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Human Polyclonal MEFV Primary Antibody für WB - ABIN1881537
Cosan, Ustek, Oku, Duymaz-Tozkir, Cakiris, Abaci, Ocal, Aral, Gül: Association of familial Mediterranean fever-related MEFV variations with ankylosing spondylitis. in Arthritis and rheumatism 2010
Show all 4 Pubmed References
Human Polyclonal MEFV Primary Antibody für IP, WB - ABIN1169260
Papin, Cuenin, Agostini, Martinon, Werner, Beer, Grütter, Grütter, Tschopp: The SPRY domain of Pyrin, mutated in familial Mediterranean fever patients, interacts with inflammasome components and inhibits proIL-1beta processing. in Cell death and differentiation 2007
Human Polyclonal MEFV Primary Antibody für ELISA, WB - ABIN269824
Rabinovich, Livneh, Langevitz, Brezniak, Shinar, Pras, Shinar: Severe disease in patients with rheumatoid arthritis carrying a mutation in the Mediterranean fever gene. in Annals of the rheumatic diseases 2005
Human Polyclonal MEFV Primary Antibody für ELISA, WB - ABIN561791
Taskiran, Cetinkaya, Balci-Peynircioglu, Akkaya, Yilmaz: The effect of colchicine on pyrin and pyrin interacting proteins. in Journal of cellular biochemistry 2012
This article summarizes the broad spectrum of clinical presentations associated with MEFV mutations and analyzes the effect of the gene dose on the phenotypical expression. Furthermore, the impact of the molecular genetic analysis on the diagnostics of a patient and on the individualized management of the disease is discussed.
Case Report: autoinflammatory syndrome with relapsing aseptic neutrophilic meningitis and chronic myelitis associated with MEFV/TNFRSF1A (zeige TNFRSF1A Antikörper) mutations.
The mutations of p.R42W, p.L110P, p.E148Q, p.R202Q, p.E230K, p.369PS, and p.R408Q, which have been reported in many Familial Mediterranean Fever patients, had significant allele frequency differences with the disease-causing mutations.
Contrary to the NLRP3 (zeige NLRP3 Antikörper) mutations described in cryopyrin (zeige NLRP3 Antikörper)-associated periodic syndrome, FMF-associated MEFV mutations do not lead to a constitutive activation of Pyrin. Rather, FMF-associated mutations are hypermorphic mutations that specifically decrease the activation threshold of the Pyrin inflammasome without affecting other canonical inflammasomes.
There was a statistically significant different response to surgical treatment between patients with periodic fever, aphthosis, pharyngitis, and adenitis (PFAPA) Syndrome with and without coexistence of Familial Mediterranean Fever features and MEFV mutations.
The study indicates that the MEFV M694V mutation may contribute to the pathogenesis of ankylosing spondylitis. (Meta-analysis)
The authors evaluated the distribution of MEFV mutations in a Turkish population. Their findings confirm the correlation between M694V and FMF associated amyloidosis found in earlier studies.
we found a significant association between genotypes of variants in rs3743930 with increased Henoch-Schonlein purpura risk, after covariates adjustment. The carriers of homozygous mutant of rs3743930 polymorphisms revealed increased HSP risk than those with wild-type homozygotes.
MEFV gene variations in exons 2, 3, 5 and 10 associate with major clinical symptoms of familial Mediterranean fever. Arthritis was high in K695R heterozygous genotype.
These results provide a novel mechanism underlying the anti-inflammatory effects of carbon monoxide, involving the IL-10 (zeige IL10 Antikörper)-dependent upregulation of pyrin expression.
Mechanistically, Yersinia pseudotuberculosis YopM recruits and activates the mouse host kinases PRK1 (zeige PKN1 Antikörper) and PRK2 (zeige PKN2 Antikörper) to negatively regulate pyrin by phosphorylation.
These results are consistent with a model in which pyrin acts to limit the release of IL-1beta (zeige IL1B Antikörper) generated by activation and assembly of inflammasomes in response to subclinical immune challenges.
pyrin has a critical role in the innate immune response, possibly by acting on ASC (zeige STS Antikörper), a known caspase-1 (zeige CASP1 Antikörper) activator
This gene encodes a protein, also known as pyrin or marenostrin, that is an important modulator of innate immunity. Mutations in this gene are associated with Mediterranean fever, a hereditary periodic fever syndrome.
Mediterranean fever protein
, Mediterranean fever
, familial mediterranean fever