(Q34388792)

English

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

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22912713%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

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

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22912713%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Alexandre S Stephens

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22912713%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

7

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11 February 2020

Geoffrey C. Nicholson

14

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11 February 2020

Stuart H Ralston

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Stuart H Ralston

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11 February 2020

8

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Julie Pasco

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11 February 2020

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Nigel A Morrison

1

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11 February 2020

Motomi Osato

3

1 reference

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11 February 2020

Patsie Polly

4

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11 February 2020

Timothy C Tan

5

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11 February 2020

Namiko Yamashita

6

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11 February 2020

Nicolette Fozzard

9

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Europe PubMed Central

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11 February 2020

Philip N Sambrook

12

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11 February 2020

Richard L Prince

13

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11 February 2020

Graeme Jones

10

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11 February 2020

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13 August 2012

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11 February 2020

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22912713%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

7

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22912713%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

8

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22912713%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

e42617

1 reference

Europe PubMed Central

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11 February 2020

copyright license

Creative Commons Attribution 4.0 International

13 August 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Building strong bones: molecular regulation of the osteoblast lineage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Bovine proteins containing poly-glutamine repeats are often polymorphic and enriched for components of transcriptional regulatory complexes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Mechanisms of trinucleotide repeat instability during human development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Perspectives of Kennedy's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

A Draft Sequence of the Neandertal Genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Effects of calcium supplementation on clinical fracture and bone structure: results of a 5-year, double-blind, placebo-controlled trial in elderly women.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Molecular origins of rapid and continuous morphological evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Bone-specific transcription factor Runx2 interacts with the 1alpha,25-dihydroxyvitamin D3 receptor to up-regulate rat osteocalcin gene expression in osteoblastic cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Amyloid fibers are water-filled nanotubes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Cbfa1 is a positive regulatory factor in chondrocyte maturation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

pEF-BOS, a powerful mammalian expression vector

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

6 July 2018

Polyglutamine tracts as modulators of transcriptional activation from yeast to mammals.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

Molecular dynamics simulation study on the structural stabilities of polyglutamine peptides.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

Association between leptin, body composition, sex and knee cartilage morphology in older adults: the Tasmanian older adult cohort (TASOAC) study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

The correlated evolution of Runx2 tandem repeats, transcriptional activity, and facial length in Carnivora

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

Genetic effects on bone loss in peri- and postmenopausal women: a longitudinal twin study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

Association of functionally different RUNX2 P2 promoter alleles with BMD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

Vitamin D receptor genotypes influence the success of calcitriol therapy for recurrent vertebral fracture in osteoporosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

RUNX2 alleles associated with BMD in Scottish women; interaction of RUNX2 alleles with menopausal status and body mass index

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

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

1 reference

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27 October 2018

A noncommercial dual luciferase enzyme assay system for reporter gene analysis

1 reference

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27 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418257

27 October 2018

The population burden of fractures originates in women with osteopenia, not osteoporosis

1 reference

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Treatment of postmenopausal osteoporosis with calcitriol or calcium

1 reference

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inferred from PubMed ID database lookup

The diagnosis of osteoporosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22912713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Perspectives on RUNX genes: an update

1 reference

https://pubmed.ncbi.nlm.nih.gov/22912713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22912713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22912713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22912713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PEBP2alphaA/CBFA1 mutations in Japanese cleidocranial dysplasia patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/22912713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

VDR-Alien: a novel, DNA-selective vitamin D(3) receptor-corepressor partnership

1 reference

https://pubmed.ncbi.nlm.nih.gov/22912713

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of Osteoporosis in Australian Women

1 reference

https://pubmed.ncbi.nlm.nih.gov/22912713

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inferred from PubMed ID database lookup

COL1A1 Sp1 polymorphism predicts perimenopausal and early postmenopausal spinal bone loss

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based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0042617

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22912713%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

2012PLoSO...742617M

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22912713%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22912713%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

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