(Q42409873)

English

The low-penetrance R92Q mutation of the tumour necrosis factor superfamily 1A gene is neither a major risk factor for Wegener's granulomatosis nor multiple sclerosis

scientific article published on September 2007

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

The low-penetrance R92Q mutation of the tumour necrosis factor superfamily 1A gene is neither a major risk factor for Wegener's granulomatosis nor multiple sclerosis (English)

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

0 references

0 references

author name string

Dieter E Jenne

1

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

Peer M Aries

2

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

Simon Einwächter

3

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

Amer D Akkad

4

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

Stefan Wieczorek

5

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

Peter Lamprecht

6

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

Wolfgang L Gross

7

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

language of work or name

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publication date

1 September 2007

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

Annals of the Rheumatic Diseases

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

66

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

9

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

1266-1267

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

Clinical significance of P46L and R92Q substitutions in the tumour necrosis factor superfamily 1A gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955148

28 May 2018

Stable incidence of primary systemic vasculitides over five years: results from the German vasculitis register

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955148

28 May 2018

Small vessel vasculitis and relapsing panniculitis in tumour necrosis factor receptor associated periodic syndrome (TRAPS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955148

28 May 2018

The TNF receptor-associated periodic syndrome (TRAPS): emerging concepts of an autoinflammatory disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955148

28 May 2018

Tumour necrosis factor receptor associated periodic syndrome (TRAPS) with central nervous system involvement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955148

16 August 2018

Polymorphism R92Q of the tumour necrosis factor receptor 1 gene is associated with myocardial infarction and carotid intima-media thickness--the ECTIM, AXA, EVA and GENIC Studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1955148

16 August 2018

A polymorphic microsatellite marker in the human p55 TNF receptor, CD120a

1 reference

https://pubmed.ncbi.nlm.nih.gov/17693606

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of evidence for an association between two genetic polymorphisms in the tumor necrosis factor receptor 1 gene and multiple sclerosis in Ashkenazi Jews

1 reference

https://pubmed.ncbi.nlm.nih.gov/17693606

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variants in the tumor necrosis factor receptor 1 gene in patients with MS

1 reference

https://pubmed.ncbi.nlm.nih.gov/17693606

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the R92QTNFRSF1Amutation and extracranial deep vein thrombosis in patients with Behçet's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17693606

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/ARD.2006.065987

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

30 October 2017

ResearchGate publication ID

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