About: Mito-Omics and immune function: Applying novel mitochondrial omic techniques to the context of the aging immune system

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About: Mito-Omics and immune function: Applying novel mitochondrial omic techniques to the context of the aging immune system Goto Sponge NotDistinct Permalink

An Entity of Type : schema:ScholarlyArticle, within Data Space : covidontheweb.inria.fr associated with source document(s)

Attributes	Values
type	Academic Article research paper schema:ScholarlyArticle
isDefinedBy	Covid-on-the-Web dataset
has title	Mito-Omics and immune function: Applying novel mitochondrial omic techniques to the context of the aging immune system
Creator	Cohen, Affiliations, Ana Cohen, Pinchas Davis, Leonard Flores, Brendan Flores, Melanie Kim, Kelvin Kim, Su-Jeong Mehta, Hemal Mehta, Pinchas Miller, Brendan Miller, Su-Jeong Silverstein, Ana Silverstein, Melanie Yen, Hemal Yen, Kelvin
Source	Elsevier; Medline; PMC
abstract	Recent advancements in genomic, transcriptomic, proteomic, and metabolomic techniques have prompted fresh inquiry in the field of aging. Here, we outline the application of these techniques in the context of the mitochondrial genome and suggest their potential for use in exploring the biological mechanisms of the aging immune system.
has issue date	2020-08-21(xsd:dateTime)
bibo:doi	10.1016/j.tma.2020.08.001
bibo:pmid	32844137
has license	no-cc
sha1sum (hex)	16208527e08a23b2f9f615065f6767b5d6ff058e
schema:url	https://doi.org/10.1016/j.tma.2020.08.001
resource representing a document's title	Mito-Omics and immune function: Applying novel mitochondrial omic techniques to the context of the aging immune system
has PubMed Central identifier	PMC7441040
has PubMed identifier	32844137
schema:publication	Transl Med Aging
resource representing a document's body	covid:16208527e08a23b2f9f615065f6767b5d6ff058e#body_text
is schema:about of	named entity 'omic' named entity 'FRESH' named entity 'MECHANISMS' named entity 'THESE' named entity 'open reading frame' named entity 'metabolomic' named entity 'proteomic' named entity 'immune system' named entity 'proteomic' named entity 'mitochondrial genome' named entity 'mitochondrial' named entity 'pathology' named entity 'genomic variants' named entity 'heteroplasmy' named entity 'mitochondrial dysfunction' named entity 'NLRP3' named entity 'metabolomics' named entity 'peptide' named entity 'IL-18' named entity 'experimental design' named entity 'healthy aging' named entity 'mtDNA' named entity 'mitochondria' named entity 'oncogenes' named entity 'GWAS' named entity 'Mitochondria' named entity 'proinflammatory state' named entity 'rRNAs' named entity 'cancer development' named entity 'proteomics' named entity 'mtDNA' named entity 'mitochondrial' named entity 'mitochondrial' named entity 'Alzheimer's disease' named entity 'humanin' named entity 'mitochondrial genome' named entity 'age-related diseases' named entity 'obesity' named entity 'mutation' named entity 'mice' named entity 'mtDNA' named entity 'pathogenesis' named entity 'diseases of aging' named entity 'immunosenescence' named entity 'cellular metabolism' named entity 'mtDNA' named entity 'genome' named entity 'pathology' named entity 'transcriptomic' named entity 'tRNAs' named entity 'proinflammatory' named entity 'mtDNA' named entity 'humanin' named entity 'glutathione' named entity 'immune dysfunction' named entity 'age-related diseases' named entity 'age-related' named entity 'mitochondrial' named entity 'peptides' named entity 'proteomic' named entity 'diabetes' named entity 'mitochondrial' named entity 'nuclear genes' named entity 'heteroplasmy' named entity 'cell damage' named entity 'innate immune'

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