(Q63729182)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22707062%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

title

Functional polymorphisms in the P2X7 receptor gene are associated with osteoporosis (English)

1 reference

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5 February 2020

5

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5 February 2020

author name string

L B Husted

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22707062%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

T Harsløf

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22707062%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

L Stenkjær

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22707062%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

M Carstens

4

1 reference

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5 February 2020

B L Langdahl

6

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5 February 2020

language of work or name

English

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publication date

16 June 2012

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22707062%20AND%20SRC:MED&resulttype=core&format=json

Osteoporosis International

5 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22707062%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

volume

24

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22707062%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

issue

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22707062%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

page(s)

949-959

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https://scigraph.springernature.com/pub.10.1007/s00198-012-2035-5

5 February 2020

exact match

0 references

cites work

A 5' intronic splice site polymorphism leads to a null allele of the P2X7 gene in 1-2% of the Caucasian population.

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12 December 2020

Expression of P2 receptors in bone and cultured bone cells

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Nucleotide receptors: an emerging family of regulatory molecules in blood cells

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An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor.

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A genome-wide association study of global gene expression

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P2X receptors as cell-surface ATP sensors in health and disease

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Human P2X7 pore function predicts allele linkage disequilibrium.

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A Thr357 to Ser polymorphism in homozygous and compound heterozygous subjects causes absent or reduced P2X7 function and impairs ATP-induced mycobacterial killing by macrophages

1 reference

12 December 2020

Expression of a P2X7 receptor by a subpopulation of human osteoblasts

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12 December 2020

Intercellular Calcium Signaling Occurs between Human Osteoblasts and Osteoclasts and Requires Activation of Osteoclast P2X7 Receptors

1 reference

12 December 2020

A His-155 to Tyr polymorphism confers gain-of-function to the human P2X7 receptor of human leukemic lymphocytes.

1 reference

12 December 2020

P2X7 receptor drives osteoclast fusion by increasing the extracellular adenosine concentration.

1 reference

12 December 2020

Extracellular nucleotides act through P2X7 receptors to activate NF-kappaB in osteoclasts

1 reference

12 December 2020

Rapid ATP-induced release of matrix metalloproteinase 9 is mediated by the P2X7 receptor

1 reference

12 December 2020

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

12 December 2020

Two haplotypes of the P2X(7) receptor containing the Ala-348 to Thr polymorphism exhibit a gain-of-function effect and enhanced interleukin-1beta secretion

1 reference

12 December 2020

Single-nucleotide polymorphisms in the P2X7 receptor gene are associated with post-menopausal bone loss and vertebral fractures

1 reference

12 December 2020

Risk of Wrist Fracture in Women Is Heritable and Is Influenced by Genes That Are Largely Independent of Those Influencing BMD

1 reference

12 December 2020

Functional variants of the P2RX7 gene, aseptic osteolysis, and revision of the total hip arthroplasty: A preliminary study

1 reference

12 December 2020

A Glu-496 to Ala polymorphism leads to loss of function of the human P2X7 receptor

1 reference

12 December 2020

Crystal structure of the ATP-gated P2X(4) ion channel in the closed state

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12 December 2020

Multinucleated osteoclast formation in vivo and in vitro by P2X7 receptor-deficient mice

1 reference

12 December 2020

Adenosine triphosphate-induced shedding of CD23 and L-selectin (CD62L) from lymphocytes is mediated by the same receptor but different metalloproteases.

1 reference

12 December 2020

Polymorphisms in the P2X7 receptor gene are associated with low lumbar spine bone mineral density and accelerated bone loss in post-menopausal women

1 reference

12 December 2020

P2X7 receptors on osteoblasts couple to production of lysophosphatidic acid: a signaling axis promoting osteogenesis

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12 December 2020

The assessment of vertebral deformity: a method for use in population studies and clinical trials

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12 December 2020

The diagnosis of osteoporosis

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12 December 2020

Altered cytokine production in mice lacking P2X(7) receptors

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12 December 2020

The P2X7 nucleotide receptor mediates skeletal mechanotransduction

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12 December 2020

Universal standardization for dual x-ray absorptiometry: patient and phantom cross-calibration results

1 reference

12 December 2020

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

1 reference

12 December 2020

Haploview: analysis and visualization of LD and haplotype maps

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12 December 2020

Activity-dependent development of P2X7 current and Ca2+ entry in rabbit osteoclasts

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12 December 2020

Deletion of the P2X7 nucleotide receptor reveals its regulatory roles in bone formation and resorption

1 reference

12 December 2020

P2Z purinoreceptor ligation induces activation of caspases with distinct roles in apoptotic and necrotic alterations of cell death

1 reference

12 December 2020

Glu496Ala polymorphism of human P2X7 receptor does not affect its electrophysiological phenotype

1 reference

12 December 2020

Risk factors for hip fracture in white women. Study of Osteoporotic Fractures Research Group.

1 reference

12 December 2020

An Ile-568 to Asn polymorphism prevents normal trafficking and function of the human P2X7 receptor

1 reference

12 December 2020

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

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12 December 2020

Segregation analysis and variance components analysis of bone mineral density in healthy families.

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12 December 2020

No association between hip geometry and four common polymorphisms associated with fracture: the Danish osteoporosis prevention study.

1 reference

12 December 2020

Single nucleotide polymorphisms that were identified in affective mood disorders affect ATP-activated P2X7 receptor functions

1 reference

12 December 2020

Identification and characterization of a novel variant of the human P2X(7) receptor resulting in gain of function

1 reference

12 December 2020

The cytolytic P2Z receptor for extracellular ATP identified as a P2X receptor (P2X7)

1 reference

12 December 2020

Blockade of the pore-forming P2X7 receptor inhibits formation of multinucleated human osteoclasts in vitro

1 reference

12 December 2020

Molecular physiology of P2X receptors

1 reference

12 December 2020

Gated access to the pore of a P2X receptor: structural implications for closed-open transitions.

1 reference

12 December 2020

Stress-activated protein kinase/JNK activation and apoptotic induction by the macrophage P2X7 nucleotide receptor

1 reference

12 December 2020

P2X7 nucleotide receptors mediate blebbing in osteoblasts through a pathway involving lysophosphatidic acid

1 reference

12 December 2020

Single nucleotide polymorphisms in the P2X7 gene are associated to fracture risk and to effect of estrogen treatment

1 reference

12 December 2020