Mostrando 1 - 18 Resultados de 18 Para Buscar 'Stefan Offermanns', tiempo de consulta: 0.04s Limitar resultados
  1. 1
    20-HETE promotes glucose-stimulated insulin secretion in an autocrine manner through FFAR1
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  2. 2
    Semaphorin 4C Plexin-B2 signaling in peripheral sensory neurons is pronociceptive in a model of inflammatory pain
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  3. 3
    The G2A receptor (GPR132) contributes to oxaliplatin-induced mechanical pain hypersensitivity
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  4. 4
    In vivo modulation of endothelial polarization by Apelin receptor signalling
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  5. 5
    YAP and TAZ protect against white adipocyte cell death during obesity
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  6. 6
    Helix 8 is the essential structural motif of mechanosensitive GPCRs
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  7. 7
    Angiopoietin-2–integrin α5β1 signaling enhances vascular fatty acid transport and prevents ectopic lipid-induced insulin resistance
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  8. 8
    Constitutive smooth muscle tumour necrosis factor regulates microvascular myogenic responsiveness and systemic blood pressure
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  9. 9
    Tanycytes control the hormonal output of the hypothalamic-pituitary-thyroid axis
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  10. 10
    G-protein-coupled receptor P2Y10 facilitates chemokine-induced CD4 T cell migration through autocrine/paracrine mediators
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  11. 11
    Conditional deletion of Rcan1 predisposes to hypertension-mediated intramural hematoma and subsequent aneurysm and aortic rupture
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  12. 12
    Adipocyte Piezo1 mediates obesogenic adipogenesis through the FGF1/FGFR1 signaling pathway in mice
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  13. 13
    The potassium channel KCNJ13 is essential for smooth muscle cytoskeletal organization during mouse tracheal tubulogenesis
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  14. 14
    Lactate released by inflammatory bone marrow neutrophils induces their mobilization via endothelial GPR81 signaling
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  15. 15
    Myh10 deficiency leads to defective extracellular matrix remodeling and pulmonary disease
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  16. 16
    Exercise induces cerebral VEGF and angiogenesis via the lactate receptor HCAR1
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  17. 17
    Mechanochemical control of epidermal stem cell divisions by B-plexins
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  18. 18
    Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndrome
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