Atoh1 drives the heterogeneity of the pontine nuclei neurons and promotes their differentiation

por Wu, Sih-Rong, Butts, Jessica C., Caudill, Matthew S., Revelli, Jean-Pierre, Dhindsa, Ryan S., Durham, Mark A., Zoghbi, Huda Y.
Publicado 2023

Presence of a pre-hospital enhanced care team reduces on scene time and improves triage compliance for stab trauma

por Cowley, Alan, Durham, Mark, Aldred, Duncan, Crabb, Richard, Crouch, Paul, Heywood, Adam, McBride, Andy, Williams, Julia, Lyon, Richard
Publicado 2019

MeCP2 regulates Gdf11, a dosage-sensitive gene critical for neurological function

por Bajikar, Sameer S, Anderson, Ashley G, Zhou, Jian, Durham, Mark A, Trostle, Alexander J, Wan, Ying-Wooi, Liu, Zhandong, Zoghbi, Huda Y
Publicado 2023

Critical care paramedics’ experiences of performing an emergency scalpel cricothyroidotomy: a qualitative study

por Aldred, Duncan, Durham, Mark, Prokop, Nora, Balderston, Gary, Crabb, Richard, Crouch, Paul, Pike, Lewis, Children, John, McBride, Andy, Heywood, Adam, Williams, Julia, Cowley, Alan
Publicado 2022

Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1

por Coffin, Stephanie L., Durham, Mark A., Nitschke, Larissa, Xhako, Eder, Brown, Amanda M., Revelli, Jean-Pierre, Gonzalez, Esmeralda Villavicencio, Lin, Tao, Handler, Hillary P., Dai, Yanwan, Trostle, Alexander J., Wan, Ying-Wooi, Liu, Zhandong, Sillitoe, Roy V., Orr, Harry T., Zoghbi, Huda Y.
Publicado 2023

Losing Dnmt3a dependent methylation in inhibitory neurons impairs neural function by a mechanism impacting Rett syndrome

por Lavery, Laura A, Ure, Kerstin, Wan, Ying-Wooi, Luo, Chongyuan, Trostle, Alexander J, Wang, Wei, Jin, Haijing, Lopez, Joanna, Lucero, Jacinta, Durham, Mark A, Castanon, Rosa, Nery, Joseph R, Liu, Zhandong, Goodell, Margaret, Ecker, Joseph R, Behrens, M Margarita, Zoghbi, Huda Y
Publicado 2020

Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1

por Coffin, Stephanie L., Durham, Mark A., Nitschke, Larissa, Xhako, Eder, Brown, Amanda M., Revelli, Jean-Pierre, Gonzalez, Esmeralda Villavicencio, Lin, Tao, Handler, Hillary P., Dai, Yanwan, Trostle, Alexander J., Wan, Ying-Wooi, Liu, Zhandong, Sillitoe, Roy V., Orr, Harry T., Zoghbi, Huda Y.
Publicado 2023

Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder

por Bedoyan, Jirair Krikor, Schaibley, Valerie M, Peng, Weiping, Bai, Yongsheng, Mondal, Kajari, Shetty, Amol C, Durham, Mark, Micucci, Joseph A, Dhiraaj, Arti, Skidmore, Jennifer M, Kaplan, Julie B, Skinner, Cindy, Schwartz, Charles E, Antonellis, Anthony, Zwick, Michael E, Cavalcoli, James D, Li, Jun Z, Martin, Donna M
Publicado 2012

Disruption of MeCP2–TCF20 complex underlies distinct neurodevelopmental disorders

por Zhou, Jian, Hamdan, Hamdan, Yalamanchili, Hari Krishna, Pang, Kaifang, Pohodich, Amy E., Lopez, Joanna, Shao, Yingyao, Oses-Prieto, Juan A., Li, Lifang, Kim, Wonho, Durham, Mark A., Bajikar, Sameer S., Palmer, Donna J., Ng, Philip, Thompson, Michelle L., Bebin, E. Martina, Müller, Amelie J., Kuechler, Alma, Kampmeier, Antje, Haack, Tobias B., Burlingame, Alma L., Liu, Zhandong, Rasband, Matthew N., Zoghbi, Huda Y.
Publicado 2022