A quantitative study of TWiki at CERN after ten years of use

por Jones, Peter L
Publicado 2016

The application of knowledge-based techniques to the monitoring of computers in a large heterogeneous distributed environment

por Jones, Peter L, Harrison, Alan
Publicado 2006

TWiki a collaboration tool for the LHC

por Jones, Peter L, Høimyr, Nils
Publicado 2011

A cre-inducible DUX4 transgenic mouse model for investigating facioscapulohumeral muscular dystrophy

por Jones, Takako, Jones, Peter L.
Publicado 2018

An analysis of TWiki performance following computer simulation of overuse

por Jones, Peter L, Høimyr, Nils-Joar
Publicado 2008

FSHD Therapeutic Strategies: What Will It Take to Get to Clinic?

por Himeda, Charis L., Jones, Peter L.
Publicado 2022

Association of modified cytosines and the methylated DNA-binding protein MeCP2 with distinctive structural domains of lampbrush chromatin

por Morgan, Garry T, Jones, Peter L, Bellini, Michel
Publicado 2013

Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD)

por Jones, Takako I., Parilla, Megan, Jones, Peter L.
Publicado 2016

Precise Epigenetic Analysis Using Targeted Bisulfite Genomic Sequencing Distinguishes FSHD1, FSHD2, and Healthy Subjects

por Gould, Taylor, Jones, Takako I., Jones, Peter L.
Publicado 2021

Targeted epigenetic repression by CRISPR/dSaCas9 suppresses pathogenic DUX4-fl expression in FSHD

por Himeda, Charis L., Jones, Takako I., Jones, Peter L.
Publicado 2020

Identification of candidate miRNA biomarkers for facioscapulohumeral muscular dystrophy using DUX4-based mouse models

por Nunes, Andreia M., Ramirez, Monique, Jones, Takako I., Jones, Peter L.
Publicado 2021

Identification of Epigenetic Regulators of DUX4-fl for Targeted Therapy of Facioscapulohumeral Muscular Dystrophy

por Himeda, Charis L., Jones, Takako I., Virbasius, Ching-Man, Zhu, Lihua Julie, Green, Michael R., Jones, Peter L.
Publicado 2018

Transient high glucose causes persistent epigenetic changes and altered gene expression during subsequent normoglycemia

por El-Osta, Assam, Brasacchio, Daniella, Yao, Dachun, Pocai, Alessandro, Jones, Peter L., Roeder, Robert G., Cooper, Mark E., Brownlee, Michael
Publicado 2008

Transient high glucose causes persistent epigenetic changes and altered gene expression during subsequent normoglycemia

por El-Osta, Assam, Brasacchio, Daniella, Yao, Dachun, Pocai, Alessandro, Jones, Peter L., Roeder, Robert G., Cooper, Mark E., Brownlee, Michael
Publicado 2008

Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing

por Jones, Takako I, Yan, Chi, Sapp, Peter C, McKenna-Yasek, Diane, Kang, Peter B, Quinn, Colin, Salameh, Johnny S, King, Oliver D, Jones, Peter L
Publicado 2014

Transgenic mice expressing tunable levels of DUX4 develop characteristic facioscapulohumeral muscular dystrophy-like pathophysiology ranging in severity

por Jones, Takako I., Chew, Guo-Liang, Barraza-Flores, Pamela, Schreier, Spencer, Ramirez, Monique, Wuebbles, Ryan D., Burkin, Dean J., Bradley, Robert K., Jones, Peter L.
Publicado 2020

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

por Jones, Takako I, King, Oliver D, Himeda, Charis L, Homma, Sachiko, Chen, Jennifer C J, Beermann, Mary Lou, Yan, Chi, Emerson, Charles P, Miller, Jeffrey B, Wagner, Kathryn R, Jones, Peter L
Publicado 2015

Identification of Serum Interleukin 6 Levels as a Disease Severity Biomarker in Facioscapulohumeral Muscular Dystrophy

por Gros, Marilyn, Nunes, Andreia M., Daoudlarian, Douglas, Pini, Jonathan, Martinuzzi, Emanuela, Barbosa, Susana, Ramirez, Monique, Puma, Angela, Villa, Luisa, Cavalli, Michele, Grecu, Nicolae, Garcia, Jérémy, Siciliano, Gabriele, Solé, Guilhem, Juntas-Morales, Raul, Jones, Peter L., Jones, Takako, Glaichenhaus, Nicolas, Sacconi, Sabrina
Publicado 2022

Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype Studies

por Nikolic, Ana, Jones, Takako I, Govi, Monica, Mele, Fabiano, Maranda, Louise, Sera, Francesco, Ricci, Giulia, Ruggiero, Lucia, Vercelli, Liliana, Portaro, Simona, Villa, Luisa, Fiorillo, Chiara, Maggi, Lorenzo, Santoro, Lucio, Antonini, Giovanni, Filosto, Massimiliano, Moggio, Maurizio, Angelini, Corrado, Pegoraro, Elena, Berardinelli, Angela, Maioli, Maria Antonetta, D’Angelo, Grazia, Di Muzio, Antonino, Siciliano, Gabriele, Tomelleri, Giuliano, D’Esposito, Maurizio, Della Ragione, Floriana, Brancaccio, Arianna, Piras, Rachele, Rodolico, Carmelo, Mongini, Tiziana, Magdinier, Frederique, Salsi, Valentina, Jones, Peter L., Tupler, Rossella
Publicado 2020