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Pyrin
Known as:
TRIM20 Protein
, MEFV Protein
, Pyrin [Chemical/Ingredient]
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A tripartite motif protein that consists of an N-terminal pyrin domain, a central coiled-coil region and B-box type ZINC FINGER, and C-terminal…
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National Institutes of Health
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Related topics
Related topics
11 relations
In Blood
MEFV gene
Process of secretion
Pyrin Domain
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Narrower (1)
MEFV protein, human
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Ron receptor-dependent gene regulation of Kupffer cells during endotoxemia.
Rishikesh M. Kulkarni
,
W. Stuart
,
S. Waltz
Hepatobiliary & Pancreatic Diseases International
2014
Corpus ID: 24362636
2014
2014
Detecting “different”: Pyrin senses modified GTPases
M. R. D. Zoete
,
R. Flavell
Cell Research
2014
Corpus ID: 1295141
Pathogenic bacteria secrete effector proteins that target host cell Rho GTPases to manipulate the actin cytoskeleton. A recent…
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Review
2013
Review
2013
Gene hunting in autoinflammation
A. Standing
,
E. Omoyinmi
,
P. Brogan
Clinical and Translational Allergy
2013
Corpus ID: 15760220
Steady progress in our understanding of the genetic basis of autoinflammatory diseases has been made over the past 16 years…
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2013
2013
Decreased vitamin D levels in patients with familial mediterranean fever
B. Kısacık
,
S. Kaya
,
Y. Pehlivan
,
Turker Tasliyurt
,
M. Sayarlıoğlu
,
A. Onat
Rheumatology International
2013
Corpus ID: 6086105
Familial mediterranean fever (FMF) is an autosomal recessive disorder caused by mutations in the FMF gene (MEFV). The gene…
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2009
2009
The spectrum of FMF mutations and genotypes in the referrals to molecular genetic laboratory at Kırıkkale University in Turkey
A. Gunel-Ozcan
,
D. B. Sayın
,
E. Mısırlıoğlu
,
S. Güliter
,
F. Yakaryilmaz
,
C. Ensari
Molecular Biology Reports
2009
Corpus ID: 325168
Familial Mediterranean Fever (FMF) is an autosomal recessive genetic disorder characterised by recurrent and self-limited…
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2008
2008
Expression of ASC in Renal Tissues of Familial Mediterranean Fever Patients with Amyloidosis: Postulating a Role for ASC in AA Type Amyloid Deposition
B. Balcı-Peynircioğlu
,
A. Waite
,
+7 authors
E. Yılmaz
Experimental biology and medicine
2008
Corpus ID: 37696739
Familial Mediterranean fever (FMF) is characterized by recurrent attacks of fever and serositis; in some cases, ensuing…
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2008
2008
Screening of family members of children with Familial Mediterranean Fever: true-autosomal and pseudo-autosomal inheritance.
M. K. Cağlar
,
F. S. Altugan
,
H. Ozyurt
,
H. Atasoy
Acta Reumatológica Portuguesa
2008
Corpus ID: 39680514
OBJECTIVES Screening of family members of children with Familial Mediterranean Fever (FMF) has been carried out to detect new…
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2004
2004
Subcellular localisation of marenostrin/pyrin isoforms carrying the most common mutations involved in familial Mediterranean fever in the presence or absence of its binding partner ASC
C. Cazeneuve
,
S. Papin
,
I. Jéru
,
P. Duquesnoy
,
S. Amselem
Journal of Medical Genetics
2004
Corpus ID: 27002480
Familial Mediterranean fever (FMF) is an autosomal recessive disorder characterised by recurrent episodes of fever and serosal…
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Highly Cited
2002
Highly Cited
2002
Mutation of a New Gene Encoding a Putative Pyrin-Like Protein Causes Familial Cold Autoinflammatory Syndrome and Muckle-Wells Syndrome
A. Thatayatikom
,
A. Liu
Pediatrics
2002
Corpus ID: 73053977
Purpose of the Study. Some patients with severe congenital neutropenia harbor mutations in the carboxyl terminus of the…
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Highly Cited
1998
Highly Cited
1998
Assessment of pyrin gene mutations in Turks with familial Mediterranean fever (FMF)
Xiaoguang Chen
,
N. Fischel‐Ghodsian
,
+5 authors
M. Shohat
Human Mutation
1998
Corpus ID: 36901043
Familial Mediterranean fever (FMF) is an autosomal recessive disease clinically characterized by recurrent short self‐limited…
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