- Dentinogenesis imperfecta type II: A case report with 17 years of follow-up
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Gama FJ, Corrêa IS, Valerio CS, Ferreira E, Manzi FR
- KMID: 2389894
- Imaging Sci Dent.
- 2017 Jun;47(2):129-133.
- doi: 10.5624/isd.2017.47.2.129
Dentinogenesis imperfecta is a dominant autosomal hereditary disorder of dentin formation that affects the deciduous and permanent teeth. Its etiology is characterized by inadequate cell differentiation during odontogenesis. The clinical... -
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- The Blue Sclera in Osteogenesis Imperfecta
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Kim SE, Lim KH, Ahn CS
- KMID: 2336654
- J Korean Ophthalmol Soc.
- 1998 Jan;39(1):204-208.
Osteogenesis imperfecta is relatively rare hereditary disease. It is characterized by frequent multiple bone fractures, spine scoliosis due to fragility of bone and is often associated with blue sclera, deafness... -
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- The role of nuclear factor I-C in tooth and bone development
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Roh SY, Park JC
- KMID: 2377007
- J Korean Assoc Oral Maxillofac Surg.
- 2017 Apr;43(2):63-69.
- doi: 10.5125/jkaoms.2017.43.2.63
Nuclear factor I-C (NFI-C) plays a pivotal role in various cellular processes such as odontoblast and osteoblast differentiation. Nfic-deficient mice showed abnormal tooth and bone formation. The transplantation of Nfic-expressing... -
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- Osteogenesis Imperfecta (Correction of Anterior Tibial Bowing): A case report
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Seo JS, Ihn JC
- KMID: 2373929
- Yeungnam Univ J Med.
- 1987 Aug;4(1):157-163.
- doi: 10.12701/yujm.1987.4.1.157
Osteogenesis imperfecta has been categorized as a heritable disorder of connective tissue affecting both bone and soft tissues and is characterized by fragility of bone, blue sclera, and deafness, less... -
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- Full-mouth rehabilitation with CAD/CAM monolithic zirconia in dentinogenesis imperfecta: a case report
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Kim MK, Kim SH, Lee JB, Han JS, Yeo IS, Ha SR
- KMID: 2321794
- J Korean Acad Prosthodont.
- 2014 Oct;52(4):317-323.
- doi: 10.4047/jkap.2014.52.4.317
Dentinogenesis Imperfecta, with a high incidence rate of 1 : 6 - 8000, is inherited by autosomal dominant genetic transmission. This dental disorder causes discoloration of the teeth and the... -
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- The comparison of gene expression from human dental pulp cells and periodontal ligament cells
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So H, Park SH, Choi GW
- KMID: 1986606
- J Korean Acad Conserv Dent.
- 2009 Sep;34(5):430-441.
- doi: 10.5395/JKACD.2009.34.5.430
The purpose of this study was to characterize functional distinction between human dental pulp cells(PC) and periodontal ligament cells(PDLC) using cDNA microarray assay and to confirm the results of the... -
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- A Case of Neurofibromatosis Type I with Osteogenesis Imperfecta Type I
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Lee EJ, Kim WS
- KMID: 2329595
- J Korean Child Neurol Soc.
- 2006 Nov;14(2):369-374.
Neurofibromatosis type I is one of the most common autosomal dominant disorders, characterized by cafe au-lait spots, axillary freckling, Lisch nodules in the iris, multiple neurofibromas and the bone involvement... -
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- Histological Study of Reparative Dentin Formation after Direct Pulp Capping and Pulpotomy using MTA
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Park SH, Hwang HK, Kim HJ, Park JC
- KMID: 2224474
- Korean J Anat.
- 2006 Jun;39(3):235-243.
The ultimate goal of a regenerative pulp treatment strategy is to reconstitute normal tissue continuum at the pulp-dentin border, regulating tissue-specific processes of reparative dentinogenesis. However, little is known about the molecular... -
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- The Role of Autonomous Wntless in Odontoblastic Differentiation of Mouse Dental Pulp Cells
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Choi H, Kim TH, Ko SO, Cho ES
- KMID: 2382973
- J Korean Dent Sci.
- 2016 Jun;9(1):9-18.
- doi: 10.5856/JKDS.2016.9.1.9
PURPOSE: Wnt signaling plays an essential role in the dental epithelium and mesenchyme during tooth morphogenesis. Deletion of the Wntless (Wls) gene in odontoblasts appears to reduce canonical Wnt activity,... -
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- A Case of Type I Osteogenesis Imperfecta Differentially Diagnosed as a Cause of a Spinal Compression Fracture
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Rhee SY, Moon SY, Chon S, Jeong IK, Oh S, Ahn KJ, Chung HY, Woo JT, Kim SW, Kim YS, Kim JW
- KMID: 1958910
- J Korean Endocr Soc.
- 2007 Dec;22(6):446-452.
- doi: 10.3803/jkes.2007.22.6.446
Osteogenesis imperfecta (OI) is a genetic disease that is caused by a synthetic anomaly of type I collagen. It is characterized by such features as low bone density, multiple fractures,... -
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- Requirement of Smad4-mediated signaling in odontoblast differentiation and dentin matrix formation
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Yun CY, Choi H, You YJ, Yang JY, Baek JA, Cho ES
- KMID: 2353345
- Anat Cell Biol.
- 2016 Sep;49(3):199-205.
- doi: 10.5115/acb.2016.49.3.199
Dentin is the major part of tooth and formed by odontoblasts. Under the influence of the inner enamel epithelium, odontoblasts differentiate from ectomesenchymal cells of the dental papilla and secrete... -
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- Clinical Characteristics of 10 Cases of Korean Osteogenesis Imperfecta
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Lee HS, Kim HJ, Cho JH, Lee SW, Kim HA, Choi JH, Song YJ, Kim DJ, Lee KW, Chung YS
- KMID: 2331188
- J Korean Soc Endocrinol.
- 2003 Oct;18(5):496-503.
Osteogenesis Imperfecta (OI) is a relatively rare hereditary disease, which is characterized by multiple bone fractures and spine scoliosis, due to the fragility of bone, and is often associated with... -
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- Prevalence of dental anomalies among 7- to 35-year-old people in Hamadan, Iran in 2012-2013 as observed using panoramic radiographs
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Shokri A, Poorolajal J, Khajeh S, Faramarzi , Kahnamoui
- KMID: 1974468
- Imaging Sci Dent.
- 2014 Mar;44(1):7-13.
- doi: 10.5624/isd.2014.44.1.7
PURPOSE: This study was performed to evaluate the prevalence of all types and subtypes of dental anomalies among 7- to 35-year-old patients by using panoramic radiographs. MATERIALS AND METHODS: This cross-sectional... -
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- Expression and functional characterization of odontoblast-derived gene: OD314
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Kim DH, Kim HJ, Jeong MJ, Son HH, Park JC
- KMID: 2175634
- J Korean Acad Conserv Dent.
- 2004 Jul;29(4):399-408.
- doi: 10.5395/JKACD.2004.29.4.399
Odontoblasts are responsible for the formation and maintenance of dentin. They are known to synthesize unique gene products including dentin sialophosphoprotein (DSPP). Another unique genes of the cells remain unclear. OD314... -
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