Gene expression and epigenetic markers of prion diseases

por Viré, Emmanuelle A., Mead, Simon
Publicado 2022

Prion protein gene mutation detection using long-read Nanopore sequencing

por Kroll, François, Dimitriadis, Athanasios, Campbell, Tracy, Darwent, Lee, Collinge, John, Mead, Simon, Vire, Emmanuelle
Publicado 2022

Epigenetic age acceleration is associated with oligodendrocyte proportions in MSA and control brain tissue

por Murthy, Megha, Shireby, Gemma, Miki, Yasuo, Viré, Emmanuelle, Lashley, Tammaryn, Warner, Thomas T., Mill, Jonathan, Bettencourt, Conceição
Publicado 2023

DNA methylation analysis of archival lymphoreticular tissues in Creutzfeldt–Jakob disease

por Guntoro, Fernando, Viré, Emmanuelle, Giordani, Chiara, Darwent, Lee, Hummerich, Holger, Linehan, Jacqueline, Sinka, Katy, Jaunmuktane, Zane, Brandner, Sebastian, Collinge, John, Mead, Simon
Publicado 2022

The Breast Cancer Oncogene EMSY Represses Transcription of Antimetastatic microRNA miR-31

por Viré, Emmanuelle, Curtis, Christina, Davalos, Veronica, Git, Anna, Robson, Samuel, Villanueva, Alberto, Vidal, August, Barbieri, Isaia, Aparicio, Samuel, Esteller, Manel, Caldas, Carlos, Kouzarides, Tony
Publicado 2014

The Breast Cancer Oncogene EMSY Represses Transcription of Antimetastatic microRNA miR-31

por Viré, Emmanuelle, Curtis, Christina, Davalos, Veronica, Git, Anna, Robson, Samuel, Villanueva, Alberto, Vidal, August, Barbieri, Isaia, Aparicio, Samuel, Esteller, Manel, Caldas, Carlos, Kouzarides, Tony
Publicado 2014

White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy

por Bettencourt, Conceição, Foti, Sandrine C., Miki, Yasuo, Botia, Juan, Chatterjee, Aparajita, Warner, Thomas T., Revesz, Tamas, Lashley, Tammaryn, Balazs, Robert, Viré, Emmanuelle, Holton, Janice L.
Publicado 2019

Epigenomics and transcriptomics analyses of multiple system atrophy brain tissue supports a role for inflammatory processes in disease pathogenesis

por Bettencourt, Conceição, Piras, Ignazio S., Foti, Sandrine C., Talboom, Joshua, Miki, Yasuo, Lashley, Tammaryn, Balazs, Robert, Viré, Emmanuelle, Warner, Thomas T., Huentelman, Matt J., Holton, Janice L.
Publicado 2020

A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis

por Norsworthy, Penny J., Thompson, Andrew G. B., Mok, Tze H., Guntoro, Fernando, Dabin, Luke C., Nihat, Akin, Paterson, Ross W., Schott, Jonathan M., Collinge, John, Mead, Simon, Viré, Emmanuelle A.
Publicado 2020

Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt–Jakob disease

por Dabin, Luke C., Guntoro, Fernando, Campbell, Tracy, Bélicard, Tony, Smith, Adam R., Smith, Rebecca G., Raybould, Rachel, Schott, Jonathan M., Lunnon, Katie, Sarkies, Peter, Collinge, John, Mead, Simon, Viré, Emmanuelle
Publicado 2020

MOBP and HIP1 in multiple system atrophy: New α‐synuclein partners in glial cytoplasmic inclusions implicated in the disease pathogenesis

por Bettencourt, Conceição, Miki, Yasuo, Piras, Ignazio S., de Silva, Rohan, Foti, Sandrine C., Talboom, Joshua S., Revesz, Tamas, Lashley, Tammaryn, Balazs, Robert, Viré, Emmanuelle, Warner, Thomas T., Huentelman, Matt J., Holton, Janice L.
Publicado 2021

Synthetic viability genomic screening defines Sae2 function in DNA repair

por Puddu, Fabio, Oelschlaegel, Tobias, Guerini, Ilaria, Geisler, Nicola J, Niu, Hengyao, Herzog, Mareike, Salguero, Israel, Ochoa-Montaño, Bernardo, Viré, Emmanuelle, Sung, Patrick, Adams, David J, Keane, Thomas M, Jackson, Stephen P
Publicado 2015

Genomic positional conservation identifies topological anchor point RNAs linked to developmental loci

por Amaral, Paulo P., Leonardi, Tommaso, Han, Namshik, Viré, Emmanuelle, Gascoigne, Dennis K., Arias-Carrasco, Raúl, Büscher, Magdalena, Pandolfini, Luca, Zhang, Anda, Pluchino, Stefano, Maracaja-Coutinho, Vinicius, Nakaya, Helder I., Hemberg, Martin, Shiekhattar, Ramin, Enright, Anton J., Kouzarides, Tony
Publicado 2018