Novel C1QB Variant Causes Functional Complement Deficiency in Lupus Case Study
Researchers identified a novel homozygous C1QB variant causing functional complement deficiency alongside a somatic TNFAIP3 variant in a pediatric lupus ...
Tag: Type I interferon signature
Type I Interferon Signature Unlinked to Blau Syndrome Activity
In the evolving landscape of autoinflammatory disorders, Blau syndrome presents a conundrum that challenges our understanding of inflammatory pathways and ...
Type I Interferon Signature Enables Early Bacterial Infection Diagnosis
In recent years, the challenge of diagnosing serious bacterial infections (SBIs) in febrile infants has posed a formidable obstacle for ...
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Mothers who receive childcare support from maternal grandparents show more parental warmth, finds NTU Singapore study
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University of Seville Breaks 120-Year-Old Mystery, Revises a Key Einstein Concept
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Bee body mass, pathogens and local climate influence heat tolerance
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Researchers record first-ever images and data of a shark experiencing a boat strike
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Groundbreaking Clinical Trial Reveals Lubiprostone Enhances Kidney Function
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