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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2013, Volume 110, Issue 20, pp. 8134 - 8139
Journal Article
PLoS genetics, ISSN 1553-7404, 2019, Volume 15, Issue 4, p. e1008038
Journal Article
Nature Genetics, ISSN 1061-4036, 1997, Volume 17, Issue 1, pp. 25 - 31
Journal Article
by Tunca, Mehmet and Ozdogan, Huri and Kasapcopur, Ozgur and Yalcinkaya, Fatos and Tutar, Ercan and Topaloglu, Rezan and Yilmaz, Engin and Arici, Mustafa and Bakkaloglu, Aysin and Besbas, Nesrin and Akpolat, Tekin and Dinc, Ayhan and Erken, Eren and Tirpan, Kazim and Ozer, Huseyin TE and Soyturk, Mujde and Senturk, Taskin and Balci, Banu and Ozguc, Meral and Dundar, Munis and Akar, Ece and Ozel, Duygu and Dundar, Munis and Gunesacar, Ramazan and Booth, David R and Hawkins, Philip N and Touitou, Isabelle and Aksentijevich, Ivona and Matzner, Yakov and Arslan, Serap and Balaban, Yasemin and Batman, Figen and Bayraktar, Yusuf and Apras, Sule and Calguneri, Meral and Duzova, Ali and Kav, Taylan and Ozaltin, Fatih and Simsek, Halis and Sivri, Bulent and Tatar, Gonca and Akkoc, Nurullah and Kavukcu, Salih and Soylu, Alper and Turkmen, Mehmet and Unsal, Erbil and Arisoy, Nil and Caliskan, Salim and Gogus, Feride and Masatlioglu, Seval and Sever, Lale and Akkok, Nermin and Cakar, Nilgun and Kara, Nazli and Kocak, Hulusi and Ozalp, Sila and Bilge, Ilmay and Sevinc, Emre and Gul, Ahmet and Kamali, Sevil and Sadikoglu, Banu and Selcukbiricik, Fatih and Sirin, Aydan and Sucu, Aysegul and Bek, Kenan and Bulbul, Mehmet and Delibas, Ali and Demircin, Gulay and Erdogan, Ozlem and Oner, Ayse and Mesiha, Ekim and Ozkaya, Nuray and Tekin, Mustafa and Demirkaya, Erkan and Erdem, Hakan and Gok, Faysal and Pay, Salih and Islek, Ismail and Kabasakal, Yasemin and Keser, Gokhan and Ozmen, Mustafa and Akoglu, Emel and Atagunduz, Pamir and Direskeneli, Haner and Temel, Musa and Tuglular, Serhan and Buyan, Necla and Bakkaloglu, Sevcan and Derici, Ulver and Goker, Berna and Kalman, Suleyman and Ozkaya, Ozan and Dusunsel, Ruhan and Gunduz, Zubeyde and Poyrazoglu, M. Hakan and Korkmaz, Cengiz and Baskin, Esra and Koseoglu, Hamide Kart and Saatci, Umit and Yucel, Eftal and ... and Turkish FMF Study Grp and Turkish FMF Study Group
Medicine, ISSN 0025-7974, 01/2005, Volume 84, Issue 1, pp. 1 - 11
Journal Article
Proceedings of the National Academy of Sciences - PNAS, ISSN 1091-6490, 2011, Volume 108, Issue 17, pp. 7148 - 7153
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2017, Volume 76, Issue Suppl 2, p. 1399
BackgroundFamilial Mediterranean Fever (FMF) is an inherited autoinflammatory disorder caused by mutations in the MEFV gene encoding pyrine, characterized by recurrent episodes of fever and serositis... 
Knee | Pericarditis | Serositis | Arthritis | Joint diseases | Fever | Genetic screening | Abdomen | Myocarditis | Pyrin protein | Pain | Pleurisy | Point mutation | Familial Mediterranean fever | Mutation | Colchicine | Heart diseases | Age
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2009, Volume 4, Issue 9, p. e7154
Background and Aims: The familial Mediterranean fever (FMF) gene (MEFV) encodes pyrin, a major regulator of the inflammasome platform controlling caspase-1 activation and IL-1 beta processing... 
FLIP-FLOP | CONTRIBUTE | INFLAMMATORY-BOWEL-DISEASE | CASPASE-1 | INTERACTS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | MUTATIONS | EXPRESSION | GENOME-WIDE ASSOCIATION | PYRIN | Crohn Disease - genetics | Genetic Predisposition to Disease | Cytoskeletal Proteins - genetics | Humans | Middle Aged | Colitis, Ulcerative - genetics | Familial Mediterranean Fever - genetics | Child, Preschool | Caspase 1 - metabolism | Male | Pyrin | Genetic Variation | Epistasis, Genetic | Interleukin-1beta - metabolism | Adolescent | Inflammatory Bowel Diseases - genetics | Aged, 80 and over | Adult | Cytoskeletal Proteins - metabolism | Female | Aged | Enzyme Activation | Child | Cohort Studies | Genes | Genetic research | Disease susceptibility | Genetic aspects | Familial Mediterranean fever | Colitis | Gene expression | Risk factors | Genetic screening | Haplotypes | Animal models | Inflammatory bowel diseases | DNA polymerase | Pathogenesis | Mucosa | Risk | Single-nucleotide polymorphism | Caspase-1 | Jews | Intestine | Rodents | Gastroenterology | Colon | Medical research | Cytokines | Cryopyrin | Research & development--R&D | Health risks | Caspase | Inflammation | Genetic diversity | IL-1β | Fever | Crohns disease | Medicine | Inflammatory bowel disease | Polymerase chain reaction | Crohn's Disease | Hospitals | Pyrin protein | Genotyping | Gene frequency | Alleles | Mutation | Ulcerative colitis | Research & development | R&D
Journal Article
Autoimmunity Reviews, ISSN 1568-9972, 2012, Volume 12, Issue 1, pp. 31 - 37
Abstract Familial Mediterranean fever (FMF) is an inherited autosomal recessive disorder, ethnically restricted and commonly found among individuals of Mediterranean descent, caused by MEditerranean FeVer gene (MEFV... 
Allergy and Immunology | Phenotypes | Familial Mediterranean fever | Mediterranean fever gene | Genotypes | DIAGNOSTIC-VALUE | PEDIATRIC CRITERIA | MANIFESTATION | CLINICAL-FEATURES | IMMUNOLOGY | ARTHRITIS | CHILDREN | MEFV GENE | RENAL AMYLOIDOSIS | DISEASE | MUTATIONS | Phenotype | Genetic aspects
Journal Article