Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation (Q35156029)

6 August 2017

title

Long-term clinical outcome and carrier phenotype in autosomal recessive hypophosphatemia caused by a novel DMP1 mutation (English)

1 reference

6 August 2017

Serap Turan

4

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Outi Mäkitie

object named as

Outi Mäkitie

1

0 references

Harald Jüppner

9

object named as

Harald Jüppner

1 reference

6 August 2017

5

Murat Bastepe

1 reference

6 August 2017

Renata C Pereira

2

1 reference

6 August 2017

Ilkka Kaitila

3

1 reference

6 August 2017

Tero Laine

6

1 reference

6 August 2017

Heikki Kröger

7

1 reference

6 August 2017

William G Cole

8

1 reference

6 August 2017

language of work or name

1 reference

1 October 2010

1 reference

Journal of Bone and Mineral Research

6 August 2017

published in

1 reference

6 August 2017

volume

25

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6 August 2017

issue

10

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6 August 2017

page(s)

2165-2174

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Bone formation regulates circulating concentrations of fibroblast growth factor 23.

6 August 2017

cites work

1 reference

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Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia

28 July 2018

1 reference

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Patterns of FGF-23, DMP1, and MEPE expression in patients with chronic kidney disease

28 July 2018

1 reference

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Molecular analysis of DMP1 mutants causing autosomal recessive hypophosphatemic rickets

28 July 2018

1 reference

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Studies of the DMP1 57-kDa functional domain both in vivo and in vitro

28 July 2018

1 reference

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PHEX, FGF23, DMP1 and beyond

28 July 2018

1 reference

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Pathogenic role of Fgf23 in Dmp1-null mice.

28 July 2018

1 reference

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

28 July 2018

1 reference

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Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype

28 July 2018

1 reference

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MRI of the axial skeletal manifestations of ankylosing spondylitis

28 July 2018

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

28 July 2018

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28 July 2018

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Bone histomorphometry: standardization of nomenclature, symbols, and units. Report of the ASBMR Histomorphometry Nomenclature Committee

28 July 2018

1 reference

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Therapeutic effects of anti-FGF23 antibodies in hypophosphatemic rickets/osteomalacia

28 July 2018

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Prevalence of dural ectasia in 63 gene-mutation-positive patients with features of Marfan syndrome type 1 and Loeys-Dietz syndrome and report of 22 novel FBN1 mutations

27 September 2018

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Usefulness of a quick decalcification of bone sections embedded in methyl methacrylate[corrected]: an improved method for immunohistochemistry

27 September 2018

1 reference

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

27 September 2018

1 reference

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DMP1 depletion decreases bone mineralization in vivo: an FTIR imaging analysis

27 September 2018

1 reference

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Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS

27 September 2018

1 reference

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The Dentin Matrix Protein 1 (Dmp1) is Specifically Expressed in Mineralized, but not Soft, Tissues during Development

27 September 2018

1 reference

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

27 September 2018

1 reference

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Gene expression patterns of murine dentin matrix protein 1 (Dmp1) and dentin sialophosphoprotein (DSPP) suggest distinct developmental functions in vivo

27 September 2018

1 reference

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A type I collagen defect leads to rapidly progressive osteoarthritis in a mouse model

27 September 2018

1 reference

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Bone mineral density in Marfan syndrome. A large case-control study

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20499351

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/JBMR.105

1 reference

6 August 2017

1 reference

6 August 2017

1 reference