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  1. Tel1 is recruited at chromosomal loop/axis contact sites to modulate meiotic DNA double-strand breaks interference
  2. Tel1 is recruited at chromosomal loop/axis contact sites to regulate meiotic DNA double-strand breaks interference
  3. The COMPASS subunit Spp1 protects nascent DNA at the Tus/Ter replication fork barrier by limiting DNA availability to nucleases
  4. NPCs and APBs: two HUBs of non-canonical homology-based recombination at telomeres?
  5. The COMPASS subunit Spp1 protects nascent DNA at stalled replication fork barrier by limiting DNA availability to nucleases
  6. A proto-telomere is elongated by telomerase in a shelterin-dependent manner in quiescent fission yeast cells
  7. Telomeric C‐circles localize at nuclear pore complexes in Saccharomyces cerevisiae
  8. Set1-dependent H3K4 methylation becomes critical for limiting DNA damage in response to changes in S-phase dynamics in Saccharomyces cerevisiae
  9. RAP1 moonlights to activate NF-κB and Notch in ALT
  10. Rad52 SUMOylation functions as a molecular switch that determines a balance between the Rad51- and Rad59-dependent survivors
  11. Set1-dependent H3K4 methylation becomes critical for DNA replication fork progression in response to changes in S phase dynamics inSaccharomyces cerevisiae
  12. The Set1 N-terminal domain and Swd2 interact with RNA polymerase II CTD to recruit COMPASS
  13. Histone stress: an unexplored source of chromosomal instability in cancer?
  14. Nuclear dynamics of the Set1C subunit Spp1 prepares meiotic recombination sites for break formation
  15. High levels of histones promote whole-genome-duplications and trigger a Swe1WEE1-dependent phosphorylation of Cdc28CDK1
  16. Eroded telomeres are rearranged in quiescent fission yeast cells through duplications of subtelomeric sequences
  17. De novo telomere addition at chromosome breaks: Dangerous Liaisons
  18. Histone Purification from Saccharomyces cerevisiae
  19. Coordination of Cell Cycle Progression and Mitotic Spindle Assembly Involves Histone H3 Lysine 4 Methylation by Set1/COMPASS
  20. Replication stress as a source of telomere recombination during replicative senescence in Saccharomyces cerevisiae
  21. TERRA Incognitaat chromosome ends
  22. SUMO-Dependent Relocalization of Eroded Telomeres to Nuclear Pore Complexes Controls Telomere Recombination
  23. Posttranslational marks control architectural and functional plasticity of the nuclear pore complex basket
  24. Recombinational DNA repair is regulated by compartmentalization of DNA lesions at the nuclear pore complex
  25. RPA prevents G-rich structure formation at lagging-strand telomeres to allow maintenance of chromosome ends
  26. Rad59-Facilitated Acquisition of Y′ Elements by Short Telomeres Delays the Onset of Senescence
  27. Sgs1 and Sae2 promote telomere replication by limiting accumulation of ssDNA
  28. Seismic precursors linked to super-critical fluids at oceanic transform faults
  29. Abstract 4055: Non-canonical telomere maintenance mechanism in B-cell chronic lymphocytic leukemia.
  30. Spp1 at the crossroads of H3K4me3 regulation and meiotic recombination
  31. Two Distinct Repressive Mechanisms for Histone 3 Lysine 4 Methylation through Promoting 3′-End Antisense Transcription
  32. RPA facilitates telomerase activity at chromosome ends in budding and fission yeasts
  33. CST Meets Shelterin to Keep Telomeres in Check
  34. Cdc13 and Telomerase Bind through Different Mechanisms at the Lagging- and Leading-Strand Telomeres
  35. FACT Prevents the Accumulation of Free Histones Evicted from Transcribed Chromatin and a Subsequent Cell Cycle Delay in G1
  36. A two-step model for senescence triggered by a single critically short telomere
  37. The fate of irreparable DNA double-strand breaks and eroded telomeres at the nuclear periphery
  38. The fate of irreparable DNA double-strand breaks and eroded telomeres at the nuclear periphery
  39. Cotranslational assembly of the yeast SET1C histone methyltransferase complex
  40. The DNA damage response at eroded telomeres and tethering to the nuclear pore complex
  41. A two-step model for senescence triggered by a single critically short telomere
  42. Histone H3 lysine 4 trimethylation marks meiotic recombination initiation sites
  43. Ubiquitylation of the COMPASS component Swd2 links H2B ubiquitylation to H3K4 trimethylation
  44. How telomeres are replicated
  45. The multiple faces of Set1This paper is one of a selection of papers published in this Special Issue, entitled 27th International West Coast Chromatin and Chromosome Conference, and has undergone the Journal's usual peer review process.
  46. The finger subdomain of yeast telomerase cooperates with Pif1p to limit telomere elongation
  47. Subtelomeric proteins negatively regulate telomere elongation in budding yeast
  48. Histone H3 Lysine 4 Mono-methylation does not Require Ubiquitination of Histone H2B
  49. Set1 is required for meiotic S-phase onset, double-strand break formation and middle gene expression
  50. RPA regulates telomerase action by providing Est1p access to chromosome ends
  51. The Fission Yeast spSet1p is a Histone H3-K4 Methyltransferase that Functions in Telomere Maintenance and DNA Repair in an ATM Kinase Rad3-dependent Pathway
  52. The MYST Domain Acetyltransferase Chameau Functions in Epigenetic Mechanisms of Transcriptional Repression
  53. Bacteriocins
  54. Colicins
  55. Cleavage of Colicin D Is Necessary for Cell Killing and Requires the Inner Membrane Peptidase LepB
  56. The AprX protein of Pseudomonas aeruginosa: a new substrate for the Apr type I secretion system
  57. Integration of the colicin A pore-forming domain into the cytoplasmic membrane of Escherichia coli 1 1Edited by I. B. Holland
  58. The mitochondrial processing peptidase behaves as a zinc-metallopeptidase
  59. Development of a Positive Screen for the Identification of Suppressive Mutations in Secretion Defective Strains of Pseudomonas aeruginosa
  60. Functional cooperation of the mitochondrial processing peptidase subunits
  61. The mitochondrial processing peptidase: Function and specificity
  62. Transmembrane α-Helix Interactions are Required for the Functional Assembly of theEscherichia coliTol Complex
  63. Immunity proteins to pore-forming colicins: structure-function relationships
  64. The colicin A pore-forming domain fused to mitochondrial intermembrane space sorting signals can be functionally inserted into the Escherichia coli plasma membrane by a mechanism that bypasses the Tol proteins
  65. Recognition of the colicin A N-terminal epitope 1C11 in vitro and in vivo in Escherichia coli by its cognate monoclonal antibody
  66. Acidic interaction of the colicin A pore-forming domain with model membranes of Escherichia coli lipids results in a large perturbation of acyl chain order and stabilization of the bilayer
  67. Study of the Import Mechanisms of Colicins Through Protein Engineering and K+ Efflux Kinetics
  68. Import of Colicins into Escherichia Coli
  69. Synthesis and sequence-specific proteolysis of a hybrid protein (colicin A :: growth hormone releasing factor) produced in Escherichia coli
  70. Purification and reconstitution into liposomes of an integral membrane protein conferring immunity to colicin A
  71. Isolation and molecular and functional properties of the amino-terminal domain of colicin A
  72. Interactions of colicin A domains with phospholipid monolayers and liposomes relevance to the mechanism of action
  73. The membrane channel-forming colicin A: synthesis, secretion, structure, action and immunity
  74. A molecular genetic approach to the functioning of the immunity protein to colicin A