162 results on '"Furuichi, Tatsuya"'
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2. Mice lacking nucleotide sugar transporter SLC35A3 exhibit lethal chondrodysplasia with vertebral anomalies and impaired glycosaminoglycan biosynthesis
3. Follistatin-like 1 (Fstl1) is a bone morphogenetic protein (BMP) 4 signaling antagonist in controlling mouse lung development
4. Zinc signal: a new player in osteobiology
5. ENU-induced missense mutation in the C-propeptide coding region of Col2a1 creates a mouse model of platyspondylic lethal skeletal dysplasia, Torrance type
6. A compound heterozygote of novel and recurrent DTDST mutations results in a novel intermediate phenotype of Desbuquois dysplasia, diastrophic dysplasia, and recessive form of multiple epiphyseal dysplasia
7. Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese
8. A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with Lumbar-disc herniation
9. Nucleotide-sugar transporter SLC35D1 is critical to chondroitin sulfate synthesis in cartilage and skeletal development in mouse and human
10. CANT1 mutation is also responsible for Desbuquois dysplasia, type 2 and Kim variant
11. CANT1 deficiency in a mouse model of Desbuquois dysplasia impairs glycosaminoglycan synthesis and chondrocyte differentiation in growth plate cartilage
12. Loss-of-Function Mutations of CHST14 in a New Type of Ehlers-Danlos Syndrome
13. Association of KLOTHO Gene Polymorphisms with Knee Osteoarthritis in Greek Population
14. A functional SNP in EDG2 increases susceptibility to knee osteoarthritis in Japanese
15. A novel dominant-negative mutation in Gdf5 generated by ENU mutagenesis impairs joint formation and causes osteoarthritis in mice
16. Effects of i.v. and oral 1,25-dihydroxy-22-oxavitamin D3 on secondary hyperparathyroidism in dogs with chronic renal failure
17. Crim1C140S mutant mice reveal the importance of cysteine 140 in the internal region 1 of CRIM1 for its physiological functions
18. Crim1C140S mutant mice reveal the importance of cysteine 140 in the internal region 1 of CRIM1 for its physiological functions.
19. Disruption of the mouse Slc39a14 gene encoding zinc transporter ZIP 14 is associated with decreased bone mass, likely caused by enhanced bone resorption
20. An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes
21. Runx2 and Runx3 are essential for chondrocyte maturation, and Runx2 regulates limb growth through induction of Indian hedgehog
22. Overexpression ofBCLXLin Osteoblasts Inhibits Osteoblast Apoptosis and Increases Bone Volume and Strength
23. Endoplasmic reticulum stress-mediated apoptosis contributes to a skeletal dysplasia resembling platyspondylic lethal skeletal dysplasia, Torrance type, in a novel Col2a1 mutant mouse line
24. Disruption of the mouse <italic>Slc39a14</italic> gene encoding zinc transporter ZIP14 is associated with decreased bone mass, likely caused by enhanced bone resorption.
25. SP7 Inhibits Osteoblast Differentiation at a Late Stage in Mice
26. Overexpression of bcl2 in osteoblasts inhibits osteoblast differentiation and induces osteocyte apoptosis.
27. New sequence variants in HLA Class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study
28. Overexpression of BCLXL in Osteoblasts Inhibits Osteoblast Apoptosis and Increases Bone Volume and Strength.
29. Zinc signal: a new player in osteobiology
30. SP7 Inhibits Osteoblast Differentiation at a Late Stage in Mice
31. Overexpression of Bcl2 in Osteoblasts Inhibits Osteoblast Differentiation and Induces Osteocyte Apoptosis
32. A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia
33. SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice
34. Chondroitin sulfate N-acetylgalactosaminyltransferase-1 is required for normal cartilage development
35. A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility
36. New Sequence Variants in HLA Class II/III Region Associated with Susceptibility to Knee Osteoarthritis Identified by Genome-Wide Association Study
37. Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation
38. Regulation of endoplasmic reticulum stress response by a BBF2H7-mediated Sec23a pathway is essential for chondrogenesis
39. Association of the Tag SNPs in the HumanSKTGene (KIAA1217) With Lumbar Disc Herniation
40. 糖ヌクレオチド輸送体SLC35D1 の機能不全は，マウスとヒトにおいて重度の骨格形成異常を引き起こす (第127回成医会総会一般演題)
41. Correction: The Zinc Transporter SLC39A13/ZIP13 Is Required for Connective Tissue Development; Its Involvement in BMP/TGF-β Signaling Pathways
42. The Zinc Transporter SLC39A13/ZIP13 Is Required for Connective Tissue Development; Its Involvement in BMP/TGF-β Signaling Pathways
43. Runx2 determines bone maturity and turnover rate in postnatal bone development and is involved in bone loss in estrogen deficiency
44. Runx2 regulates FGF2-inducedBmp2 expression during cranial bone development
45. Evaluation of 9.4-T MR microimaging in assessing normal and defective fetal bone development: comparison of MR imaging and histological findings
46. Runx2deficiency in chondrocytes causes adipogenic changes in vitro
47. Induction of Osteoclast Differentiation by Runx2 through Receptor Activator of Nuclear Factor-κB Ligand (RANKL) and Osteoprotegerin Regulation and Partial Rescue of Osteoclastogenesis in Runx2–/– Mice by RANKL Transgene
48. Core-binding factor β interacts with Runx2 and is required for skeletal development
49. EFFECT OF DNA METHYLATION ON GENE EXPRESSION FROM THE MAREK'S DISEASE VIRUS GENOME IN THE LYMPHOBLASTOID CELL LINE, MDCC-MSB1
50. DIFFERENTIAL TIME COURSE OF INDUCTION OF 1α,25-DIHYDROXYVITAMIN D3-24-HYDROXYLASE mRNA EXPRESSION IN RATS BY 1α,25-DIHYDROXYVITAMIN D3 AND ITS ANALOGS
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