CIAS1


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CIAS1

This is a retired HUGO symbol for what is now designated NLRP3.
References in periodicals archive ?
We observed a case (case 11) where the patient presented with two separate heterozygous mutations in the CIAS1 gene and the MEFV gene.
New mutations of CIAS1 that are responsible for Muckle-Wells Syndrome and Familial Cold Urticaria: A novel mutation underlies both syndromes.
For instance, the CIAS1 gene in the pyrin domain is responsible for three different conditions: familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal onset multisystem inflammatory disease (NOMID)/chronic infantile neurologic cutaneous articular syndrome (CINCA).
Prieur et al., "Molecular basis of the spectral expression of CIAS1 mutations associated with phagocytic cell-mediated autoinflammatory disorders CINCA/NOMID, MWS, and FCU," Blood, vol.
Carta et al., "Pattern of interleukin-1[beta] secretion in response to lipopolysaccharide and ATP before and after interleukin-1 blockade in patients with CIAS1 mutations," Arthritis & Rheumatism, vol.