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Human Monocytic Models Reveal Genotype‐Dependent Inflammatory Programs in VEXAS Syndrome
Objective VEXAS syndrome is a severe X‐linked autoinflammatory disorder caused by somatic mutations in ubiquitin‐like modifier activating enzyme 1 (UBA1), with clinical outcomes that vary by UBA1 genotype. We aimed to elucidate genotype‐specific inflammatory programs and identify potential therapeutic targets.
Kana Higashitani +10 more
wiley +1 more source
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THE VOLUNTARY HOSPITALS: Payment for Disabled Pensioners in Voluntary Hospitals
BMJ, 1919openaire +1 more source
Reliability of measurements of muscle strength and voluntary activation using twitch interpolation
Muscle and Nerve, 1995G M Allen
exaly

