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Submissions from 2020

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Additional file 3 of Integrated Puncture Score: force–displacement weighted rind penetration tests improve stalk lodging resistance estimations in maize, Christopher J. Stubbs, Douglas D. Cook, Daniel J. Robertson, Christopher McMahan, and Will Seegmiller

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Additional file 1 of Integrated Puncture Score: force–displacement weighted rind penetration tests improve stalk lodging resistance estimations in maize, Christopher J. Stubbs, Will Seegmiller, Douglas D. Cook, Christopher McMahan, and Daniel J. Robertson

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The promise and the perils of resurveying to understand global change impacts, Katharine Stuble, Sharon Bewick, Arthur Shapiro, Susan Harrison, Mark Fisher, Matthew Forister, Andrew Latimer, and Laurel Fox

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The effects of climate change on floral anthocyanin polymorphisms, Cierra Sullivan and Matthew Koski

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Additional file 2 of AsHSP26.8a, a creeping bentgrass small heat shock protein integrates different signaling pathways to modulate plant abiotic stress response, Xinbo Sun, Liebao Han, Hong Luo, Zhigang Li, Junfei Zhu, and Xin Li

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CCDC 1958147: Experimental Crystal Structure Determination, Maria I. Swasy, Kristopher G. Gross, Beau R. Brummel, William T. Pennington, Timothy R. Lex, Soham Panda, Lauren N. Giambalvo, Daniel C. Whitehead, Colin D. McMillen, and Khadijatul Kobra

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A case of anti- pityriasis versicolor therapy that preserves healthy mycobiome, Jacek C. Szepietowski, Ewa Leniak, Sebastian Gnat, Lukasz Kozubowski, and Mariusz Dyląg

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Data for the GMG Stokes paper, Clevenger T.C. and Heister Timo

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Additional file 1 of Isolation and characterization of diverse microbial representatives from the human skin microbiome, Collin M. Timm, Thomas Mehoke, William Stone, David K. Karig, Matthew Pellicore, Bryan Brensinger, Seema Nayak, Curtisha Charles, Kristin Loomis, and Phillip P.A. Staniczenko

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The deal.II tutorial step-50: Geometric Multigrid on adaptive meshes distributed in parallel, Heister Timo and C. Clevenger Thomas

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dealii/candi: 9.2.0-r2, Heister Timo, Köcher Uwe, Rudolph Max, fvanmaele, Turcksin Bruno, Gassmoeller Rene, Corum Curt, WEI Xiaoyu, tcclevenger, Arndt Daniel, and Bangerth Wolfgang

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Figure 10 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 15 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 17 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 18 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 19 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 1 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 21 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 25 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 29 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 30 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 32 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 33 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 34 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 37 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 38 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 39 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 3 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 5 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 6 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 7 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Figure 8 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 10 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 11 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 13 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 1 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 3 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 5 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 6 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 7 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 8 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Map 9 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Supplementary material 1 from: Caterino MS, Tishechkin AK (2020) Recognition and revision of the Phelister blairi group (Histeridae, Histerinae, Exosternini). ZooKeys 1001: 1-154. https://doi.org/10.3897/zookeys.1001.58447, Alexey K. Tishechkin and Michael S. Caterino

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Political System Attitudes Study - Pilot Wave, Stephen Utych, Matthew Rhodes-Purdy, Rachel Navarre, and Matthew Rhodes-Purdy

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Identification and characterization of QTLs for fruit quality traits in peach through a multi-family approach, Eric Van De Weg, David H. Byrne, Silvia Carpenedo, Cassia Da Silva Linge, Zena J. Rawandoozi, Ksenija Gasic, Timothy P. Hartmann, and Lichun Cai

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VidyaSamadi/WaccamawData: WaccamawData, Samadi Vidya

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Combined Geotechnical and Geophysical Investigation of Texas Rivers Post Hurricane Harvey., Tech Virginia, Ravi Ravichandran, Nina Stark, University Clemson, Reem Jaber, Navid Jafari, and State University Louisiana

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Disentangling interactions among mercury, immunity, and infection in a Neotropical bat community, Dmitriy Volokhov, Hannah Droke, Alexis Brown, Ticha Padgett-Stewart, Brock Fenton, Matthew Chumchal, Daniel Becker, Hugh Broders, Catherene Baijnauth, Thomas Rainwater, Nancy Simmons, Raina Plowright, Kelly Speer, and Jennifer Korstian

