Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Meena Sethuraman"'
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100873- (2024)
Externí odkaz:
https://doaj.org/article/6f9c4f4f1c77463993f8d73625ad267e
Autor:
Meena Sethuraman, Nagadhara Dronadula, Lianxiang Bi, Bradley K. Wacker, Ethan Knight, Pieter De Bleser, David A. Dichek
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Transduction of endothelial cells (EC) with a vector that expresses apolipoprotein A-I (APOAI) reduces atherosclerosis in arteries of fat-fed rabbits. However, the effects on atherosclerosis are partial and might be enhanced if APOAI express
Externí odkaz:
https://doaj.org/article/2ad6ece108b24aa594c3f46484bd534d
Autor:
Olivia M. D'Annibale, Erik A. Koppes, Meena Sethuraman, Kaitlyn Bloom, Al‐Walid Mohsen, Jerry Vockley
Publikováno v:
J Inherit Metab Dis
Very long-chain acyl-CoA dehydrogenase deficiency (VLCADD) is an autosomal recessive disease resulting from mutations in the ACADVL gene and is among the disorders tested for in newborn screening (NBS). Confirmatory sequencing following suspected VLC
Autor:
Lianxiang Bi, David A. Dichek, Alexis Stamatikos, Meena Sethuraman, Bradley K. Wacker, Kaushik Komandur
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology
Supplemental Digital Content is available in the text.
Objective: Efficient gene transfer to the vascular wall via intravenous vector injection would be useful for experimental vascular biology and gene therapy. Initial studies of lentiviral vec
Objective: Efficient gene transfer to the vascular wall via intravenous vector injection would be useful for experimental vascular biology and gene therapy. Initial studies of lentiviral vec
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 42
Background: Altered transforming growth factor beta (TGF-β) signaling in aortic SMC is implicated as a cause of aortic aneurysms and dissections (AAD), with AAD attributed both to increased and decreased TGF-β signaling. Loss of TGF-β signaling in
Publikováno v:
Genetics in Medicine. 24:S334-S335