The genome sequence of the thick-headed fly,  Myopa tessellatipennis (Motschulsky, 1859)

por Ashworth, Michael, Falk, Steven, Clements, David K.
Publicado 2023

Diffuse lung disease of infancy: a pattern-based, algorithmic approach to histological diagnosis

por Armes, Jane E, Mifsud, William, Ashworth, Michael
Publicado 2015

The genome sequence of the Figwort Cheilosia, Cheilosia variabilis (Panzer, 1798)

por Crowley, Liam M., Sivell, Olga, Ashworth, Michael, Poole, Oliver
Publicado 2023

Herbicide Resistance Management: Recent Developments and Trends

por Beckie, Hugh J., Ashworth, Michael B., Flower, Ken C.
Publicado 2019

Farming without Glyphosate?

por Beckie, Hugh J., Flower, Ken C., Ashworth, Michael B.
Publicado 2020

Diagnostic accuracy of post-mortem cardiovascular magnetic resonance imaging in fetuses, newborns, and children

por Thayyil, Sudhin, Sebire, Neil, Ashworth, Michael A, Taylor, Andrew M
Publicado 2012

Micro-CT of tracheal stenosis in trisomy 21

por Shelmerdine, Susan C, Ashworth, Michael T, Calder, Alistair D, Muthialu, Nagarajan, Arthurs, Owen J
Publicado 2019

Reference ranges for organ weights of infants at autopsy: results of >1,000 consecutive cases from a single centre

por Pryce, Jeremy W, Bamber, Andrew R, Ashworth, Michael T, Kiho, Liina, Malone, Marian, Sebire, Neil J
Publicado 2014

Directional selection for flowering time leads to adaptive evolution in Raphanus raphanistrum (Wild radish)

por Ashworth, Michael B., Walsh, Michael J., Flower, Ken C., Vila‐Aiub, Martin M., Powles, Stephen B.
Publicado 2016

Postmortem microfocus computed tomography for noninvasive autopsies: experience in >250 human fetuses

por Shelmerdine, Susan C., Simcock, Ian C., Hutchinson, John Ciaran, Guy, Anna, Ashworth, Michael T., Sebire, Neil J., Arthurs, Owen J.
Publicado 2021

Assessing the Capability and Potential of LiDAR for Weed Detection

por Shahbazi, Nooshin, Ashworth, Michael B., Callow, J. Nikolaus, Mian, Ajmal, Beckie, Hugh J., Speidel, Stuart, Nicholls, Elliot, Flower, Ken C.
Publicado 2021

Micro-CT Imaging of Pediatric Thyroglossal Duct Cysts: A Prospective Case Series

por Frauenfelder, Claire, Shelmerdine, Susan C., Simcock, Ian C., Hall, Andrew, Hutchinson, John Ciaran, Ashworth, Michael T., Arthurs, Owen J., Butler, Colin R.
Publicado 2021

Reappraising myocardial fibrosis in severe aortic stenosis: an invasive and non-invasive study in 133 patients

por Treibel, Thomas A, López, Begoña, González, Arantxa, Menacho, Katia, Schofield, Rebecca S, Ravassa, Susana, Fontana, Marianna, White, Steven K, DiSalvo, Carmelo, Roberts, Neil, Ashworth, Michael T, Díez, Javier, Moon, James C
Publicado 2018

Occult senile cardiac amyloid in severe calcific aortic stenosis is not rare and has a poor prognosis: a 146 patient CMR biopsy study

por Treibel, Thomas A, Fontana, Marianna, Gilbertson, Janet A, Boniface, Karen A, White, Steven K, Abdel-Gadir, Amna, Rosmini, Stefania, Hutt, David F, Whelan, Carol J, Gillmore, Julian D, Wechalekar, Ashutosh, Hayward, Martin P, Ashworth, Michael A, Hawkins, Philip N, Moon, James C
Publicado 2016

Preclinical Optimization and Safety Studies of a New Lentiviral Gene Therapy for p47(phox)-Deficient Chronic Granulomatous Disease

por Schejtman, Andrea, Vetharoy, Winston, Choi, Uimook, Rivat, Christine, Theobald, Narda, Piras, Giuseppa, Leon-Rico, Diego, Buckland, Karen, Armenteros-Monterroso, Elena, Benedetti, Sara, Ashworth, Michael T., Rothe, Michael, Schambach, Axel, Gaspar, Hubert Bobby, Kang, Elizabeth M., Malech, Harry L., Thrasher, Adrian J., Santilli, Giorgia
Publicado 2021

