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Publications by Michihiro Kono
A Child With Epidermolytic Ichthyosis From a Parent With Epidermolytic Nevus: Risk Evaluation of Transmission From Mosaic to Germline
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
PLoS ONE
Multidisciplinary
Related publications
Annular Epidermolytic Ichthyosis
Autosomal Dominant Epidermolytic Ichthyosis
Mutation p.R156H of KRT10 Responsible for Severe Phenotype of Epidermolytic Ichthyosis in a Chinese Family
Therapeutics and Clinical Risk Management
Histopathologic Characterization of Epidermolytic Hyperkeratosis: A Systematic Review of Histology From the National Registry for Ichthyosis and Related Skin Disorders
Journal of the American Academy of Dermatology
Dermatology
198 TALEN-mediated Gene Editing in Epidermolytic Ichthyosis Patient-Derived Keratinocytes
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Gene Editing-Mediated Disruption of Epidermolytic Ichthyosis-Associated KRT10 Alleles Restores Filament Stability in Keratinocytes
Journal of Investigative Dermatology
Biochemistry
Dermatology
Cell Biology
Molecular Biology
Plasmids in Epidermolytic Strains of Staphylococcus Aureus
Microbiology
Microbiology
Mutations in the Keratin 9 Gene in Pakistani Families With Epidermolytic Palmoplantar Keratoderma
Clinical and Experimental Dermatology
Dermatology
Comparing Histopathology From Patients With X-Linked Recessive Ichthyosis and Autosomal Recessive Congenital Ichthyosis With Transglutaminase 1 Mutation: A Report From the National Registry for Ichthyosis and Related Skin Disorders
Journal of the American Academy of Dermatology
Dermatology
