Dermatology News

Dermatology

sponsor

Your Article Summary

(Click the title below to leave the MDLinx Network and go to the Journal's Website)

Uitto J - Epidermolysis bullosa, a group of blistering disorders, serves as the paradigm of the tremendous progress made in understanding the molecular genetics of heritable skin diseases. Mutations in 10 distinct genes have been disclosed in the classic forms of epidermolysis bullosa, and the level of expression of the mutated genes within the cutaneous basement membrane zone, the types and combinations of mutations and their consequences at the mRNA and protein levels, when placed in the context of the individual's genetic background and exposure to environmental trauma, all determine the subtype and the phenotypic severity in each case.

Related Articles

A case of epidermolysis bullosa acquisita with unusual clinical features
Clinical and Experimental Dermatology, 10/16/09    Relevance Score: 68%

Successful radiation therapy for supratentorial primitive neuroectodermal tumor and epidermolysis bullosa simplex
Pediatric Blood & Cancer, 10/07/09    Relevance Score: 64%

Study of relationship of concha bullosa to nasal septal deviation and sinusitis
Indian Journal of Otolaryngology and Head & Neck Surgery, 10/01/09    Relevance Score: 42%

Today in Autoimmune/Bullous Dz...keeping you current

Potential role of interleukin-17 in the pathogenesis of bullous pemphigoid
Medical Hypotheses, 12/09/09

Genetic basis of oculocutaneous albinism
Expert Review of Dermatology, 12/08/09

Hyper IgE syndrome with umbilical hernia
Indian Journal of Dermatology, 11/25/09

Today in Basic Science/Genetics...keeping you current

Analysis of family history of palmoplantar hyperhidrosis in Japan
Journal of Dermatology, 12/08/09

Evidence for a Founder Mutation in the Cathepsin C Gene in Three Families with Papillon-Lefevre Syndrome
Dermatology, 12/08/09

Adult T-cell leukemia-lymphoma associated with follicular mucinosis
Journal of Dermatology, 12/08/09