Fine-Mapping and Phenotypic Analysis of the Ity3 Salmonella Susceptibility Locus Identify a Complex Genetic Structure

por Khan, Rabia T., Yuki, Kyoko E., Malo, Danielle
Publicado 2014

Genetic Dissection of the Ity3 Locus Identifies a Role for Ncf2 Co-Expression Modules and Suggests Selp as a Candidate Gene Underlying the Ity3.2 Locus

por Khan, Rabia Tahir, Chevenon, Marie, Yuki, Kyoko E., Malo, Danielle
Publicado 2014

Characterization of Two ENU-Induced Mutations Affecting Mouse Skeletal Morphology

por Dauphinee, Shauna M., Eva, Megan M., Yuki, Kyoko E., Herman, Melissa, Vidal, Silvia M., Malo, Danielle
Publicado 2013

Identification of TIA1 mRNA targets during human neuronal development

por Byres, Loryn P., Mufteev, Marat, Yuki, Kyoko E., Wei, Wei, Piekna, Alina, Wilson, Michael D., Rodrigues, Deivid C., Ellis, James
Publicado 2021

MON-725 Transcriptome Profiling in Postnatal Pituitary Gland Identifies Cell Type-Driven Sex-Specific Changes

por Hou, Huayun, Chan, Cadia, Uusküla-Reimand, Liis, Yuki, Kyoko E, Sokolowski, Dustin, Roy, Anna R, Zhang, Zhaolei, Wilson, Michael D, Palmert, Mark
Publicado 2020

Suppression of Hepcidin Expression and Iron Overload Mediate Salmonella Susceptibility in Ankyrin 1 ENU-Induced Mutant

por Yuki, Kyoko E., Eva, Megan M., Richer, Etienne, Chung, Dudley, Paquet, Marilène, Cellier, Mathieu, Canonne-Hergaux, François, Vaulont, Sophie, Vidal, Silvia M., Malo, Danielle
Publicado 2013

Transcriptional buffering and 3ʹUTR lengthening are shaped during human neurodevelopment by shifts in mRNA stability and microRNA load

por Mufteev, Marat, Rodrigues, Deivid C., Yuki, Kyoko E., Narula, Ashrut, Wei, Wei, Piekna, Alina, Liu, Jiajie, Pasceri, Peter, Rissland, Olivia S., Wilson, Michael D., Ellis, James
Publicado 2023

Buffering of transcription rate by mRNA half-life is a conserved feature of Rett syndrome models

por Rodrigues, Deivid C., Mufteev, Marat, Yuki, Kyoko E., Narula, Ashrut, Wei, Wei, Piekna, Alina, Liu, Jiajie, Pasceri, Peter, Rissland, Olivia S., Wilson, Michael D., Ellis, James
Publicado 2023

R-Spondin 2 signaling mediates susceptibility to fatal infectious diarrhea

por Papapietro, Olivier, Teatero, Sarah, Thanabalasuriar, Ajitha, Yuki, Kyoko E., Diez, Eduardo, Zhu, Lei, Kang, Eugene, Dhillon, Sandeep, Muise, Aleixo M., Durocher, Yves, Marcinkiewicz, Martin M., Malo, Danielle, Gruenheid, Samantha
Publicado 2013

Alternative polyadenylation is a determinant of oncogenic Ras function

por Subramanian, Aishwarya, Hall, Mathew, Hou, Huayun, Mufteev, Marat, Yu, Bin, Yuki, Kyoko E., Nishimura, Haruka, Sathaseevan, Anson, Lant, Benjamin, Zhai, Beibei, Ellis, James, Wilson, Michael D., Daugaard, Mads, Derry, W. Brent
Publicado 2021

Postnatal developmental trajectory of sex-biased gene expression in the mouse pituitary gland

por Hou, Huayun, Chan, Cadia, Yuki, Kyoko E., Sokolowski, Dustin, Roy, Anna, Qu, Rihao, Uusküla-Reimand, Liis, Faykoo-Martinez, Mariela, Hudson, Matt, Corre, Christina, Goldenberg, Anna, Zhang, Zhaolei, Palmert, Mark R., Wilson, Michael D.
Publicado 2022

