性表皮水疱症 ,  治療