The effects of work division and technology on auditor engagement and performance von Pearson, Christopher A.

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Online Worker Fraud and Evolving Threats to the Integrity of MTurk Data: A Discussion of Virtual Private Servers and the Limitations of IP-Based Screening Procedures von Dennis, Sean A., Goodson, Brian M., Pearson, Christopher A.

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Facioscapulohumeral dystrophy: incomplete suppression of a retrotransposed gene von Snider, Lauren, Geng, Linda N, Lemmers, Richard J L F, Kyba, Michael, Ware, Carol B, Nelson, Angelique M, Tawil, Rabi, Filippova, Galina N, van der Maarel, Silvère M, Tapscott, Stephen J, Miller, Daniel G

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Integrating 5-hydroxymethylcytosine into the epigenomic landscape of human embryonic stem cells von Szulwach, Keith E, Li, Xuekun, Li, Yujing, Song, Chun-Xiao, Han, Ji Woong, Kim, SangSung, Namburi, Sandeep, Hermetz, Karen, Kim, Julie J, Rudd, M Katharine, Yoon, Young-Sup, Ren, Bing, He, Chuan, Jin, Peng

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Genome instability and transcription elongation impairment in human cells depleted of THO/TREX von Domínguez-Sánchez, María S, Barroso, Sonia, Gómez-González, Belén, Luna, Rosa, Aguilera, Andrés

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The role of the mammalian DNA end-processing enzyme polynucleotide kinase 3'-phosphatase in spinocerebellar ataxia type 3 pathogenesis von Chatterjee, Arpita, Saha, Saikat, Chakraborty, Anirban, Silva-Fernandes, Anabela, Mandal, Santi M, Neves-Carvalho, Andreia, Liu, Yongping, Pandita, Raj K, Hegde, Muralidhar L, Hegde, Pavana M, Boldogh, Istvan, Ashizawa, Tetsuo, Koeppen, Arnulf H, Pandita, Tej K, Maciel, Patricia, Sarkar, Partha S, Hazra, Tapas K

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A pathogenic mechanism in Huntington's disease involves small CAG-repeated RNAs with neurotoxic activity von Bañez-Coronel, Mónica, Porta, Silvia, Kagerbauer, Birgit, Mateu-Huertas, Elisabet, Pantano, Lorena, Ferrer, Isidre, Guzmán, Manuel, Estivill, Xavier, Martí, Eulàlia

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RNA gain-of-function in spinocerebellar ataxia type 8 von Daughters, Randy S, Tuttle, Daniel L, Gao, Wangcai, Ikeda, Yoshio, Moseley, Melinda L, Ebner, Timothy J, Swanson, Maurice S, Ranum, Laura P W

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Ku regulates the non-homologous end joining pathway choice of DNA double-strand break repair in human somatic cells von Fattah, Farjana, Lee, Eu Han, Weisensel, Natalie, Wang, Yongbao, Lichter, Natalie, Hendrickson, Eric A

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Inactivation of PNKP by mutant ATXN3 triggers apoptosis by activating the DNA damage-response pathway in SCA3 von Gao, Rui, Liu, Yongping, Silva-Fernandes, Anabela, Fang, Xiang, Paulucci-Holthauzen, Adriana, Chatterjee, Arpita, Zhang, Hang L, Matsuura, Tohru, Choudhary, Sanjeev, Ashizawa, Tetsuo, Koeppen, Arnulf H, Maciel, Patricia, Hazra, Tapas K, Sarkar, Partha S

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Methylation of histone H3 on lysine 79 associates with a group of replication origins and helps limit DNA replication once per cell cycle von Fu, Haiqing, Maunakea, Alika K, Martin, Melvenia M, Huang, Liang, Zhang, Ya, Ryan, Michael, Kim, RyangGuk, Lin, Chii Meil, Zhao, Keji, Aladjem, Mirit I

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Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD von Krom, Yvonne D, Thijssen, Peter E, Young, Janet M, den Hamer, Bianca, Balog, Judit, Yao, Zizhen, Maves, Lisa, Snider, Lauren, Knopp, Paul, Zammit, Peter S, Rijkers, Tonnie, van Engelen, Baziel G M, Padberg, George W, Frants, Rune R, Tawil, Rabi, Tapscott, Stephen J, van der Maarel, Silvère M

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Mismatch repair balances leading and lagging strand DNA replication fidelity von Lujan, Scott A, Williams, Jessica S, Pursell, Zachary F, Abdulovic-Cui, Amy A, Clark, Alan B, Nick McElhinny, Stephanie A, Kunkel, Thomas A

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Restarted replication forks are error-prone and cause CAG repeat expansions and contractions von Gold, Michaela A, Whalen, Jenna M, Freon, Karine, Hong, Zixin, Iraqui, Ismail, Lambert, Sarah A E, Freudenreich, Catherine H

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Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus von Huguet, Aline, Medja, Fadia, Nicole, Annie, Vignaud, Alban, Guiraud-Dogan, Céline, Ferry, Arnaud, Decostre, Valérie, Hogrel, Jean-Yves, Metzger, Friedrich, Hoeflich, Andreas, Baraibar, Martin, Gomes-Pereira, Mário, Puymirat, Jack, Bassez, Guillaume, Furling, Denis, Munnich, Arnold, Gourdon, Geneviève

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Evidence for sequential and increasing activation of replication origins along replication timing gradients in the human genome von Guilbaud, Guillaume, Rappailles, Aurélien, Baker, Antoine, Chen, Chun-Long, Arneodo, Alain, Goldar, Arach, d'Aubenton-Carafa, Yves, Thermes, Claude, Audit, Benjamin, Hyrien, Olivier

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A MutSβ-Dependent Contribution of MutSα to Repeat Expansions in Fragile X Premutation Mice? von Zhao, Xiao-Nan, Lokanga, Rachel, Allette, Kimaada, Gazy, Inbal, Wu, Di, Usdin, Karen

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The role of interruptions in polyQ in the pathology of SCA1 von Menon, Rajesh P, Nethisinghe, Suran, Faggiano, Serena, Vannocci, Tommaso, Rezaei, Human, Pemble, Sally, Sweeney, Mary G, Wood, Nicholas W, Davis, Mary B, Pastore, Annalisa, Giunti, Paola

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Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice von Goula, Agathi-Vassiliki, Berquist, Brian R, Wilson, 3rd, David M, Wheeler, Vanessa C, Trottier, Yvon, Merienne, Karine

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Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome von Todd, Peter K, Oh, Seok Yoon, Krans, Amy, Pandey, Udai B, Di Prospero, Nicholas A, Min, Kyung-Tai, Taylor, J Paul, Paulson, Henry L

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