Arama Sonuçları - Quesnel-Vallières, Mathieu

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

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Rapid and Scalable Profiling of Nascent RNA with fastGRO Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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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