(Q24610376)

11

0 references

Philippe M. Campeau

object named as

Philippe M Campeau

16

0 references

Richard A Gibbs

14

object named as

Richard A Gibbs

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author name string

Jay R Shapiro

1

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Monica Grover

3

0 references

James T Lu

4

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Sandesh Cs Nagamani

5

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Brian C Dawson

6

0 references

Dustin M Baldridge

7

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Matthew N Bainbridge

8

0 references

Dan H Cohn

9

0 references

Maria Blazo

10

0 references

Feng-Shu Brennen

12

0 references

Yimei Wu

13

0 references

Pamela Melvin

15

0 references

Brendan H Lee

Journal of Bone and Mineral Research

17

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language of work or name

English

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publication date

July 2013

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published in

0 references

volume

28

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issue

7

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page(s)

1523-30

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cites work

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Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndrome

7 April 2017

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Genetic heterogeneity in osteogenesis imperfecta

7 April 2017

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7 April 2017

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7 April 2017

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Characterization of the osteoblast-specific transmembrane protein IFITM5 and analysis of IFITM5-deficient mice

7 April 2017

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Bril: a novel bone-specific modulator of mineralization

7 April 2017

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7 April 2017

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7 April 2017

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7 April 2017

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7 April 2017

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A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus

27 September 2017

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A single recurrent mutation in the 5'-UTR of IFITM5 causes osteogenesis imperfecta type V.

27 September 2017

1 reference

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Hearing loss in osteogenesis imperfecta: characteristics and treatment considerations

27 September 2017

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Osteogenesis imperfecta: questions and answers

27 September 2017

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Effects of bisphosphonates in children with osteogenesis imperfecta: an AACPDM systematic review

27 September 2017

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Osteogenesis Imperfecta: update on presentation and management

27 September 2017

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27 September 2017

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The effect of cyclical intravenous pamidronate in children and adolescents with osteogenesis imperfecta type V.

27 September 2017

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27 September 2017

Osteogenesis imperfecta

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27 September 2017

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Osteogenesis imperfecta and hyperplastic callus formation in a family: a report of three cases and a review of the literature

27 September 2017

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Type V osteogenesis imperfecta: a new form of brittle bone disease

27 September 2017

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Distinct biochemical phenotypes predict clinical severity in nonlethal variants of osteogenesis imperfecta

27 September 2017

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Osteoblast-enriched membrane protein IFITM5 regulates the association of CD9 with an FKBP11-CD81-FPRP complex and stimulates expression of interferon-induced genes

27 September 2017

1 reference

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30 May 2018

1 reference

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Radial head dislocation and subluxation in osteogenesis imperfecta.

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FJBMR.1891

Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.-14C>T mutation in all patients.

21 January 2018

1 reference

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https://api.crossref.org/works/10.1002%2FJBMR.1891

Hereditary congenital posterior dislocation of radial heads

21 January 2018

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12 December 2020

MRI and CT features of hyperplastic callus in osteogenesis imperfecta tarda

1 reference

12 December 2020

Hyperplastic callus formation in osteogenesis imperfecta type V: follow-up of three generations over ten years

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12 December 2020

[Osteogenesis imperfecta in childhood and adolescence]

1 reference

12 December 2020