| Part I: Gametes, Maturation, Fertilization and Modes of Reproduction |
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1 Marine Nemertean Worms for Studies of Oocyte Maturation and Aging |
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3 | (12) |
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3 | (2) |
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5 | (4) |
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1.2.1 Collection Procedures |
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5 | (1) |
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1.2.2 Maintaining Adult Specimens in the Laboratory |
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6 | (1) |
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1.2.3 Obtaining Gametes and Generating Cultures of Embryos |
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6 | (3) |
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1.2.4 General Cell Biological Applications |
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9 | (1) |
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1.3 Results and Discussion |
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9 | (3) |
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1.3.1 Using Nemertean Oocytes in Analyses of Maturation and Aging Processes |
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9 | (1) |
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1.3.2 AMP Kinase (AMPK) Deactivation During Oocyte Maturation |
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10 | (1) |
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1.3.3 c-Jun N-terminal Kinase (JNK) Activation During Oocyte Degradation |
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11 | (1) |
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12 | (1) |
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13 | (2) |
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2 Sperm Nuclear Basic Proteins of Marine Invertebrates |
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15 | (18) |
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2.1 Diversity of Sperm Nuclear Basic Proteins (SNBPs) |
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16 | (1) |
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2.2 Evolutionary Origin of SNBPs |
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17 | (4) |
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2.3 SNBPs in Marine Invertebrates |
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21 | (4) |
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2.3.1 P-Type and PL-Type SNBPs Contribute to Sperm Chromatin Compaction and Often Replace Somatic Histones Entirely During Spermatogenesis |
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21 | (1) |
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2.3.2 Porifera, Ctenophora and Crustacea Exclusively Use Somatic Histones to Pack Sperm DNA |
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21 | (1) |
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2.3.3 Echinoidea (Phylum Echinodermata) and Hydrozoa (Phylum Cnidaria) Lack SNBPs but Evolved Novel Nucleosomal Histone Variants with Specific Roles in Spermatogenesis |
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22 | (3) |
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2.4 Conclusion, Discussion and Outstanding Questions |
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25 | (2) |
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27 | (6) |
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3 Fertilization in Starfish and Sea Urchin: Roles of Actin |
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33 | (16) |
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33 | (1) |
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3.2 Actin in Sperm Acrosome Reaction |
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34 | (2) |
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3.3 Actin in Oocyte Maturation |
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36 | (2) |
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3.4 Actin in Fertilized Eggs |
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38 | (3) |
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3.5 Modulation of Intracellular Ca2+ Signaling by the Actin Cytoskeleton |
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41 | (2) |
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43 | (1) |
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43 | (6) |
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4 Starfish as a Model System for Analyzing Signal Transduction During Fertilization |
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49 | (20) |
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49 | (2) |
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4.2 Understanding the Regulation of Meiosis at the Cellular Level |
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51 | (8) |
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4.2.1 Future Contributions of the Starfish |
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52 | (1) |
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4.2.2 Signaling at Cell Surface |
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52 | (4) |
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4.2.3 Moving Inside the Egg During Fertilization |
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56 | (1) |
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4.2.4 Understanding Calcium Signaling |
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57 | (1) |
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4.2.5 Microinjection of the Live Oocyte and Egg |
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58 | (1) |
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4.3 Genomics in the Starfish (the Exciting Future!) |
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59 | (4) |
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4.3.1 Validation of the Existing Starfish Transcriptome Data |
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60 | (1) |
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4.3.2 Finding Novel Signaling Genes and Their RNA |
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60 | (2) |
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4.3.3 Applying CRISPR Technology to Studying Signaling in the Starfish |
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62 | (1) |
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4.4 Connections to Human Health |
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63 | (1) |
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64 | (5) |
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5 Toward Multiscale Modeling of Molecular and Biochemical Events Occurring at Fertilization Time in Sea Urchins |
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69 | (22) |
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70 | (1) |
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5.2 From Ca2+ Signaling Pathway to Sperm Navigation |
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71 | (3) |
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5.3 From Ca2+ Wave to Fertilization Envelope Elevation |
