| Name | Last modified | Size | Description |
|
| Parent Directory | | - | |
| asset/ | 2019-05-09 20:37 | - | |
| css/ | 2019-05-09 20:37 | - | |
| hlw_0207_hydrogen_bonds.html | 2019-05-09 20:37 | 3.1K | |
| hlw_0207_hydrogen_bonds_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_0303_the_central_dogma.html | 2019-05-09 20:37 | 3.1K | |
| hlw_0303_the_central_dogma_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_0310_dna_structure_and_stabilization.html | 2019-05-09 20:37 | 3.1K | |
| hlw_0310_dna_structure_and_stabilization_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_04_trna_synthetase.html | 2019-05-09 20:37 | 3.1K | |
| hlw_04_trna_synthetase_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_0418_translation_elongation.html | 2019-05-09 20:37 | 3.0K | |
| hlw_0418_translation_elongation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_0510_diffusion.html | 2019-05-09 20:37 | 3.0K | |
| hlw_0510_diffusion_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_0511_osmosis.html | 2019-05-09 20:37 | 3.0K | |
| hlw_0511_osmosis_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_0512_active_transport.html | 2019-05-09 20:37 | 3.0K | |
| hlw_0512_active_transport_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_0517_fluid_mosaic_model.html | 2019-05-09 20:37 | 3.0K | |
| hlw_0517_fluid_mosaic_model_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_06_activation_energy.html | 2019-05-09 20:37 | 3.0K | |
| hlw_06_activation_energy_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_06_activation_energy copy.html | 2019-05-09 20:37 | 3.0K | |
| hlw_06_activation_energy copy_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_0608_chemical_reactions.html | 2019-05-09 20:37 | 3.0K | |
| hlw_0608_chemical_reactions_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_07_oxidation_reduction_reactions.html | 2019-05-09 20:37 | 3.0K | |
| hlw_07_oxidation_reduction_reactions_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_08_chlorophyll.html | 2019-05-09 20:37 | 3.1K | |
| hlw_08_chlorophyll_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_08_energy_transfer.html | 2019-05-09 20:37 | 3.0K | |
| hlw_08_energy_transfer_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_08_photosynthetic_electron_transport_chain.html | 2019-05-09 20:37 | 3.1K | |
| hlw_08_photosynthetic_electron_transport_chain_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_08_rubisco_as_oxygenase.html | 2019-05-09 20:37 | 3.1K | |
| hlw_08_rubisco_as_oxygenase_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_0814_atp_synthase_and_nadph_synthesis.html | 2019-05-09 20:37 | 3.1K | |
| hlw_0814_atp_synthase_and_nadph_synthesis_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_09_cell_signaling.html | 2019-05-09 20:37 | 3.1K | |
| hlw_09_cell_signaling_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_09_g_protein_coupled_receptors.html | 2019-05-09 20:37 | 3.2K | |
| hlw_09_g_protein_coupled_receptors_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_09_signal_amplification.html | 2019-05-09 20:37 | 3.2K | |
| hlw_09_signal_amplification_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_10_actin_filaments.html | 2019-05-09 20:37 | 3.1K | |
| hlw_10_actin_filaments_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_10_microtubules.html | 2019-05-09 20:37 | 3.1K | |
| hlw_10_microtubules_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_10_molecular_motors.html | 2019-05-09 20:37 | 3.2K | |
| hlw_10_molecular_motors_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_11_meiotic_cell_division.html | 2019-05-09 20:37 | 3.1K | |
| hlw_11_meiotic_cell_division_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_11_mitotic_cell_division.html | 2019-05-09 20:37 | 3.1K | |
| hlw_11_mitotic_cell_division_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_12_dna_replication.html | 2019-05-09 20:37 | 3.1K | |
| hlw_12_dna_replication_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_12_proofreading.html | 2019-05-09 20:37 | 3.1K | |
| hlw_12_proofreading_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_13_sequence_assembly.html | 2019-05-09 20:37 | 3.1K | |