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Data and supplemental tables from Colour dimorphism in labrid fishes as an adaptation to life on coral reefs, P.C. Wainwright, F. Santini, and J.R. Hodge

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Data and supplemental tables from Colour dimorphism in labrid fishes as an adaptation to life on coral reefs, P.C. Wainwright, F. Santini, and J.R. Hodge

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Divergent processes drive parallel evolution in marine and freshwater fishes, Peter Wainwright, Mike Collyer, Samantha Price, and Sarah Friedman

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Additional file 2 of Prediction and prioritization of autism-associated long non-coding RNAs using gene expression and sequence features, Jun Wang and Liangjiang Wang

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Additional file 3 of Prediction and prioritization of autism-associated long non-coding RNAs using gene expression and sequence features, Jun Wang and Liangjiang Wang

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Prediction and prioritization of autism-associated long non-coding RNAs using gene expression and sequence features, Liangjiang Wang and Jun Wang

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Supplemental Material for Brenton et al., 2020, Xiaoyun Wang, Erin L. Connolly, Zachary W. Brenton, Kathleen E. Jordan, Jeffrey C. Glaubitz, Matthew T. Myers, Brendon T. Juengst, Savanah M. Dale, Elizabeth A. Cooper, and Richard E. Boyles

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Additional file 11 of Transcriptomic profiles of non-embryogenic and embryogenic callus cells in a highly regenerative upland cotton line (Gossypium hirsutum L.), Li Wen, John Lawson, Zhigang Li, Christopher A. Saski, Michael Smathers, Wei Li, Shuangxia Jin, Matthew West, Don Jones, and Stephen Parris

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Additional file 5 of Transcriptomic profiles of non-embryogenic and embryogenic callus cells in a highly regenerative upland cotton line (Gossypium hirsutum L.), Li Wen, Michael Smathers, Don Jones, Stephen Parris, John Lawson, Zhigang Li, Shuangxia Jin, Matthew West, Wei Li, and Christopher A. Saski

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CSD 1881440: Experimental Crystal Structure Determination, Yimei Wen, Tiffany M. Smith Pellizzeri, Rachel B. Getman, Steven Pellizzeri, Joseph W. Kolis, Colin D. McMillen, and George Chumanov

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Additional file 9 of Transcriptomic profiles of non-embryogenic and embryogenic callus cells in a highly regenerative upland cotton line (Gossypium hirsutum L.), Matthew West, John Lawson, Michael Smathers, Stephen Parris, Li Wen, Don Jones, Christopher A. Saski, Wei Li, Shuangxia Jin, and Zhigang Li

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Additional file 3 of Transcriptomic profiles of non-embryogenic and embryogenic callus cells in a highly regenerative upland cotton line (Gossypium hirsutum L.), Matthew West, Li Wen, Stephen Parris, Shuangxia Jin, Christopher A. Saski, John Lawson, Wei Li, Don Jones, Michael Smathers, and Zhigang Li

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CCDC 1883834: Experimental Crystal Structure Determination, Modi Wetzler, Megan M. Sibley, Matthew S. Wasilewski, Alexandra M. North, Ian R. Ruohoniemi, and Colin D. Mcmillen

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CCDC 1954260: Experimental Crystal Structure Determination, Daniel C. Whitehead, Joseph W. Kolis, Beau R. Brummel, Kinsey G. Lee, and Colin D. McMillen

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CCDC 1954259: Experimental Crystal Structure Determination, Daniel C. Whitehead, Colin D. McMillen, Beau R. Brummel, Joseph W. Kolis, and Kinsey G. Lee

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CCDC 1954262: Experimental Crystal Structure Determination, Daniel C. Whitehead, Colin D. McMillen, Beau R. Brummel, Kinsey G. Lee, and Joseph W. Kolis

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CSD 1790459: Experimental Crystal Structure Determination, Daniel Willett, Garlea V. Ovidiu, Joseph W. Kolis, Michael A. McGuire, Tiffany M. Smith Pellizzeri, Liurukara D. Sanjeewa, Colin D. McMillen, and George Chumanov

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Importance of Regional-Scale Auroral Precipitation and Electrical Field Variability to the Storm-Time Thermospheric Temperature Enhancement and Inversion Layer (TTEIL) in the Antarctic E Region, Haonan Wu and Xian Lu

