Kay Davies
Kay Davies
Professor of Genetics University of Oxford
Verified email at
Cited by
Cited by
Function and genetics of dystrophin and dystrophin-related proteins in muscle
DJ Blake, A Weir, SE Newey, KE Davies
Physiological reviews 82 (2), 291-329, 2002
Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy
AE Deconinck, JA Rafael, JA Skinner, SC Brown, AC Potter, L Metzinger, ...
Cell 90 (4), 717-727, 1997
A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16
ST Reeders, MH Breuning, KE Davies, RD Nicholls, AP Jarman, ...
Nature 317 (6037), 542-544, 1985
A functional genetic link between distinct developmental language disorders
SC Vernes, DF Newbury, BS Abrahams, L Winchester, J Nicod, M Groszer, ...
New England Journal of Medicine 359 (22), 2337-2345, 2008
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets
F Francis, S Hennig, B Korn, R Reinhardt, P De Jong, A Poustka, ...
Nature genetics 11 (2), 130-136, 1995
Expression of full-length utrophin prevents muscular dystrophy in mdx mice
J Tinsley, N Deconinck, R Fisher, D Kahn, S Phelps, JM Gillis, K Davies
Nature medicine 4 (12), 1441-1444, 1998
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse
PM Nolan, J Peters, M Strivens, D Rogers, J Hagan, N Spurr, IC Gray, ...
Nature genetics 25 (4), 440-443, 2000
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3
LM Brzustowicz, T Lehner, LH Castilla, GK Penchaszadeh, ...
Nature 344 (6266), 540-541, 1990
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin
SB England, LVB Nicholson, MA Johnson, SM Forrest, DR Love, ...
Nature 343 (6254), 180-182, 1990
Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs
G Acsadi, G Dickson, DR Love, A Jani, FS Walsh, A Gurusinghe, JA Wolff, ...
Nature 352 (6338), 815-818, 1991
Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
SJL Knight, AV Flannery, MC Hirst, L Campbell, Z Christodoulou, ...
Cell 74 (1), 127-134, 1993
An autosomal transcript in skeletal muscle with homology to dystrophin
DR Love, DF Hill, G Dickson, NK Spurr, BC Byth, RF Marsden, FS Walsh, ...
Nature 339 (6219), 55-58, 1989
Incidence of severe critical events in paediatric anaesthesia (APRICOT): a prospective multicentre observational study in 261 hospitals in Europe
W Habre, N Disma, K Virag, K Becke, TG Hansen, M Jöhr, B Leva, ...
The Lancet Respiratory Medicine 5 (5), 412-425, 2017
Amelioration of the dystrophic phenotype of mdx mice using a truncated utrophin transgene
JM Tinsley, AC Potter, SR Phelps, R Fisher, JI Trickett, KE Davies
Nature 384 (6607), 349-353, 1996
PDZ domains: targeting signalling molecules to sub‐membranous sites
CP Ponting, C Phillips, KE Davies, DJ Blake
Bioessays 19 (6), 469-479, 1997
Primary structure of dystrophin-related protein
JM Tinsley, DJ Blake, A Roche, U Fairbrother, J Riss, BC Byth, AE Knight, ...
Nature 360 (6404), 591-593, 1992
Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome
KE Davies, PL Pearson, PS Harper, JM Murray, T O'Brien, M Sarfarazi, ...
Nucleic Acids Research 11 (8), 2303-2312, 1983
Mutations in α-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans
DA Keays, G Tian, K Poirier, GJ Huang, C Siebold, J Cleak, PL Oliver, ...
Cell 128 (1), 45-57, 2007
The dual specificity phosphatases M3/6 and MKP-3 are highly selective for inactivation of distinct mitogen-activated protein kinases
M Muda, A Theodosiou, N Rodrigues, U Boschert, M Camps, C Gillieron, ...
Journal of Biological Chemistry 271 (44), 27205-27208, 1996
Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome
MV Bell, MC Hirst, Y Nakahori, RN MacKinnon, A Roche, TJ Flint, ...
Cell 64 (4), 861-866, 1991
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