Barth syndrome

por Clarke, Sarah LN, Bowron, Ann, Gonzalez, Iris L, Groves, Sarah J, Newbury-Ecob, Ruth, Clayton, Nicol, Martin, Robin P, Tsai-Goodman, Beverly, Garratt, Vanessa, Ashworth, Michael, Bowen, Valerie M, McCurdy, Katherine R, Damin, Michaela K, Spencer, Carolyn T, Toth, Matthew J, Kelley, Richard I, Steward, Colin G
Publicado 2013

Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11

por Rea, Gillian, Homfray, Tessa, Till, Jan, Roses-Noguer, Ferran, Buchan, Rachel J., Wilkinson, Sam, Wilk, Alicja, Walsh, Roddy, John, Shibu, McKee, Shane, Stewart, Fiona J., Murday, Victoria, Taylor, Robert W., Ashworth, Michael, Baksi, A. John, Daubeney, Piers, Prasad, Sanjay, Barton, Paul J.R., Cook, Stuart A., Ware, James S.
Publicado 2017

LUBAC is essential for embryogenesis by preventing cell death and enabling haematopoiesis

por Peltzer, Nieves, Darding, Maurice, Montinaro, Antonella, Draber, Peter, Draberova, Helena, Kupka, Sebastian, Rieser, Eva, Fisher, Amanda, Hutchinson, Ciaran, Taraborrelli, Lucia, Hartwig, Torsten, Lafont, Elodie, Haas, Tobias L., Shimizu, Yutaka, Böiers, Charlotta, Sarr, Aida, Rickard, James, Alvarez-Diaz, Silvia, Ashworth, Michael T., Beal, Allison, Enver, Tariq, Bertin, John, Kaiser, William, Strasser, Andreas, Silke, John, Bouillet, Philippe, Walczak, Henning
Publicado 2018

Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study

por Balestrini, Simona, Mikati, Mohamad A., Álvarez-García-Rovés, Reyes, Carboni, Michael, Hunanyan, Arsen S., Kherallah, Bassil, McLean, Melissa, Prange, Lyndsey, De Grandis, Elisa, Gagliardi, Alessandra, Pisciotta, Livia, Stagnaro, Michela, Veneselli, Edvige, Campistol, Jaume, Fons, Carmen, Pias-Peleteiro, Leticia, Brashear, Allison, Miller, Charlotte, Samões, Raquel, Brankovic, Vesna, Padiath, Quasar S., Potic, Ana, Pilch, Jacek, Vezyroglou, Aikaterini, Bye, Ann M.E., Davis, Andrew M., Ryan, Monique M., Semsarian, Christopher, Hollingsworth, Georgina, Scheffer, Ingrid E., Granata, Tiziana, Nardocci, Nardo, Ragona, Francesca, Arzimanoglou, Alexis, Panagiotakaki, Eleni, Carrilho, Inês, Zucca, Claudio, Novy, Jan, Dzieżyc, Karolina, Parowicz, Marek, Mazurkiewicz-Bełdzińska, Maria, Weckhuysen, Sarah, Pons, Roser, Groppa, Sergiu, Sinden, Daniel S., Pitt, Geoffrey S., Tinker, Andrew, Ashworth, Michael, Michalak, Zuzanna, Thom, Maria, Cross, J. Helen, Vavassori, Rosaria, Kaski, Juan P., Sisodiya, Sanjay M.
Publicado 2020

Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy

por Lopes, Luis R, Garcia-Hernández, Soledad, Lorenzini, Massimiliano, Futema, Marta, Chumakova, Olga, Zateyshchikov, Dmitry, Isidoro-Garcia, Maria, Villacorta, Eduardo, Escobar-Lopez, Luis, Garcia-Pavia, Pablo, Bilbao, Raquel, Dobarro, David, Sandin-Fuentes, Maria, Catalli, Claudio, Gener Querol, Blanca, Mezcua, Ainhoa, Garcia Pinilla, Jose, Bloch Rasmussen, Torsten, Ferreira-Aguar, Ana, Revilla-Martí, Pablo, Basurte Elorz, Maria Teresa, Bautista Paves, Alicia, Ramon Gimeno, Juan, Figueroa, Ana Virginia, Franco-Gutierrez, Raul, Fuentes-Cañamero, Maria Eugenia, Martinez Moreno, Marina, Ortiz-Genga, Martin, Piqueras-Flores, Jesus, Analia Ramos, Karina, Rudzitis, Ainars, Ruiz-Guerrero, Luis, Stein, Ricardo, Triguero-Bocharán, Mayte, de la Higuera, Luis, Ochoa, Juan Pablo, Abu-Bonsrah, Dad, Kwok, Cecilia Y T, Smith, Jacob B, Porrello, Enzo R, Akhtar, Mohammed M, Jager, Joanna, Ashworth, Michael, Syrris, Petros, Elliott, David A, Monserrat, Lorenzo, Elliott, Perry M
Publicado 2021