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74 | (3) |
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5.4 From Translation Regulation to the First Mitotic Division Following Fertilization |
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77 | (5) |
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5.5 Conclusions and Perspectives |
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82 | (1) |
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83 | (8) |
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91 | (14) |
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91 | (1) |
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92 | (1) |
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6.3 How to Generate Monosex? |
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92 | (1) |
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6.4 Sex Determination and Sexual Differentiation |
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93 | (2) |
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6.4.1 Sex Determination: Heterogamecy |
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94 | (1) |
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6.4.2 Sexual Differentiation |
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94 | (1) |
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6.5 Hormonal Regulation of Sex Differentiation in Vertebrates |
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95 | (2) |
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96 | (1) |
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6.6 Sex Reversal Induction in Vertebrates |
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97 | (1) |
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6.7 The Case of Macrobrachium rosenbergii: The Commercially Most Important Freshwater Prawn |
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98 | (1) |
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6.8 Sex Reversal Induction in Other Crustaceans |
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99 | (1) |
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100 | (1) |
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100 | (5) |
| Part II: Embryonic and Post-Embryonic Development, and the Evolution of the Body Plan |
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7 Medusa: A Review of an Ancient Cnidarian Body Form |
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105 | (32) |
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7.1 Medusozoa: Emergence of the Medusa Body Form |
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105 | (5) |
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7.1.1 Appeal of the Medusa |
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105 | (1) |
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7.1.2 Systematics and Evolutionary Position |
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106 | (1) |
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107 | (3) |
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7.2 Evolution of an Innovative Bauplan |
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110 | (5) |
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110 | (2) |
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7.2.2 Medusa Feeding and Digestion |
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112 | (3) |
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7.3 Nematocysts: Novel Stinging Structures |
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115 | (1) |
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115 | (1) |
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7.3.2 Cellular and Molecular Classification of Nematocysts |
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116 | (1) |
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116 | (3) |
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117 | (1) |
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7.4.2 Sensory Perception and Balance: The Medusa Pacemaker |
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117 | (2) |
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119 | (3) |
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7.5.1 Sexual Reproduction |
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119 | (1) |
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7.5.2 Metagenetic Life Cycles |
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119 | (2) |
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7.5.3 Exceptions to Metagenesis |
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121 | (1) |
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122 | (3) |
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7.6.1 Jellyfish Proliferations |
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122 | (1) |
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7.6.2 Jellyfish Blooms: A Bad Rap |
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123 | (1) |
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7.6.3 Ecological and Societal Benefits of Medusae |
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124 | (1) |
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7.6.4 Medusa-Inspired Robotics |
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124 | (1) |
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7.7 Emerging Medusa Model Systems: Insights to Be Gained |
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125 | (1) |
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126 | (11) |
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8 Sea Urchin Larvae as a Model for Postembryonic Development |
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137 | (26) |
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8.1 Larval Forms as Experimental Models in Physiology and Development |
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138 | (1) |
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8.2 A Framework for Hormonal Action in Larval Development and Metamorphosis of the Sea Urchin |
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139 | (4) |
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8.2.1 The Hypothesized Endocrine and Neuroendocrine Network of Sea Urchin Larval Development |
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140 | (1) |
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8.2.2 Putative Function of TH Signaling in Skeletogenesis |
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141 | (1) |
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8.2.3 Function of Hormonal Signaling in Programmed Cell Death (PCD) |
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142 | (1) |
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8.3 Sea Urchin Larvae as an Experimental Model for Bacterial Colonization and Host-Microbe Interactions in Postembryonic Development |
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143 | (4) |
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8.4 Sea Urchin Immunity in Larval Development |
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147 | (6) |
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8.4.1 The Larval Immune Gene Response and IL-17 |
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151 | (1) |
