Caspase-1 inhibitor ameliorates experimental autoimmune myasthenia gravis by innate dendric cell IL-1-IL-17 pathway

Congcong Wang, Heng Li, Min Zhang, +8

Journal of Neuroinflammation

WDFY4 Is Involved in Symptoms of Systemic Lupus Erythematosus by Modulating B Cell Fate via Noncanonical Autophagy

Qianqian Yuan, Yan Li, Jiangxia Li, +10

The Journal of Immunology

Smek1 deficiency exacerbates experimental autoimmune encephalomyelitis by activating proinflammatory microglia and suppressing the IDO1-AhR pathway

Ruonan Duan, Chunlin Yang, Tong Du, +7

Journal of Neuroinflammation

A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus

Ruonan Duan, Qi Liu, Jiangxia Li, +11

Journal of Clinical Immunology

Autoimmune DiseaseLupusGeneticsLupus NephritisImmunology +3

A SMOC2 variant inhibits BMP signaling by competitively binding to BMPR1B and causes growth plate defects

Feng Long, Hongbiao Shi, Pengyu Li, +14

Bone

Signal TransductionDevelopmental BiologyBone Morphogenic ProteinSignaling PathwayCell Regulation +5

Cervical Spinal Involvement in a Chinese Pedigree With Pontine Autosomal Dominant Microangiopathy and Leukoencephalopathy Caused by a 3′ Untranslated Region Mutation of <i>COL4A1</i> Gene

Yuying Zhao, Ruonan Duan, Lin Ji, +2

Stroke

Family MembersGeneticsPathologyMolecular GeneticsDisease Gene Identification +18

Deficiency in WDFY4 reduces the number of CD8+ T cells via reactive oxygen species-induced apoptosis

Yan Li, Jiangxia Li, Qianqian Yuan, +11

Molecular Immunology

InflammationT-regulatory CellApoptosisImmunologyCell Death +7

Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in &lt;b&gt;&lt;i&gt;NEFH&lt;/i&gt;&lt;/b&gt; in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in &lt;b&gt;&lt;i&gt;NEFH&lt;/i&gt;&lt;/b&gt; for Charcot-Marie-Tooth 2

Xianli Bian, Pengfei Lin, Jiangxia Li, +12

Neurodegenerative Diseases

Generation of a human induced pluripotent stem cell line (SDUBMSi001-A) from a hereditary spastic paraplegia patient carrying kif1a c.773C&gt;T missense mutation

Xiaojing Wang, Ma Yanyan, Ruonan Duan, +6

Stem Cell Research

Kif1a GeneGeneticsDisease Gene IdentificationRegenerative MedicineT Missense Mutation +15

Interactions between Beta-Amyloid and Pericytes in Alzheimer’s Disease

You-Yue Li, Dandan Guo, Ruonan Duan, +1

Frontiers in Bioscience-Landmark