Literature DB >> 4516067

A proposed classification for heritable human dentine defects with a description of a new entity.

E D Shields, D Bixler, A M el-Kafrawy.   

Abstract

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Year:  1973        PMID: 4516067     DOI: 10.1016/0003-9969(73)90075-7

Source DB:  PubMed          Journal:  Arch Oral Biol        ISSN: 0003-9969            Impact factor:   2.633


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  71 in total

1.  Klf10 regulates odontoblast differentiation and mineralization via promoting expression of dentin matrix protein 1 and dentin sialophosphoprotein genes.

Authors:  Zhuo Chen; Wentong Li; Han Wang; Chunyan Wan; Daoshu Luo; Shuli Deng; Hui Chen; Shuo Chen
Journal:  Cell Tissue Res       Date:  2015-08-28       Impact factor: 5.249

2.  Multiple pulp stones: a case report.

Authors:  Nurhat Ozkalayci; A Zeynep Zengin; Selma Elekdag Turk; A Pinar Sumer; Bilinc Bulucu; Tugrul Kirtiloglu
Journal:  Eur J Dent       Date:  2011-04

3.  Disorders of human dentin.

Authors:  P Suzanne Hart; Thomas C Hart
Journal:  Cells Tissues Organs       Date:  2007       Impact factor: 2.481

4.  Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III.

Authors:  M MacDougall; M Zeichner-David; J Murray; M Crall; A Davis; H Slavkin
Journal:  Am J Hum Genet       Date:  1992-01       Impact factor: 11.025

5.  Hereditary opalescent dentin.

Authors:  Kaushal Mahendra Shah
Journal:  BMJ Case Rep       Date:  2013-04-03

6.  Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP.

Authors:  Zofia von Marschall; Seeun Mok; Matthew D Phillips; Dianalee A McKnight; Larry W Fisher
Journal:  J Bone Miner Res       Date:  2012-06       Impact factor: 6.741

7.  Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21.

Authors:  M L Beattie; J-W Kim; S-G Gong; C A Murdoch-Kinch; J P Simmer; J C-C Hu
Journal:  J Dent Res       Date:  2006-04       Impact factor: 6.116

8.  A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II.

Authors:  J W Kim; S H Nam; K T Jang; S H Lee; C C Kim; S H Hahn; J C C Hu; J P Simmer
Journal:  Hum Genet       Date:  2004-07-06       Impact factor: 4.132

Review 9.  Site-specific function and regulation of Osterix in tooth root formation.

Authors:  Y D He; B D Sui; M Li; J Huang; S Chen; L A Wu
Journal:  Int Endod J       Date:  2016-01-04       Impact factor: 5.264

10.  Root anomalies and dentin dysplasia in autosomal recessive hyperphosphatemic familial tumoral calcinosis (HFTC).

Authors:  Alexandre R Vieira; Moses Lee; Filippo Vairo; Julio Cesar Loguercio Leite; Maria Cristina Munerato; Fernanda Visioli; Stéphanie Rodrigues D'Ávila; Shih-Kai Wang; Murim Choi; James P Simmer; Jan C-C Hu
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol       Date:  2015-05-28
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