Transcriptome-wide Regulation of Pre-mRNA Splicing and mRNA Localization by Muscleblind Proteins von Wang, Eric T., Cody, Neal A.L., Jog, Sonali, Biancolella, Michela, Wang, Thomas T., Treacy, Daniel J., Luo, Shujun, Schroth, Gary P., Housman, David E., Reddy, Sita, Lécuyer, Eric, Burge, Christopher B.

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A large-scale binding and functional map of human RNA-binding proteins von Van Nostrand, Eric L., Freese, Peter, Pratt, Gabriel A., Wang, Xiaofeng, Wei, Xintao, Xiao, Rui, Blue, Steven M., Chen, Jia-Yu, Cody, Neal A. L., Dominguez, Daniel, Olson, Sara, Sundararaman, Balaji, Zhan, Lijun, Bazile, Cassandra, Bouvrette, Louis Philip Benoit, Bergalet, Julie, Duff, Michael O., Garcia, Keri E., Gelboin-Burkhart, Chelsea, Hochman, Myles, Lambert, Nicole J., Li, Hairi, McGurk, Michael P., Nguyen, Thai B., Palden, Tsultrim, Rabano, Ines, Sathe, Shashank, Stanton, Rebecca, Su, Amanda, Wang, Ruth, Yee, Brian A., Zhou, Bing, Louie, Ashley L., Aigner, Stefan, Fu, Xiang-Dong, Lécuyer, Eric, Burge, Christopher B., Graveley, Brenton R., Yeo, Gene W.

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CeFra-seq reveals broad asymmetric mRNA and noncoding RNA distribution profiles in Drosophila and human cells von Benoit Bouvrette, Louis Philip, Cody, Neal A L, Bergalet, Julie, Lefebvre, Fabio Alexis, Diot, Cédric, Wang, Xiaofeng, Blanchette, Mathieu, Lécuyer, Eric

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CeFra-seq: Systematic mapping of RNA subcellular distribution properties through cell fractionation coupled to deep-sequencing von Lefebvre, Fabio Alexis, Cody, Neal A.L., Bouvrette, Louis Philip Benoit, Bergalet, Julie, Wang, Xiaofeng, Lécuyer, Eric

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DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients von Urreizti, Roser, Mayer, Klaus, Evrony, Gilad D, Said, Edith, Castilla-Vallmanya, Laura, Cody, Neal A L, Plasencia, Guillem, Gelb, Bruce D, Grinberg, Daniel, Brinkmann, Ulrich, Webb, Bryn D, Balcells, Susanna

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Developmentally regulated elimination of damaged nuclei involves a Chk2-dependent mechanism of mRNA nuclear retention von Iampietro, Carole, Bergalet, Julie, Wang, Xiaofeng, Cody, Neal A L, Chin, Ashley, Lefebvre, Fabio Alexis, Douziech, Mélanie, Krause, Henry M, Lécuyer, Eric

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DPH1 syndrome: Two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients von Urreizti, Roser, Mayer, Klaus, Evrony, Gilad D, Said, Edith, Castilla-Vallmanya, Laura, Cody, Neal A.L, Plasencia, Guillem, Gelb, Bruce D, Grinberg Vaisman, Daniel Raúl, Brinkmann, Ulrich, Webb, Bryn D, Balcells Comas, Susana

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Characterization of the 3p12.3-pcen region associated with tumor suppression in a novel ovarian cancer cell line model genetically modified by chromosome 3 fragment transfer von Cody, Neal A.L., Shen, Zhen, Ripeau, Jean-Sebastien, Provencher, Diane M., Mes-Masson, Anne-Marie, Chevrette, Mario, Tonin, Patricia N.

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Characterization of the 3p12.3‐p cen region associated with tumor suppression in a novel ovarian cancer cell line model genetically modified by chromosome 3 fragment transfer von Cody, Neal A.L., Shen, Zhen, Ripeau, Jean‐Sebastien, Provencher, Diane M., Mes‐Masson, Anne‐Marie, Chevrette, Mario, Tonin, Patricia N.

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