Results 111 to 120 of about 6,236 (217)
1Novel MEFV transcripts in Familial Mediterranean fever patients and controls
, 2010 Background Familial Mediterranean fever is a recessive autoinflammatory disease frequently encountered in Armenians, Jews, Arabs and Turks. The MEFV gene is responsible for the disease.
Myrna Medlej-Hashim +4 more
core +1 more source
Frequency of MEFV gene mutations in child patients who had the diagnosis of henoch-schönlein purpura
, 2012 Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Ana Bilim DalıHenoch-Schönlein Purpurası (HSP) çocukluk çağının en sık görülen sistemik vasküliti, MEFV ise Ailevi Akdeniz Ateşi' nden (AAA) sorumlu gendir.
Özdemir, Göktuğ
core
HeliyonObjective: Henoch-Schönlein purpura (HSP) is the most common systemic vasculitis in children. HSP is a multifactorial inflammatory disease, but its pathogenesis is still unclear.
Yang Ruan, Longlong Xie
doaj +1 more source
, 2015 Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disease with autosomal recessive inheritance pattern often seen around the Mediterranean Sea. It is characterized by recurrent episodes of fever and polyserositis and rash.
Sepideh Jahangiri +4 more
core
Caspase-1 (CASP-1) activity is not elevated in Mefv−/− macrophages.
, 2013 A, rpMΦs from Mefv+/+ and Mefv−/− littermate mice were exposed to LPS and ATP as indicated in the method section. Levels of caspase-1 (upper panel) and IL-1β (middle panel) were detected by western blot in cell lysates (lanes 1 and 2) and cell culture ...
MyTrang Nguyen (296629) +4 more
core +1 more source
MEFV Mutations in Behcet's Disease
, 2000 Familial Mediterranean fever (FMF) and Behcet's disease (BD), both inflammatory diseases, are highly prevalent in the Middle Eastern and Mediterranean populations. FMF is a Mendelian autosomic recessive disease linked to MEFV, a gene of unknown function.
Garnier, Jean Marc +12 more
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Analysis of blood collected from Mefv+/+ and Mefv−/− mice.
, 2013 Blood was collected by cardiac puncture. Whole blood containing 5 mM EDTA was used for analysis on the Heska Hematology Analyzer by the Animal Clinical Chemistry and Gene Expression Laboratory at UNC-Chapel Hill. n = 13 and 13 mice.
MyTrang Nguyen (296629) +4 more
core +1 more source
European Journal of Case Reports in Internal MedicineFamilial Mediterranean fever (FMF) is traditionally associated with biallelic mutations in the MEFV gene; however, heterozygous mutations may also contribute to disease phenotypes.
Marcus Villander Barros de Oliveira Sá +4 more
doaj +1 more source
MEFV Gene Profile in Northwest of Iran, Twelve Common MEFV Gene Mutations Analysis in 216 Patients with Familial Mediterranean Fever [PDF]
Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disease with autosomal recessive inheritance pattern often seen around the Mediterranean Sea. It is characterized by recurrent episodes of fever and polyserositis and rash.
حسینی اصل, سید سعید +4 more
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MEFV gene 3'-UTR Alu repeat polymorphisms in patients with familial Mediterranean fever
, 2008 Objective. Familial Mediterranean fever (FMF), an autosomal recessively inherited outoinflammatory disorder, is caused by missense mutations in the pyrin-encoding MEFV gene. The MEFV initiations can be detected in the majority of FMF patients.
Kamali, S. +19 more
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