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8.4.2 Partitioning the Immune System Between Embryo, Larva, and Adult |
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152 | (1) |
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8.5 Asexual Reproduction and Regeneration |
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153 | (1) |
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8.5.1 Regeneration in Echinoderm Larvae |
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153 | (1) |
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8.5.2 Asexual Reproduction Via Budding in Sea Urchins |
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153 | (1) |
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154 | (1) |
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155 | (8) |
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9 The Ciona Notochord Gene Regulatory Network |
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163 | (22) |
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9.1 Ciona as a Model for Chordate GRN Analysis |
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163 | (2) |
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9.2 The Ciona Notochord as a Model for Understanding Morphogenesis and Differentiation |
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165 | (3) |
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9.3 Establishing Primary Notochord Fate |
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168 | (2) |
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9.4 Secondary Notochord Induction |
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170 | (2) |
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9.5 The Notochord Transcriptome |
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172 | (2) |
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9.6 Cis-regulatory Control of Brachyury Expression |
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174 | (1) |
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9.7 Notochord Effector Gene Regulation |
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174 | (2) |
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9.8 Fine Spatial Patterning |
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176 | (1) |
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9.9 Is Brachyury a True Master Regulator Gene? |
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177 | (1) |
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9.10 Current Questions in Ciona Notochord Gene Regulation |
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178 | (1) |
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179 | (6) |
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10 Model Systems for Exploring the Evolutionary Origins of the Nervous System |
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185 | (12) |
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185 | (1) |
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10.2 A Minimal Nervous System |
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186 | (1) |
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10.3 Uncertainty in the Metazoan Phylogeny |
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187 | (1) |
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10.4 Nervous System Evolution at the Base of the Metazoan Tree |
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188 | (5) |
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10.4.1 The Proto-Synaptic Scaffolding of Sponges |
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188 | (1) |
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10.4.2 The Ctenophore Nervous System |
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189 | (2) |
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191 | (1) |
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10.4.4 Cnidarian Nervous Systems |
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192 | (1) |
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193 | (1) |
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10.5.1 Evolution of Synapses from Ancient Chemosensory Cells |
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193 | (1) |
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10.5.2 Origin and Evolution of the Nervous System |
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193 | (1) |
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194 | (3) |
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11 Nonprotein-Coding RNAs as Regulators of Development in Tunicates |
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197 | (32) |
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Cristian A. Velandia-Huerto |
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Clara I. Bermudez-Santana |
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198 | (1) |
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11.2 miRNA Families Origin and Evolutionary Perspective |
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199 | (10) |
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11.2.1 Origins and Evolution of MicroRNAs |
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199 | (2) |
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11.2.2 miRNA Identification and Validation |
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201 | (1) |
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11.2.2.1 High-Throughput Studies of Ciona miRNAs |
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202 | (1) |
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11.2.2.2 High-Throughput miRNA Searches in Other Urochordates |
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204 | (1) |
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204 | (5) |
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11.3 miRNAs and Its Role in Development |
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209 | (9) |
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11.3.1 miRNA Discovery and Its Role in Development |
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209 | (5) |
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11.3.2 Neuronal Fate Determination and Regulation by miR-124 |
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214 | (1) |
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11.3.2.1 Muscle Development and the Polycistronic miR-1/miR-133 Cluster |
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216 | (1) |
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11.3.2.2 miRNA Expression During Oral Siphon (OS) Regeneration |
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217 | (1) |
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11.3.2.3 miRNA Expression During O. dioica Development |
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217 | (1) |
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11.4 Other ncRNAs Associated with Development |
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218 | (3) |
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11.4.1 Yellow Crescent RNA |
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218 | (1) |
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11.4.2 MicroRNA-Offset RNAs |
