متابعة
Kay Davies
Kay Davies
Professor of Genetics University of Oxford
بريد إلكتروني تم التحقق منه على dpag.ox.ac.uk
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
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
15052002
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
9601985
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
9581997
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
8661995
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
8522008
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
7651998
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
7592000
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
7541990
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
7381991
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
7371990
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
6651993
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
6331989
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
5862017
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
5781996
PDZ domains: targeting signalling molecules to sub‐membranous sites
CP Ponting, C Phillips, KE Davies, DJ Blake
Bioessays 19 (6), 469-479, 1997
5391997
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
5181992
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
5041983
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
4772007
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
4581996
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
4511991
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مقالات 1–20