Eric Dec
Overview
Explore the profile of Eric Dec including associated specialties, affiliations and a list of published articles.
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7
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242
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Recent Articles
1.
Dec E, Clement J, Cheng K, Church G, Fossel M, Rehkopf D, et al.
Geroscience
. 2023 Mar;
45(3):1817-1835.
PMID: 36964402
Claims surrounding exceptional longevity are sometimes disputed or dismissed for lack of credible evidence. Here, we present three DNA methylation-based age estimators (epigenetic clocks) for verifying age claims of centenarians....
2.
Perkins B, Caskey C, Brar P, Dec E, Karow D, Kahn A, et al.
Proc Natl Acad Sci U S A
. 2018 Mar;
115(14):3686-3691.
PMID: 29555771
Reducing premature mortality associated with age-related chronic diseases, such as cancer and cardiovascular disease, is an urgent priority. We report early results using genomics in combination with advanced imaging and...
3.
Brodehl A, Dieding M, Klauke B, Dec E, Madaan S, Huang T, et al.
Circ Cardiovasc Genet
. 2013 Nov;
6(6):615-23.
PMID: 24200904
Background: The intermediate filament protein desmin is encoded by the gene DES and contributes to the mechanical stabilization of the striated muscle sarcomere and cell contacts within the cardiac intercalated...
4.
Dec E, Rana P, Katheria V, Dec R, Khare M, Nalbandian A, et al.
Clin Transl Sci
. 2013 Oct;
7(1):29-32.
PMID: 24119107
Valosin containing protein (VCP) disease (also known as Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia [IBMPFD] syndrome) is caused by mutations in the gene encoding VCP classically...
5.
Nalbandian A, Ghimbovschi S, Radom-Aizik S, Dec E, Vesa J, Martin B, et al.
Clin Transl Sci
. 2012 Jun;
5(3):226-34.
PMID: 22686199
Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is an autosomal dominant disorder caused by mutations in the Valosin-containing protein (VCP) gene on chromosome 9p12-13....
6.
Nalbandian A, Donkervoort S, Dec E, Badadani M, Katheria V, Rana P, et al.
J Mol Neurosci
. 2011 Sep;
45(3):522-31.
PMID: 21892620
Inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD) is a progressive, fatal genetic disorder with variable penetrance, predominantly affecting three main tissue types: muscle (IBM),...
7.
Badadani M, Nalbandian A, Watts G, Vesa J, Kitazawa M, Su H, et al.
PLoS One
. 2010 Oct;
5(10).
PMID: 20957154
Dominant mutations in the valosin containing protein (VCP) gene cause inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia (IBMPFD). We have generated a knock-in mouse model...