| hlw_13_sequence_assembly_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_14_base_excision_repair.html | 2019-05-09 20:37 | 3.1K | |
| hlw_14_base_excision_repair_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_14_cancer_from_somatic_mutations.html | 2019-05-09 20:37 | 3.1K | |
| hlw_14_cancer_from_somatic_mutations_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_15_nondisjunction.html | 2019-05-09 20:37 | 3.1K | |
| hlw_15_nondisjunction_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_15_snp_genotyping.html | 2019-05-09 20:37 | 3.1K | |
| hlw_15_snp_genotyping_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_16_principle_of_independent_assortment.html | 2019-05-09 20:37 | 3.1K | |
| hlw_16_principle_of_independent_assortment_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_16_principle_of_segregation.html | 2019-05-09 20:37 | 3.2K | |
| hlw_16_principle_of_segregation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_17_linkage_and_recombination.html | 2019-05-09 20:37 | 3.1K | |
| hlw_17_linkage_and_recombination_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_17_x_linkage.html | 2019-05-09 20:37 | 3.1K | |
| hlw_17_x_linkage_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_18_regression_toward_the_mean.html | 2019-05-09 20:37 | 3.1K | |
| hlw_18_regression_toward_the_mean_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_19_lac_operon_induction.html | 2019-05-09 20:37 | 3.1K | |
| hlw_19_lac_operon_induction_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_19_lac_operon_repression.html | 2019-05-09 20:37 | 3.2K | |
| hlw_19_lac_operon_repression_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_19_x_inactivation.html | 2019-05-09 20:37 | 3.2K | |
| hlw_19_x_inactivation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_20_abc_model_for_floral_development.html | 2019-05-09 20:37 | 3.2K | |
| hlw_20_abc_model_for_floral_development_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_21_genetic_drift.html | 2019-05-09 20:37 | 3.1K | |
| hlw_21_genetic_drift_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_21_mutation_and_recombination.html | 2019-05-09 20:37 | 3.2K | |
| hlw_21_mutation_and_recombination_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_21_stabilizing_directional_and_disruptive_stabilization.html | 2019-05-09 20:37 | 3.2K | |
| hlw_21_stabilizing_directional_and_disruptive_stabilization_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_22_speciation.html | 2019-05-09 20:37 | 3.1K | |
| hlw_22_speciation_by_vicariance.html | 2019-05-09 20:37 | 3.1K | |
| hlw_22_speciation_by_vicariance_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_22_speciation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_23_carbon_dating.html | 2019-05-09 20:37 | 3.1K | |
| hlw_23_carbon_dating_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_23_monophyletic_paraphyletic_and_polyphyletic_groups.html | 2019-05-09 20:37 | 3.2K | |
| hlw_23_monophyletic_paraphyletic_and_polyphyletic_groups_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_23_phylogenies_and_depicting_sister_groups.html | 2019-05-09 20:37 | 3.1K | |
| hlw_23_phylogenies_and_depicting_sister_groups_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_24_evidence_for_human_evolution_heteroduplex_denaturation.html | 2019-05-09 20:37 | 3.2K | |
| hlw_24_evidence_for_human_evolution_heteroduplex_denaturation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_24_evidence_for_human_migration_mitochondrial_dna.html | 2019-05-09 20:37 | 3.2K | |
| hlw_24_evidence_for_human_migration_mitochondrial_dna_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_25_carbon_cycle.html | 2019-05-09 20:37 | 3.1K | |
| hlw_25_carbon_cycle_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_25_glaciation.html | 2019-05-09 20:37 | 3.1K | |
| hlw_25_glaciation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_26_horizontal_gene_transfer.html | 2019-05-09 20:37 | 3.1K | |
| hlw_26_horizontal_gene_transfer_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_26_stromatolite_formation.html | 2019-05-09 20:37 | 3.1K | |
