All Stories

  1. Recombinant SpTrf proteins illustrate putative functions of native SpTrf proteins: from immune response to resolution in sea urchins
  2. SpEchinoidin, a C-type lectin and a member of an expanded CTL family, is up-regulated by phagocytes in sea urchins responding to immune challenge
  3. Ultrafiltration and Fluid Excretion in Echinoids Involves the Axial Organ with Elimination via the Intestine
  4. Recombinant SpTransformer proteins bind to specific sites on sea urchin phagocytes and modulate SpTransformer gene expression and immune responsiveness
  5. The marine sponge, Hymeniacidon sinapium, displays allorecognition of siblings during post-larval settling and metamorphosis to juveniles
  6. Recombinant SpTransformer proteins are functionally diverse for binding and phagocytosis by three subtypes of sea urchin phagocytes
  7. Local Genomic Instability of the SpTransformer Gene Family in the Purple Sea Urchin Inferred from BAC Insert Deletions
  8. Spotting disease disrupts the microbiome of infected purple sea urchins, Strongylocentrotus purpuratus
  9. The echinoid complement system inferred from genome sequence searches
  10. Bald sea urchin disease shifts the surface microbiome on purple sea urchins in an aquarium
  11. The complex set of internal repeats in SpTransformer protein sequences result in multiple but limited alternative alignments
  12. Coelomocyte populations in the sea urchin, Strongylocentrotus purpuratus, undergo dynamic changes in response to immune challenge
  13. Lipofection mediated transfection fails for sea urchin coelomocytes
  14. A flow cytometry based approach to identify distinct coelomocyte subsets of the purple sea urchin, Strongylocentrotus purpuratus
  15. Echinoderm diseases and pathologies
  16. Ecological outcomes of echinoderm disease, mass die-offs, and pandemics
  17. Host defences of invertebrates to pathogens and parasites
  18. Sequence Diversity, Locus Structure, and Evolutionary History of the SpTransformer Genes in the Sea Urchin Genome
  19. Guardian of the Genome: An Alternative RAG/Transib Co-Evolution Hypothesis for the Origin of V(D)J Recombination
  20. Individual Sea Urchin Coelomocytes Undergo Somatic Immune Gene Diversification
  21. The Axial Organ and the Pharynx Are Sites of Hematopoiesis in the Sea Urchin
  22. Methods for collection, handling, and analysis of sea urchin coelomocytes
  23. SpTransformer proteins from the purple sea urchin opsonize bacteria, augment phagocytosis, and retard bacterial growth
  24. Echinodermata: The Complex Immune System in Echinoderms
  25. The SpTransformer Gene Family (Formerly Sp185/333) in the Purple Sea Urchin and the Functional Diversity of the Anti-Pathogen rSpTransformer-E1 Protein
  26. The Recombinant Sea Urchin Immune Effector Protein, rSpTransformer-E1, Binds to Phosphatidic Acid and Deforms Membranes
  27. Multitasking Immune Sp185/333 Protein, rSpTransformer-E1, and Its Recombinant Fragments Undergo Secondary Structural Transformation upon Binding Targets
  28. Short tandem repeats, segmental duplications, gene deletion, and genomic instability in a rapidly diversified immune gene family
  29. A recombinant Sp185/333 protein from the purple sea urchin has multitasking binding activities towards certain microbes and PAMPs
  30. Conference Report: The 13th Congress of the International Society of Developmental and Comparative Immunology
  31. Genomic Instability and Shared Mechanisms for Gene Diversification in Two Distant Immune Gene Families: The Plant NBS-LRR Genes and the Echinoid 185/333 Genes
  32. Research Highlight: rSp0032 has multitasking, anti-pathogen binding activities that predicts a flexible and effective immune response in sea urchins mediated by the Sp185/333 system
  33. Extraordinary Diversity of Immune Response Proteins among Sea Urchins: Nickel-Isolated Sp185/333 Proteins Show Broad Variations in Size and Charge
  34. Bacterial and fungal pattern recognition receptors in homologous innate signaling pathways of insects and mammals
  35. Single Sea Urchin Phagocytes Express Messages of a Single Sequence from the DiverseSp185/333Gene Family in Response to Bacterial Challenge
  36. Corrigendum to “Shotgun proteomics of coelomic fluid from the purple sea urchin, Strongylocentrotus purpuratus” [DCI 40 (1) (2013) 35–50]
  37. Shotgun proteomics of coelomic fluid from the purple sea urchin, Strongylocentrotus purpuratus
  38. Aggregation of Sea Urchin Phagocytes Is Augmented In Vitro by Lipopolysaccharide
  39. TheSp185/333immune response genes and proteins are expressed in cells dispersed within all major organs of the adult purple sea urchin
  40. Innate immune complexity in the purple sea urchin: diversity of the Sp185/333 system
  41. Invertebrate immune diversity
  42. An Sp185/333 gene cluster from the purple sea urchin and putative microsatellite-mediated gene diversification
