Cameron A Ackerley
Overview
Explore the profile of Cameron A Ackerley including associated specialties, affiliations and a list of published articles.
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Articles
31
Citations
1379
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Recent Articles
1.
Mastrangelo P, Chin A, Tan S, Jeon A, Ackerley C, Siu K, et al.
Viruses
. 2021 Feb;
13(2).
PMID: 33567674
Nucleolin is an essential cellular receptor to human respiratory syncytial virus (RSV). Pharmacological targeting of the nucleolin RNA binding domain RBD1,2 can inhibit RSV infections in vitro and in vivo;...
2.
Turnbull J, Tiberia E, Striano P, Genton P, Carpenter S, Ackerley C, et al.
Epileptic Disord
. 2016 Oct;
18(S2):38-62.
PMID: 27702709
Lafora disease (LD) is an autosomal recessive progressive myoclonus epilepsy due to mutations in the EPM2A (laforin) and EPM2B (malin) genes, with no substantial genotype-phenotype differences between the two. Founder...
3.
Ackerley C, Cooper M, Munoz D, Minassian B
Neurology
. 2016 Aug;
87(13):1417-9.
PMID: 27566744
No abstract available.
4.
Turnbull J, Epp J, Goldsmith D, Zhao X, Pencea N, Wang P, et al.
Ann Neurol
. 2014 Jan;
75(3):442-6.
PMID: 24419970
Ubiquitin ligases regulate quantities and activities of target proteins, often pleiotropically. The malin ubiquitin E3 ligase is reported to regulate autophagy, the misfolded protein response, microRNA silencing, Wnt signaling, neuronatin-mediated...
5.
Turnbull J, Tiberia E, Pereira S, Zhao X, Pencea N, Wheeler A, et al.
J Biol Chem
. 2013 Oct;
288(48):34627-37.
PMID: 24142699
Glycogen synthesis is a major component of the insulin response, and defective glycogen synthesis is a major portion of insulin resistance. Insulin regulates glycogen synthase (GS) through incompletely defined pathways...
6.
Pederson B, Turnbull J, Epp J, Weaver S, Zhao X, Pencea N, et al.
Ann Neurol
. 2013 Aug;
74(2):297-300.
PMID: 23913475
Lafora disease (LD) is a fatal progressive myoclonus epilepsy characterized neuropathologically by aggregates of abnormally structured glycogen and proteins (Lafora bodies [LBs]), and neurodegeneration. Whether LBs could be prevented by...
7.
Ramachandran N, Munteanu I, Wang P, Ruggieri A, Rilstone J, Israelian N, et al.
Acta Neuropathol
. 2013 Jan;
125(3):439-57.
PMID: 23315026
X-linked Myopathy with Excessive Autophagy (XMEA) is a childhood onset disease characterized by progressive vacuolation and atrophy of skeletal muscle. We show that XMEA is caused by hypomorphic alleles of...
8.
Turnbull J, Girard J, Lohi H, Chan E, Wang P, Tiberia E, et al.
Brain
. 2012 Sep;
135(Pt 9):2684-98.
PMID: 22961547
The most common progressive myoclonus epilepsies are the late infantile and late infantile-variant neuronal ceroid lipofuscinoses (onset before the age of 6 years), Unverricht-Lundborg disease (onset after the age of...
9.
Tiberia E, Turnbull J, Wang T, Ruggieri A, Zhao X, Pencea N, et al.
J Biol Chem
. 2012 Jun;
287(30):25650-9.
PMID: 22669944
The solubility of glycogen, essential to its metabolism, is a property of its shape, a sphere generated through extensive branching during synthesis. Lafora disease (LD) is a severe teenage-onset neurodegenerative...
10.
Girard J, Stone S, Lohi H, Blaszykowski C, Teixeira C, Turnbull J, et al.
Neurology
. 2012 May;
79(1):100-2.
PMID: 22622857
No abstract available.