GOTO Maki | Department of Dermatology, Hokkaido University Graduate School of Medicine

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概要

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著作論文

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
COL7A1 mutation G2037E causes epidermal retention of type VII collagen
In vivo transfer of TGF-α and β genes to keratinocytes
Required Transient Dose Escalation of Tacrolimus in Living-Donor Liver Transplant Recipients with High Concentrations of a Minor Metabolite M-II in Bile
Common single nucleotide polymorphisms of the MDR1 gene have on influence on its mRNA expression level of normal kidney cortex and renal cell carcinoma in Japanese nephrectomized patients
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

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