No differential gene expression for CD4
CD4+ T cells
Genetics
RNA sequencing
gene expression
multiple sclerosis
Journal
Multiple sclerosis journal - experimental, translational and clinical
ISSN: 2055-2173
Titre abrégé: Mult Scler J Exp Transl Clin
Pays: United States
ID NLM: 101668877
Informations de publication
Date de publication:
Historique:
received:
07
12
2018
revised:
30
04
2019
accepted:
20
05
2019
entrez:
22
6
2019
pubmed:
22
6
2019
medline:
22
6
2019
Statut:
epublish
Résumé
Multiple sclerosis-associated genetic variants indicate that the adaptive immune system plays an important role in the risk of developing multiple sclerosis. It is currently not well understood how these multiple sclerosis-associated genetic variants contribute to multiple sclerosis risk. CD4 We aim to identify CD4 We applied RNA sequencing on CD4 We did not identify significantly differentially expressed genes in CD4 We conclude that CD4
Sections du résumé
BACKGROUND
BACKGROUND
Multiple sclerosis-associated genetic variants indicate that the adaptive immune system plays an important role in the risk of developing multiple sclerosis. It is currently not well understood how these multiple sclerosis-associated genetic variants contribute to multiple sclerosis risk. CD4
OBJECTIVE
OBJECTIVE
We aim to identify CD4
METHODS
METHODS
We applied RNA sequencing on CD4
RESULTS
RESULTS
We did not identify significantly differentially expressed genes in CD4
CONCLUSION
CONCLUSIONS
We conclude that CD4
Identifiants
pubmed: 31223483
doi: 10.1177/2055217319856903
pii: 10.1177_2055217319856903
pmc: PMC6566490
doi:
Types de publication
Journal Article
Langues
eng
Pagination
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