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Dentinogenesis imperfecta without osteogenesis imperfecta
Known as:
DENTINOGENESIS IMPERFECTA 1
, OPALESCENT DENTIN
, DGI-II
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National Institutes of Health
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Related topics
Related topics
6 relations
Autosomal dominant inheritance
DSPP, ALA15VAL
DSPP, GLN45TER
DSPP, VAL18PHE
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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
B. Carrasco
,
Tribhuwan Yadav
,
Ester Serrano
,
J. Alonso
Nucleic acids research
2015
Corpus ID: 16073371
Genetic data have revealed that the absence of Bacillus subtilis RecO and one of the end-processing avenues (AddAB or RecJ…
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Highly Cited
2010
Highly Cited
2010
Quantification and characterization of subvisible proteinaceous particles in opalescent mAb formulations using micro-flow imaging.
D. K. Sharma
,
Peter Oma
,
Mark Pollo
,
M. Sukumar
Journal of pharmaceutical sciences
2010
Corpus ID: 206148777
Micro-flow imaging (MFI) has been shown to be more sensitive than light obscuration (LO) methods for measuring subvisible…
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Review
2008
Review
2008
Dentinogenesis imperfecta: a review and case report of a family over four generations.
S. Bhandari
,
K. Pannu
Indian journal of dental research : official…
2008
Corpus ID: 19787018
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal…
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Review
2006
Review
2006
STM-theory: Image potential, chemistry and surface relaxation
J. Blanco
,
F. Flores
,
R. Pérez
2006
Corpus ID: 12837536
Highly Cited
2001
Highly Cited
2001
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
S. Xiao
,
Chuan Yu
,
+15 authors
Xiangyin Kong
Nature Genetics
2001
Corpus ID: 22276124
Dentinogenesis imperfecta 1 (DGI1, MIM 125490) is an autosomal dominant dental disease characterized by abnormal dentin…
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2001
2001
Use of water uptake and capillary suction time measures for evaluation of the anti-diarrhoeic properties of fibrous clays
P. Cerezo
,
C. V. Iborra
,
A. López-Galindo
,
F. Ferrari
,
C. Caramella
2001
Corpus ID: 73581264
Review
2000
Review
2000
Tools for tissue engineering of mineralized oral structures
M. Dard
,
A. Sewing
,
J. Meyer
,
S. Verrier
,
S. Roessler
,
D. Scharnweber
Clinical Oral Investigations
2000
Corpus ID: 2644192
Abstract This paper presents a short review of three groups of tools which can be or are used for the tissue engineering of…
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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.
H. Aplin
,
K. L. Hirst
,
A. Crosby
,
M. Dixon
Genomics
1995
Corpus ID: 38118161
Dentinogenesis imperfecta type II (DGI1) is an autosomal dominant disorder of dentin formation, which has been mapped to human…
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1985
1985
An unusual presentation of opalescent dentin and Brandywine isolate hereditary opalescent dentin in an Ashkenazic Jewish family.
A. Heimler
,
J. Sciubba
,
E. Lieber
,
S. Kamen
Oral surgery, oral medicine, and oral pathology
1985
Corpus ID: 8435441
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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