Trio RNA sequencing in a cohort of medically complex children

por Deshwar, Ashish R., Yuki, Kyoko E., Hou, Huayun, Liang, Yijing, Khan, Tayyaba, Celik, Alper, Ramani, Arun, Mendoza-Londono, Roberto, Marshall, Christian R., Brudno, Michael, Shlien, Adam, Meyn, M. Stephen, Hayeems, Robin Z., McKinlay, Brandon J., Klentrou, Panagiota, Wilson, Michael D., Kyriakopoulou, Lianna, Costain, Gregory, Dowling, James J.
Publicado 2023

X-linked myotubular myopathy is associated with epigenetic alterations and is ameliorated by HDAC inhibition

por Volpatti, Jonathan R., Ghahramani-Seno, Mehdi M., Mansat, Mélanie, Sabha, Nesrin, Sarikaya, Ege, Goodman, Sarah J., Chater-Diehl, Eric, Celik, Alper, Pannia, Emanuela, Froment, Carine, Combes-Soia, Lucie, Maani, Nika, Yuki, Kyoko E., Chicanne, Gaëtan, Uusküla-Reimand, Liis, Monis, Simon, Alvi, Sana Akhtar, Genetti, Casie A., Payrastre, Bernard, Beggs, Alan H., Bonnemann, Carsten G., Muntoni, Francesco, Wilson, Michael D., Weksberg, Rosanna, Viaud, Julien, Dowling, James J.
Publicado 2022

Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome

por McQuaid, Mary E., Ahmed, Kashif, Tran, Stephanie, Rousseau, Justine, Shaheen, Ranad, Kernohan, Kristin D., Yuki, Kyoko E., Grover, Prerna, Dreseris, Ema S., Ahmed, Sameen, Dupuis, Lucie, Stimec, Jennifer, Shago, Mary, Al-Hassnan, Zuhair N., Tremblay, Roch, Maass, Philipp G., Wilson, Michael D., Grunebaum, Eyal, Boycott, Kym M., Boisvert, François-Michel, Maddirevula, Sateesh, Faqeih, Eissa A., Almanjomi, Fahad, Khan, Zaheer Ullah, Alkuraya, Fowzan S., Campeau, Philippe M., Kannu, Peter, Campos, Eric I., Wurtele, Hugo
Publicado 2022

Lineage-defined leiomyosarcoma subtypes emerge years before diagnosis and determine patient survival

por Anderson, Nathaniel D., Babichev, Yael, Fuligni, Fabio, Comitani, Federico, Layeghifard, Mehdi, Venier, Rosemarie E., Dentro, Stefan C., Maheshwari, Anant, Guram, Sheena, Wunker, Claire, Thompson, J. Drew, Yuki, Kyoko E., Hou, Huayun, Zatzman, Matthew, Light, Nicholas, Bernardini, Marcus Q., Wunder, Jay S., Andrulis, Irene L., Ferguson, Peter, Razak, Albiruni R. Abdul, Swallow, Carol J., Dowling, James J., Al-Awar, Rima S., Marcellus, Richard, Rouzbahman, Marjan, Gerstung, Moritz, Durocher, Daniel, Alexandrov, Ludmil B., Dickson, Brendan C., Gladdy, Rebecca A., Shlien, Adam
Publicado 2021

The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations

por Villani, Anita, Davidson, Scott, Kanwar, Nisha, Lo, Winnie W., Li, Yisu, Cohen-Gogo, Sarah, Fuligni, Fabio, Edward, Lisa-Monique, Light, Nicholas, Layeghifard, Mehdi, Harripaul, Ricardo, Waldman, Larissa, Gallinger, Bailey, Comitani, Federico, Brunga, Ledia, Hayes, Reid, Anderson, Nathaniel D., Ramani, Arun K., Yuki, Kyoko E., Blay, Sasha, Johnstone, Brittney, Inglese, Cara, Hammad, Rawan, Goudie, Catherine, Shuen, Andrew, Wasserman, Jonathan D., Venier, Rosemarie E., Eliou, Marianne, Lorenti, Miranda, Ryan, Carol Ann, Braga, Michael, Gloven-Brown, Meagan, Han, Jianan, Montero, Maria, Spatare, Famida, Whitlock, James A., Scherer, Stephen W., Chun, Kathy, Somerville, Martin J., Hawkins, Cynthia, Abdelhaleem, Mohamed, Ramaswamy, Vijay, Somers, Gino R., Kyriakopoulou, Lianna, Hitzler, Johann, Shago, Mary, Morgenstern, Daniel A., Tabori, Uri, Meyn, Stephen, Irwin, Meredith S., Malkin, David, Shlien, Adam
Publicado 2022