SPINK5, the Defective Gene in Netherton Syndrome, Encodes Multiple LEKTI Isoforms Derived from Alternative Pre-mRNA Processing
- 1 February 2006
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 126 (2) , 315-324
- https://doi.org/10.1038/sj.jid.5700015
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Nova regulates brain-specific splicing to shape the synapseNature Genetics, 2005
- Characterization and expression analysis of the Spink5 gene, the mouse ortholog of the defective gene in Netherton syndromeGenomics, 2005
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivityNature Genetics, 2004
- Lethal, neonatal ichthyosis with increased proteolytic processing of filaggrin in a mouse model of Netherton syndromeHuman Molecular Genetics, 2004
- Epidermal detachment, desmosomal dissociation, and destabilization of corneodesmosin in Spink5-/- miceGenes & Development, 2004
- LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndromeHuman Molecular Genetics, 2003
- The human integrin β4B and β4C variants are not expressed in a tissue‐specific mannerFEBS Letters, 2002
- A new mathematical model for relative quantification in real-time RT-PCRNucleic Acids Research, 2001
- Regulation and Regulatory Role of Proteinase InhibitorsCritical Reviews™ in Eukaryotic Gene Expression, 1995
- Isolation of a Crystalline Trypsin Inhibitor-Anticoagulant Protein from Pancreas1aJournal of the American Chemical Society, 1948