![]() | Hidemitsu HaradaDivision of Developmental Biology and Regenerative Medicine, Department of Anatomy, Iwate Medical University, 1-1-1, Idaidori, Yahaba, Iwate 028-3694, Japan. | Division of ... |
KOL Resume for Hidemitsu Harada
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2022 | Division of Developmental Biology and Regenerative Medicine, Department of Anatomy, Iwate Medical University, 1-1-1, Idaidori, Yahaba, Iwate 028-3694, Japan. |
2021 | Division of Developmental Biology and Regenerative Medicine, Department of Anatomy, Iwate Medical University, 1-1-1, Idaidori, Yahaba, Iwate 028-3694, Japan |
2020 | Division of Developmental Biology and Regenerative Medicine, Department of Anatomy, Iwate Medical University, Shiwa‐gun, Japan |
2019 | Department of Anatomy, Division of Developmental Biology & Regenerative Medicine, Iwate Medical University, 2‐1‐1 Nishitokuda, Yahaba, Iwate, Japan |
2018 | Division of Developmental Biology and Regenerative Medicine, Department of Anatomy, Iwate Medical University |
2017 | Department of Anatomy, Iwate Medical University, Iwate, Japan |
2016 | Division of Developmental Biology and Regenerative Medicine Department of Anatomy Iwate Medical University Iwate Japan |
2015 | Division of Oral Histology and Developmental Biology, School of Dentistry, Iwate Medical University, Iwate, Japan |
2014 | Division of Developmental Biology and Regenerative Medicine, Department of Anatomy, Iwate Medical University, 2-1-1, Nishitokuta, Yahaba, Iwate 028-3694, Japan |
2013 | Division of Developmental Biology & Regenerative Medicine, Department of Anatomy, Iwate Medical University, 2-1-1, Nishitokuda, Yahaba, Shiwa-gun, Iwate 020-3694, Japan |
2012 | Department of Oral Anatomy II, School of Dentistry, Iwate Medical University, Morioka, Iwate, Japan |
2011 | Division of Developmental Biology and Regenerative Medicine, Department of Anatomy, Iwate Medical University, Yahaba, Iwate, Japan |
2010 | Department of Oral Histology and Developmental Biology, Iwate Medical University, School of Dentistry, 1-3-27 Chuodori, 020-8505, Morioka, Iwate, Japan |
2009 | Department of Oral Anatomy II, School of Dentistry, Iwate Medical University, Morioka, Iwate 020-8505, Japan National Institute for the Control of Pharmaceutical & Biological Products, No. 2 Tiantan Xili, Beijing, 100050 China; |
2008 | Department of Oral Anatomy II, School of Dentistry, Iwate Medical University 1-3-27, Chuo-dori, Morioka, Iwate 020-8505, Japan |
2007 | Department of Oral Anatomy II, Iwate Medical College School of Dentistry, Morioka, Iwate 020-8505, Japan. |
2006 | Department of Oral Anatomy and Developmental Biology, Osaka University Graduate School of Dentistry, Suita, Japan |
2005 | Department of Oral Anatomy and Developmental Biology, Osaka University Graduate School of Dentistry, 1-8, Yamadaoka, Suita, Osaka 565-0871, Japan |
2004 | Department of Oral Anatomy and Cell Biology, Kyushu Dental College, 2-6-1, Manazuru, Kokurakita-ku, Kitakyushu, Japan, 803-8580; Section of Oral and Maxillofacial Oncology, Division of Maxillofacial Diagnostic and Surgical Sciences, Faculty of Dental Science, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, Japan, 812-8582; |
2003 | Department of Oral Anatomy and Developmental Biology, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka 565-0871, the |
2002 | Department of Oral Anatomy and Cell Biology, Kyushu Dental College, 2-6-1, Manazuru, Kokurakita-ku, Kitakyushu, Japan 803-8580 |
