K E Davies
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Explore the profile of K E Davies including associated specialties, affiliations and a list of published articles.
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317
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Recent Articles
11.
Culle M, Walsh J, Tinsle J, Fisher R, Davies K
Histochem J
. 2002 May;
33(9-10):579-83.
PMID: 12005030
It has been shown previously that when utrophin is highly expressed in mice which lack dystrophin, the muscle pathology is prevented. Immunohistochemical evidence strongly suggests that utrophin in these transgenic...
12.
Cole M, Rafael J, Taylor D, Lodi R, Davies K, Styles P
Neuromuscul Disord
. 2002 Jan;
12(3):247-57.
PMID: 11801396
Muscle energetics and function were investigated in the hindlimb of mice lacking dystrophin (mdx), utrophin and dystrophin (utr-dys) and controls (C57Bl/10) using 31P and 1H magnetic resonance techniques, electrical nerve...
13.
PERKINS K, Burton E, Davies K
Nucleic Acids Res
. 2001 Dec;
29(23):4843-50.
PMID: 11726694
Duchenne muscular dystrophy (DMD) is an X-linked recessive muscle wasting disease caused by the absence of a muscle cytoskeletal protein, dystrophin. Utrophin is the autosomal homologue of dystrophin. We previously...
14.
Davies K, Houghton K, Montgomery J
Anaesthesia
. 2001 Nov;
56(11):1112-5.
PMID: 11703247
Day-case surgery is increasing in popularity and more patients with multiple medical problems are being considered as suitable for this approach. However, the current recommendations exclude morbidly obese patients (body...
15.
Fisher R, Tinsley J, Phelps S, Squire S, Townsend E, Martin J, et al.
Neuromuscul Disord
. 2001 Oct;
11(8):713-21.
PMID: 11595513
Duchenne muscular dystrophy (DMD) is an inherited, severe muscle wasting disease caused by the loss of the cytoskeletal protein, dystrophin. Patients usually die in their late teens or early twenties...
16.
Loh N, Blake D, Smith A, Davies K
Mol Cell Biol
. 2001 Oct;
21(21):7442-8.
PMID: 11585924
beta-Dystrobrevin is a dystrophin-related and -associated protein that is highly expressed in brain, kidney, and liver. Recent studies with the kidneys of the mdx3Cv mouse, which lacks all dystrophin isoforms,...
17.
Talbot K, Davies K
Semin Neurol
. 2001 Jul;
21(2):189-97.
PMID: 11442327
The spinal muscular atrophies are a group of mostly inherited disorders selectively affecting the lower motor neuron. There is a wide degree of clinical and genetic heterogeneity that must be...
18.
Skordis L, Dunckley M, Burglen L, Campbell L, Talbot K, Patel S, et al.
Hum Genet
. 2001 May;
108(4):356-7.
PMID: 11379882
We report two novel mutations in three cases of spinal muscular atrophy (SMA), including two distant cousins who followed an unexpectedly severe course. Diagnosis was confirmed by reduced SMN protein...
19.
Nakamura A, Harrod G, Davies K
Neuromuscul Disord
. 2001 Apr;
11(3):251-9.
PMID: 11297940
Dilated cardiomyopathy is a common complication of Duchenne and Becker muscular dystrophies, which are caused by mutations in the dystrophin gene. The mdx mouse is an animal model for Duchenne...
20.
Hopkins J, Bia B, Crilley J, Boehm E, Sang A, Tinsley J, et al.
MAGMA
. 2001 Feb;
11(1-2):7-9.
PMID: 11186993
No abstract available.