スポンサーリンク
Department of Anatomy, School of Medicine, Tokushima University | 論文
- A novel P gene missense mutation in a Japanese patient with oculocutaneous albinism type II (OCA2)
- 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
- Genome-Wide Analysis of the Effects of Location and Number of Stress Response Elements on Gene Expression in Saccharovyces cerevisiae(BIOINFORMATICS)
- Distinct Roles of Two Anaplerotic Pathways in Glutamate Production Induced by Biotin Limitation in Corynebacterium glutamicum(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)
- Comparison of Transcriptional Responses to Osmotic Stresses Induced by NaCl and Sorbitol Additions in Saccharomyces cerevisiae Using DNA Microarray(BIOINFORMATICS)
- Dietary glucosylceramide improves skin barrier function in hairless mice
- Effect of Dietary Phosphate on Na^+-Dependent Phosphate Cotransporters Function and Expression in the Rat Kidney
- Dietary regulation of renal phosphate transporters in hypophosphatemic mice
- Radial glial cells in the developing brain of mice prenatally exposed to γ-irradiation
- Acute Regulation by Dietary Phosphate of the Sodium-Dependent Phosphate Transporter (NaP_i-2) in Rat Kidney^1
- 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
- Nonisothermal Crystallization Kinetics of Biodegradable Random Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) and Block One
- 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
- Occupational factors, smoking habits and tobacco withdrawal symptoms among male Japanese employees
- Pemphigus : from immunofluorescence to molecular biology
- Compound heterozygosity for premature termination codon and glycine substitution mutations in the COL7A1 gene in Korean siblings with a moderately severe phenotype of recessive dystrophic epidermolysis bullosa