Sökresultat - Quesnel-Vallières, Mathieu

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

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Rapid and Scalable Profiling of Nascent RNA with fastGRO av 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 av 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 av 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 av 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 av 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 av 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 av 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 av 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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