about
Interferon-alpha induces nmi-IFP35 heterodimeric complex formation that is affected by the phosphorylation of IFP35Keratin 20 helps maintain intermediate filament organization in intestinal epitheliaKeratin 20 serine 13 phosphorylation is a stress and intestinal goblet cell markerPhosphorylation of human keratin 8 in vivo at conserved head domain serine 23 and at epidermal growth factor-stimulated tail domain serine 431Phosphorylation of human keratin 18 serine 33 regulates binding to 14-3-3 proteinsKeratin binding to 14-3-3 proteins modulates keratin filaments and hepatocyte mitotic progressionMutation of human keratin 18 in association with cryptogenic cirrhosisNew consensus nomenclature for mammalian keratinsPost-translational modifications of intermediate filament proteins: mechanisms and functionsToll like receptor 3 plays a critical role in the progression and severity of acetaminophen-induced hepatotoxicityKeratin 8 phosphorylation by p38 kinase regulates cellular keratin filament reorganization: modulation by a keratin 1-like disease causing mutationCharacterization of in vivo keratin 19 phosphorylation on tyrosine-391Ethanol and Acetaminophen Synergistically Induce Hepatic Aggregation and TCH346-Insensitive Nuclear Translocation of GAPDHKeratin 8 phosphorylation by protein kinase C delta regulates shear stress-mediated disassembly of keratin intermediate filaments in alveolar epithelial cellsKeratin-8 null mice have different gallbladder and liver susceptibility to lithogenic diet-induced injuryNot All Mice Are the Same: Standardization of Animal Research Data Presentation.Characterization of the major physiologic phosphorylation site of human keratin 19 and its role in filament organization.Type II keratins are phosphorylated on a unique motif during stress and mitosis in tissues and cultured cells.Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies.Hemin-activated macrophages home to the pancreas and protect from acute pancreatitis via heme oxygenase-1 inductionUnique amino acid signatures that are evolutionarily conserved distinguish simple-type, epidermal and hair keratinsKeratin hypersumoylation alters filament dynamics and is a marker for human liver disease and keratin mutation.Heme oxygenase-1 is induced in peripheral blood mononuclear cells of patients with acute pancreatitis: a potential therapeutic targetAbsence of keratin 8 confers a paradoxical microflora-dependent resistance to apoptosis in the colon.Mouse hepatocyte overexpression of NF-κB-inducing kinase (NIK) triggers fatal macrophage-dependent liver injury and fibrosis.Fibrinogen-γ proteolysis and solubility dynamics during apoptotic mouse liver injury: heparin prevents and treats liver damage.Keratin 8 modulates β-cell stress responses and normoglycaemiaKeratin variants predispose to acute liver failure and adverse outcome: race and ethnic associations.PKC412 normalizes mutation-related keratin filament disruption and hepatic injury in mice by promoting keratin-myosin binding.Keratin 8 absence down-regulates colonocyte HMGCS2 and modulates colonic ketogenesis and energy metabolism.Prevalence of genetic variants of keratins 8 and 18 in patients with drug-induced liver injuryHuman keratin 8 variants promote mouse acetaminophen hepatotoxicity coupled with c-jun amino-terminal kinase activation and protein adduct formation.Ambient Light Promotes Selective Subcellular Proteotoxicity after Endogenous and Exogenous Porphyrinogenic StressMallory-Denk bodies are associated with outcomes and histologic features in patients with chronic hepatitis C.A disease- and phosphorylation-related nonmechanical function for keratin 8.Cellular integrity plus: organelle-related and protein-targeting functions of intermediate filaments.Absence of keratin 8 or 18 promotes antimitochondrial autoantibody formation in aging male miceKeratins turn over by ubiquitination in a phosphorylation-modulated fashionMutation of a major keratin phosphorylation site predisposes to hepatotoxic injury in transgenic miceT200 cell surface glycoprotein of the mouse. Polymorphism defined by the Ly-5 system of alloantigens.
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P496
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