Alternative utrophin mRNAs contribute to phenotypic differences between dystrophin‐deficient mice and Duchenne muscular dystrophy

Por Perkins, Kelly J., Davies, Kay E.
Publicado no FEBS Lett (2018)

Recent advances in Duchenne muscular dystrophy

Por Perkins, Kelly J, Davies, Kay E
Publicado no Degener Neurol Neuromuscul Dis (2012)

The role of basal and myogenic factors in the transcriptional activation of utrophin promoter A: implications for therapeutic up-regulation in Duchenne muscular dystrophy

Por Perkins, Kelly J., Burton, Edward A., Davies, Kay E.
Publicado em 2001

An arylsulphatase A (ARSA) frameshift mutation (289insG) in metachromatic leukodystrophy (MLD)

Por Perkins, Kelly J, Carey, William F, Morris, C Phillip
Publicado em 2005

Transcription-Dependent Gene Looping of the HIV-1 Provirus Is Dictated by Recognition of Pre-mRNA Processing Signals

Por Perkins, Kelly J., Lusic, Marina, Mitar, Ivonne, Giacca, Mauro, Proudfoot, Nick J.
Publicado em 2008

Ets-2 Repressor Factor Silences Extrasynaptic Utrophin by N-Box–mediated Repression in Skeletal Muscle

Por Perkins, Kelly J., Basu, Utpal, Budak, Murat T., Ketterer, Caroline, Baby, Santhosh M., Lozynska, Olga, Lunde, John A., Jasmin, Bernard J., Rubinstein, Neal A., Khurana, Tejvir S.
Publicado em 2007

Emulating Natural Disturbances for Declining Late-Successional Species: A Case Study of the Consequences for Cerulean Warblers (Setophaga cerulea)

Por Boves, Than J., Buehler, David A., Sheehan, James, Wood, Petra Bohall, Rodewald, Amanda D., Larkin, Jeffrey L., Keyser, Patrick D., Newell, Felicity L., George, Gregory A., Bakermans, Marja H., Evans, Andrea, Beachy, Tiffany A., McDermott, Molly E., Perkins, Kelly A., White, Matthew, Wigley, T. Bently
Publicado em 2013

Chemical Proteomics and Phenotypic Profiling Identifies the Aryl Hydrocarbon Receptor as a Molecular Target of the Utrophin Modulator Ezutromid

Por Wilkinson, Isabel V. L., Perkins, Kelly J., Dugdale, Hannah, Moir, Lee, Vuorinen, Aini, Chatzopoulou, Maria, Squire, Sarah E., Monecke, Sebastian, Lomow, Alexander, Geese, Marcus, Charles, Philip D., Burch, Peter, Tinsley, Jonathan M., Wynne, Graham M., Davies, Stephen G., Wilson, Francis X., Rastinejad, Fraydoon, Mohammed, Shabaz, Davies, Kay E., Russell, Angela J.
Publicado no Angew Chem Int Ed Engl (2020)

GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia

Por Roberts, Irene, Alford, Kate, Hall, Georgina, Juban, Gaetan, Richmond, Helen, Norton, Alice, Vallance, Grant, Perkins, Kelly, Marchi, Emanuele, McGowan, Simon, Roy, Anindita, Cowan, Gillian, Anthony, Mark, Gupta, Amit, Ho, John, Uthaya, Sabita, Curley, Anna, Rasiah, Shree Vishna, Watts, Timothy, Nicholl, Richard, Bedford-Russell, Alison, Blumberg, Raoul, Thomas, Angela, Gibson, Brenda, Halsey, Chris, Lee, Pek-Wan, Godambe, Sunit, Sweeney, Connor, Bhatnagar, Neha, Goriely, Anne, Campbell, Peter, Vyas, Paresh
Publicado em 2013

Mechanisms of Progression of Myeloid Preleukemia to Transformed Myeloid Leukemia in Children with Down Syndrome

Por Labuhn, Maurice, Perkins, Kelly, Matzk, Sören, Varghese, Leila, Garnett, Catherine, Papaemmanuil, Elli, Metzner, Marlen, Kennedy, Alison, Amstislavskiy, Vyacheslav, Risch, Thomas, Bhayadia, Raj, Samulowski, David, Hernandez, David Cruz, Stoilova, Bilyana, Iotchkova, Valentina, Oppermann, Udo, Scheer, Carina, Yoshida, Kenichi, Schwarzer, Adrian, Taub, Jeffrey W., Crispino, John D., Weiss, Mitchell J., Hayashi, Yasuhide, Taga, Takashi, Ito, Etsuro, Ogawa, Seishi, Reinhardt, Dirk, Yaspo, Marie-Laure, Campbell, Peter J., Roberts, Irene, Constantinescu, Stefan N., Vyas, Paresh, Heckl, Dirk, Klusmann, Jan-Henning
Publicado no Cancer Cell (2019)