Results 71 to 80 of about 4,864,129 (252)
From mice to humans—divergent strategies for intestinal homeostasis and regeneration
Recent advances such as organoid genome editing, xenotransplantation, imaging, and whole‐genome sequencing have enabled direct studies of human intestinal stem cells (ISCs). These studies reveal species‐specific features, including slower ISC proliferation, distinct injury responses, slower somatic mutation accumulation in humans, and an inverse ...
Keiko Ishikawa +2 more
wiley +1 more source
Adult-onset Still’s disease: pathogenesis, symptoms, diagnostics and treatment. [PDF]
Adult-onset Still’s disease (AoSD) is a rare but clinically well-known, polygenic, systemic autoinflammatory disease. Typically this disease occurs by four main symptoms: spiking fever ≥ 39 °C, arthralgia or arthritis, skin rash, and leukocytosis (≥ 10 ...
Kaušaitė, Dominyka,
core
Still’s Disease in the Constellation of Hyperinflammatory Syndromes: A Link with Kawasaki Disease?
Still’s disease and Kawasaki disease (KD) today belong to the group of cytokine storm syndromes, a pathophysiological set related to excessive activation of the innate immune response. We present here a personal vision of what can link these two diseases,
Perrine Dusser, Isabelle Koné-Paut
core +1 more source
Modelling stem cell differentiation related processes—A practical overview for biologists
Stem cell differentiation is complex and difficult to control experimentally. This review introduces suitable computational modelling approaches that can support stem cell research, from mechanistic ODE and abstract models to multiscale and deep learning methods.
Ricco Zeegelaar +4 more
wiley +1 more source
The paper considers a case of adult-onset Still's disease that occurred as acute pericarditis, two-spike hectic fever, and neutrophilic leukocytosis in a young man.
V. Yu. Myachikova +5 more
doaj +1 more source
Мета роботи – на прикладі клінічного випадку ознайомити лікарів з особливостями клінічного перебігу хвороби Стілла. Наведено витяг з історії хвороби пацієнтки, госпіталізованої в інфекційне відділення ОКНП «Чернівецька обласна клінічна лікарня», в якої ...
Сhernetska, N.V. +11 more
core +1 more source
Mixed results with baricitinib in biological-resistant adult-onset Still’s disease and undifferentiated systemic autoinflammatory disease [PDF]
This clinical case series describes our experience with the use of Janus kinase 1/2 inhibitor baricitinib in two patients suffering from refractory adult-onset Still’s disease (AOSD) as well as in one case suffering from AOSD-like autoinflammatory ...
Fitton, J +5 more
core +1 more source
Investigating transcription factor dynamics in health and disease using FRAP
FRAP analysis of GFP‐tagged transcription factors reveals how molecular mobility and target engagement change in response to drug treatment. By combining live‐cell imaging, quantitative model fitting, and statistical analysis, this approach uncovers transcription factor dynamics linked to disease mechanisms, providing a powerful framework for ...
Kannan Govindaraj +3 more
wiley +1 more source
Still’s disease has long been divided by age at onset into systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD). The 2024 evidence synthesis prepared for the European Alliance of Associations for Rheumatology/Pediatric ...
Ivica Jeremić
core +1 more source
EULAR/PReS recommendations for the diagnosis and management of Still’s disease, comprising systemic juvenile idiopathic arthritis and adult-onset Still’s disease [PDF]
Systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still’s disease (AOSD) are considered the same disease, but a common approach for diagnosis and management is still missing.
Feist, Eugen +105 more
core +1 more source