2000 | Department of Oral Anatomy and Cell Biology, Kyusyu Dental College, 2-6-1 Manazuru, Kokurakita-ku, Kitakyushu, 803-8580, Japan |
1999 | Developmental Biology Programme, Institute of Biotechnology, Viikki Biocenter, University of Helsinki, 00014 Helsinki, Finland |
1998 | Department of Oral Anatomy and Neurobiology, Kyushu Dental College, Kitakyushu, Japan |
1997 | Department of Oral Anatomy II, Kyushu Dental College, Kokurakita-ku, Kitakyushu 803, Japan |
1996 | Department of Agricultural Chemistry, Tokyo University of Agriculture, Setagayaku, Japan. |
1995 | Department of Agricultural Chemistry, Faculty of Agriculture, Tokyo University of Agriculture, Japan. |
1994 | First Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Kyushu University, Fukuoka, Japan |
1993 | Department of Oral Surgery Faculty of Dentistry, Kyushu University, Fukuoka, Japan |
1992 | Second Department of Anatomy, Faculty of Dentistry, Kyushu University, Fukuoka, Japan |
Hidemitsu Harada: Influence Statistics
Concept | World rank |
---|---|
cultured ameloblastoma | #1 |
cell collagen membrane | #1 |
anomaly root length | #1 |
powerful tool teeth | #1 |
submicron titanium | #1 |
incisors fgf10 | #1 |
mouse rat molar | #1 |
cell hers01a | #1 |
bulbous epithelial protrusion | #1 |
ki67 immunostaining oee | #1 |
root formation development | #1 |
epithelium mesenchyme sw | #1 |
apical tooth development | #1 |
glut1 dental epithelium | #1 |
identification suppressor element | #1 |
βcatenin root formation | #1 |
suppressor element | #1 |
transduction ameloblasts | #1 |
rho‐kinase ameloblast differentiation | #1 |
tooth emt | #1 |
notch stratum intermedium | #1 |
pig premolars | #1 |
lamp3 amelogenin | #1 |
tgfβ1 treatment hers01a | #1 |
enamel knotlike structure | #1 |
tooth differentiation culture | #1 |
polarity amelogenin | #1 |
harada tamaki | #1 |
incisor ki67 | #1 |
gingival epithelium pathway | #1 |
mice mice nclc | #1 |
ameloblast differentiation gtpases | #1 |
amelogenin protein lamp1 | #1 |
bmp signaling ameloblasts | #1 |
ameloblastoma mapk | #1 |
hers01a cell cultures | #1 |
cultured am1 | #1 |
enhanced mrna stabilization | #1 |
ameloblastlike cell | #1 |
sema4d rhoa | #1 |
collagen membrane differentiation | #1 |
Open the FULL List in Excel | |
Prominent publications by Hidemitsu Harada
In tooth development matrix metalloproteinases (MMPs) are under the control of several regulatory mechanisms including the upregulation of expression by inducers and downregulation by inhibitors. The aim of the present study was to monitor the occurrence and distribution pattern of the extracellular matrix metalloproteinase inducer (EMMPRIN), the metalloproteinases MMP-2 and MT1-MMP and caveolin-1 during the cap and bell stage of rat molar tooth germs by means of immunocytochemistry. ...
Known for Dental Epithelial Cells | Rat Tooth Germ | Membrane Rafts | Expression Emmprin | Enamel Organ |
Localization of Putative Stem Cells in Dental Epithelium and Their Association with Notch and Fgf Signaling
[ PUBLICATION ]
The continuously growing mouse incisor is an excellent model to analyze the mechanisms for stem cell lineage. We designed an organ culture method for the apical end of the incisor and analyzed the epithelial cell lineage by 5-bromo-2'-deoxyuridine and DiI labeling. Our results indicate that stem cells reside in the cervical loop epithelium consisting of a central core of stellate reticulum cells surrounded by a layer of basal epithelial cells, and that they give rise to ...
