Zoekresultaten - Quesnel-Vallières, Mathieu

Essential roles for the splicing regulator nSR100/SRRM4 during nervous system development door Quesnel-Vallières, Mathieu, Irimia, Manuel, Cordes, Sabine P., Blencowe, Benjamin J.

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Rapid and Scalable Profiling of Nascent RNA with fastGRO door Barbieri, Elisa, Hill, Connor, Quesnel-Vallières, Mathieu, Zucco, Avery J., Barash, Yoseph, Gardini, Alessandro

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Identifying common transcriptome signatures of cancer by interpreting deep learning models door Jha, Anupama, Quesnel-Vallières, Mathieu, Wang, David, Thomas-Tikhonenko, Andrei, Lynch, Kristen W, Barash, Yoseph

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Seronegative Hepatitis C Virus Infection in a Child Infected via Mother-to-Child Transmission door Larouche, Ariane, Gaëtan, Geneviève, El-Bilali, Nabil, Quesnel-Vallières, Mathieu, Martin, Steven R., Alvarez, Fernando, Shoukry, Naglaa H., Soudeyns, Hugo

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Alternative splicing redefines landscape of commonly mutated genes in acute myeloid leukemia door Rivera, Osvaldo D., Mallory, Michael J., Quesnel-Vallières, Mathieu, Chatrikhi, Rakesh, Schultz, David C., Carroll, Martin, Barash, Yoseph, Cherry, Sara, Lynch, Kristen W.

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Novel HIV-1 Recombinant Forms in Antenatal Cohort, Montreal, Quebec, Canada door Quesnel-Vallières, Mathieu, Kouzayha, Iman, Tran, Evelyne, Barry, Issatou, Lasgi, Charlène, Merindol, Natacha, Monteil, Vanessa, Ransy, Doris G., Boucher, Marc, Lapointe, Normand, Soudeyns, Hugo

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An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms door Tapial, Javier, Ha, Kevin C.H., Sterne-Weiler, Timothy, Gohr, André, Braunschweig, Ulrich, Hermoso-Pulido, Antonio, Quesnel-Vallières, Mathieu, Permanyer, Jon, Sodaei, Reza, Marquez, Yamile, Cozzuto, Luca, Wang, Xinchen, Gómez-Velázquez, Melisa, Rayon, Teresa, Manzanares, Miguel, Ponomarenko, Julia, Blencowe, Benjamin J., Irimia, Manuel

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A highly conserved program of neuronal microexons is misregulated in autistic brains door Irimia, Manuel, Weatheritt, Robert J., Ellis, Jonathan, Parikshak, Neelroop N., Gonatopoulos-Pournatzis, Thomas, Babor, Mariana, Quesnel-Vallières, Mathieu, Tapial, Javier, Raj, Bushra, O’Hanlon, Dave, Barrios-Rodiles, Miriam, Sternberg, Michael J.E., Cordes, Sabine P., Roth, Frederick P., Wrana, Jeffrey L., Geschwind, Daniel H., Blencowe, Benjamin J.

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Missense Mutations in NKAP Cause a Disorder of Transcriptional Regulation Characterized by Marfanoid Habitus and Cognitive Impairment door Fiordaliso, Sarah K., Iwata-Otsubo, Aiko, Ritter, Alyssa L., Quesnel-Vallières, Mathieu, Fujiki, Katsunori, Nishi, Eriko, Hancarova, Miroslava, Miyake, Noriko, Morton, Jenny E.V., Lee, Sangmoon, Hackmann, Karl, Bando, Masashige, Masuda, Koji, Nakato, Ryuichiro, Arakawa, Michiko, Bhoj, Elizabeth, Li, Dong, Hakonarson, Hakon, Takeda, Ryojun, Harr, Margaret, Keena, Beth, Zackai, Elaine H., Okamoto, Nobuhiko, Mizuno, Seiji, Ko, Jung Min, Valachova, Alica, Prchalova, Darina, Vlckova, Marketa, Pippucci, Tommaso, Seiler, Christoph, Choi, Murim, Matsumoto, Naomichi, Di Donato, Nataliya, Barash, Yoseph, Sedlacek, Zdenek, Shirahige, Katsuhiko, Izumi, Kosuke

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