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Chromatin Remodeling Factors and DNA Replication |
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1 | (30) |
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1 | (1) |
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Chromatin and Chromatin Remodeling Factors |
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2 | (3) |
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2 | (1) |
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Histone Modification Enzymes |
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3 | (1) |
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ATP-Dependent Chromatin Remodeling Factors |
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4 | (1) |
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Chromatin Structure and DNA Replication |
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5 | (2) |
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7 | (6) |
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7 | (2) |
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Chromatin Assembly Factor 1, a Replication-Coupled Histone Chaperone |
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9 | (1) |
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CAF-1 Functions in the Inheritance of Chromatin States |
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9 | (1) |
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10 | (1) |
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Histone Chaperones and Heterochromatin Replication |
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11 | (1) |
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11 | (1) |
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DNA Replication-Independent Chromatin Assembly |
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12 | (1) |
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Histone Modifications and Chromatin Replication |
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13 | (1) |
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Histone Deacetylation During Chromatin Replication |
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13 | (1) |
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Histone Acetylation at the Replication Site |
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13 | (1) |
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ATP-Dependent Chromatin Remodeling Factors in Chromatin Replication |
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14 | (5) |
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ISWI Complexes in Chromatin Assembly in Vitro |
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14 | (3) |
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ISWI Complexes and Their Role in Chromatin Replication in Vivo |
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17 | (2) |
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The Assembly of Higher Order Chromatin Structures |
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19 | (1) |
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PCNA, a Central Coordinator of Epigenetic Inheritance |
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20 | (1) |
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Mechanisms of Epigenetic Inheritance Through Chromatin: Conclusion |
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21 | (10) |
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21 | (10) |
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Epigenetic Inheritance of Chromatin States Mediated by Polycomb and Trithorax Group Proteins in Drosophila |
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31 | (34) |
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31 | (2) |
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Proteins of the Polycomb Group of Genes |
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33 | (13) |
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33 | (1) |
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33 | (2) |
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The Polycomb Repressive Complex 1 |
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35 | (1) |
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Other Identified PcG Proteins and Partners |
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36 | (1) |
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Targeting of PcG-Mediated Repression |
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37 | (1) |
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37 | (2) |
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Chromatin Determinants Associated with Targeting |
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39 | (4) |
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43 | (1) |
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43 | (1) |
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Proposed Silencing Mechanisms |
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44 | (2) |
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Proteins of the Trithorax Group |
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46 | (8) |
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48 | (1) |
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The Trithorax Acetylation Complex (TAC1) |
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48 | (1) |
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48 | (1) |
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49 | (1) |
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Other trxG Complexes and Partners |
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49 | (1) |
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Targeting of trxG Complexes at TREs |
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49 | (2) |
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51 | (3) |
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54 | (1) |
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55 | (10) |
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56 | (9) |
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How to Pack the Genome for a Safe Trip |
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65 | (26) |
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65 | (2) |
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Synthesis of Histone Variants |
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67 | (4) |
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Non-Testis-Specific Core Histone Variants |
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68 | (1) |
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Testis-Specific Histone Variants |
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69 | (1) |
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69 | (1) |
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70 | (1) |
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71 | (3) |
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72 | (1) |
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73 | (1) |
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73 | (1) |
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74 | (1) |
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74 | (1) |
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Final Components of the Sperm Chromatin |
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75 | (2) |
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76 | (1) |
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77 | (1) |
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Mechanisms Controlling Post-Meiotic Chromatin Reorganization: A General Discussion |
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77 | (5) |
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Active Transcription Followed by Repression in Round Spermatids |
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78 | (1) |
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Functional Link Between Histone Acetylation and Chromatin Condensation and Histone Replacement |
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79 | (1) |
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Does Histone Ubiquitination Play a Role in Spermatid-Specific Chromatin Remodeling? |
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80 | (1) |
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Is There a Spermiogenesis-Specific Histone Code? |
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81 | (1) |
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Do Histone Variants Play a Role in Spermatid-Specific Chromatin Remodeling? |
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82 | (1) |
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82 | (9) |
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84 | (7) |
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Chromatin Modifications on the Inactive X Chromosome |
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91 | (32) |
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91 | (1) |
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92 | (9) |
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Histone H3 Lysine 9 Methylation |
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92 | (2) |
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Histone H3 Lysine 27 Methylation |
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94 | (1) |
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Methylation at Other Histone H3 Residues |
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95 | (1) |
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96 | (1) |
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97 | (1) |
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98 | (1) |
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98 | (1) |
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98 | (1) |
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99 | (1) |
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100 | (1) |
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101 | (1) |
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Redundant Mechanisms Maintain Silencing |
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101 | (1) |
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101 | (2) |
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102 | (1) |
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102 | (1) |
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103 | (1) |
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Genes that Escape X-Inactivation |
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103 | (2) |
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103 | (1) |
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104 | (1) |
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104 | (1) |
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104 | (1) |
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Developmental Regulation of X-Inactivation |
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105 | (6) |
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Three Stages of X-Inactivation |
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105 | (2) |
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107 | (1) |
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108 | (1) |
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109 | (2) |
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Chromatin Features of the X Chromosomes Prior to X-Inactivation |
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111 | (3) |
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111 | (1) |
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112 | (2) |
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114 | (9) |
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115 | (8) |
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Chromatin Mechanisms in Drosophila Dosage Compensation |
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123 | (28) |
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123 | (1) |
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124 | (9) |
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126 | (1) |
