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β-Glucan-induced reprogramming of human macrophages inhibits NLRP3 inflammasome activation in cryopyrinopathies.
Not available
S-EPMC7456248
|
biostudies-literature
Cite
Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.
Not available
S-EPMC1288238
|
biostudies-literature
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Expression of SAA1, SAA2 and SAA4 genes in human primary monocytes and monocyte-derived macrophages.
Not available
S-EPMC6524798
|
biostudies-literature
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Hemodynamic and biological correlates of glomerular hyperfiltration in sickle cell patients before and under renin-angiotensin system blocker.
Not available
S-EPMC8175337
|
biostudies-literature
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New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.
Not available
S-EPMC379138
|
biostudies-literature
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Impact of human monocyte and macrophage polarization on NLR expression and NLRP3 inflammasome activation.
Not available
S-EPMC5389804
|
biostudies-literature
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VLITL is a major cross-β-sheet signal for fibrinogen Aα-chain frameshift variants.
Not available
S-EPMC5843806
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biostudies-literature
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Identification of MEFV-independent modifying genetic factors for familial Mediterranean fever.
Not available
S-EPMC1288556
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biostudies-literature
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The NLRP3 p.A441V Mutation in
NLRP3
-AID Pathogenesis: Functional Consequences, Phenotype-Genotype Correlations and Evidence for a Recurrent Mutational Event.
Not available
S-EPMC6857991
|
biostudies-literature
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D25V apolipoprotein C-III variant causes dominant hereditary systemic amyloidosis and confers cardiovascular protective lipoprotein profile.
Not available
S-EPMC4735822
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biostudies-literature
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