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Disorders of human dentin
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
title
Disorders of human dentin
(English)
1 reference
stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
author name string
P Suzanne Hart
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
Thomas C Hart
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
publication date
1 January 2007
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stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
published in
Cells Tissues Organs
1 reference
stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
volume
186
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stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
issue
1
1 reference
stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
page(s)
70-77
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stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
cites work
Abnormal dentin structure in two novel gene mutations [COL1A1, Arg134Cys] and [ADAMTS2, Trp795-to-ter] causing rare type I collagen disorders
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Hyperphosphatemic familial tumoral calcinosis caused by a mutation in GALNT3 in a European kindred
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
MMP20 active-site mutation in hypomaturation amelogenesis imperfecta
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Dentin glycoprotein: the protein in the middle of the dentin sialophosphoprotein chimera
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Post-translational modifications of sibling proteins and their roles in osteogenesis and dentinogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Odontoblasts: the cells forming and maintaining dentine
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Dentin extracellular matrix (ECM) proteins: comparison to bone ECM and contribution to dynamics of dentinogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
DSPP mutation in dentinogenesis imperfecta Shields type II
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Flexible structures of SIBLING proteins, bone sialoprotein, and osteopontin
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Classical Ehlers-Danlos syndrome caused by a mutation in type I collagen
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
The carboxyl-terminal domain of phosphophoryn contains unique extended triplet amino acid repeat sequences forming ordered carboxyl-phosphate interaction ridges that may be essential in the biomineralization process
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Dentinogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
A proposed classification for heritable human dentine defects with a description of a new entity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Genetic heterogeneity in osteogenesis imperfecta
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
1 October 2017
Seckel syndrome associated with oligodontia, microdontia, enamel hypoplasia, delayed eruption, and dentin dysmineralization: a new variant?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
2 July 2018
Dentinogenesis imperfecta in the Brandywine isolate (DI type III): clinical, radiologic, and scanning electron microscopic studies of the dentition
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
2 July 2018
Dentin sialophosphoprotein is processed by MMP-2 and MMP-20 in vitro and in vivo.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Matrix metalloproteinase-8 (MMP-8) is the major collagenase in human dentin.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Expression of HMGB1 during tooth development.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Expression and potential role of dentin phosphophoryn (DPP) in mouse embryonic tissues involved in epithelial-mesenchymal interactions and branching morphogenesis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Phenotypes and genotypes in 2 DGI families with different DSPP mutations.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Dentinogenesis imperfecta associated with short stature, hearing loss and mental retardation: a new syndrome with autosomal recessive inheritance?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
A novel GALNT3 mutation in a pseudoautosomal dominant form of tumoral calcinosis: evidence that the disorder is autosomal recessive
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Dentin sialophosphoprotein knockout mouse teeth display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta type III.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Odontoblasts enhance the maturation of enamel crystals by secreting EMSP1 at the enamel-dentin junction
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Novel COL1A1 mutation (G559C) [correction of G599C] associated with mild osteogenesis imperfecta and dentinogenesis imperfecta
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4617234
retrieved
22 September 2018
Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17627120
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Hereditary defects in enamel and dentin
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17627120
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
An autosomal-dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17627120
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1159/000102682
1 reference
stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
PMCID
4617234
1 reference
stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
PubMed ID
17627120
1 reference
stated in
Europe PubMed Central
PMCID
4617234
retrieved
12 August 2017
ResearchGate publication ID
6211317
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