  43. SpTie1/2 is expressed in coelomocytes, axial organ and embryos of the sea urchin Strongylocentrotus purpuratus, and is an orthologue of vertebrate Tie1 and Tie2
  44. Diversification of innate immune genes: lessons from the purple sea urchin
  45. Sp185/333: A novel family of genes and proteins involved in the purple sea urchin immune response
  46. Two recombinant peptides, SpStrongylocins 1 and 2, from Strongylocentrotus purpuratus, show antimicrobial activity against Gram-positive and Gram-negative bacteria
  47. Echinoderm Immunity
  48. A method for identifying alternative or cryptic donor splice sites within gene and mRNA sequences. Comparisons among sequences from vertebrates, echinoderms and other groups
  49. Highly Variable Immune-Response Proteins (185/333) from the Sea Urchin,Strongylocentrotus purpuratus: Proteomic Analysis Identifies Diversity within and between Individuals
  50. Sequence Variations in 185/333 Messages from the Purple Sea Urchin Suggest Posttranscriptional Modifications to Increase Immune Diversity
  51. The 185/333 Gene Family Is a Rapidly Diversifying Host-Defense Gene Cluster in the Purple Sea Urchin Strongylocentrotus purpuratus
  52. Localization and diversity of 185/333 proteins from the purple sea urchin – unexpected protein-size range and protein expression in a new coelomocyte type
  53. Brief review of McDowell and Simon
  54. Distinctive expression patterns of 185/333 genes in the purple sea urchin, Strongylocentrotus purpuratus: an unexpectedly diverse family of transcripts in response to LPS, β-1,3-glucan, and dsRNA
  55. Extraordinary diversity among members of the large gene family, 185/333, from the purple sea urchin, Strongylocentrotus purpuratus
  56. The immune gene repertoire encoded in the purple sea urchin genome
  57. The Genome of the Sea Urchin Strongylocentrotus purpuratus
  58. Genomic Insights into the Immune System of the Sea Urchin
  59. Unexpected diversity displayed in cDNAs expressed by the immune cells of the purple sea urchin,Strongylocentrotus purpuratus
  60. Macroarray analysis of coelomocyte gene expression in response to LPS in the sea urchin. Identification of unexpected immune diversity in an invertebrate
  61. Constitutive expression and alternative splicing of the exons encoding SCRs in Sp152, the sea urchin homologue of complement factor B. Implications on the evolution of the Bf/C2 gene family
  62. The sea urchin complement homologue, SpC3, functions as an opsonin
  63. Two cDNAs from the purple sea urchin, Strongylocentrotus purpuratus, encoding mosaic proteins with domains found in factor H, factor I, and complement components C6 and C7
  64. The gene encoding the sea urchin complement protein, SpC3, is expressed in embryos and can be upregulated by bacteria
  65. Workshop report: evolutionary immunobiology—new approaches, new paradigms
  66. Evolutionary immunobiology: new approaches, new paradigms
  67. Thioester function is conserved in SpC3, the sea urchin homologue of the complement component C3
  68. The ancestral complement system in sea urchins
  69. Origin and Evolution of the Vertebrate Immune System. L. Du Pasquier , G. W. Litman
  70. The Complement System in Sea Urchins
  71. Expression of SpC3, the sea urchin complement component, in response to lipopolysaccharide
  72. SpC3, the complement homologue from the purple sea urchin, Strongylocentrotus purpuratus , is expressed in two subpopulations of the phagocytic coelomocytes
  73. L.C. Smith, C. Baier-Anderson, L.A. Clow, D.P. Terwilliger and C.M. Adema. Conference report.
  74. Meeting review: Mid Atlantic Society of Developmental and Comparative Immunology
  75. Erratum
  76. Echinoderm immunity and the evolution of the complement system
  77. Complement systems in invertebrates. The ancient alternative and lectin pathways
  78. HP7 The sea urchin complement C3 protein: Expression and function
  79. Lipopolysaccharide activates the sea urchin immune system
  80. The sea urchin profilin gene is specifically expressed in mesenchyme cells during gastrulation
  81. The Echinoderm Immune System
  82. Ligand-dependent stimulation of introduced mammalian brain receptors alters spicule symmetry and other morphogenetic events in sea urchin embryos
  83. Reply by Smith and Davidson
  84. The echinoid immune system and the phylogenetic occurrence of immune mechanisms in deuterostomes
  85. SpCoel1: a sea urchin profilin gene expressed specifically in coelomocytes in response to injury.
  86. A gene (Spcoel) expressed in sea urchin coelomocytes shows an increase in transcripts after immune challenge
  87. The Role of Mesohyl Cells in Sponge Allograft Rejections
  88. Report from the I.S.D.C.I. committee on graduate student/post-doctoral affairs
  89. Allogeneic cell interactions during graft rejection inCallyspongia diffusa(Porifera, Demospongia); a study with monoclonal antibodies
  90. Allograft rejection, autograft fusion and inflammatory responses to injury inCallyspongia diffusa(Porifera; Demospongia)