Challenges to oligonucleotides-based therapeutics for Duchenne muscular dystrophy

por Goyenvalle, Aurélie, Davies, Kay E
Publicado 2011

Regenerative biomarkers for Duchenne muscular dystrophy

por Guiraud, Simon, Davies, Kay E.
Publicado 2019

Evaluating the potential of novel genetic approaches for the treatment of Duchenne muscular dystrophy

por Himič, Vratko, Davies, Kay E.
Publicado 2021

Interaction between environmental and genetic factors modulates schizophrenic endophenotypes in the Snap-25 mouse mutant blind-drunk

por Oliver, Peter L., Davies, Kay E.
Publicado 2009

New insights into behaviour using mouse ENU mutagenesis

por Oliver, Peter L., Davies, Kay E.
Publicado 2012

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

por Perkins, Kelly J., Davies, Kay E.
Publicado 2018

Safety, tolerability, and pharmacokinetics of SMT C1100, a 2‐arylbenzoxazole utrophin modulator, following single‐ and multiple‐dose administration to healthy male adult volunteers...

por Tinsley, Jon, Robinson, Neil, Davies, Kay E.
Publicado 2015

Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease

por Oliver, Peter L., Bitoun, Emmanuelle, Davies, Kay E.
Publicado 2007

The antioxidant protein Oxr1 influences aspects of mitochondrial morphology

por Wu, Yixing, Davies, Kay E., Oliver, Peter L.
Publicado 2016

A Motor Function for the DEAD-Box RNA Helicase, Gemin3, in Drosophila

por Cauchi, Ruben J., Davies, Kay E., Liu, Ji-Long
Publicado 2008

Advances in genetic therapeutic strategies for Duchenne muscular dystrophy

por Guiraud, Simon, Chen, Huijia, Burns, David T., Davies, Kay E.
Publicado 2015

The Cellular Processing Capacity Limits the Amounts of Chimeric U7 snRNA Available for Antisense Delivery

por Eckenfelder, Agathe, Tordo, Julie, Babbs, Arran, Davies, Kay E, Goyenvalle, Aurélie, Danos, Olivier
Publicado 2012

Oxr1 improves pathogenic cellular features of ALS-associated FUS and TDP-43 mutations

por Finelli, Mattéa J., Liu, Kevin X., Wu, Yixing, Oliver, Peter L., Davies, Kay E.
Publicado 2015

Temporal transcriptomics suggest that twin-peaking genes reset the clock

por Pembroke, William G, Babbs, Arran, Davies, Kay E, Ponting, Chris P, Oliver, Peter L
Publicado 2015

Rescue of severely affected dystrophin/utrophin-deficient mice through scAAV-U7snRNA-mediated exon skipping

por Goyenvalle, Aurélie, Babbs, Arran, Wright, Jordan, Wilkins, Vivienne, Powell, Dave, Garcia, Luis, Davies, Kay E.
Publicado 2012

The Evolutionarily Conserved Tre2/Bub2/Cdc16 (TBC), Lysin Motif (LysM), Domain Catalytic (TLDc) Domain Is Neuroprotective against Oxidative Stress

por Finelli, Mattéa J., Sanchez-Pulido, Luis, Liu, Kevin X, Davies, Kay E., Oliver, Peter L.
Publicado 2016

In vivo MRI Characterization of Progressive Cardiac Dysfunction in the mdx Mouse Model of Muscular Dystrophy

por Stuckey, Daniel J., Carr, Carolyn A., Camelliti, Patrizia, Tyler, Damian J., Davies, Kay E., Clarke, Kieran
Publicado 2012

Identification of valid housekeeping genes for quantitative RT-PCR analysis of cardiosphere-derived cells preconditioned under hypoxia or with prolyl-4-hydroxylase inhibitors

por Tan, Suat Cheng, Carr, Carolyn A., Yeoh, Kar Kheng, Schofield, Christopher J., Davies, Kay E., Clarke, Kieran
Publicado 2011

Analysis of skeletal muscle function in the C57BL6/SV129 syncoilin knockout mouse

por McCullagh, Karl J. A., Edwards, Ben, Kemp, Matthew W., Giles, Laura C., Burgess, Matthew, Davies, Kay E.
Publicado 2008

Laf4/Aff3, a Gene Involved in Intellectual Disability, Is Required for Cellular Migration in the Mouse Cerebral Cortex

por Moore, Justin M., Oliver, Peter L., Finelli, Mattéa J., Lee, Sheena, Lickiss, Tom, Molnár, Zoltán, Davies, Kay E.
Publicado 2014