(Q46379662)

21 December 2017

title

Functional splicing assay of DSPP mutations in hereditary dentin defects (English)

1 reference

21 December 2017

author name string

K-E Lee

1

1 reference

21 December 2017

S-K Lee

2

1 reference

21 December 2017

S-E Jung

3

1 reference

21 December 2017

Zh Lee

4

1 reference

21 December 2017

J-W Kim

5

1 reference

21 December 2017

publication date

8 July 2011

1 reference

21 December 2017

published in

Oral Diseases

1 reference

21 December 2017

volume

17

1 reference

21 December 2017

issue

7

1 reference

21 December 2017

page(s)

690-695

1 reference

21 December 2017

A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.X

Disorders of human dentin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.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.1601-0825.2011.01825.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.1601-0825.2011.01825.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.1601-0825.2011.01825.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.1601-0825.2011.01825.X

Novel dentin phosphoprotein frameshift mutations in dentinogenesis imperfecta type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.X

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 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.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.1601-0825.2011.01825.X

Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.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.1601-0825.2011.01825.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.1601-0825.2011.01825.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.1601-0825.2011.01825.X

Messenger RNA regulation: to translate or to degrade

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.X

Phenotypes and genotypes in 2 DGI families with different DSPP mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.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.1601-0825.2011.01825.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.1601-0825.2011.01825.X

DSPP mutation in dentinogenesis imperfecta Shields type II

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.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.1601-0825.2011.01825.X

Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-0825.2011.01825.X

10.1111/J.1601-0825.2011.01825.X

21 January 2018

Identifiers

DOI

1 reference

21 December 2017

1 reference

21 December 2017