檢索結果 - Quesnel-Vallières, Mathieu

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

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