44 results on '"Tachikawa, Kanako"'
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2. Growth-related skeletal changes and alterations in phosphate metabolism
3. Clonal osteoblastic cell lines with CRISPR/Cas9-mediated ablation of Pit1 or Pit2 show enhanced mineralization despite reduced osteogenic gene expression
4. Novel mutation in the ALPL gene with a dominant negative effect in a Japanese family
5. Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients
6. The Effect of Asfotase Alfa on Plasma and Urine Pyrophosphate Levels and Pseudofractures in a Patient With Adult‐Onset Hypophosphatasia
7. A unique case of childhood hypophosphatasia caused by a novel heterozygous 51-bp in-frame deletion in the ALPL gene
8. Discordant fetal phenotype of hypophosphatasia in two siblings
9. Cover Image, Volume 176A, Number 1, January 2018
10. Interleukin-1-induced acute bone resorption facilitates the secretion of fibroblast growth factor 23 into the circulation
11. Vinculin Functions as Regulator of Chondrogenesis
12. Benign prenatal hypophosphatasia: a treatable disease not to be missed
13. Signaling of extracellular inorganic phosphate up-regulates cyclin D1 expression in proliferating chondrocytes via the Na +/Pi cotransporter Pit-1 and Raf/MEK/ERK pathway
14. Novel mutation in the ALPL gene with a dominant negative effect in a Japanese family
15. Involvement of nuclear factor I transcription/replication factor in the early stage of chondrocytic differentiation
16. Common mutations F310L and T1559del in the tissue-nonspecific alkaline phosphatase gene are related to distinct phenotypes in Japanese patients with hypophosphatasia
17. Sodium-coupled neutral amino acid transporter 4 functions as a regulator of protein synthesis during liver development
18. Czech Dysplasia Occurring in a Japanese Family
19. A case of osteopathia striata with cranial sclerosis with facial nerve palsies.
20. Hypophosphatasia in Japan: ALPL Mutation Analysis in 98 Unrelated Patients
21. Findings of amplitude-integrated electroencephalogram recordings and serum vitamin B6 metabolites in perinatal lethal hypophosphatasia during enzyme replacement therapy
22. Hypophosphatasia in Japan: ALPL mutation analysis in 98 patients
23. Glycosylated tris-bipyridine ferrous complexes as molecular mimics of densely packed glycoclusters on cell surfaces: spatial carbohydrate packing of glycoclusters changes on additions of salts
24. CREB activation in hypertrophic chondrocytes is involved in the skeletal overgrowth in epiphyseal chondrodysplasia Miura type caused by activating mutations of natriuretic peptide receptor B
25. Cover Image, Volume 176A, Number 1, January 2018
26. Discordant fetal phenotype of hypophosphatasia in two siblings
27. CREB activation in hypertrophic chondrocytes is involved in the skeletal overgrowth in epiphyseal chondrodysplasia Miura type caused by activating mutations of natriuretic peptide receptor B.
28. Extracellular Phosphate Induces the Expression of Dentin Matrix Protein 1 Through the FGF Receptor in Osteoblasts
29. Reversible Deterioration in Hypophosphatasia Caused by Renal Failure With Bisphosphonate Treatment
30. Interleukin-1-induced acute bone resorption facilitates the secretion of fibroblast growth factor 23 into the circulation
31. Elevated Fibroblast Growth Factor 23 Exerts Its Effects on Placenta and Regulates Vitamin D Metabolism in Pregnancy of Hyp Mice
32. Dysregulated Gene Expression in the Primary Osteoblasts and Osteocytes Isolated from Hypophosphatemic Hyp Mice
33. Benign prenatal hypophosphatasia: a treatable disease not to be missed
34. Phenotypic change in a patient with hypophosphatasia with the onset of renal failure
35. A case of autosomal dominant osteopetrosis type II with a novel TCIRG1 gene mutation
36. Both FGF23 and extracellular phosphate activate Raf/MEK/ERK pathway via FGF receptors in HEK293 cells
37. Signaling of extracellular inorganic phosphate up-regulates cyclin D1 expression in proliferating chondrocytes via the Na+/Pi cotransporter Pit-1 and Raf/MEK/ERK pathway
38. Clinical Characteristics of Perinatal Lethal Hypophosphatasia: A Report of 6 Cases
39. PTH/cAMP/PKA signaling facilitates canonical Wnt signaling via inactivation of glycogen synthase kinase‐3β in osteoblastic Saos‐2 cells
40. Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome
41. Dysregulated Gene Expression in the Primary Osteoblasts and Osteocytes Isolated from Hypophosphatemic Hyp Mice.
42. PTH/cAMP/PKA signaling facilitates canonical Wnt signaling via inactivation of glycogen synthase kinase-3β in osteoblastic Saos-2 cells.
43. A case of autosomal dominant osteopetrosis type II with a novel TCIRG1gene mutation
44. Efficacy of asfotase alfa in a patient with adult-onset hypophosphatasia without obvious bone lesions: a case report with review of literature.
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