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Dentinogenesis imperfecta without osteogenesis imperfecta

Known as: DENTINOGENESIS IMPERFECTA 1, OPALESCENT DENTIN, DGI-II 
National Institutes of Health

Related topics

Related topics

6 relations
Autosomal dominant inheritanceDSPP, ALA15VALDSPP, GLN45TERDSPP, VAL18PHE

Broader (1)

Dentinogenesis Imperfecta

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Bacillus subtilis RecO and SsbA are crucial for RecA-mediated recombinational DNA repair
Genetic data have revealed that the absence of Bacillus subtilis RecO and one of the end-processing avenues (AddAB or RecJ… 
Highly Cited
2010
Highly Cited
2010
Quantification and characterization of subvisible proteinaceous particles in opalescent mAb formulations using micro-flow imaging.
Micro-flow imaging (MFI) has been shown to be more sensitive than light obscuration (LO) methods for measuring subvisible… 
Review
2008
Review
2008
Dentinogenesis imperfecta: a review and case report of a family over four generations.
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal… 
Review
2006
Review
2006
STM-theory: Image potential, chemistry and surface relaxation
Highly Cited
2001
Highly Cited
2001
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
Dentinogenesis imperfecta 1 (DGI1, MIM 125490) is an autosomal dominant dental disease characterized by abnormal dentin… 
2001
2001
Use of water uptake and capillary suction time measures for evaluation of the anti-diarrhoeic properties of fibrous clays
Review
2000
Review
2000
Tools for tissue engineering of mineralized oral structures
Abstract This paper presents a short review of three groups of tools which can be or are used for the tissue engineering of… 
Highly Cited
1995
Highly Cited
1995
Mapping of the human dentin matrix acidic phosphoprotein gene (DMP1) to the dentinogenesis imperfecta type II critical region at chromosome 4q21.
Dentinogenesis imperfecta type II (DGI1) is an autosomal dominant disorder of dentin formation, which has been mapped to human… 
1985
1985
An unusual presentation of opalescent dentin and Brandywine isolate hereditary opalescent dentin in an Ashkenazic Jewish family.
1971
1971
Dentinogenesis imperfecta.
  • R. Jorgenson
  • Birth defects original article series
  • 1971
  • Corpus ID: 423287
Researchers have described three types of dentinogenesis imperfecta with similar dental abnormalities. Type I occurs in people… 
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