(Q51896986)

17 April 2018

title

Identification of the DSPP mutation in a new kindred and phenotype-genotype correlation. (English)

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17 April 2018

author name string

S-K Lee

1

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17 April 2018

K-E Lee

2

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17 April 2018

Y-H Hwang

3

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17 April 2018

M Kida

4

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17 April 2018

T Tsutsumi

5

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17 April 2018

T Ariga

6

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17 April 2018

J-C Park

7

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17 April 2018

J-W Kim

8

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17 April 2018

publication date

28 October 2010

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17 April 2018

published in

Oral Diseases

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17 April 2018

volume

17

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17 April 2018

issue

3

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17 April 2018

page(s)

314-319

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17 April 2018

Dentin sialoprotein, dentin phosphoprotein, enamelysin and ameloblastin: tooth-specific molecules that are distinctively expressed during murine dental differentiation

cites work

1 reference

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Abnormal dentin structure in two novel gene mutations [COL1A1, Arg134Cys] and [ADAMTS2, Trp795-to-ter] causing rare type I collagen disorders

21 January 2018

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Disorders of human dentin

21 January 2018

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An unusual presentation of opalescent dentin and Brandywine isolate hereditary opalescent dentin in an Ashkenazic Jewish family

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

Hereditary dentin defects

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

A dentin sialophosphoprotein mutation that partially disrupts a splice acceptor site causes type II dentin dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

A novel mutation in the DSPP gene associated with dentinogenesis imperfecta type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

Dentin phosphoprotein frameshift mutations in hereditary dentin disorders and their variation patterns in normal human population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

Epithelial-mesenchymal signalling regulating tooth morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

A novel splice site mutation in the dentin sialophosphoprotein gene in a Chinese family with dentinogenesis imperfecta type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

DSPP mutation in dentinogenesis imperfecta Shields type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2010.01760.X

10.1111/J.1601-0825.2010.01760.X

21 January 2018

Identifiers

DOI

1 reference

17 April 2018

PubMed ID

21029264

1 reference

17 April 2018