Comparison of the regressor within the regression model of SD-TOPSIS technique results across groups of combinations - B1-B5 vs. C1-C10 vs. D1-D10. by Roman Vavrek (13200141)

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(a) Average absolute percentage relative error (AAPRE), and, (b) Coefficient of determination (R²) of the models. by Fahd Saeed Alakbari (10701871)

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Mod is expressed throughout the larval CNS and is primarily nuclear. by Amalia S. Parra (4173004)

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RNA targets and biological process GO terms associated with Mod RiP-Seq analysis. by Amalia S. Parra (4173004)

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Mod antibody and RNAi validations. by Amalia S. Parra (4173004)

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Mod is required to maintain nucleolar architecture. by Amalia S. Parra (4173004)

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Loss of Mod causes cell cycle defects. by Amalia S. Parra (4173004)

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NBs in Mod-depleted brains display defects in expression of key cell identity factors. by Amalia S. Parra (4173004)

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Mod localizes both within and outside the nucleolus in NBs. by Amalia S. Parra (4173004)

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Mod loss is associated with a reduction of central brain NBs. by Amalia S. Parra (4173004)

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Differential gene expression analysis following Mod knockdown. by Amalia S. Parra (4173004)

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Loss of Mod does not affect NB asymmetric cell division. by Amalia S. Parra (4173004)

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Data for Fig 1. by Rachael M. Giersch (22331947)

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Development of <i>Drosophila</i> Neuroblasts (NB). by Amalia S. Parra (4173004)

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Anecdotal case of regression in a clam with naturally acquired BTN. by Rachael M. Giersch (22331947)

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Negative (Prednisone) and basal (ATP) control compounds binding to ALK protein. by Richard Junior Zapata Dongo (17912565)

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Length distribution and condition factors <i>K</i> of <i>E. erythropterus</i> (A) before and (B) after the NRE opening. by Jeong-Soo Gim (18058588)

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Distribution of zooplankton abundance by depth (A) before and (B) after and phytoplankton abundance by depth (C) before and (D) after the opening of the NRE. by Jeong-Soo Gim (18058588)

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S1 Data - by Richard Junior Zapata Dongo (17912565)

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Study-related adverse events. by Benjamin R. Lewis (22279166)

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