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10 in total

1. Dentin phosphoprotein (DPP) activates integrin-mediated anchorage-dependent signals in undifferentiated mesenchymal cells.

Authors: Asha Eapen; Amsaveni Ramachandran; Anne George
Journal: J Biol Chem Date: 2011-12-01 Impact factor: 5.157

2. Failure to process dentin sialophosphoprotein into fragments leads to periodontal defects in mice.

Authors: Monica Prasad Gibson; Priyam Jani; Ying Liu; Xiaofang Wang; Yongbo Lu; Jian Q Feng; Chunlin Qin
Journal: Eur J Oral Sci Date: 2013-09-25 Impact factor: 2.612

3. DSPP contains an IRES element responsible for the translation of dentin phosphophoryn.

Authors: Y Zhang; Y Song; S Ravindran; Q Gao; C C Huang; A Ramachandran; A Kulkarni; A George
Journal: J Dent Res Date: 2013-12-18 Impact factor: 6.116

4. Rescue of odontogenesis in Dmp1-deficient mice by targeted re-expression of DMP1 reveals roles for DMP1 in early odontogenesis and dentin apposition in vivo.

Authors: Yongbo Lu; Ling Ye; Shibin Yu; Shubin Zhang; Yixia Xie; Marc D McKee; Yan Chun Li; Juan Kong; J David Eick; Sarah L Dallas; Jian Q Feng
Journal: Dev Biol Date: 2006-11-07 Impact factor: 3.582

5. 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

Assignment of dentin sialophosphoprotein (DSPP) to the critical DGI2 locus on human chromosome 4 band q21.3 by in situ hybridization.

1. Dentin phosphoprotein (DPP) activates integrin-mediated anchorage-dependent signals in undifferentiated mesenchymal cells.

2. Failure to process dentin sialophosphoprotein into fragments leads to periodontal defects in mice.

3. DSPP contains an IRES element responsible for the translation of dentin phosphophoryn.

4. Rescue of odontogenesis in Dmp1-deficient mice by targeted re-expression of DMP1 reveals roles for DMP1 in early odontogenesis and dentin apposition in vivo.

5. 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.

6. Acidic domain in dentin phosphophoryn facilitates cellular uptake: implications in targeted protein delivery.

7. A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene.

8. DSPP Is Essential for Normal Development of the Dental-Craniofacial Complex.

Review 9. Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.

10. Transgenic expression of dentin phosphoprotein inhibits skeletal development.