J A Beck
Overview
Explore the profile of J A Beck including associated specialties, affiliations and a list of published articles.
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Articles
28
Citations
727
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Recent Articles
1.
Mason N, Selmic L, Ruple A, London C, Barber L, Weishaar K, et al.
Mol Ther
. 2025 Feb;
PMID: 39955616
A clinical trial in dogs with spontaneous osteosarcoma was performed to assess a recombinant Listeria expressing a chimeric human HER2/neu (ADXS31-164) as an adjunctive vaccine strategy to prevent metastatic disease...
2.
Silver K, Patkar S, Mazcko C, Berger E, Beck J, LeBlanc A
Vet Comp Oncol
. 2023 Aug;
21(4):646-655.
PMID: 37592810
Osteosarcoma is a highly metastatic primary bone tumour that occurs spontaneously in both pet dogs and humans. Patterns of metastasis to organs beyond the most common site (lung) are poorly...
3.
Beck J, Budgell G, Roberts D, Evans P
Med Phys
. 2009 Jun;
36(5):1859-66.
PMID: 19544805
An amorphous silicon EPID has been investigated to determine whether it is capable of quality control constancy measurements for linear accelerator electron beams. The EPID grayscale response was found to...
4.
Beck J, Campbell T, Adamson G, Poulter M, Uphill J, Molou E, et al.
J Med Genet
. 2008 Sep;
45(12):813-7.
PMID: 18805828
Background: No susceptibility genes have been identified in human prion disase, apart from the prion protein gene (PRNP). The gene SPRN, encodes Shadoo (Sho, shadow of prion protein) which has...
5.
Barrs V, Nicoll R, Churcher R, Beck J, Beatty J
J Small Anim Pract
. 2007 Jun;
48(8):449-54.
PMID: 17543019
Objectives: To review the literature on intracranial empyema and report two new cases in cats. Methods: Literature review and case reports. Results: Intracranial empyema has been rarely reported in small...
6.
Kovacs T, Beck J, Papp M, Lantos P, Aranyi Z, Szirmai I, et al.
J Neurol Neurosurg Psychiatry
. 2007 Feb;
78(3):321-3.
PMID: 17308293
About 15% of human prion diseases are inherited, and are associated with point or insertional mutations of the prion protein gene (PRNP). Four families with six octapeptide repeat insertions (OPRI)...
7.
Godbolt A, Beck J, Collinge J, Cipolotti L, Fox N, Rossor M
Neurology
. 2006 Mar;
66(4):611-2.
PMID: 16505331
No abstract available.
8.
Godbolt A, Beck J, Collinge J, Garrard P, Warren J, Fox N, et al.
Neurology
. 2004 Nov;
63(9):1702-4.
PMID: 15534260
Presenilin (PSEN)1 mutations are responsible for many cases of autosomal dominant Alzheimer disease (AD), although the clinical spectrum has not been fully defined. The authors describe two members of a...
9.
Janssen J, Beck J, Campbell T, Dickinson A, Fox N, Harvey R, et al.
Neurology
. 2003 Jan;
60(2):235-9.
PMID: 12552037
Background: Three causative genes have been identified for autosomal dominant AD. Objective: To determine the proportion of patients with early onset AD with a positive family history accounted for by...
10.
Jackson G, Beck J, Navarrete C, Brown J, Sutton P, Contreras M, et al.
Nature
. 2001 Nov;
414(6861):269-70.
PMID: 11713518
No abstract available.