In Vitro and Rapid In Situ Transglutaminase Assays for Congenital Ichthyoses – A Comparative Study
- 1 March 1998
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 110 (3), 268-271
- https://doi.org/10.1046/j.1523-1747.1998.00132.x
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Direct Evidence That Involucrin Is a Major Early Isopeptide Cross-linked Component of the Keratinocyte Cornified Cell EnvelopeJournal of Biological Chemistry, 1997
- Mapping of a second locus for lamellar ichthyosis to chromosome 2q33-35 [published erratum appears in Hum Mol Genet 1996 Jun;5(6):862-3]Human Molecular Genetics, 1996
- Lamellar Ichthyosis Is Genetically Heterogeneous–Cases with Normal Keratinocyte TransglutaminaseJournal of Investigative Dermatology, 1995
- Autosomal recessive lamellar ichthyosis: identification of a new mutation in transglutaminase 1 and evidence for genetic heterogeneityHuman Molecular Genetics, 1995
- Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosisNature Genetics, 1995
- Expression of Transglutaminase 1 in Human EpidermisJournal of Investigative Dermatology, 1995
- Structure and Organization of the Human Transglutaminase 3 Gene: Evolutionary Relationship to the Transglutaminase FamilyJournal of Investigative Dermatology, 1994
- Transglutaminase factor XIII uses proteinase‐like catalytic triad to crosslink macromoleculesProtein Science, 1994
- Covalently Bound Lipids of Human Stratum CorneumJournal of Investigative Dermatology, 1989
- Elevated n-alkanes in congenital ichthyosiform erythroderma. Phenotypic differentiation of two types of autosomal recessive ichthyosis.Journal of Clinical Investigation, 1984