2023 - Research.com Genetics in United Kingdom Leader Award
2022 - Research.com Best Female Scientist Award
2015 - William Allan Award, the American Society of Human Genetics
2003 - Fellow of the Royal Society, United Kingdom
Her main research concerns Genetics, Duchenne muscular dystrophy, Dystrophin, Utrophin and Muscular dystrophy. Her study in Gene, X chromosome, Locus, Mutation and Genetic linkage is done as part of Genetics. Her research investigates the link between Duchenne muscular dystrophy and topics such as Transgene that cross with problems in Downregulation and upregulation.
Her Dystrophin research incorporates elements of Sarcolemma, Molecular biology, ITGA7 and Cell biology. As a part of the same scientific family, she mostly works in the field of Utrophin, focusing on Gene expression and, on occasion, Regulation of gene expression. Her work deals with themes such as Exon skipping, Genetic enhancement, Bioinformatics and Myopathy, which intersect with Muscular dystrophy.
Kay E. Davies focuses on Genetics, Duchenne muscular dystrophy, Utrophin, Dystrophin and Molecular biology. Her research related to X chromosome, Gene, Locus, Genetic linkage and Gene mapping might be considered part of Genetics. Her X chromosome study integrates concerns from other disciplines, such as Chromosomal fragile site and Restriction fragment length polymorphism.
Her work focuses on many connections between Duchenne muscular dystrophy and other disciplines, such as Muscular dystrophy, that overlap with her field of interest in Pathology. Her study in Utrophin is interdisciplinary in nature, drawing from both mdx mouse, ITGA7 and Cell biology. Kay E. Davies interconnects Sarcolemma, Exon skipping, Neuromuscular junction and Transgene in the investigation of issues within Dystrophin.
Kay E. Davies mainly focuses on Duchenne muscular dystrophy, Utrophin, Dystrophin, Muscular dystrophy and Bioinformatics. Her Duchenne muscular dystrophy study combines topics in areas such as Exon skipping, Cancer research, Clinical trial and Disease. The study incorporates disciplines such as mdx mouse, Downregulation and upregulation, Molecular biology, Pharmacology and In vivo in addition to Utrophin.
Kay E. Davies has included themes like Context, Proteomics and Cell biology, Myosin in her Dystrophin study. Her Muscular dystrophy research is under the purview of Genetics. Her study looks at the intersection of Bioinformatics and topics like Wasting with Muscle weakness.
Her primary areas of study are Muscular dystrophy, Duchenne muscular dystrophy, Dystrophin, Utrophin and Genetics. The Muscular dystrophy study combines topics in areas such as Exon skipping, Cardiomyopathy, Gene and Pathology. She combines subjects such as Endocrinology, Clinical trial, Bioinformatics and Transgene with her study of Duchenne muscular dystrophy.
Her research in Dystrophin intersects with topics in Muscle weakness, Disease, ITGA7 and Pathogenesis. Her Utrophin study incorporates themes from Cancer research, Downregulation and upregulation, Molecular biology and Pharmacology, Dosing. Her Genetics study combines topics from a wide range of disciplines, such as Oxidative stress and Cell biology.
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Function and genetics of dystrophin and dystrophin-related proteins in muscle
Derek J. Blake;Andrew Weir;Sarah E. Newey;Kay E. Davies.
Physiological Reviews (2002)
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16
S. T. Reeders;M. H. Breuning;K. E. Davies;R. D. Nicholls.
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets
F. Francis;S. Hennig;B. Korn;R. Reinhardt.
Nature Genetics (1995)
Utrophin-Dystrophin-Deficient Mice as a Model for Duchenne Muscular Dystrophy
Anne E Deconinck;Jill A Rafael;Judith A Skinner;Susan C Brown.
Report of the committee on the genetic constitution of the X chromosome
K E Davies;J L Mandel;A P Monaco;R L Nussbaum.
Cytogenetic and Genome Research (1988)
A functional genetic link between distinct developmental language disorders.
Sonja C. Vernes;Dianne F. Newbury;Brett S. Abrahams;Laura Winchester.
The New England Journal of Medicine (2008)
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.
P M Nolan;J Peters;M Strivens;D Rogers.
Nature Genetics (2000)
International SMA consortium meeting. (26-28 June 1992, Bonn, Germany).
Theodore L. Munsat;Kay E. Davies.
Neuromuscular Disorders (1992)
Human dystrophin expression in mdx mice after intramuscular injection of dna constructs
Gyula Acsadi;George Dickson;Donald R. Love;Agnes Jani.
Expression of full-length utrophin prevents muscular dystrophy in mdx mice
Jonathon Tinsley;Nicolas Deconinck;Rosie Fisher;David Kahn.
Nature Medicine (1998)
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