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Life Science Alliance|March 25, 2024
Type I interferon regulates interleukin-1beta and IL-18 production and secretion in human macrophagesRodrigo Díaz-Pino, Gillian I Rice, Diego San Felipe, et al.
Lupus|May 9, 2013
Systemic lupus erythematosus due to C1q deficiency with progressive encephalopathy, intracranial calcification and acquired moyamoya cerebral vasculopathyC Troedson, M Wong, J Dalby-Payne, et al.
JAMA Dermatology|May 21, 2015
Stimulator of Interferon Genes-Associated Vasculopathy With Onset in Infancy: A Mimic of Childhood Granulomatosis With PolyangiitisJustine Munoz, Michel Rodière, Nadia Jeremiah, et al.
Chest|November 12, 2002
Oximeter performance: the influence of acquisition parametersDavid G Davila, Kathy C Richards, Buddy L Marshall, et al.
Nature Immunology|July 28, 2014
The SKIV2L RNA exosome limits activation of the RIG-I-like receptorsSterling C Eckard, Gillian I Rice, Alexandre Fabre, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|November 19, 2016
Expression of Cyclic GMP-AMP Synthase in Patients With Systemic Lupus ErythematosusJie An, Laura Durcan, Reynold M Karr, et al.
Plos One|February 1, 2020
Genetic polymorphism in C3 is associated with progression in chronic kidney disease (CKD) patients with IgA nephropathy but not in other causes of CKDSara T Ibrahim, Rajkumar Chinnadurai, Ibrahim Ali, et al.
RMD Open|June 3, 2016
ADA2 deficiency: case report of a new phenotype and novel mutation in two sistersF Uettwiller, G Sarrabay, M P Rodero, et al.
Orphanet Journal of Rare Diseases|June 16, 2026
Refining Human Phenotype Ontology (HPO) to enable better phenotype-genotype integration in systemic autoimmune rheumatic diseasesAnastasia-Vasiliki Madenidou, Gillian I Rice, Sarah Dyball, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 11, 2007
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathyS Orcesi, A Pessagno, R Biancheri, et al.
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