Effects of Keratin 14 Ablation on the Clinical and Cellular Phenotype in a Kindred with Recessive Epidermolysis Bullosa Simplex-Reference-Cited by-同舟云学术

Effects of Keratin 14 Ablation on the Clinical and Cellular Phenotype in a Kindred with Recessive Epidermolysis Bullosa Simplex

Published:1996-11 Issue:5 Volume:107 Page:764-769
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Jonkman Marcel F.,Heeres Klaas,Pas Hendri H.,van Luyn Marja J.A.,Elema Job D.,Corden Laura D.,Smith Frances J.D.,McLean W.H. Irwin,Ramaekers Frans C.S.,Burton Margaret,Scheffer Hans

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference31 articles.

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2. A human keratin 14 'knockout': the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein;Chan;Genes Der,1995

3. The genetic basis of epidemolytic hyperkeratosis: a disorder of differentiation-sperific epidermal keratin genes;Cheng;Cell,1992

4. Human gene mutations affecting RNA processing and translation;Cooper;Ann Med,1993

5. Identification and characterization of genes that are required for the accelerated degradation of mRNAs containing a premature translational termination codon;Cui;Genes Dev,1995

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