(Q35004670)

5 August 2017

Polyalanine repeat polymorphism in RUNX2 is associated with site-specific fracture in post-menopausal females (English)

1 reference

5 August 2017

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Alexandre S Stephens

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Geoffrey C. Nicholson

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

6

Gary S Stein

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

4

Julie A Pasco

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

author name string

Nigel A Morrison

1

1 reference

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31 May 2020

Motomi Osato

3

1 reference

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31 May 2020

Nicolette Fozzard

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

Patsie Polly

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

language of work or name

English

0 references

publication date

23 September 2013

1 reference

5 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

issue

9

1 reference

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31 May 2020

page(s)

e72740

1 reference

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Creative Commons Attribution 4.0 International

31 May 2020

copyright license

start time

23 September 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Glutamine repeat variants in human RUNX2 associated with decreased femoral neck BMD, broadband ultrasound attenuation and target gene transactivation

8 July 2018

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RUNX2 tandem repeats and the evolution of facial length in placental mammals

8 July 2018

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Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

8 July 2018

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8 July 2018

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8 July 2018

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Bone turnover markers for osteoporotic status assessment? A systematic review of their diagnosis value at baseline in osteoporosis

8 July 2018

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Runx2 protein expression utilizes the Runx2 P1 promoter to establish osteoprogenitor cell number for normal bone formation

8 July 2018

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Induction and patterning of intramembranous bone

8 July 2018

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A Draft Sequence of the Neandertal Genome

8 July 2018

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Dose-dependent effects of Runx2 on bone development.

8 July 2018

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A Runx2 threshold for the cleidocranial dysplasia phenotype

8 July 2018

1 reference

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Mutations and promoter SNPs in RUNX2, a transcriptional regulator of bone formation.

8 July 2018

1 reference

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Selective Runx2-II deficiency leads to low-turnover osteopenia in adult mice

8 July 2018

1 reference

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Molecular origins of rapid and continuous morphological evolution

8 July 2018

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Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations

8 July 2018

1 reference

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Alleles of RUNX2/CBFA1 gene are associated with differences in bone mineral density and risk of fracture

8 July 2018

1 reference

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A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia

8 July 2018

1 reference

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Serum CTX: a new marker of bone resorption that shows treatment effect more often than other markers because of low coefficient of variability and large changes with bisphosphonate therapy

8 July 2018

1 reference

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Identification of incident fractures: the Geelong Osteoporosis Study

8 July 2018

1 reference

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Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

8 July 2018

1 reference

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Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

8 July 2018

1 reference

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Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

8 July 2018

1 reference

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Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

8 July 2018

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New approaches for interpreting projected bone densitometry data

8 July 2018

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Genetic and environmental determinants of peak bone mass in young men and women.

8 July 2018

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Cbf beta regulates Runx2 function isoform-dependently in postnatal bone development.

21 January 2018

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A noncommercial dual luciferase enzyme assay system for reporter gene analysis

21 January 2018

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Association of functionally different RUNX2 P2 promoter alleles with BMD.

21 January 2018

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Family-based association study of polymorphisms in the RUNX2 locus with hand bone length and hand BMD.

21 January 2018

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Association of a RUNX2 promoter polymorphism with bone mineral density in postmenopausal Korean women.

21 January 2018

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Variation in femoral length is associated with polymorphisms in RUNX2 gene

21 January 2018

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Selective deficiency of the "bone-related" Runx2-II unexpectedly preserves osteoblast-mediated skeletogenesis.

21 January 2018

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21 January 2018

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The Exclusion of High Trauma Fractures May Underestimate the Prevalence of Bone Fragility Fractures in the Community: The Geelong Osteoporosis Study

21 January 2018

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Prevalence of Osteoporosis in Australian Women

21 January 2018

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Promoter 2 -1025 T/C Polymorphism in the RUNX2 Gene Is Associated with Femoral Neck BMD in Spanish Postmenopausal Women

21 January 2018

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The diagnosis of osteoporosis

21 January 2018

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12 December 2020

Perspectives on RUNX genes: an update

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12 December 2020

Common polymorphisms rather than rare genetic variants of the Runx2 gene are associated with femoral neck BMD in Spanish women

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12 December 2020

Age- and Gender-Specific Rate of Fractures in Australia: A Population-Based Study

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12 December 2020

Absolute Fracture-Risk Prediction by a Combination of Calcaneal Quantitative Ultrasound and Bone Mineral Density

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12 December 2020

10.1371/JOURNAL.PONE.0072740

Identifiers

DOI

1 reference

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31 May 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json

31 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24086263%20AND%20SRC:MED&resulttype=core&format=json