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218 | (1) |
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11.4.3 Long Noncoding RNA RMST |
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219 | (1) |
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11.4.4 Spliced-Leader RNA |
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220 | (1) |
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221 | (8) |
| Part III: Differentiation, Regeneration and Stemness |
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12 Differentiation and Transdifferentiation of Sponge Cells |
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229 | (26) |
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229 | (1) |
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12.2 Cell Types in Sponges: Ancient Characters? |
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230 | (2) |
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12.3 Sponge Body Plans: Is There Similarity to Other Animals? |
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232 | (2) |
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12.4 Germline and Stem Cell Systems in Sponges |
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234 | (1) |
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12.5 Cell Differentiation and Transdifferentiation During Embryonic Development and Metamorphosis: Diversity and Plasticity |
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235 | (6) |
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12.5.1 Formation and Metamorphosis of the Amphiblastula: Embryonically Determined Cell Fate? |
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236 | (3) |
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12.5.2 Formation and Metamorphosis of the Cinctoblastula: Position-Dependent Cell Fate? |
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239 | (1) |
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12.5.3 Formation and Metamorphosis of the Parenchymella: Lability of Cell Fate? |
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240 | (1) |
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12.6 Cell Differentiation and Transdifferentiation During Growth and Asexual Reproduction |
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241 | (2) |
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12.7 Cell Differentiation and Transdifferentiation During Regeneration |
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243 | (3) |
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12.8 Do Sponges Have Differentiated Cells and What Can We Learn from Them? |
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246 | (2) |
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248 | (7) |
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13 Holothurians as a Model System to Study Regeneration |
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255 | (30) |
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256 | (1) |
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256 | (1) |
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13.1.2 Regeneration in Echinoderms |
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256 | (1) |
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13.2 Digestive Tract Regeneration |
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257 | (13) |
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13.2.1 Holothurian Digestive Tract |
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258 | (2) |
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260 | (2) |
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13.2.3 Regeneration of the Digestive Tract |
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262 | (1) |
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262 | (1) |
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13.2.3.2 Cellular Mechanisms |
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262 | (1) |
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13.2.3.3 Species Differences |
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267 | (1) |
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13.2.3.4 Molecular Basis of Intestinal Regeneration |
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267 | (1) |
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13.2.3.5 Gene Expression Patterns |
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269 | (1) |
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13.2.3.6 Functional Studies |
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270 | (1) |
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270 | (9) |
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13.3.1 Holothurian Nervous System |
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270 | (2) |
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13.3.2 Radial Nerve Cord Transection |
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272 | (1) |
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13.3.3 Regeneration of the Nervous System |
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273 | (1) |
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13.3.3.1 Neurodegeneration |
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273 | (1) |
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274 | (1) |
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275 | (1) |
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13.3.3.4 Differentiation and Growth |
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275 | (1) |
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13.3.3.5 Cellular Mechanisms |
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276 | (1) |
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277 | (1) |
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13.3.3.7 Gene Expression Patterns |
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277 | (1) |
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13.3.3.8 Functional Studies |
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278 | (1) |
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279 | (6) |
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14 Regeneration in Stellate Echinoderms: Crinoidea, Asteroidea and Ophiuroidea |
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285 | (36) |
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Maria Daniela Candia Carnevali |
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14.1 A Phylogenetic Perspective of Echinoderms |
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286 | (2) |
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14.2 Echinoderm Regeneration: Not Only a Replacement |
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288 | (2) |
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14.3 Arm Regeneration: The Cellular and Tissue Perspective |
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290 | (16) |
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14.3.1 Regenerative Phases |
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291 | (6) |
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14.3.2 Blastema or Not Blastema? |
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297 | (1) |
