Akiyama Masashi | Department Of Dermatology Hokkaido Graduate University School Of Medicine

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概要

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著作論文

Novel ABCA12 mutations identified in two cases of non-bullous congenital ichthyosiform erythroderma associated with multiple skin malignant neoplasia
Keratin 1 Gene Mutation Detected in Epidermal Nevus with Epidermolytic Hyperkeratosis
A novel OSMR mutation in familial primary localized cutaneous amyloidosis in a Japanese family
2P166 A comparison of structural properties in N-terminal domain of connexin26 associated to KID syndrome(34. Membrane protein,Poster Session,Abstract,Meeting Program of EABS & BSJ 2006)
Compound heterozygous mutations including a de novo missense mutation in ABCA12 led to a case of harlequin ichthyosis with moderate clinical severity
COL7A1 mutation G2037E causes epidermal retention of type VII collagen
Correlation of clinical severity and ELISA indices for the NC16A domain of BP180 measured using BP180 ELISA kit in bullous pemphigoid
In vivo transfer of TGF-α and β genes to keratinocytes
High expression of Ki-67 and cyclin D1 in invasive extramammary Paget's disease
Low-grade myxofibrosarcoma invaded into the underlying skeletal muscle
Remodeling of desmosomal and hemidesmosomal adhesion systems during human hair follicle development
Chromosome 11q13.5 variant : No association with atopic eczema in the Japanese population

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