Words similar to conduction
Example sentences for: conduction
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The development of well-characterized cardiac progenitor cells offers the promise of using real genetic-based approaches to rapidly define the complex pathways that guide cardiac contractility, excitability, and lineage diversification into atrial, ventricular, and conduction system myocyte cell lineages.
Genotyping of patients with conduction disease and DCM may provide important information regarding device implantation.
Those afferents that exhibited a pause in discharge frequency as the extrafusal fibers contracted ("silent period") were classified as muscle spindles [ 24 25 ] . Primary muscle spindles were differentiated from secondary muscle spindles with the satisfaction of at least two out of three criteria tested on every afferent: 1) a conduction velocity > 75 m/sec; 2) an increase in discharge frequency at 100 μm displacement reflecting a low stretch threshold; 3) an abrupt decrease in frequency discharge at the end of stretch that returned to L init static discharge levels.
These include urokinase-type plasminogen activator receptor (PLAUR; MIM 173391, see Online Mendelian Inheritance in Man http://www.ncbi.nlm.nih.gov/omim/) [ 44 ] , apolipoproteins E (MIM 107741), CII (MIM 207750) and CI (MIM 107710), human brain-specific Na(+)-dependent inorganic phosphate cotransporter (hBNPI, 19q13) [ 45 ] , cardiac troponin I (TnIc, 19q; MIM 191044) [ 46 47 ] , cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL, caused by mutations in the Notch3 gene, 19q12; MIM 602275) [ 48 ] , isolated cardiac conduction disease (19q13.
Cardiac conduction disturbance has also been recognized in the mitochondrial cytopathy, Kearns-Sayre syndrome (Mendelian inheritance in Man database *530000), characterized as progressive external ophthalmoplegia and retinopathy [ 16 ] . Clinical manifestations of cardiac disease occur in 57% of patients with Kearns-Sayre syndrome [ 17 ] . The complete AV block in Kearns-Sayre syndrome may also be associated less commonly with ventricular tachycardia, torsade de pointes and ventricular fibrillation as the ultimate and often fatal stage of the condition [ 18 ] . However, to our knowledge, ventricular tachycardia as a presenting feature has not been described in the context of mitochondrial cytopathies in the neonatal period.
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