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14.3.3 Regeneration-Competent Cells |
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298 | (4) |
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14.3.4 Distalization-Intercalary Regeneration |
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302 | (1) |
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14.3.5 Coelom and Nervous Tissue as the Key Players of Echinoderm Regeneration |
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303 | (1) |
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14.3.5.1 The Coelomic Epithelium as Organogenetic Tissue |
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303 | (1) |
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14.3.5.2 Nervous System as Coordinator |
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304 | (2) |
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14.4 Arm Regeneration: The Molecular Perspective |
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306 | (8) |
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306 | (1) |
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307 | (2) |
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309 | (5) |
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314 | (1) |
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314 | (7) |
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15 Solitary Ascidians as Model Organisms in Regenerative Biology Studies |
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321 | (16) |
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322 | (3) |
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323 | (2) |
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15.1.2 Polycarpa mytiligera |
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325 | (1) |
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15.2 Solitary Ascidians as Model System for Regenerative Studies |
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325 | (2) |
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15.3 Regeneration of Internal Organ |
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327 | (4) |
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15.3.1 Regeneration and Aging |
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329 | (2) |
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15.4 Ecological Significance of Regeneration |
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331 | (1) |
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15.5 Summary and Future Directions |
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332 | (1) |
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333 | (4) |
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16 Whole-Body Regeneration in the Colonial Tunicate Botrylloides leachii |
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337 | (22) |
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338 | (1) |
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16.2 The Biology of Botrylloides leachii |
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339 | (3) |
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16.3 Current State of Research on WBR in B. leachii |
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342 | (2) |
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16.4 Inferences from WBR and Asexual Reproduction in Other Colonial Ascidians |
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344 | (5) |
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16.4.1 Differences in WBR Ability Between Colonial Ascidians |
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344 | (2) |
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16.4.2 Insights from Asexual Reproduction |
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346 | (1) |
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16.4.3 The Origin of the Progenitor Cells Driving WBR |
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347 | (1) |
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16.4.4 The Role of Immune-Associated Cells During WBR |
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347 | (1) |
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16.4.5 Genes Involved in WBR Have Multiple Roles in Colonial Ascidian |
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348 | (1) |
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349 | (2) |
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351 | (8) |
| Part IV: Biomolecules, Secretion, Symbionts and Feeding |
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17 Beach to Bench to Bedside: Marine Invertebrate Biochemical Adaptations and Their Applications in Biotechnology and Biomedicine |
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359 | (18) |
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17.1 Marine Biotechnology and the Ocean as a Source of Chemical Diversity |
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360 | (3) |
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17.2 Biochemical Innovations of Marine Invertebrates |
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363 | (4) |
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17.2.1 Marine Invertebrate Toxins |
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363 | (2) |
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17.2.2 Marine Mollusk Ink Secretions |
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365 | (1) |
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17.2.3 Viscoelastic Adhesive Gels |
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366 | (1) |
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17.2.4 Light-Producing Compounds |
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366 | (1) |
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17.3 Biotechnological and Biomedical Applications |
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367 | (3) |
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17.3.1 Pharmacological Applications of Venom Peptides |
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367 | (1) |
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17.3.2 Applications of Light-Producing Molecules in Biophotonics |
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368 | (1) |
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17.3.3 Biomaterials Derived from Marine Invertebrates |
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369 | (1) |
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370 | (1) |
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371 | (6) |
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18 Coral Food, Feeding, Nutrition, and Secretion: A Review |
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377 | (46) |
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378 | (1) |
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18.2 Autotrophic Nutrition: A Brief Overview |
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379 | (3) |
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380 | (2) |
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18.3 Heterotrophic Nutrition in Scleractinians |
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382 | (10) |
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18.3.1 From the Water Column |
