Transglutaminase 1 Mutations in Lamellar Ichthyosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference46 articles.
1. Autosomal dominant lamellar ichthyosis: a new skin disorder*
2. Heterogeneity in Autosomal Recessive Ichthyosis
3. Clinical, Histologic, and Cell Kinetic Discriminants Between Lamellar Ichthyosis and Nonbullous Congenital Ichthyosiform Erythroderma
4. The Ichthyoses: A Guide to Clinical Diagnosis, Genetic Counseling, and Therapy;Traupe,1989
5. Ichthyosis: Mechanisms of Disease
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1. Cornification of keratinocytes is associated with differential changes in the catalytic activity and the immunoreactivity of transglutaminase-1;Scientific Reports;2023-12-06
2. Increased Osteoclastogenesis in Absence of TG2 Is Reversed by Transglutaminase Inhibition—Evidence for the Role for TG1 in Osteoclast Formation;Cells;2023-08-24
3. Identification and In Silico Analysis of a Homozygous Nonsense Variant in TGM1 Gene Segregating with Congenital Ichthyosis in a Consanguineous Family;Medicina;2023-01-02
4. Transglutaminase 3 is expressed in basal cell carcinoma of the skin;European Journal of Dermatology;2019-10
5. A Tunisian family with a novel mutation in the gene CYP 4F22 for lamellar ichthyosis and co‐occurrence of hearing loss in a child due to mutation in the SLC 26A4 gene;International Journal of Dermatology;2019-04-25
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