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Additional file 1 of The chromosome-level wintersweet (Chimonanthus praecox) genome provides insights into floral scent biosynthesis and flowering in winter, Zhongping Xu, Christopher A. Saski, Huihui Cheng, Lin Xiang, Jingpu Tian, Qiaomu Yan, Junzhong Shang, Kaige Zhao, Abbas Jamal, Longqing Chen, Xiuqun Liu, Shuangxia Jin, and Lai Li

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The chromosome-level wintersweet (Chimonanthus praecox) genome provides insights into floral scent biosynthesis and flowering in winter, Zhongping Xu, Jingpu Tian, Huihui Cheng, Qiaomu Yan, Kaige Zhao, Abbas Jamal, Lai Li, Christopher A. Saski, Xiuqun Liu, Junzhong Shang, Shuangxia Jin, Longqing Chen, and Lin Xiang

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CCDC 1987586: Experimental Crystal Structure Determination, Ashok Yadav, Dillip K. Panda, Sourav Saha, Shiyu Zhang, and Wei Zhou

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Additional file 1 of Autonomous replication sequences from the Amaranthus palmeri eccDNA replicon enable replication in yeast, Allison Yaguchi, William T. Molin, Mark Blenner, and Christopher A. Saski

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Additional file 2 of Autonomous replication sequences from the Amaranthus palmeri eccDNA replicon enable replication in yeast, Allison Yaguchi, William T. Molin, Mark Blenner, and Christopher A. Saski

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Additional file 5 of Autonomous replication sequences from the Amaranthus palmeri eccDNA replicon enable replication in yeast, Allison Yaguchi, William T. Molin, Christopher A. Saski, and Mark Blenner

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Additional file 5 of Autonomous replication sequences from the Amaranthus palmeri eccDNA replicon enable replication in yeast, Allison Yaguchi, Christopher A. Saski, William T. Molin, and Mark Blenner

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Supplemental Material for Yanagawa et al., 2020, Aya Yanagawa, Coby Schal, Wen Huang, Trudy F.C. Mackay, Akihiko Yamamoto, and Ayako Wada-Katsumata

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FIGURE 4. Ceraclea spp. n., female genitalia. 4A–4C in Interesting new Chinese species of Leptoceridae and Odontoceridae (Insecta: Trichoptera) from several recent collecting efforts, Lian-Fang Yang, Ben-Jin Hu, and John C. Morse

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FIGURE 6 in Interesting new Chinese species of Leptoceridae and Odontoceridae (Insecta: Trichoptera) from several recent collecting efforts, Lian-Fang Yang, Ben-Jin Hu, and John C. Morse

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FIGURE 7. Oecetis spp. n., female genitalia. 7A–7C in Interesting new Chinese species of Leptoceridae and Odontoceridae (Insecta: Trichoptera) from several recent collecting efforts, Lian-Fang Yang, Ben-Jin Hu, and John C. Morse

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FIGURE 3 in Interesting new Chinese species of Leptoceridae and Odontoceridae (Insecta: Trichoptera) from several recent collecting efforts, Lian-Fang Yang, John C. Morse, and Ben-Jin Hu

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Data from: Climate and soil nutrients differentially drive multidimensional fine root traits in ectomycorrhizal‐dominated alpine coniferous forests, Huajun Yin, JunXiang Ding, Ziliang Zhang, Qing Liu, Deliang Kong, Qin Cai, and Juan Xiao

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CSD 2006494: Experimental Crystal Structure Determination, Eric Zhang, Shani Egodawatte, Navindra Keerthisinghe, Mark D. Smith, Vladislav V. Klepov, Hans-Conrad zur Loye, and Stephen H. Foulger

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CSD 2006491: Experimental Crystal Structure Determination, Eric Zhang, Mark D. Smith, Navindra Keerthisinghe, Hans-Conrad zur Loye, Vladislav V. Klepov, Stephen H. Foulger, and Shani Egodawatte

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The role of surgery type in postoperative atrial fibrillation and in-hospital mortality in esophageal cancer patients with preserved left ventricular ejection fraction, Lu Zhang, Chenyang Jiang, Laite Chen, Guosheng Fu, and Lu Shi