| hlw_26_stromatolite_formation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_27_eukaryotic_life_cycles.html | 2019-05-09 20:37 | 3.1K | |
| hlw_27_eukaryotic_life_cycles_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_27_evolution_of_photosynthesis_in_eykaryotes.html | 2019-05-09 20:37 | 3.2K | |
| hlw_27_evolution_of_photosynthesis_in_eykaryotes_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_29_c4_photosynthesis.html | 2019-05-09 20:37 | 3.1K | |
| hlw_29_c4_photosynthesis_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_29_cam_photosynthesis.html | 2019-05-09 20:37 | 3.2K | |
| hlw_29_cam_photosynthesis_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_29_phloem_transport.html | 2019-05-09 20:37 | 3.1K | |
| hlw_29_phloem_transport_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_29_xylem_transport_and_cavitation.html | 2019-05-09 20:37 | 3.1K | |
| hlw_29_xylem_transport_and_cavitation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_30_algal_and_bryophyte_life_cycles.html | 2019-05-09 20:37 | 3.2K | |
| hlw_30_algal_and_bryophyte_life_cycles_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_30_angiosperms_and_double_fertilization.html | 2019-05-09 20:37 | 3.2K | |
| hlw_30_angiosperms_and_double_fertilization_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_31_shoot_growth_and_leaf_arrangement.html | 2019-05-09 20:37 | 3.2K | |
| hlw_31_shoot_growth_and_leaf_arrangement_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_31_vascular_cambium.html | 2019-05-09 20:37 | 3.1K | |
| hlw_31_vascular_cambium_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_32_density_dependent_mortality_and_diversity.html | 2019-05-09 20:37 | 3.2K | |
| hlw_32_density_dependent_mortality_and_diversity_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_32_plant_immune_system.html | 2019-05-09 20:37 | 3.2K | |
| hlw_32_plant_immune_system_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_34_ascomycete_life_cycle.html | 2019-05-09 20:37 | 3.2K | |
| hlw_34_ascomycete_life_cycle_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_34_basidomycete_life_cycle.html | 2019-05-09 20:37 | 3.2K | |
| hlw_34_basidomycete_life_cycle_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_34_hyphal_growth.html | 2019-05-09 20:37 | 3.1K | |
| hlw_34_hyphal_growth_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_35_action_potential.html | 2019-05-09 20:37 | 3.1K | |
| hlw_35_action_potential_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_35_action_potential_propagation.html | 2019-05-09 20:37 | 3.1K | |
| hlw_35_action_potential_propagation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_35_chemical_synapses.html | 2019-05-09 20:37 | 3.1K | |
| hlw_35_chemical_synapses_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_35_knee_jerk_reflex.html | 2019-05-09 20:37 | 3.1K | |
| hlw_35_knee_jerk_reflex_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_35_sensing_stimulus_strength_and_location.html | 2019-05-09 20:37 | 3.1K | |
| hlw_35_sensing_stimulus_strength_and_location_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_36_sensing_gravity.html | 2019-05-09 20:37 | 3.1K | |
| hlw_36_sensing_gravity_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_36_vertebrate_vision.html | 2019-05-09 20:37 | 3.1K | |
| hlw_36_vertebrate_vision_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_37_hierarchical_organization_of_muscle.html | 2019-05-09 20:37 | 3.1K | |
| hlw_37_hierarchical_organization_of_muscle_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_37_sarcomere_shortening_and_lengthening.html | 2019-05-09 20:37 | 3.1K | |
| hlw_37_sarcomere_shortening_and_lengthening_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_38_amplification_of_hormone_signals.html | 2019-05-09 20:37 | 3.2K | |
| hlw_38_amplification_of_hormone_signals_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_38_cellular_action_of_peptide_hormones_and_steroid_hormones.html | 2019-05-09 20:37 | 3.2K | |
