All Stories

  1. Ferroptosis in Human Diseases: Fundamental Roles and Emerging Therapeutic Perspectives
  2. Redox Imbalance in Cystic Fibrosis: The Multifaceted Role of Oxidative Stress
  3. Structural determinants of phosphorylation‐dependent nuclear transport of HCMV DNA polymerase processivity factor UL44
  4. Double Attack to Oxidative Stress in Neurodegenerative Disorders: MAO-B and Nrf2 as Elected Targets
  5. From Monoamine Oxidase Inhibition to Antiproliferative Activity: New Biological Perspectives for Polyamine Analogs
  6. From Monoamine Oxidases Inhibition to Antiproliferative Activity: New Biological Perspective for Polyamine Analogs
  7. Monitoring Nrf2/ARE Pathway Activity with a New Zebrafish Reporter System
  8. An Iron Shield to Protect Epigallocatehin-3-Gallate from Degradation: Multifunctional Self-Assembled Iron Oxide Nanocarrier Enhances Protein Kinase CK2 Intracellular Targeting and Inhibition
  9. In Silico Predicted Antifungal Peptides: In Vitro and In Vivo Anti-Candida Activity
  10. Lack of glutathione peroxidase-8 in the ER impacts on lipid composition of HeLa cells microsomal membranes
  11. Insight into the mechanism of ferroptosis inhibition by ferrostatin-1
  12. Biochemical and cellular mechanism of protein kinase CK2 inhibition by deceptive curcumin
  13. Inactivation of the glutathione peroxidase GPx4 by the ferroptosis‐inducing molecule RSL3 requires the adaptor protein 14‐3‐3ε
  14. Benextramine and derivatives as novel human monoamine oxidases inhibitors: an integrated approach
  15. Pharmacophore-guided discovery of CDC25 inhibitors causing cell cycle arrest and tumor regression
  16. Stealth Iron Oxide Nanoparticles for Organotropic Drug Targeting
  17. A pathogenic role for cystic fibrosis transmembrane conductance regulator in celiac disease
  18. The Golgi ‘casein kinase’ Fam20C is a genuine ‘phosvitin kinase’ and phosphorylates polyserine stretches devoid of the canonical consensus
  19. Hydrophobic Derivatives of Glycopeptide Antibiotics as Inhibitors of Protein Kinases
  20. Development of a yeast-based system to identify new hBRAFV600E functional interactors
  21. Developmental phosphoproteomics identifies the kinase CK2 as a driver of Hedgehog signaling and a therapeutic target in medulloblastoma
  22. The Acidophilic Kinases PLK2 and PLK3: Structure, Substrate Targeting and Inhibition
  23. TG2 regulates the heat‐shock response by the post‐translational modification of HSF1
  24. The importance of negative determinants as modulators of CK2 targeting. The lesson of Akt2 S131
  25. Covalently bound DNA on naked iron oxide nanoparticles: Intelligent colloidal nano-vector for cell transfection
  26. Glutathione peroxidase 4-catalyzed reduction of lipid hydroperoxides in membranes: The polar head of membrane phospholipids binds the enzyme and addresses the fatty acid hydroperoxide group toward the redox center
  27. The landscape of BRAF transcript and protein variants in human cancer
  28. Fam20C is under the control of sphingolipid signaling in human cell lines
  29. The Development of CK2 Inhibitors: From Traditional Pharmacology to in Silico Rational Drug Design
  30. Role of Interaction and Nucleoside Diphosphate Kinase B in Regulation of the Cystic Fibrosis Transmembrane Conductance Regulator Function by cAMP-Dependent Protein Kinase A
  31. Casein kinases as potential therapeutic targets
  32. A new role for sphingosine: Up-regulation of Fam20C, the genuine casein kinase that phosphorylates secreted proteins
  33. Chimeric peptides as modulators of CK2-dependent signaling: Mechanism of action and off-target effects
  34. “Genuine” Casein Kinase (Fam20C): The Mother of the Phosphosecretome
  35. Design, validation and efficacy of bisubstrate inhibitors specifically affecting ecto-CK2 kinase activity
  36. A chemogenomic screening identifies CK2 as a target for pro-senescence therapy in PTEN-deficient tumours
  37. Understanding mammalian glutathione peroxidase 7 in the light of its homologs
  38. Casein kinase 2 (CK2) phosphorylates the deubiquitylase OTUB1 at Ser16to trigger its nuclear localization
  39. ALK Kinase Domain Mutations in Primary Anaplastic Large Cell Lymphoma: Consequences on NPM-ALK Activity and Sensitivity to Tyrosine Kinase Inhibitors
