Shimizu Hiroshi | Department Of Dermatology Hokkaido University Graduate School Of Medicine

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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
Animation as a useful tool for assessing functional status in psoriatic arthritis
Amicrobial pustulosis associated with IgA nephropathy and Sjögren's syndrome
ITGB4 missense mutation in a transmembrane domain causes non-lethal variant of junctional epidermolysis bullosa with pyloric atresia
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
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
Multiple skin metastases of amelanotic melanoma originating from the sinonasal mucosa
Macrophage migration inhibitory factor (MIF) in bullous pemphigoid
Interleukin-1β and macrophage migration inhibitory factor (MIF) in dermal fibroblasts mediate UVA-induced matrix metalloproteinase-1 expression
Increase in macrophage migration inhibitory factor levels in lacrimal fluid of patients with severe atopic dermatitis
Coexistence of a systemic lupus erythematosus and porphyria cutanea tarda : case successfully improved by avoidance of sun exposure
Clinical and genetic analysis of Fabry disease : report of six cases including three heterozygous females
Novel mutation in a fumalate hydratase gene of a Japanese patient with multiple cutaneous and uterine leiomyomatosis
Polymorphisms in the muscarinic receptor 1 gene confer susceptibility to asthma in Japanese subjects.
Epithelioid sarcoma presenting as pulmonary cysts with cancer antigen 125 expression
Dietary glucosylceramide improves skin barrier function in hairless mice
A unique monoclonal antibody 29A stains the cytoplasm of amniotic epithelia and cutaneous basement membrane
Possible role of endoplasmic reticulum stress in the pathogenesis of Darier's disease
Tyrosinase gene analysis in Japanese patients with oculocutaneous albinism
Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa
The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa
ABCA12 dysfunction causes a disorder in glucosylceramide accumulation during keratinocyte differentiation
Chromosome 11q13.5 variant : No association with atopic eczema in the Japanese population
Topical application of anti-angiogenic peptides based on pigment epithelium-derived factor can improve psoriasis
Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome

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