31 results on '"Ishii, Norito"'
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2. Cross-sectional survey on disease severity in Japanese patients with harlequin ichthyosis/ichthyosis: Syndromic forms and quality-of-life analysis in a subgroup
3. Plectin deficient epidermolysis bullosa simplex with 27-year-history of muscular dystrophy
4. Application and limitations of three-dimensional reconstruction of the epidermal–dermal junction using electron microscopy
5. A founder deletion of corneodesmosin gene (CDSN) is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases
6. Prevalence of filaggrin gene mutations in patients with atopic dermatitis and ichthyosis vulgaris in Kyushu area of Japan and South Korea
7. A possible example of an inverse intramolecular epitope-spreading phenomenon in bullous pemphigoid associated with psoriasis
8. Isolation of all CD44 transcripts in human epidermis and regulation of their expression by various agents
9. Molecular diagnosis of Nagashima-type palmoplantar keratoderma
10. Identification of CD44 transcripts that segregate with proliferation, redox and differentiation activities in human epidermal keratinocytes
11. Mutation and pathogenic study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia
12. Detection of IgE anti BP180 and anti BP230 autoantibodies in patients with bullous pemphigoid
13. Establishment of IgA ELISAs of mammalian recombinant proteins of human desmocollins 1–3
14. Corrigendum to ‘Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia’ [Journal of Dermatological Science 78 (2015) 82–85]
15. Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia
16. N-linked glycosylation on laminin γ1 influences recognition of anti-laminin γ1 pemphigoid autoantibodies
17. Homozygous deletion of six genes including corneodesmosin on chromosome 6p21.3 is associated with generalized peeling skin disease
18. An attempt to develop mouse model for anti-laminin γ1 pemphigoid
19. Studies of cultured Hailey-Hailey disease keratinocytes revealed pathogenic role of the mutations and novel mechanism in Ca2+ homeostasis
20. Newly developed IgA ELISAs of eukaryotic recombinant proteins of desmocollins 1-3 are more sensitive and specific than baculoprotein ELISAs
21. Isolation of mouse monoclonal antibodies reactive with maturation-related unique epitope(s) on human type VII collagen
22. An attempt to identify antigen for IgA pemphigus accidentally showed the presence of transmembrane secretory component in keratinocytes
23. Molecular studies of six pemphigus vulgaris cases in remission stage showed paradoxical changes of high titer anti-desmoglein 3 antibodies
24. Interaction of plectin and intermediate filaments
25. Development of NC1 and NC2 domains of Type VII collagen ELISA for the diagnosis and analysis of the time course of epidermolysis bullosa acquisita patients
26. The compound heterozygote for new/recurrent COL7A1 mutations in a Japanese patient with bullous dermolysis of the newborn
27. A Japanese family with dominant pretibial dystrophic epidermolysis bullosa: Identification of a new glycine substitution in the triple-helical collagenous domain of type VII collagen
28. Genotype–phenotype correlation in non-Hallopeau-Siemens recessive dystrophic epidermolysis bullosa: The splice site mutation c.6216+5G>T in the COL7A1 gene results in aberrant and normal splicings
29. A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases.
30. Studies of cultured Hailey-Hailey disease keratinocytes revealed pathogenic role of the mutations and novel mechanism in Ca2+ homeostasis
31. Genotype-phenotype correlation in non-Hallopeau-Siemens recessive dystrophic epidermolysis bullosa: the splice site mutation c.6216+5G > T in the COL7A1 gene results in aberrant and normal splicings.
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