  40. The Selectivity of CK2 Inhibitor Quinalizarin: A Reevaluation
  41. “Genuine” Casein Kinase: The False Sister of CK2 That Phosphorylates Secreted Proteins at S-x-E/pS Motifs
  42. The lysine-specific demethylase 1 is a novel substrate of protein kinase CK2
  43. Synthesis and Properties of a Selective Inhibitor of Homeodomain–Interacting Protein Kinase 2 (HIPK2)
  44. Cell-permeable dual inhibitors of protein kinases CK2 and PIM-1: structural features and pharmacological potential
  45. Novel polyamine analogues: From substrates towards potential inhibitors of monoamine oxidases
  46. Detection of Phospho-Sites Generated by Protein Kinase CK2 in CFTR: Mechanistic Aspects of Thr1471 Phosphorylation
  47. Exploiting the repertoire of CK2 inhibitors to target DYRK and PIM kinases
  48. Protein disulfide isomerase and glutathione are alternative substrates in the one Cys catalytic cycle of glutathione peroxidase 7
  49. Kinase CK2 Inhibition: An Update
  50. Investigation on PLK2 and PLK3 substrate recognition
  51. Protein kinase CK2 inhibitors: a patent review
  52. Inhibition of Protein Kinase CK2 by Flavonoids and Tyrphostins. A Structural Insight
  53. Tools to discriminate between targets of CK2 vs PLK2/PLK3 acidophilic kinases
  54. Casein hydrolysate for uterine infection treatment: a patent evaluation (WO2011132191)
  55. Urolithin as a Converging Scaffold Linking Ellagic acid and Coumarin Analogues: Design of Potent Protein Kinase CK2 Inhibitors
  56. Unprecedented Selectivity and Structural Determinants of a New Class of Protein Kinase CK2 Inhibitors in Clinical Trials for the Treatment of Cancer
  57. A Comparison of Thiol Peroxidase Mechanisms
  58. Structural features underlying the selectivity of the kinase inhibitors NBC and dNBC: role of a nitro group that discriminates between CK2 and DYRK1A
  59. The Dark Side of Protein Kinase CK2 Inhibition
  60. The Role of the N-Terminal Domain in the Regulation of the “Constitutively Active” Conformation of Protein Kinase CK2α: Insight from a Molecular Dynamics Investigation
  61. 8-Hydroxynaphthalene-1,4-dione derivative as novel compound for glioma treatment
  62. Erratum to: Isoform specific phosphorylation of p53 by protein kinase CK1
  63. Glutathione Peroxidase-4
  64. A novel glucosyltransferase from Catharanthus roseus cell suspensions
  65. Cystic fibrosis transmembrane regulator fragments with the Phe 508 deletion exert a dual allosteric control over the master kinase CK2
  66. Isoform specific phosphorylation of p53 by protein kinase CK1
  67. Tetraiodobenzimidazoles are potent inhibitors of protein kinase CK2
  68. ATP Non-Competitive Ser/Thr Kinase Inhibitors as Potential Anticancer Agents
  69. Quinalizarin as a potent, selective and cell-permeable inhibitor of protein kinase CK2
  70. A novel splicing variant encoding putative catalytic α subunit of maize protein kinase CK2
  71. How druggable is protein kinase CK2?
  72. Medicinal Chemistry and the Molecular Operating Environment (MOE): Application of QSAR and Molecular Docking to Drug Discovery
  73. The selectivity of inhibitors of protein kinase CK2: an update
  74. Identification of novel protein kinase CK1 delta (CK1δ) inhibitors through structure-based virtual screening
  75. The Regulatory β Subunit of Protein Kinase CK2 Contributes to the Recognition of the Substrate Consensus Sequence. A Study with an eIF2β-Derived Peptide†
  76. Coumarin as Attractive Casein Kinase 2 (CK2) Inhibitor Scaffold: An Integrate Approach To Elucidate the Putative Binding Motif and Explain Structure–Activity Relationships
  77. Elucidation of the ribonuclease a aggregation process mediated by 3D domain swapping: A computational approach reveals possible new multimeric structures
  78. Tetrabromocinnamic Acid (TBCA) and Related Compounds Represent a New Class of Specific Protein Kinase CK2 Inhibitors
  79. Pyrazoloquinazoline Tricyclic System as Novel Scaffold to Design New Kinase CK2 Inhibitors
  80. Identification of Ellagic Acid as Potent Inhibitor of Protein Kinase CK2:  A Successful Example of a Virtual Screening Application
  81. Autophosphorylation at the regulatory β subunit reflects the supramolecular organization of protein kinase CK2
  82. Inhibition of Protein Kinase CK2 by Condensed Polyphenolic Derivatives. An in Vitro and in Vivo Study†