Known for Stem Cells | Dental Epithelium | Lunatic Fringe | Proteins Cell | Fibroblast Growth |
Mouse, rat and human molars begin to form root after the completion of crown formation. In these teeth, fibroblast growth factor (Fgf) 10 disappears in the transitional stage from crown formation to root. By contrast, rodent incisors and vole molars demonstrate continuous growth, owing to the formation and maintenance of a stem cell compartment by the constant expression of Fgf10. To clarify the relationship between root formation and disappearance of Fgf10, we carried out two ...
Known for Root Formation | Epithelial Stem | Fgf10 Signaling | Transition Crown | Rodent Incisors |
Critical Role of Heparin Binding Domains of Ameloblastin for Dental Epithelium Cell Adhesion and Ameloblastoma Proliferation*
[ PUBLICATION ]
AMBN (ameloblastin) is an enamel matrix protein that regulates cell adhesion, proliferation, and differentiation of ameloblasts. In AMBN-deficient mice, ameloblasts are detached from the enamel matrix, continue to proliferate, and form a multiple cell layer; often, odontogenic tumors develop in the maxilla with age. However, the mechanism of AMBN functions in these biological processes remains unclear. By using recombinant AMBN proteins, we found that AMBN had heparin binding domains at ...
Known for Cell Adhesion | Heparin Binding | Msx2 Expression | Enamel Matrix | Dental Epithelial |
Epithelial-mesenchymal interactions regulate the growth and morphogenesis of ectodermal organs such as teeth. Dental pulp stem cells (DPSCs) are a part of dental mesenchyme, derived from the cranial neural crest, and differentiate into dentin forming odontoblasts. However, the interactions between DPSCs and epithelium have not been clearly elucidated. In this study, we established a mouse dental pulp stem cell line (SP) comprised of enriched side population cells that displayed a ...
Known for Stem Cell | Dental Epithelial | Bone Morphogenetic | Ameloblast Markers | Dentin Sialophosphoprotein |
Neurotrophic Factor Neurotrophin-4 Regulates Ameloblastin Expression via Full-length TrkB *
[ PUBLICATION ]
Neurotrophic factors play an important role in the development and maintenance of not only neural but also nonneural tissues. Several neurotrophic factors are expressed in dental tissues, but their role in tooth development is not clear. Here, we report that neurotrophic factor neurotrophin (NT)-4 promotes differentiation of dental epithelial cells and enhances the expression of enamel matrix genes. Dental epithelial cells from 3-day-old mice expressed NT-4 and three variants of TrkB ...
Known for Neurotrophic Factor | Ameloblastin Expression | Erk1 2 | Hat7 Cells | Dental Epithelial |
Dental pulp is assumed to possess the capacity to elaborate both bone and dentin matrix under the pathological conditions following tooth injury. This study was undertaken to clarify the mechanism inducing bone formation in the dental pulp by investigating the pulpal healing process, after tooth replantation, by micro-computed tomography (μ-CT), immunocytochemistry for heat-shock protein (HSP)-25 and cathepsin K (CK), and histochemistry for both alkaline phosphatase (ALP) and ...
Known for Tooth Replantation | Dental Pulp | Healing Process | Rat Molars | Tissue Formation |
Expression of the Metabotropic Glutamate Receptor, mGluR4a, in the Taste Hairs of Taste Buds in Rat Gustatory Papillae
[ PUBLICATION ]
Taste-mGluR4, cloned from taste tissues, is a truncated variant of brain-expressed mGluR4a (brain-mGluR4), and is known to be a candidate for the receptor involved in the umami taste sense. Although the expression patterns of taste- and brain-mGluR4 mRNAs have been demonstrated, no mention has so far been made of the expression of these two mGluR4 proteins in taste tissues. The present study examined the expression of taste-mGluR4 and brain-mGluR4 proteins in rat taste tissues by using a ...
Known for Taste Buds | Metabotropic Glutamate | Rat Gustatory Papillae | Brain Mglur4 | Dawley Receptors |
A cementoblast progenitor cell line designated BCPb8 was successfully isolated from dental follicle cells immortalized with Bmi-1 and hTERT. BCPb8 showed the potential to differentiate into cementoblasts on implantation into immunodeficient mice. BCPb8 was confirmed to be the first established cementoblast progenitor cell line and will provide a useful model for investigating cementogenesis.
