(Q83157612)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

title

A novel nonsense mutation in the DMP1 gene in a Japanese family with autosomal recessive hypophosphatemic rickets (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

autosomal recessive hypophosphatemic rickets

19 January 2020

main subject

0 references

author name string

Ryusuke Koshida

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Hideki Yamaguchi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Koji Yamasaki

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Wakaba Tsuchimochi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Tadato Yonekawa

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

Masamitsu Nakazato

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

publication date

9 March 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

Journal of Bone and Mineral Metabolism

19 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

volume

28

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

page(s)

585-590

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

Dentin matrix protein 1 regulates dentin sialophosphoprotein gene transcription during early odontoblast differentiation

19 January 2020

cites work

1 reference

12 December 2020

A novel recessive mutation in fibroblast growth factor-23 causes familial tumoral calcinosis

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel mutation in fibroblast growth factor 23 gene as a cause of tumoral calcinosis

1 reference

12 December 2020

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

1 reference

12 December 2020

Nucleation of apatite crystals in vitro by self-assembled dentin matrix protein 1.

1 reference

12 December 2020

Characterization of a novel dentin matrix acidic phosphoprotein. Implications for induction of biomineralization

1 reference

12 December 2020

Clinical usefulness of measurement of fibroblast growth factor 23 (FGF23) in hypophosphatemic patients: proposal of diagnostic criteria using FGF23 measurement

1 reference

12 December 2020

Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics

1 reference

12 December 2020

Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalacia

1 reference

12 December 2020

Differentiation of embryonic mesenchymal cells to odontoblast-like cells by overexpression of dentin matrix protein 1.

1 reference

12 December 2020

DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.

1 reference

12 December 2020

Flexible structures of SIBLING proteins, bone sialoprotein, and osteopontin

1 reference

12 December 2020

Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulation

1 reference

12 December 2020

Circulating concentration of FGF-23 increases as renal function declines in patients with chronic kidney disease, but does not change in response to variation in phosphate intake in healthy volunteers

1 reference

12 December 2020

Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism.

1 reference

12 December 2020

Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia

1 reference

12 December 2020

Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23

1 reference

12 December 2020

Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic rickets

1 reference

12 December 2020

How fibroblast growth factor 23 works

1 reference

12 December 2020

Nomogram for derivation of renal threshold phosphate concentration

1 reference

12 December 2020

A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium

1 reference

12 December 2020

Mutant FGF-23 responsible for autosomal dominant hypophosphatemic rickets is resistant to proteolytic cleavage and causes hypophosphatemia in vivo.

1 reference

12 December 2020

Dentin matrix protein 1 (DMP1): new and important roles for biomineralization and phosphate homeostasis

1 reference

12 December 2020

Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia

1 reference

12 December 2020

10.1007/S00774-010-0169-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20213538%20AND%20SRC:MED&resulttype=core&format=json

19 January 2020

1 reference