| hlw_38_cellular_action_of_peptide_hormones_and_steroid_hormones_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_39_concurrent_and_countercurrent_exchange.html | 2019-05-09 20:37 | 3.1K | |
| hlw_39_concurrent_and_countercurrent_exchange_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_40_glucose_absorption_in_the_small_intestine.html | 2019-05-09 20:37 | 3.2K | |
| hlw_40_glucose_absorption_in_the_small_intestine_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_41_concentration_gradient_in_the_nephron.html | 2019-05-09 20:37 | 3.2K | |
| hlw_41_concentration_gradient_in_the_nephron_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_41_countercurrent_multiplication.html | 2019-05-09 20:37 | 3.1K | |
| hlw_41_countercurrent_multiplication_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_41_filtration_reabsorption_secretion.html | 2019-05-09 20:37 | 3.2K | |
| hlw_41_filtration_reabsorption_secretion_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_42_gastrulation.html | 2019-05-09 20:37 | 3.1K | |
| hlw_42_gastrulation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_44_radial_and_bilateral_symmetry.html | 2019-05-09 20:37 | 3.1K | |
| hlw_44_radial_and_bilateral_symmetry_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_44_vertebrate_tree_with_characters.html | 2019-05-09 20:37 | 3.1K | |
| hlw_44_vertebrate_tree_with_characters_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_46_age_structure.html | 2019-05-09 20:37 | 3.1K | |
| hlw_46_age_structure_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_46_life_cycles_and_survivorship_curves.html | 2019-05-09 20:37 | 3.1K | |
| hlw_46_life_cycles_and_survivorship_curves_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_46_logistic_growth.html | 2019-05-09 20:37 | 3.1K | |
| hlw_46_logistic_growth_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_47_competition_mediated_by_predation.html | 2019-05-09 20:37 | 3.2K | |
| hlw_47_competition_mediated_by_predation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_47_funcamental_and_realized_niches.html | 2019-05-09 20:37 | 3.2K | |
| hlw_47_funcamental_and_realized_niches_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_47_fundamental_and_realized_niches.html | 2019-05-09 20:37 | 3.2K | |
| hlw_47_fundamental_and_realized_niches_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_48_dead_zone.html | 2019-05-09 20:37 | 3.1K | |
| hlw_48_dead_zone_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_48_greenhouse_effect.html | 2019-05-09 20:37 | 3.2K | |
| hlw_48_greenhouse_effect_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_2604_horizontal_gene_transfer.html | 2019-05-09 20:37 | 3.2K | |
| hlw_2604_horizontal_gene_transfer_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_2621_stromatolite_formation.html | 2019-05-09 20:37 | 3.2K | |
| hlw_2621_stromatolite_formation_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_3003_alternation_generations.html | 2019-05-09 20:37 | 3.1K | |
| hlw_3003_alternation_generations_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_3801_ecdysone.html | 2019-05-09 20:37 | 3.1K | |
| hlw_3801_ecdysone_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_simple_animations.xml | 2019-05-09 20:37 | 44K | |
| hlw_xxxx_activation_energy.html | 2019-05-09 20:37 | 2.7K | |
| hlw_xxxx_activation_energy_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_xxxx_cell_signaling.html | 2019-05-09 20:37 | 2.7K | |
| hlw_xxxx_cell_signaling_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_xxxx_energy_transfer.html | 2019-05-09 20:37 | 3.1K | |
| hlw_xxxx_energy_transfer_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_xxxx_oxidation_reduction_reactions.html | 2019-05-09 20:37 | 3.1K | |
| hlw_xxxx_oxidation_reduction_reactions_dlap.xml | 2019-05-09 20:37 | 120 | |
| hlw_xxxx_photosynthetic_electron_transport_chain.html | 2019-05-09 20:37 | 3.1K | |
| hlw_xxxx_photosynthetic_electron_transport_chain_dlap.xml | 2019-05-09 20:37 | 120 | |
| js/ | 2019-05-09 20:37 | - | |
| manifest-51c0c9a4757a2e374a000005.html | 2019-05-09 20:37 | 634 | |
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