A mouse model for human osteogenesis imperfecta type VI. (Q41956895)

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24 February 2020

title

A mouse model for human osteogenesis imperfecta type VI (English)

1 reference

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24 February 2020

main subject

osteogenesis imperfecta

0 references

author

Adele L. Boskey

7

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24 February 2020

author name string

Rosalind Bogan

1

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24 February 2020

Ryan C Riddle

2

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24 February 2020

Zhu Li

3

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24 February 2020

Sarvesh Kumar

4

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24 February 2020

Anjali Nandal

5

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24 February 2020

Marie-Claude Faugere

6

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24 February 2020

Susan E Crawford

8

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24 February 2020

Thomas L Clemens

9

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24 February 2020

publication date

1 July 2013

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Journal of Bone and Mineral Research

24 February 2020

published in

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volume

28

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24 February 2020

issue

7

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24 February 2020

page(s)

1531-1536

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Standardized nomenclature, symbols, and units for bone histomorphometry: a 2012 update of the report of the ASBMR Histomorphometry Nomenclature Committee

24 February 2020

cites work

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Mutations in SERPINF1 cause osteogenesis imperfecta type VI

5 June 2018

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New perspectives on osteogenesis imperfecta

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Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta

5 June 2018

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Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding

5 June 2018

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Characterization of PEDF: a multi-functional serpin family protein

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Aberrant Phex function in osteoblasts and osteocytes alone underlies murine X-linked hypophosphatemia

5 June 2018

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Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

5 June 2018

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Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta

5 June 2018

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Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.

5 June 2018

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CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta

5 June 2018

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Identification of a lipase-linked cell membrane receptor for pigment epithelium-derived factor

5 June 2018

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5 June 2018

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5 June 2018

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5 June 2018

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5 June 2018

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5 June 2018

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5 June 2018

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5 June 2018

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5 June 2018

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5 June 2018

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Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen

5 June 2018

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18 August 2018

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Osteogenesis imperfecta type VI: a form of brittle bone disease with a mineralization defect

18 August 2018

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18 August 2018

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A co-occurrence of osteogenesis imperfecta type VI and cystinosis

18 August 2018

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12 December 2020

Bone brittleness varies with genetic background in A/J and C57BL/6J inbred mice

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12 December 2020

Osteoblast-specific knockout of the insulin-like growth factor (IGF) receptor gene reveals an essential role of IGF signaling in bone matrix mineralization

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12 December 2020

Osteogenesis imperfecta type VI in childhood and adolescence: effects of cyclical intravenous pamidronate treatment

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12 December 2020

Identifiers

DOI

10.1002/JBMR.1892

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23413146 AND SRC:MED&resulttype=core&format=json

24 February 2020

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24 February 2020

PubMed publication ID

23413146

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23413146 AND SRC:MED&resulttype=core&format=json