Site-1 protease deficiency causes human skeletal dysplasia due to defective inter-organelle protein trafficking.
Enhancer histone-QTLs are enriched on autoimmune risk haplotypes and influence gene expression within chromatin networks.
Evidence of Alternative Modes of B Cell Activation Involving Acquired Fab Regions of N-Glycosylation in Antibody-Secreting Cells Infiltrating the Labial Salivary Glands of Patients With Sjögren’s Syndrome.
Unique clinical characteristics, autoantibodies and medication use in Native American patients with systemic lupus erythematosus.
Accumulation of Antigen-Driven Lymphoproliferations in Complement Receptor 2/CD21-/low B Cells From Patients With Sjögren’s Syndrome.
