Physiological data (mean ± s.e.m.) for the four groups that constituted our control mice (pooled hereafter) and the eight groups of mutant/pharmacologically treated mice. Myh11+/+, Fbln5+/+ and Fbn1+/+ were generated as a by-product by breeding heterozygous mutant mice to produce homozygous mutant mice; wild-type (WT) refers to inbred mice maintained through sibling matings. Background, age, body mass and blood pressure (systolic/diastolic) are indicated for each group. Differences in background and age were dictated by prior individual studies that focused on the effect of each mutation [16–18,20,22]. The value of systolic pressure was adjusted (adj) to conscious mouse conditions depending on the protocol and apparatus used for data acquisition [23,24]. Note that elastase was applied to WT C57BL/6J ascending aortas; hence, donor mice are not listed as a separate group. Note: C, indwelling (aortic) polyethylene catheter in the conscious mouse; M, Millar ascending aortic catheter in the anaesthetized mouse (1.2% isoflurane); S, Scisense ascending aortic catheter in the anaesthetized mouse (1.5% isoflurane); T, non-invasive tail cuff method in the conscious mouse. By mild phenotype, we mean that the aortic properties were nearly, though not precisely, normal.