Analysis of NOD-like receptor NLRP1 in multiple sclerosis families

Common genetic etiology between “multiple sclerosis-like” single-gene disorders and familial multiple sclerosis

(2017) Anthony L. Traboulsee et al.   HUMAN GENETICS

Purinergic receptors P2RX4 and P2RX7 in familial multiple sclerosis

(2017) A Dessa Sadovnick et al.   HUMAN MUTATION

Modulating inflammation and neuroprotection in multiple sclerosis

(2017) Heather Yong et al.   JOURNAL OF NEUROSCIENCE RESEARCH

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

(2017) Ales Maver et al.   Scientific Reports

Analysis of protein-coding genetic variation in 60,706 humans

(2016) Monkol Lek et al.   NATURE

Nuclear Receptor NR1H3 in Familial Multiple Sclerosis

(2016) Zhe Wang et al.   NEURON

The Inflammasomes and Autoinflammatory Syndromes

(2015) Lori Broderick et al.   Annual Review of Pathology-Mechanisms of Disease

Activation and Regulation of Cellular Inflammasomes: Gaps in Our Knowledge for Central Nervous System Injury

(2014) Juan Pablo de Rivero Vaccari et al.   JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM

Genetic variants in IL2RA and IL7R affect multiple sclerosis disease risk and progression

(2014) Anthony L. Traboulsee et al.   NEUROGENETICS

C3a modulates IL-1  secretion in human monocytes by regulating ATP efflux and subsequent NLRP3 inflammasome activation

(2013) E. Asgari et al.   BLOOD

STX6 rs1411478 is not associated with increased risk of Parkinson's disease

(2013) Joanne Trinh et al.   PARKINSONISM & RELATED DISORDERS

Recognition of Bacteria by Inflammasomes

(2012) Jakob von Moltke et al.   Annual Review of Immunology