(Q33530548)

27 July 2017

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

1 reference

dentinogenesis imperfecta

27 July 2017

0 references

1 reference

Haihua Bai

1

1 reference

27 July 2017

Hasi Agula

2

1 reference

27 July 2017

Qizhu Wu

3

1 reference

27 July 2017

Wenyu Zhou

4

1 reference

27 July 2017

Yujing Sun

5

1 reference

27 July 2017

Yue Qi

6

1 reference

27 July 2017

Suya Latu

7

1 reference

27 July 2017

Yujie Chen

8

1 reference

27 July 2017

Jiri Mutu

9

1 reference

27 July 2017

Changchun Qiu

10

1 reference

27 July 2017

10 February 2010

1 reference

27 July 2017

1 reference

27 July 2017

11

1 reference

27 July 2017

23

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-11-23

27 July 2017

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

Hereditary dentin defects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

DSPP mutation in dentinogenesis imperfecta Shields type II

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

Refined mapping of the human dentin sialophosphoprotein (DSPP) gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

Improved splice site detection in Genie

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

Genetic mapping of the dentinogenesis imperfecta type II locus.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2829541

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

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-23

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/10.1186%2F1471-2350-11-23

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/10.1186%2F1471-2350-11-23

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-23

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-23

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-23

Hereditary defects in enamel and dentin

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20146806

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20146806

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular basis of human dentin diseases

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20146806

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-11-23

1 reference

Dimensions Publication ID

27 July 2017

0 references

1 reference

27 July 2017

1 reference