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School of Health Science, Faculty of Medicine, Tottori University | 論文
- Genetic susceptibility in the neural tube defects induced by ochratoxin A in the genetic arhinencephaly mouse, Pdn/Pdn
- Exencephaly induction by valproic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn
- Effect of estrogen replacement therapy on arthritis and bone mineral density in estrogen-replete rats with collagen-induced arthritis
- Effect of ovariectomy and estrogen replacement therapy on arthritis and bone mineral density in mature rats with type II collagen-induced arthritis
- Prevention of ochratoxin A-induced neural tube defects by folic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn
- Altered signaling pathway in the dysmorphogenesis of telencephalon in the Gli3 depressed mouse embryo, Pdn/Pdn
- Knee deformity in rheumatoid arthritis is closely correlated with generalized osteoporosis
- Longitudinal change in periprosthetic, peripheral, and axial bone mineral density after total hip arthroplasty
- Influence of glucocorticoid on bone in 3-, 6-, and 12-month-old rats as determined by bone mass and histomorphometry
- Effect of parathyroid hormone on cortical bone response to in vivo external loading of the rat tibia
- The change of bone mineral density in secondary osteoporosis and vertebral fracture incidence
- Hydrocephalus manifestation in the genetic polydactyly/arhinencephaly mouse (Pdn/Pdn)
- Birth defects caused by mutations in human GLI3 and mouse Gli3 genes
- Gender-dependent differences in the incidence of ochratoxin A-induced neural tube defects in the Pdn/Pdn mouse
- Integration of a transposon into Gil3 in the genetic polydactyly/arhinencephaly mouse(Pdn/Pdn)(Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
- Over-expression of the Shh gene in the genetic polydactyly/arhinencephaly mouse (Pdn/Pdn) in which the gene responsible is Gil3(Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
- O-58 Analysis of Gli3 and Shh gene expressions in the genetic polydactyly/arhinencephaly mouse,(Pdn/Pdn)
- A-2 Cerabral abnormalities in the homozygous legless mouse (lgl/lgl).
- Exencephaly and embryonic lethality in Cbp knockout mouse embryo
- B-09 Phenotypic Similarity in Rubinstein-Taybi Syndrome and Knockout Mice in Cbp Gene.