194 results on '"Tokita, Yoshihito"'
Search Results
2. Novel WNT10A variant in a Japanese case of nonsyndromic oligodontia
3. A novel LRP6 variant in a Japanese family with oligodontia
4. Novel MSX1 frameshift mutation in a Japanese family with nonsyndromic oligodontia
5. Local application of Usag-1 siRNA can promote tooth regeneration in Runx2-deficient mice
6. Development of tooth regenerative medicine strategies by controlling the number of teeth using targeted molecular therapy
7. Identification of nuclear localization signals in the human homeoprotein MSX1
8. A novel in-frame deletion of the RUNX2 gene causes a classic form of cleidocranial dysplasia
9. Regeneration of optic nerve fibers with unoprostone, a prostaglandin-related antiglaucoma drug, in adult cats
10. Recovery of Mitogenic Activity of a Growth Factor Mutant with a Nuclear Translocation Sequence
11. Differential effects of two ROCK inhibitors, Fasudil and Y-27632, on optic nerve regeneration in adult cats
12. Neuroglycan C, A Brain-Specific Chondroitin Sulfate Proteoglycan, Interacts with Pleiotrophin, A Heparin-Binding Growth Factor
13. Reduction of Brain Injury in Neonatal Hypoxic—Ischemic Rats by Intracerebroventricular Injection of Neural Stem/Progenitor Cells Together With Chondroitinase ABC
14. Local application of Usag-1 siRNA can promote tooth regeneration in Runx2-deficient mice
15. A novel ROCK inhibitor, Y-39983, promotes regeneration of crushed axons of retinal ganglion cells into the optic nerve of adult cats
16. Neuroglycan C, a brain-specific part-time proteoglycan, with a particular multidomain structure
17. Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4
18. Developmental changes in the biochemical and immunological characters of the carbohydrate moiety of neuroglycan C, a brain-specific chondroitin sulfate proteoglycan
19. Identification of Neurite Outgrowth-promoting Domains of Neuroglycan C, a Brain-specific Chondroitin Sulfate Proteoglycan, and Involvement of Phosphatidylinositol 3-Kinase and Protein Kinase C Signaling Pathways in Neuritogenesis
20. Identification and Functions of Chondroitin Sulfate in the Milieu of Neural Stem Cells
21. R3HDM1haploinsufficiency is associated with mild intellectual disability
22. Intravitreal macrophage activation enables cat retinal ganglion cells to regenerate injured axons into the mature optic nerve
23. A highly sulfated chondroitin sulfate preparation, CS-E, prevents excitatory amino acid-induced neuronal cell death
24. Reduction of cerebral degeneration in neonatal hypoxic-ischemic rats by intracerebroventricular injection of neural stem/progenitor cells together with chondroitinase ABC: O-116
25. Ectodomain shedding of neuroglycan C, a brain-specific chondroitin sulfate proteoglycan, by TIMP-2- and TIMP-3-sensitive proteolysis
26. Fates of Cdh23/CDH23 With Mutations Affecting the Cytoplasmic Region
27. Glycosylation Site for Chondroitin Sulfate on the Neural Part-time Proteoglycan, Neuroglycan C
28. Neuroglycan C, a novel member of the neuregulin family
29. Phosphorylation of Neuroglycan C, a Brain-specific Transmembrane Chondroitin Sulfate Proteoglycan, and Its Localization in the Lipid Rafts
30. R3HDM1 haploinsufficiency is associated with mild intellectual disability.
31. Loss of Stemness, EMT, and Supernumerary Tooth Formation in Cebpb⁻/⁻Runx2⁺/⁻ Murine Incisors
32. Effects of Lipid-Derivatized Glycosaminoglycans (GAGs), a Novel Probe for Functional Analyses of GAGs, on Cell-to-Substratum Adhesion and Neurite Elongation in Primary Cultures of Fetal Rat Hippocampal Neurons
33. Molecular Interactions of Neural Chondroitin Sulfate Proteoglycans in the Brain Development
34. Genomic Organization and Expression Pattern of Mouse Neuroglycan C in the Cerebellar Development
35. Loss of Stemness, EMT, and Supernumerary Tooth Formation in Cebpb⁻/⁻Runx2⁺/⁻ Murine Incisors
36. Use of Anti-phospho-girdin Antibodies to Visualize Intestinal Tuft Cells in Free-Floating Mouse Jejunum Cryosections
37. WNT10A variants isolated from Japanese patients with congenital tooth agenesis
38. Novel RUNX2/CBFA1 mutation in the runt domain in a Japanese patient with cleidocranial dysplasia
39. Disparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23
40. Characterisation of novel RUNX2 mutation with alanine tract expansion from Japanese cleidocranial dysplasia patient
41. An Aberrant Splice Acceptor Site Due to a Novel Intronic Nucleotide Substitution in MSX1 Gene Is the Cause of Congenital Tooth Agenesis in a Japanese Family
42. Characterization of Novel MSX1 Mutations Identified in Japanese Patients with Nonsyndromic Tooth Agenesis
43. A novel PITX2 mutation causing iris hypoplasia
44. Novel nonsense mutation inMSX1in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4
45. Regeneration of optic nerve fibers with unoprostone, a prostaglandin-related antiglaucoma drug, in adult cats
46. A novel in-frame deletion of the RUNX2 gene causes a classic form of cleidocranial dysplasia
47. Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia
48. Effect of psychotropic drugs on behavior of mice which show abnormal expressions of neuroglycan C, a brain-specific chondroitin sulfate proteoglycan
49. Roles of the chondroitin sulfate chain on the core protein of neuroglycan C, a brain-specific transmembrane proteoglycan
50. A highly sulfated chondroitin sulfate preparation, CS-E, prevents excitatory amino acid-induced neuronal cell death
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.