Elizabeth M Thompson
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Explore the profile of Elizabeth M Thompson including associated specialties, affiliations and a list of published articles.
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32
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1215
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Recent Articles
11.
Miller M, Akaronu N, Thompson E, Hood S, Fogle J
J Immunol
. 2014 Dec;
194(3):990-8.
PMID: 25548225
We have previously demonstrated that CD4(+)CD25(+) regulatory T cells (Tregs) activated during the course of feline immunodeficiency virus (FIV) infection suppress CD8(+) CTL function in a TGF-β-dependent fashion, inhibiting IFN-γ...
12.
Thompson E, Towle Millard H, Moore G, Guptill L
Am J Vet Res
. 2014 Sep;
75(10):924-8.
PMID: 25255183
Objective: To evaluate the effect of multiple hydrogen peroxide gas plasma (HPGP) sterilizations on the rate of closure of ameroid constrictors. Sample: Thirty-six 5.0-mm ameroid constrictors. Procedures: Ameroid constrictors were...
13.
Ansari M, Poke G, Ferry Q, Williamson K, Aldridge R, Meynert A, et al.
J Med Genet
. 2014 Aug;
51(10):659-68.
PMID: 25125236
Background: Cornelia de Lange syndrome (CdLS) is a multisystem disorder with distinctive facial appearance, intellectual disability and growth failure as prominent features. Most individuals with typical CdLS have de novo...
14.
Bear K, Solomon B, Antonini S, Arnhold I, Franca M, Gerkes E, et al.
J Med Genet
. 2014 Apr;
51(6):413-8.
PMID: 24744436
Background: Mutations in GLI2 have been associated with holoprosencephaly (HPE), a neuroanatomic anomaly resulting from incomplete cleavage of the developing forebrain, and an HPE-like phenotype involving pituitary anomalies and polydactyly....
15.
Nicholl J, Waters W, Mulley J, Suwalski S, Brown S, Hull Y, et al.
Pathology
. 2013 Dec;
46(1):41-5.
PMID: 24300712
The aim of this study was to determine prospectively the frequency of pathogenic chromosomal microdeletions and microduplications in a large group of referred patients with developmental delay (DD), intellectual disability...
16.
Gupta V, Ravenscroft G, Shaheen R, Todd E, Swanson L, Shiina M, et al.
Am J Hum Genet
. 2013 Nov;
93(6):1108-17.
PMID: 24268659
Nemaline myopathy (NM) is a rare congenital muscle disorder primarily affecting skeletal muscles that results in neonatal death in severe cases as a result of associated respiratory insufficiency. NM is...
17.
Dobson-Stone C, Hallupp M, Loy C, Thompson E, Haan E, Sue C, et al.
PLoS One
. 2013 Feb;
8(2):e56899.
PMID: 23437264
A hexanucleotide repeat expansion in C9ORF72 has been established as a common cause of frontotemporal dementia (FTD). However, the minimum repeat number necessary for disease pathogenesis is not known. The...
18.
Dobson-Stone C, Luty A, Thompson E, Blumbergs P, Brooks W, Short C, et al.
Acta Neuropathol
. 2013 Jan;
125(4):523-33.
PMID: 23338750
Numerous families exhibiting both frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) have been described, and although many of these have been shown to harbour a repeat expansion in C9ORF72,...
19.
Miller M, Thompson E, Suter S, Fogle J
Vet Immunol Immunopathol
. 2013 Jan;
152(3-4):200-8.
PMID: 23332729
Acute lentiviral infection is characterized by early CD8(+) cytotoxic T cell (CTL) activity and a subsequent decline in plasma viremia. However, CD8(+) lymphocytes fail to eliminate the virus and a...
20.
Ravenscroft G, Thompson E, Todd E, Yau K, Kresoje N, Sivadorai P, et al.
Neuromuscul Disord
. 2012 Dec;
23(2):165-9.
PMID: 23218673
The clinically and genetically heterogenous foetal akinesias have low rates of genetic diagnosis. Exome sequencing of two siblings with phenotypic lethal multiple pterygium syndrome identified compound heterozygozity for a known...