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Catherine Moorwood
Observed name:
C. Moorwood
Institutions:
Royal Devon & Exeter NHS Foundation Trust,
Royal Devon University Healthcare NHS Foundation Trust
Observed institutions:
Royal Devon & Exeter NHS Foundation Trust,
University of Oxford,
Royal Devon University Healthcare NHS Foundation Trust,
University of Pennsylvania
ORCID:
0000-0002-0589-861X
Observed ORCID:
0000-0002-0589-861X
OpenAlex ID:
A5012373185
Isometric and Eccentric Force Generation Assessment of Skeletal Muscles Isolated from Murine Models of Muscular Dystrophies
2013
·
Catherine Moorwood
, Min Liu
, et al.
·
Journal of Visualized Experiments
·
89
Drug Discovery for Duchenne Muscular Dystrophy via Utrophin Promoter Activation Screening
2011
·
Catherine Moorwood
, Olga Lozynska
, et al.
·
PLoS ONE
·
71
PDF
Translational Regulation of Utrophin by miRNAs
2011
·
Utpal Basu
, Olga Lozynska
, et al.
·
PLoS ONE
·
56
PDF
Caspase-12 ablation preserves muscle function in the mdx mouse
2014
·
Catherine Moorwood
, Elisabeth R. Barton
·
Human Molecular Genetics
·
46
A Cell-Based High-Throughput Screening Assay for Posttranscriptional Utrophin Upregulation
2012
·
Catherine Moorwood
, Neha Soni
, et al.
·
SLAS DISCOVERY
·
32
PDF
Syncoilin modulates peripherin filament networks and is necessary for large-calibre motor neurons
2010
·
W. Thomas Clarke
, Ben Edwards
, et al.
·
Journal of Cell Science
·
27
ATP2B2 de novo variants as a cause of variable neurodevelopmental disorders that feature dystonia, ataxia, intellectual disability, behavioral symptoms, and seizures
2023
·
Elena Poggio
, Lucia Barazzuol
, et al.
·
Genetics in Medicine
·
25
PDF
Isometric and Eccentric Force Generation Assessment of Skeletal Muscles Isolated from Murine Models of Muscular Dystrophies
2013
·
Catherine Moorwood
, Min Liu
, et al.
·
Journal of Visualized Experiments
·
24
PDF
Absence of γ-sarcoglycan alters the response of p70S6 kinase to mechanical perturbation in murine skeletal muscle
2014
·
Catherine Moorwood
, Anastassios Philippou
, et al.
·
Skeletal Muscle
·
21
PDF
Syncoilin, an intermediate filament-like protein linked to the dystrophin associated protein complex in skeletal muscle
2008
·
C. Moorwood
·
Cellular and Molecular Life Sciences
·
20
Duchenne muscular dystrophy drug discovery – the application of utrophin promoter activation screening
2013
·
Catherine Moorwood
, Tejvir S Khurana
·
Expert Opinion on Drug Discovery
·
17
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations
2022
·
Kerith-Rae Dias
, Colleen M. Carlston
, et al.
·
Genetics in Medicine
·
13
Congenital Central Hypothyroidism Caused by Novel Variants in IGSF1 Gene: Case Series of 3 Patients
2024
·
Helen MacGloin
, Nadia Schoenmakers
, et al.
·
Hormone Research in Paediatrics
·
2
A large in-frame deletion of the calcium-sensing receptor extracellular domain causes familial hypocalciuric hypercalcaemia type 1 (FHH1) and is partially responsive to cinacalcet
2023
·
Kreepa Kooblall
, Fadil Hannan
, et al.
·
Endocrine Abstracts
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Works count:
15
Citation count:
443
H-index:
12
I10-index:
12
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