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Tectono-magmatic events of the Qilian orogenic belt in northern Tibet: new insights from detrital zircon geochronology of river sands, Shuo Zhang, Ling Fu, Alex Pullen, Wei Zhang, Xing Jian, Dongming Hong, and Hanghai Liang

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Effect of soil carbon amendments in reversing the legacy effect of plant invasion, Ziliang Zhang, Prasanta Bhowmik, and Vidya Suseela

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Effect of soil carbon amendments in reversing the legacy effect of plant invasion, Ziliang Zhang, Vidya Suseela, and Prasanta Bhowmik

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CCDC 1987585: Experimental Crystal Structure Determination, Wei Zhou, Ashok Yadav, Shiyu Zhang, Dillip K. Panda, and Sourav Saha

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Additional file 2 of AsHSP26.8a, a creeping bentgrass small heat shock protein integrates different signaling pathways to modulate plant abiotic stress response, Junfei Zhu, Hong Luo, Xin Li, Zhigang Li, Xinbo Sun, and Liebao Han

Submissions from 2019

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The Ambidextrous Sales Force: Aligning Salesperson Polychronicity and Selling Contexts for Sales-Service Behaviors and Customer Value, Raj Agnihotri, Zachary Hall, and Ryan Mullins

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Forecasting the Prevalence of Diabetes Mellitus Using Econometric Models, Zhanay Akanov, Amy Apon, Sanjay Kalra, Nurbek Saparkhojayev, and Assel Mukasheva

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Data from: Genetic analyses in Lake Malawi cichlids identify new roles for Fgf signaling in scale shape variation, R. Craig Albertson, Kenta C. Kawasaki, Kara E. Powder, and Emily R. Tetrault

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Data from: Genetic analyses in Lake Malawi cichlids identify new roles for Fgf signaling in scale shape variation, R. Craig Albertson, Kenta C. Kawasaki, Emily R. Tetrault, and Kara E. Powder

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Data from: White shark genome reveals ancient elasmobranch adaptations associated with wound healing and the maintenance of genome stability, Agostinho Antunes, Nicholas J. Marra, Minghui Wang, Chuck Winkler, Michael J. Stanhope, Salvador Jorgensen, Stephen J. O’Brien, Paulina Pavinski Bitar, Bryce J. Stanhope, Qi Sun, Mike Rayko, Aleksey Komissarov, Sergey Kliver, Mahmood S. Shivji, Vincent P. Richards, and Nathaniel K. Jue

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Perceived supports and evidence-based teaching in college STEM, Oriana R. Aragón, Andrew J. Cavanagh, Jennifer Frederick, Meghan E. Bathgate, Jonathan K. Waterhouse, and Mark J. Graham

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DATASET: De novo assembly and functional annotation of the heart + hemolymph transcriptome in the Caribbean spiny lobster Panulirus argus, J. Antonio Baeza and Matthew D MacManes

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Figure 4 in An integrative taxonomic and phylogenetic approach reveals a complex of cryptic species in the 'peppermint' shrimp Lysmata wurdemanni sensu stricto, J. Antonio Baeza and Sanjeevi Prakash

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The complete mitochondrial genome and description of a new cryptic species of Benedenia Diesing, 1858 (Monogenea: Capsalidae), a major pathogen infecting the yellowtail kingfish Seriola lalandi Valenciennes in the South-East Pacific, J. Antonio Baeza, Fabiola A. Sepúlveda, and M. Teresa González

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Replication Materials for Barkowski/McLaughlin JHR 2020, Scott Barkowski and Joanne Song McLaughlin

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raw data for version 2 of article " Effect of environmental and cultural conditions on medium pH and explant growth performance of Douglas-fir", Rick Bates, Chien-Chih Chen, and John Carlson

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MOESM3 of Alu insertion polymorphisms shared by Papio baboons and Theropithecus gelada reveal an intertwined common ancestry, Mark A. Batzer, Jessica M. Storer, Paulina Gonzalez-Quiroga, Jeffrey Rogers, Lydia C. Rewerts, Corey P. St. Romain, Jerilyn A. Walker, Vallmer E. Jordan, Thomas O. Beckstrom, Catherine E. Rockwell, Miriam K. Konkel, Cody J. Steely, and Clifford J. Jolly

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SystemsGenetics/ACE: Version 3.2.0, Shealy Ben, Smith Melissa, B Josh, Feltus Alex, and Ficklin Stephen