INTRODUCTION: The dental follicle is the mesenchymal tissue surrounding the developing tooth ...
Known for Progenitor Cells | Bmi1 Htert | Dental Follicle | Immunodeficient Mice | Cell Differentiation |
Mouse incisors are regenerative tissues that grow continuously throughout life. The renewal of dental epithelium-producing enamel matrix and/or induction of dentin formation by mesenchymal cells is performed by stem cells that reside in cervical loop of the incisor apex. However, little is known about the mechanisms of stem cell compartment formation. Recently, a mouse incisor was used as a model to show that fibroblast growth factor (FGF) 10 regulates mitogenesis and fate decision of ...
Known for Mouse Incisors | Stem Cell | Cervical Loop | Dental Epithelium | Incisor Mice |
Midkine (MK) is expressed during tooth development and, since ameloblastoma is thought to be arisen from the epithelium of the odontogenic apparatus or its remnant tissues, the effect of MK in ameloblastoma cell growth should be examined. The expression and function of MK were examined using 37 ameloblastoma tissues and AM-1 cells, an HPV-16DNA transfected ameloblastoma cell line. We found that MK was immunohistochemically expressed in 70% of ameloblastoma cases and AM-1 cells. By ...
Known for Akt Pathways | Midkine Mk | Am1 Cells | Tooth Development | Cell Growth |
Similar to embryonic stem cells, induced pluripotent stem (iPS) cells can differentiate into various cell types upon appropriate induction, and thus, may be valuable cell sources for regenerative medicine. However, iPS cells have not been reported to differentiate into odontogenic cells for tooth regeneration. Here we demonstrated that neural crest-like cells (NCLC) derived from mouse iPS cells have the potential to differentiate into odontogenic mesenchymal cells. We developed an ...
Known for Pluripotent Stem | Ips Cells | Tooth Regeneration | Dental Mesenchymal | Cell Differentiation |
Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood
[ PUBLICATION ]
The ablation of Apc function or the constitutive activation of beta-catenin in embryonic mouse oral epithelium results in supernumerary tooth formation, but the underlying mechanisms and whether adult tissues retain this potential are unknown. Here we show that supernumerary teeth can form from multiple regions of the jaw and that they are properly mineralized, vascularized, innervated and can start to form roots. Even adult dental tissues can form new teeth in response to either ...
Known for Supernumerary Tooth Formation | Wnt Signaling | Beta Catenin | New Teeth | Dental Tissues |
FGF10 Acts as a Major Ligand for FGF Receptor 2 IIIb in Mouse Multi-Organ Development
[ PUBLICATION ]
FGF receptor 2 isoform IIIb (FGFR2b), originally discovered as a receptor for FGF7, is known to be an important receptor in vertebrate morphogenesis, because FGFR2b null mice exhibit agenesis or dysgenesis of various organs, which undergo budding and branching morphogenesis. Since FGF7 null mice do not exhibit marked defects in organogenesis, it has been considered that other FGF(s) than FGF7 might function as a major ligand for FGFR2b during organogenesis. One of the candidate ligands ...
Known for Receptor 2 | Major Ligand | Fibroblast Growth Factor | Lung Development | Null Mice |
Key People For Stem Cells
Hidemitsu Harada:Expert Impact
Concepts for whichHidemitsu Haradahas direct influence:Stem cells, Tooth development, Ameloblast differentiation, Mouse incisors, Ips cells, Stem cell, Amelogenin protein, Dental epithelial cells.
Hidemitsu Harada:KOL impact
Concepts related to the work of other authors for whichfor which Hidemitsu Harada has influence:Stem cells, Tooth development, Dental pulp, Fibroblast growth factor, Cell proliferation, Tissue engineering, Branching morphogenesis.
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