DIPG-14. PROTEOGENOMICS PROFILING REVEALS ENRICHED NON-HISTONE PROTEIN METHYLTRANSFERASES AS NEW THERAPEUTIC TARGETS IN DIPG

por Anguraj Vadivel, Arun Kumaran, Pajovic, Sanja, Patel, Palak, Siddaway, Robert, Zhu, Sabrina, Phillips, Lauren, Hawkins, Cynthia
Publicado 2023

Tracking endothelium-dependent NO release in pressurized arteries

por Wallis, Lillian, Donovan, Lucy, Johnston, Aaron, Phillips, Lauren C., Lin, Jinheng, Garland, Christopher J., Dora, Kim A.
Publicado 2023

Methane Emission in a Specific Riparian-Zone Sediment Decreased with Bioelectrochemical Manipulation and Corresponded to the Microbial Community Dynamics

por Friedman, Elliot S., McPhillips, Lauren E., Werner, Jeffrey J., Poole, Angela C., Ley, Ruth E., Walter, M. Todd, Angenent, Largus T.
Publicado 2016

Controlled Dual Growth Factor Delivery From Microparticles Incorporated Within Human Bone Marrow-Derived Mesenchymal Stem Cell Aggregates for Enhanced Bone Tissue Engineering via E...

por Dang, Phuong N., Dwivedi, Neha, Phillips, Lauren M., Yu, Xiaohua, Herberg, Samuel, Bowerman, Caitlin, Solorio, Loran D., Murphy, William L., Alsberg, Eben
Publicado 2016

MRC Centre Neuromuscular Biobank (Newcastle and London): Supporting and facilitating rare and neuromuscular disease research worldwide

por Reza, Mojgan, Cox, Daniel, Phillips, Lauren, Johnson, Diana, Manoharan, Vaishnavi, Grieves, Michael, Davis, Becky, Roos, Andreas, Morgan, Jennifer, Hanna, Michael G., Muntoni, Francesco, Lochmüller, Hanns
Publicado 2017

Disruption of embryonic ROCK signaling reproduces the sarcomeric phenotype of hypertrophic cardiomyopathy

por Bailey, Kate E., MacGowan, Guy A., Tual-Chalot, Simon, Phillips, Lauren, Mohun, Timothy J., Henderson, Deborah J., Arthur, Helen M., Bamforth, Simon D., Phillips, Helen M.
Publicado 2019

Disruption of embryonic ROCK signaling reproduces the sarcomeric phenotype of hypertrophic cardiomyopathy

por Bailey, Kate E., MacGowan, Guy A., Tual-Chalot, Simon, Phillips, Lauren, Mohun, Timothy J., Henderson, Deborah J., Arthur, Helen M., Bamforth, Simon D., Phillips, Helen M.
Publicado 2020

Epigenetic activation of a RAS/MYC axis in H3.3K27M-driven cancer

por Pajovic, Sanja, Siddaway, Robert, Bridge, Taylor, Sheth, Javal, Rakopoulos, Patricia, Kim, Byungjin, Ryall, Scott, Agnihotri, Sameer, Phillips, Lauren, Yu, Man, Li, Christopher, Milos, Scott, Patel, Palak, Srikanthan, Dilakshan, Huang, Annie, Hawkins, Cynthia
Publicado 2020

Endochondral Ossification in Critical‐Sized Bone Defects via Readily Implantable Scaffold‐Free Stem Cell Constructs

por Dang, Phuong N., Herberg, Samuel, Varghai, Davood, Riazi, Hooman, Varghai, Daniel, McMillan, Alexandra, Awadallah, Amad, Phillips, Lauren M., Jeon, Oju, Nguyen, Minh K., Dwivedi, Neha, Yu, Xiaohua, Murphy, William L., Alsberg, Eben
Publicado 2017

Usefulness of Blood Pressure Variability Indices Derived From 24‐Hour Ambulatory Blood Pressure Monitoring in Detecting Autonomic Failure

por Lodhi, Hamza A., Peri‐Okonny, Poghni A., Schesing, Kevin, Phelps, Kamal, Ngo, Christian, Evans, Hillary, Arbique, Debbie, Price, Angela L., Vernino, Steven, Phillips, Lauren, Mitchell, Jere H., Smith, Scott A., Yano, Yuichiro, Das, Sandeep R., Wang, Tao, Vongpatanasin, Wanpen
Publicado 2019

Identification of GAA variants through whole exome sequencing targeted to a cohort of 606 patients with unexplained limb-girdle muscle weakness

por Johnson, Katherine, Töpf, Ana, Bertoli, Marta, Phillips, Lauren, Claeys, Kristl G., Stojanovic, Vidosava Rakocevic, Perić, Stojan, Hahn, Andreas, Maddison, Paul, Akay, Ela, Bastian, Alexandra E., Łusakowska, Anna, Kostera-Pruszczyk, Anna, Lek, Monkol, Xu, Liwen, MacArthur, Daniel G., Straub, Volker
Publicado 2017

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

por Töpf, Ana, Johnson, Katherine, Bates, Adam, Phillips, Lauren, Chao, Katherine R., England, Eleina M., Laricchia, Kristen M., Mullen, Thomas, Valkanas, Elise, Xu, Liwen, Bertoli, Marta, Blain, Alison, Casasús, Ana B., Duff, Jennifer, Mroczek, Magdalena, Specht, Sabine, Lek, Monkol, Ensini, Monica, MacArthur, Daniel G., Straub, Volker
Publicado 2020

Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population

por Johnson, Katherine, De Ridder, Willem, Töpf, Ana, Bertoli, Marta, Phillips, Lauren, De Jonghe, Peter, Baets, Jonathan, Deconinck, Tine, Rakocevic Stojanovic, Vidosava, Perić, Stojan, Durmus, Hacer, Jamal-Omidi, Shirin, Nafissi, Shahriar, Mongini, Tiziana, Łusakowska, Anna, Busby, Mark, Miller, James, Norwood, Fiona, Hudson, Judith, Barresi, Rita, Lek, Monkol, MacArthur, Daniel G, Straub, Volker
Publicado 2019

Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb...

por Johnson, Katherine, Bertoli, Marta, Phillips, Lauren, Töpf, Ana, Van den Bergh, Peter, Vissing, John, Witting, Nanna, Nafissi, Shahriar, Jamal-Omidi, Shirin, Łusakowska, Anna, Kostera-Pruszczyk, Anna, Potulska-Chromik, Anna, Deconinck, Nicolas, Wallgren-Pettersson, Carina, Strang-Karlsson, Sonja, Colomer, Jaume, Claeys, Kristl G., De Ridder, Willem, Baets, Jonathan, von der Hagen, Maja, Fernández-Torrón, Roberto, Zulaica Ijurco, Miren, Espinal Valencia, Juan Bautista, Hahn, Andreas, Durmus, Hacer, Willis, Tracey, Xu, Liwen, Valkanas, Elise, Mullen, Thomas E., Lek, Monkol, MacArthur, Daniel G., Straub, Volker
Publicado 2018