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382 | (1) |
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18.3.1.1 Tentacle Capture and the Use of Cnidae |
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382 | (1) |
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18.3.1.2 Feeding and Digestion by Mesenterial Filaments |
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384 | (1) |
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18.3.1.3 Capture of Mesozooplankton |
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387 | (1) |
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18.3.1.4 Capture of Micro-, Nano-, and Picoplankton |
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389 | (1) |
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18.3.1.5 The Microbial Loop, POM, and DOM in the Water Column: A Brief Overview |
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390 | (2) |
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18.4 Benthic and Epibenthic Organic Matter Production and Consumption |
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392 | (5) |
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393 | (2) |
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18.4.2 Mucus and Coral Feeding |
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395 | (1) |
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18.4.3 Feeding by Cold-Water Corals |
|
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396 | (1) |
|
18.5 Dissolved Organic and Inorganic Matter |
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397 | (5) |
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18.5.1 Mucus and the Production of Dissolved Organic Carbon |
|
|
397 | (1) |
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18.5.2 Sources of Dissolved Organic Nitrogen |
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398 | (1) |
|
18.5.3 Dissolved Inorganic Nitrogen (DIN) |
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399 | (1) |
|
18.5.4 Dissolved Forms of Phosphorus |
|
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400 | (2) |
|
18.6 Heterotrophic Feeding in the Octocorallia |
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402 | (3) |
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18.6.1 Alcyonacean Soft Corals |
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402 | (2) |
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18.6.2 Gorgonian Octocorals |
|
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404 | (1) |
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18.7 Heterotrophic Feeding in the Antipatharian Corals |
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|
405 | (1) |
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18.8 Questions for Future Research |
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406 | (1) |
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406 | (17) |
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19 The Suitability of Fishes as Models for Studying Appetitive Behavior in Vertebrates |
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423 | (16) |
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424 | (1) |
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19.2 The Endocrine Signals |
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425 | (1) |
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19.3 The Aminergic and Endocannabinoid Systems |
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426 | (1) |
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19.4 The Chemosensory Receptors and Their Affinity for Ligands |
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427 | (1) |
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428 | (3) |
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19.6 Anthropogenic Xenobiotics |
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431 | (1) |
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432 | (1) |
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433 | (6) |
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20 Glycans with Antiviral Activity from Marine Organisms |
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439 | (38) |
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441 | (3) |
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20.1.1 Antivirals: Definition and Therapeutic Activity |
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443 | (1) |
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443 | (1) |
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20.2 Marine Glycans: Structural Features and Reported Antiviral Activity |
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444 | (20) |
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20.2.1 Alginates (Sulfated Alginates) |
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454 | (1) |
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454 | (3) |
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457 | (1) |
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457 | (1) |
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20.2.5 Fucans/Sulfated Fucans |
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457 | (1) |
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20.2.6 Galactans/Sulfated Galactans |
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458 | (1) |
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20.2.7 Glycolipids/Sulfated Glycolipids |
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459 | (1) |
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20.2.8 Glycosaminoglycans |
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460 | (1) |
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460 | (1) |
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20.2.10 Glycosylated Haemocyanin |
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461 | (1) |
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461 | (1) |
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461 | (1) |
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20.2.13 Mannan/Sulfated Mannan |
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462 | (1) |
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462 | (1) |
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462 | (1) |
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20.2.16 Polysaccharide/Sulfated Polysaccharide |
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462 | (1) |
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463 | (1) |
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463 | (1) |
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463 | (1) |
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20.2.20 Xylomannan/Sulfated Xylomannan |
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463 | (1) |
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20.3 General Comments on Antiviral Activity of Glycans from Marine Organisms |
|
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464 | (1) |
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465 | (1) |
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466 | (11) |
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21 Cnidarian Jellyfish: Ecological Aspects, Nematocyst Isolation, and Treatment Methods of Sting |
