Long-Term Faithful Recapitulation of Transglutaminase 1–Deficient Lamellar Ichthyosis in a Skin-Humanized Mouse Model, and Insights from Proteomic Studies-Reference-Cited by-同舟云学术

Long-Term Faithful Recapitulation of Transglutaminase 1–Deficient Lamellar Ichthyosis in a Skin-Humanized Mouse Model, and Insights from Proteomic Studies

Published:2012-07 Issue:7 Volume:132 Page:1918-1921
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Aufenvenne Karin,Rice Robert H.,Hausser Ingrid,Oji Vinzenz,Hennies Hans Christian,Rio Marcela Del,Traupe Heiko,Larcher Fernando

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference13 articles.

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4. Novel transglutaminase-1 mutations and genotype-phenotype investigations of 104 patients with autosomal recessive congenital ichthyosis in the USA;Farasat;J Med Genet,2009

5. Development of skin-humanized models of Pachyonychia Congenita;García;J Invest Dermatol,2011

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2. Comprehensive Molecular Analysis of Disease-Related Genes as First-Tier Test for Early Diagnosis, Classification, and Management of Patients Affected by Nonsyndromic Ichthyosis;Biomedicines;2024-05-17

3. Cornification of keratinocytes is associated with differential changes in the catalytic activity and the immunoreactivity of transglutaminase-1;Scientific Reports;2023-12-06

4. A novel mutation compounded with a known mutation in TGM1 associated with severe lamellar ichthyosis and intellectual disability;European Journal of Dermatology;2023-08

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