(Q33666435)

28 July 2017

title

Phenotype characterization and DSPP mutational analysis of three Brazilian dentinogenesis imperfecta type II families (English)

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dentinogenesis imperfecta

28 July 2017

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1 reference

A C Acevedo

1

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28 July 2017

L J S Santos

2

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28 July 2017

L M Paula

3

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28 July 2017

J Dong

4

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28 July 2017

M MacDougall

5

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28 July 2017

publication date

16 September 2008

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28 July 2017

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28 July 2017

volume

189

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28 July 2017

issue

1-4

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28 July 2017

page(s)

230-236

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A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family

28 July 2017

cites work

1 reference

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Disorders of human dentin

21 June 2018

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

21 June 2018

1 reference

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Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.

21 June 2018

1 reference

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Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

21 June 2018

1 reference

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DSPP mutation in dentinogenesis imperfecta Shields type II

21 June 2018

1 reference

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Dentin phosphoprotein and dentin sialoprotein are cleavage products expressed from a single transcript coded by a gene on human chromosome 4. Dentin phosphoprotein DNA sequence determination

21 June 2018

1 reference

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Heritable dentin defects: nosology, pathology, and treatment

21 June 2018

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

21 June 2018

1 reference

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Inherited defects in tooth structure

21 June 2018

1 reference

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Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification

21 June 2018

1 reference

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Hereditary defects of dentin

21 June 2018

1 reference

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Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III.

21 June 2018

1 reference

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

30 October 2018

1 reference

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Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II.

30 October 2018

1 reference

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Dentin sialophosphoprotein knockout mouse teeth display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta type III.

30 October 2018

1 reference

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Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization

30 October 2018

1 reference

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Intrafibrillar mineral may be absent in dentinogenesis imperfecta type II (DI-II).

30 October 2018

1 reference

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Novel COL1A1 mutation (G559C) [correction of G599C] associated with mild osteogenesis imperfecta and dentinogenesis imperfecta

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2824200

Medical and dental findings in the Brandywine isolate

30 October 2018

1 reference

12 December 2020

The inorganic phase in dentinogenesis imperfecta

1 reference

12 December 2020

Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II

1 reference

12 December 2020

Molecular basis of human dentin diseases

1 reference

12 December 2020

Dentinogenesis imperfecta in a six-generation family. A clinical, radiographic and histologic comparison of two branches through three generations

1 reference

12 December 2020

Identifiers

DOI

10.1159/000152917

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28 July 2017

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28 July 2017

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