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477 | (38) |
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477 | (8) |
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21.1.1 Relationships Between Cnidarians and the Environment |
|
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477 | (2) |
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21.1.2 Cnidaria Outbreaks |
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479 | (2) |
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21.1.3 Interactions with Other Organisms and Endosymbiosis |
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481 | (3) |
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484 | (1) |
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21.2 Cnidarian Stinging and Related Aspects |
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485 | (2) |
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21.2.1 Nematocytes and Nematocysts |
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485 | (2) |
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21.3 Toxicological and Epidemiological Aspects |
|
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487 | (1) |
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21.4 Cytotoxicity of Cnidarian Venoms |
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488 | (5) |
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488 | (2) |
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21.4.2 Cytotoxicity of Cnidarian Extracts on Cultured Cells |
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490 | (3) |
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21.5 Cnidarians as an Underexploited Rich Resource for New Therapeutics |
|
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493 | (1) |
|
21.6 Management and Treatment of Cnidarian Jellyfish Stings: Review Papers |
|
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493 | (2) |
|
21.7 Management of Stings by Hydrozoans |
|
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495 | (1) |
|
21.8 Management of Stings by Scyphozoans |
|
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496 | (1) |
|
21.9 Management of Stings by Cubozoans |
|
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497 | (2) |
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21.10 Treatment and Management of Stings by Undefined Cnidarians |
|
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499 | (1) |
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500 | (1) |
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501 | (14) |
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22 These Colors Don't Run: Regulation of Pigment-Biosynthesis in Echinoderms |
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515 | (14) |
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515 | (1) |
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22.2 Pigments for Consideration |
|
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516 | (4) |
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516 | (1) |
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517 | (1) |
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517 | (1) |
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518 | (2) |
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22.3 What Is the Major Enzymatic Activity of Polyketide Synthases? |
|
|
520 | (3) |
|
22.3.1 How Is Echinochrome Synthesized? |
|
|
520 | (1) |
|
22.3.2 PKS Diversity in Sea Urchins |
|
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521 | (1) |
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521 | (1) |
|
22.3.4 The Gene Regulatory Network of PKS |
|
|
521 | (1) |
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22.3.5 What Is the Function of the PKS-Derived Pigment in Sea Urchin? |
|
|
522 | (1) |
|
22.4 Concluding Statements |
|
|
523 | (1) |
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|
524 | (5) |
| Part V: Bioinformatics, Bioengineering and Information Processing |
|
|
23 Reef-Building Corals as a Tool for Climate Change Research in the Genomics Era |
|
|
529 | (18) |
|
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|
23.1 Coral Biology: An Enigmatic Symbioses |
|
|
529 | (2) |
|
23.2 Microbial Evolution and the Coral Holobiont |
|
|
531 | (1) |
|
23.3 Climate Change and Coral Reefs |
|
|
532 | (3) |
|
23.3.1 The Coral Holobiont as a Model for Climate Change |
|
|
534 | (1) |
|
23.4 High-Resolution Profiling of the Coral Biosphere |
|
|
535 | (1) |
|
23.5 Brief Technical Guide to Microbiome Research |
|
|
536 | (2) |
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|
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538 | (1) |
|
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|
539 | (8) |
|
24 The Crown-of-Thorns Starfish: From Coral Reef Plague to Model System |
|
|
547 | (22) |
|
|
|
|
|
547 | (1) |
|
24.2 The Remarkably High Resolution of the COTS Genome |
|
|
548 | (1) |
|
24.3 The High Resolution of the COTS Genome Is Likely Due to Low Heterozygosity |
|
|
548 | (2) |
|
24.4 COTS and Echinoderms: General Biology |
|
|
550 | (2) |
|
24.5 How COTS Damage Coral Reefs: COTS Aggregations |
|
|
552 | (1) |
|
24.6 The COTS Genome Assembly Is Biologically Significant: Hox, ParaHox, and Pharyngeal Gill Slit Clusters |
|
|
553 | (1) |
|
24.7 COTS as Model System for the Study of Genomic Structure: 1-MA SBGN Example |
|
|
554 | (11) |
|
24.8 COTS, GRNS, and KERNALS |
|
|
565 | (1) |
|
|
|
566 | (1) |
|
|
|
567 | (2) |
|
25 Structures and Composition of the Crab Carapace: An Archetypal Material in Biomimetic Mechanical Design |
|
|
569 | (16) |
|
|
|
|
|
569 | (1) |
|
25.2 Materials Secreted Through Cellular Activity |
|
|
570 | (3) |
|
25.3 Fundamental Organisation of the Crab Carapace |
|
|
573 | (4) |
|
25.4 Biomechanics of the Crab Carapace and Its Influence in Biomimetic Design |
|
|
577 | (4) |
|
|
|
581 | (1) |
|
|
|
581 | (4) |
|
26 Octopus vulgaris: An Alternative in Evolution |
|
|
585 | (14) |
|
|
|
|
|
|
|
26.1 Octopus: A Sophisticated Animal |
|
|
585 | (3) |
|
26.2 Octopus Weird Pupil: How It Sees Colors |
|
|
588 | (1) |
|
26.3 Octopus Smells by Touch: Its Chemical Sensing |
|
|
589 | (1) |
|
26.4 Octopus Edits Own Genes |
|
|
590 | (1) |
|
26.5 Octopus Rejuvenates Own Brain |
|
|
591 | (1) |
|
26.6 Future of Research on Octopus |
|
|
592 | (1) |
|
|
|
593 | (6) |
|
27 Vision Made Easy: Cubozoans Can Advance Our Understanding of Systems-Level Visual Information Processing |
|
|
599 | |
|
|
|
|
|
|
|
600 | (2) |
|
27.2 External Environment |
|
|
602 | (1) |
|
27.3 Box Jellyfish Visual Ecology |
|
|
603 | (5) |
|
27.3.1 Visual System Morphology |
|
|
603 | (1) |
|
|
|
604 | (1) |
|
|
|
605 | (1) |
|
27.3.4 Spatio-Temporal Properties |
|
|
606 | (2) |
|
27.3.5 Directional Vision |
|
|
608 | (1) |
|
|
|
608 | (5) |
|
27.4.1 Rhopalial Nervous System |
|
|
608 | (1) |
|
27.4.2 Central Pattern Generators |
|
|
609 | (3) |
|
|
|
612 | (1) |
|
27.5 Integrative Approach to Behaviour |
|
|
613 | (6) |
|
27.5.1 Long-Distance Navigation |
|
|
613 | (3) |
|
27.5.2 Foraging: Light Shaft Detection |
|
|
616 | (1) |
|
27.5.3 Obstacle Avoidance |
|
|
616 | (3) |
|
27.6 Future Research Perspectives |
|
|
619 | (2) |
|
|
|
621 | |