Familial Creutzfeldt-Jakob Disease in an Indian Kindred

por Katrak, Sarosh M., Pauranik, Apoorva, Desai, Shrinivas B., Mead, Simon, Beck, Jon, Brandner, Sebastian, Collinge, John
Publicado 2019

A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia

por Lashley, Tammaryn, Rohrer, Jonathan D, Mahoney, Colin, Gordon, Elizabeth, Beck, Jon, Mead, Simon, Warren, Jason, Rossor, Martin, Revesz, Tamas
Publicado 2014

Laser Microdissection of Narrow Sheath Mutant Maize Uncovers Novel Gene Expression in the Shoot Apical Meristem

por Zhang, Xiaolan, Madi, Shahinez, Borsuk, Lisa, Nettleton, Dan, Elshire, Robert J, Buckner, Brent, Janick-Buckner, Diane, Beck, Jon, Timmermans, Marja, Schnable, Patrick S, Scanlon, Michael J
Publicado 2007

Global gene expression analysis of the shoot apical meristem of maize (Zea mays L.)

por Ohtsu, Kazuhiro, Smith, Marianne B, Emrich, Scott J, Borsuk, Lisa A, Zhou, Ruilian, Chen, Tianle, Zhang, Xiaolan, Timmermans, Marja C P, Beck, Jon, Buckner, Brent, Janick-Buckner, Diane, Nettleton, Dan, Scanlon, Michael J, Schnable, Patrick S
Publicado 2007

Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions

por Mahoney, Colin J, Downey, Laura E, Ridgway, Gerard R, Beck, Jon, Clegg, Shona, Blair, Melanie, Finnegan, Sarah, Leung, Kelvin K, Yeatman, Tom, Golden, Hannah, Mead, Simon, Rohrer, Jonathan D, Fox, Nick C, Warren, Jason D
Publicado 2012

Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey

por Gill, O Noel, Spencer, Yvonne, Richard-Loendt, Angela, Kelly, Carole, Dabaghian, Reza, Boyes, Lynnette, Linehan, Jacqueline, Simmons, Marion, Webb, Paul, Bellerby, Peter, Andrews, Nick, Hilton, David A, Ironside, James W, Beck, Jon, Poulter, Mark, Mead, Simon, Brandner, Sebastian
Publicado 2013

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

por Mahoney, Colin J., Beck, Jon, Rohrer, Jonathan D., Lashley, Tammaryn, Mok, Kin, Shakespeare, Tim, Yeatman, Tom, Warrington, Elizabeth K., Schott, Jonathan M., Fox, Nick C., Rossor, Martin N., Hardy, John, Collinge, John, Revesz, Tamas, Mead, Simon, Warren, Jason D.
Publicado 2012

High prevalence of focal and multi-focal somatic genetic variants in the human brain

por Keogh, Michael J., Wei, Wei, Aryaman, Juvid, Walker, Lauren, van den Ameele, Jelle, Coxhead, Jon, Wilson, Ian, Bashton, Matthew, Beck, Jon, West, John, Chen, Richard, Haudenschild, Christian, Bartha, Gabor, Luo, Shujun, Morris, Chris M., Jones, Nick S., Attems, Johannes, Chinnery, Patrick F.
Publicado 2018

Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia

por Fratta, Pietro, Poulter, Mark, Lashley, Tammaryn, Rohrer, Jonathan D., Polke, James M., Beck, Jon, Ryan, Natalie, Hensman, Davina, Mizielinska, Sarah, Waite, Adrian J., Lai, Mang-Ching, Gendron, Tania F., Petrucelli, Leonard, Fisher, Elizabeth M. C., Revesz, Tamas, Warren, Jason D., Collinge, John, Isaacs, Adrian M., Mead, Simon
Publicado 2013

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion()

por Fratta, Pietro, Polke, James M., Newcombe, Jia, Mizielinska, Sarah, Lashley, Tammaryn, Poulter, Mark, Beck, Jon, Preza, Elisavet, Devoy, Anny, Sidle, Katie, Howard, Robin, Malaspina, Andrea, Orrell, Richard W., Clarke, Jan, Lu, Ching-Hua, Mok, Kin, Collins, Toby, Shoaii, Maryam, Nanji, Tina, Wray, Selina, Adamson, Gary, Pittman, Alan, Renton, Alan E., Traynor, Bryan J., Sweeney, Mary G., Revesz, Tamas, Houlden, Henry, Mead, Simon, Isaacs, Adrian M., Fisher, Elizabeth M.C.
Publicado 2015