(Q47221692)

12 January 2018

title

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

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12 January 2018

dentinogenesis imperfecta

main subject

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B Malmgren

1

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12 January 2018

S Lindskog

series ordinal

2

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12 January 2018

A Elgadi

series ordinal

3

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12 January 2018

S Norgren

series ordinal

4

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12 January 2018

publication date

3 February 2004

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12 January 2018

number of pages

8

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inferred from page(s)

published in

Human Genetics

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12 January 2018

volume

114

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12 January 2018

issue

5

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12 January 2018

page(s)

491-498

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12 January 2018

https://scigraph.springernature.com/pub.10.1007/s00439-004-1084-z

exact match

0 references

cites work

Dentin matrix proteins

1 reference

12 December 2020

A novel rat 523 amino acid phosphophoryn: nucleotide sequence and genomic organization.

1 reference

12 December 2020

Six decades of dentinogenesis research. Historical and prospective views on phosphophoryn and dentin sialoprotein.

1 reference

12 December 2020

MEPE/OF45, a new dentin/bone matrix protein and candidate gene for dentin diseases mapping to chromosome 4q21.

1 reference

12 December 2020

DSPP mutation in dentinogenesis imperfecta Shields type II

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Refinement of the dentinogenesis imperfecta type II locus to an interval of less than 2 centiMorgans at chromosome 4q21 and the creation of a yeast artificial chromosome contig of the critical region

1 reference

12 December 2020

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

12 December 2020

Nomenclature for the description of human sequence variations.

1 reference

12 December 2020

Dentinogenesis imperfecta: genetic variations in a six-generation family

1 reference

12 December 2020

Inherited defects in tooth structure

1 reference

12 December 2020

The HUGO Gene Nomenclature Committee (HGNC).

1 reference

12 December 2020

Characterization of porcine dentin sialoprotein (DSP) and dentin sialophosphoprotein (DSPP) cDNA clones

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

Assessment of dysplastic dentin in osteogenesis imperfecta and dentinogenesis imperfecta

1 reference

12 December 2020

Rat dentin matrix protein 3 is a compound protein of rat dentin sialoprotein and phosphophoryn.

1 reference

12 December 2020

Genomic organization, chromosomal mapping, and promoter analysis of the mouse dentin sialophosphoprotein (Dspp) gene, which codes for both dentin sialoprotein and dentin phosphoprotein.

1 reference

12 December 2020

Manifestations of genetic diseases in the human pulp

1 reference

12 December 2020

Molecular cloning of a human dentin sialophosphoprotein gene

1 reference

12 December 2020

Six generations of hereditary opalescent dentin: report of case

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00439-004-1084-Z

Identifiers

DOI

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12 January 2018

PubMed ID

14758537

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12 January 2018