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127 | (1) |
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127 | (1) |
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128 | (1) |
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129 | (2) |
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131 | (1) |
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131 | (1) |
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roX Genes as Non-Coding RNAs |
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132 | (1) |
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roX Loci as Chromatin Entry Sites |
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132 | (1) |
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Targeting, Assembly and Spreading of the MSL Complex |
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133 | (3) |
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133 | (2) |
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135 | (1) |
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136 | (2) |
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136 | (1) |
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137 | (1) |
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Molecular Mechanism of Dosage Compensation |
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138 | (3) |
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Initiation Versus Elongation |
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138 | (1) |
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The Inverse Effect Hypothesis |
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139 | (2) |
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The Origin and Evolution of the MSL Complex |
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141 | (10) |
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143 | (8) |
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DNA Methylation in Epigenetic Control of Gene Expression |
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151 | (18) |
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151 | (2) |
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Changes in Gene-Specific Methylation Patterns During Early Embryo Development |
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153 | (1) |
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Effect of Methylation on Gene Expression |
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154 | (5) |
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Direct Transcription Inhibition |
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154 | (2) |
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Indirect Transcription Inhibition |
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156 | (3) |
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DNA Methylation and Genomic Imprinting |
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159 | (3) |
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DNA Methylation and Disease |
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162 | (1) |
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163 | (6) |
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163 | (6) |
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The Epigenetic Breakdown of Cancer Cells: From DNA Methylation to Histone Modifications |
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169 | (14) |
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169 | (2) |
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What Is Responsible for DNA Methylation and for How Deregulation Occurs? |
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171 | (2) |
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Is Methylation Specific to the Tumor Type? |
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173 | (1) |
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Connecting DNA Methylation Changes with Transcription: Chromatin Mechanisms |
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174 | (4) |
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Can We Reactivate Epigenetically Silenced Genes? Towards Epigenetic Therapy |
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178 | (5) |
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178 | (5) |
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Developmental Regulation of the β-Globin Gene Locus |
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183 | (24) |
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183 | (1) |
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The β-Globin Clusters and Their Ontogeny |
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184 | (1) |
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Models for Studying the β-Globin Locus |
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185 | (1) |
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The LCR Is Required for High-Level Expression |
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186 | (2) |
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The Role of Individual HS |
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188 | (1) |
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Gene Competition and the LCR Holocomplex |
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189 | (1) |
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The β-Globin Locus Resides in a Region of Tissue-Specific Open Chromatin |
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190 | (1) |
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191 | (1) |
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192 | (1) |
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193 | (1) |
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Histone Modification and Developmental Globin Gene Expression |
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194 | (1) |
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The Role of Intergenic Transcription |
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195 | (1) |
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The Cell Cycle Connection |
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196 | (1) |
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197 | (1) |
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Higher Order Folding and Long-Range Regulation |
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198 | (1) |
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199 | (1) |
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200 | (7) |
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201 | (6) |
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Epigenetic Regulation of Mammalian Imprinted Genes: From Primary to Functional Imprints |
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207 | (30) |
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207 | (1) |
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208 | (3) |
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Conservation of Parental Genomic Imprinting in Therian Mammals |
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208 | (1) |
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Theories on the Evolution of Parental Genomic Imprinting |
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209 | (1) |
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The Parental Conflict Theory |
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210 | (1) |
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211 | (1) |
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Characteristics of Mammalian Imprinted Genes |
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211 | (1) |
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Epigenetic Control of Imprinted Genes |
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212 | (4) |
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212 | (2) |
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214 | (1) |
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Asynchronous DNA Replication Timing |
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215 | (1) |
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216 | (1) |
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The Parental Genomic Imprinting Cycle |
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216 | (9) |
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216 | (2) |
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218 | (1) |
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218 | (1) |
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219 | (2) |
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221 | (1) |
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Monoallelic Expression of Imprinted Genes |
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222 | (1) |
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Formatting for Gene Expression |
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223 | (1) |
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Acquisition of Functional Imprints |
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223 | (2) |
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225 | (12) |
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226 | (11) |
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Seed Development and Genomic Imprinting in Plants |
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237 | (26) |
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237 | (1) |
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Seed Development in Angiosperms |
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238 | (1) |
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Development and Function of the Endosperm |
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238 | (3) |
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A Role for Genomic Imprinting in Seed Development? |
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241 | (1) |
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The Discovery of Genomic Imprinting in Maize |
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242 | (1) |
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Studies on Other Potentially Imprinted Genes in Maize |
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243 | (1) |
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Maternal Control of Early Seed Development in Arabidopsis |
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244 | (2) |
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Intragenomic Parental Conflict and the Evolution of Genomic Imprinting |
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246 | (1) |
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Imprinting of the MEDEA Locus in Arabidopsis |
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247 | (2) |
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Function of MEDEA During Gametophyte and Seed Development |
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249 | (2) |
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Imprinting of the FWA Locus in the Female Gametophyte |
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251 | (1) |
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The Role of Imprinting During Gametophyte and Seed Development |
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252 | (1) |
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253 | (1) |
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Possible Epigenetic Marks Distinguishing Maternal and Paternal Alleles |
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254 | (3) |
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254 | (1) |
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DNA Methylation During Gametogenesis |
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255 | (1) |
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DNA Methylation During Seed Development |
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256 | (1) |
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257 | (6) |
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257 | (6) |
Subject Index |
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263 | |