The Molecular Functions of MeCP2 in Rett Syndrome Pathology

por Sharifi, Osman, Yasui, Dag H.
Publicado 2021

Editorial: Epigenetic Mechanisms and Their Involvement in Rare Diseases

por Rastegar, Mojgan, Yasui, Dag H.
Publicado 2021

Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism

por Swanberg, Susan E., Nagarajan, Raman P., Peddada, Sailaja, Yasui, Dag H., LaSalle, Janine M.
Publicado 2009

MeCP2 modulates gene expression pathways in astrocytes

por Yasui, Dag H, Xu, Huichun, Dunaway, Keith W, LaSalle, Janine M, Jin, Lee-Way, Maezawa, Izumi
Publicado 2013

Placenta and fetal brain share a neurodevelopmental disorder DNA methylation profile in a mouse model of prenatal PCB exposure

por Laufer, Benjamin I., Neier, Kari, Valenzuela, Anthony E., Yasui, Dag H., Schmidt, Rebecca J., Lein, Pamela J., LaSalle, Janine M.
Publicado 2022

Sequence features accurately predict genome-wide MeCP2 binding in vivo

por Rube, H. Tomas, Lee, Wooje, Hejna, Miroslav, Chen, Huaiyang, Yasui, Dag H., Hess, John F., LaSalle, Janine M., Song, Jun S., Gong, Qizhi
Publicado 2016

A Prader–Willi locus lncRNA cloud modulates diurnal genes and energy expenditure

por Powell, Weston T., Coulson, Rochelle L., Crary, Florence K., Wong, Spencer S., Ach, Robert A., Tsang, Peter, Alice Yamada, N., Yasui, Dag H., LaSalle, Janine M.
Publicado 2013

Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex

por Coulson, Rochelle L., Yasui, Dag H., Dunaway, Keith W., Laufer, Benjamin I., Vogel Ciernia, Annie, Zhu, Yihui, Mordaunt, Charles E., Totah, Theresa S., LaSalle, Janine M.
Publicado 2018

Investigation of modifier genes within copy number variations in Rett syndrome

por Artuso, Rosangela, Papa, Filomena Tiziana, Grillo, Elisa, Mucciolo, Mafalda, Yasui, Dag H., Dunaway, Keith W., Disciglio, Vittoria, Mencarelli, Maria Antonietta, Pollazzon, Marzia, Zappella, Michele, Hayek, Giuseppe, Mari, Francesca, Renieri, Alessandra, LaSalle, Janine M., Ariani, Francesca
Publicado 2011

Sex disparate gut microbiome and metabolome perturbations precede disease progression in a mouse model of Rett syndrome

por Neier, Kari, Grant, Tianna E., Palmer, Rebecca L., Chappell, Demario, Hakam, Sophia M., Yasui, Kendra M., Rolston, Matt, Settles, Matthew L., Hunter, Samuel S., Madany, Abdullah, Ashwood, Paul, Durbin-Johnson, Blythe, LaSalle, Janine M., Yasui, Dag H.
Publicado 2021

Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome

por Veeraragavan, Surabi, Wan, Ying-Wooi, Connolly, Daniel R., Hamilton, Shannon M., Ward, Christopher S., Soriano, Sirena, Pitcher, Meagan R., McGraw, Christopher M., Huang, Sharon G., Green, Jennie R., Yuva, Lisa A., Liang, Agnes J., Neul, Jeffrey L., Yasui, Dag H., LaSalle, Janine M., Liu, Zhandong, Paylor, Richard, Samaco, Rodney C.
Publicado 2016

Placental methylome reveals a 22q13.33 brain regulatory gene locus associated with autism

por Zhu, Yihui, Gomez, J. Antonio, Laufer, Benjamin I., Mordaunt, Charles E., Mouat, Julia S., Soto, Daniela C., Dennis, Megan Y., Benke, Kelly S., Bakulski, Kelly M., Dou, John, Marathe, Ria, Jianu, Julia M., Williams, Logan A., Gutierrez Fugón, Orangel J., Walker, Cheryl K., Ozonoff, Sally, Daniels, Jason, Grosvenor, Luke P., Volk, Heather E., Feinberg, Jason I., Fallin, M. Daniele, Hertz-Picciotto, Irva, Schmidt, Rebecca J., Yasui, Dag H., LaSalle, Janine M.
Publicado 2022