The Ser82 RAGE Variant Affects Lung Function and Serum RAGE in Smokers and sRAGE Production In Vitro (Q36166108)

12 August 2017

The Ser82 RAGE Variant Affects Lung Function and Serum RAGE in Smokers and sRAGE Production In Vitro (English)

1 reference

12 August 2017

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Tracy L Rimington

6

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Amanda P Henry

Amanda P Henry

2

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Andrew Wardlaw

Andrew J Wardlaw

20

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Ian P. Hall

Ian P Hall

21

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Suzanne Miller

Suzanne Miller

1

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Stuart G. Parker

Stuart G Parker

18

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Charlotte E Bolton

Charlotte E Bolton

15

0 references

Anders Malarstig

17

Anders Malarstig

1 reference

12 August 2017

9

Erik Melén

1 reference

12 August 2017

Emily Hodge

3

1 reference

12 August 2017

Alexander K Kheirallah

4

1 reference

12 August 2017

Charlotte K Billington

5

1 reference

12 August 2017

Sangita K Bhaker

7

1 reference

12 August 2017

Ma'en Obeidat

8

1 reference

12 August 2017

Simon K Merid

10

1 reference

12 August 2017

Caroline Swan

11

1 reference

12 August 2017

Catherine Gowland

12

1 reference

12 August 2017

Carl P Nelson

13

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12 August 2017

Ceri E Stewart

14

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12 August 2017

Iain Kilty

16

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12 August 2017

Miriam F Moffatt

19

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12 August 2017

Ian Sayers

22

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12 August 2017

language of work or name

English

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publication date

18 October 2016

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12 August 2017

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12 August 2017

11

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12 August 2017

10

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12 August 2017

e0164041

1 reference

Creative Commons Attribution 4.0 International

12 August 2017

start time

18 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

limma

Limma

2 references

22 June 2022

https://europepmc.org/article/PMC/5068780

based on heuristic

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

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Circulating soluble receptor for advanced glycation end products (sRAGE) as a biomarker of emphysema and the RAGE axis in the lung

2 October 2017

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The G82S polymorphism promotes glycosylation of the receptor for advanced glycation end products (RAGE) at asparagine 81: comparison of wild-type rage with the G82S polymorphic variant.

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Advanced glycation end products and its receptor (RAGE) are increased in patients with COPD.

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Expression of high-mobility group box 1 and of receptor for advanced glycation end products in chronic obstructive pulmonary disease

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Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function

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Genome-wide association study identifies five loci associated with lung function

2 October 2017

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PLAUR polymorphisms and lung function in UK smokers

2 October 2017

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Transcriptomic analysis of human lung development

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Multiple levels of regulation determine the role of the receptor for AGE (RAGE) as common soil in inflammation, immune responses and diabetes mellitus and its complications

2 October 2017

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2 October 2017

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RAGE and amyloid-beta peptide neurotoxicity in Alzheimer's disease

2 October 2017

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2 October 2017

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Systemic soluble receptor for advanced glycation endproducts is a biomarker of emphysema and associated with AGER genetic variants in patients with chronic obstructive pulmonary disease

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Embryonic overexpression of receptors for advanced glycation end-products by alveolar epithelium induces an imbalance between proliferation and apoptosis.

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23 September 2018

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23 September 2018

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23 September 2018

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Receptor for advanced glycation end-products is a marker of type I lung alveolar cells.

23 September 2018

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RAGE and arthritis: the G82S polymorphism amplifies the inflammatory response

23 September 2018

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23 September 2018

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Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0164041

De-N-glycosylation or G82S mutation of RAGE sensitizes its interaction with advanced glycation endproducts

21 January 2018

1 reference

PubMed

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Type II alveolar epithelial cells in lung express receptor for advanced glycation end products (RAGE) gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27755550

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0164041

1 reference

12 August 2017

0 references

1 reference

12 August 2017

1 reference