Page last updated: 2024-09-04

lonafarnib and Atherogenesis

lonafarnib has been researched along with Atherogenesis in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's1 (33.33)2.80

Authors

AuthorsStudies
Abutaleb, NO; Atchison, L; Bedapudi, A; Cao, K; Choi, L; Gete, Y; Shores, K; Truskey, GA1
Brazier, J; Brown, WT; Campbell, SE; D'Agostino, RB; Gordon, LB; Kieran, MW; Kleinman, ME; Massaro, J1
Li, Y; Peng, G; Qin, J; Sun, L; Wang, J; Xie, S; Zhong, D1

Other Studies

3 other study(ies) available for lonafarnib and Atherogenesis

ArticleYear
Lonafarnib and everolimus reduce pathology in iPSC-derived tissue engineered blood vessel model of Hutchinson-Gilford Progeria Syndrome.
    Scientific reports, 2023, 03-28, Volume: 13, Issue:1

    Topics: Atherosclerosis; Calcinosis; Endothelial Cells; Everolimus; Humans; Induced Pluripotent Stem Cells; Lamin Type A; Progeria

2023
Impact of farnesylation inhibitors on survival in Hutchinson-Gilford progeria syndrome.
    Circulation, 2014, Jul-01, Volume: 130, Issue:1

    Topics: Adolescent; Adult; Alkyl and Aryl Transferases; Atherosclerosis; Cause of Death; Child; Child, Preschool; Clinical Trials as Topic; Cohort Studies; Dimethylallyltranstransferase; Diphosphonates; Drug Therapy, Combination; Female; Genes, Dominant; Genotype; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Imidazoles; Kaplan-Meier Estimate; Lamin Type A; Male; Multicenter Studies as Topic; Nuclear Proteins; Piperidines; Pravastatin; Progeria; Proportional Hazards Models; Protein Precursors; Protein Prenylation; Pyridines; Treatment Outcome; Young Adult; Zoledronic Acid

2014
Lonafarnib is a potential inhibitor for neovascularization.
    PloS one, 2015, Volume: 10, Issue:4

    Topics: Alkyl and Aryl Transferases; Animals; Apolipoproteins E; Atherosclerosis; Cell Polarity; Cell Proliferation; Cytoskeletal Proteins; Endothelial Cells; Gene Expression Regulation; Humans; Mice; Neovascularization, Pathologic; Piperidines; Pyridines

2015