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https://doi.org/10.1371/journal.pone.0001051
DC Field | Value | |
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dc.title | Ankyrin-B syndrome: Enhanced cardiac function balance by risk of cardiac death and premature senescence | |
dc.contributor.author | Mohler P.J. | |
dc.contributor.author | Healy J.A. | |
dc.contributor.author | Xue H. | |
dc.contributor.author | Puca A.A. | |
dc.contributor.author | Kline C.F. | |
dc.contributor.author | Allingham R.R. | |
dc.contributor.author | Kranias E.G. | |
dc.contributor.author | Rockman H.A. | |
dc.contributor.author | Bennett V. | |
dc.date.accessioned | 2019-11-08T00:58:22Z | |
dc.date.available | 2019-11-08T00:58:22Z | |
dc.date.issued | 2007 | |
dc.identifier.citation | Mohler P.J., Healy J.A., Xue H., Puca A.A., Kline C.F., Allingham R.R., Kranias E.G., Rockman H.A., Bennett V. (2007). Ankyrin-B syndrome: Enhanced cardiac function balance by risk of cardiac death and premature senescence. PLoS ONE 2 (10) : e1051. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0001051 | |
dc.identifier.issn | 19326203 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/161863 | |
dc.description.abstract | Here we report the unexpected finding that specific human ANK2 variants represent a new example of balanced human variants. The prevalence of certain ANK2 (encodes ankyrin-B) variants range from 2 percent of European individuals to 8 percent in individuals from West Africa. Ankyrin-B variants associated with severe human arrhythmia phenotypes (eg E1425G, V1516D, R1788W) were rare in the general population. Variants associated with less severe clinical and in vitro phenotypes were unexpectedly common. Studies with the ankyrin-B+/- mouse reveal both benefits of enhanced cardiac contractility, as well as costs in earlier senescence and reduced lifespan. Together these findings suggest a constellation of traits that we term "ankyrin-B syndrome", which may contribute to both aging-related disorders and enhanced cardiac function. � 2007 Mohler et al. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20191101 | |
dc.subject | ankyrin | |
dc.subject | ankyrin b | |
dc.subject | unclassified drug | |
dc.subject | ANK2 protein, human | |
dc.subject | Ank2 protein, mouse | |
dc.subject | ankyrin | |
dc.subject | Africa | |
dc.subject | animal cell | |
dc.subject | animal experiment | |
dc.subject | article | |
dc.subject | controlled study | |
dc.subject | disease association | |
dc.subject | disease severity | |
dc.subject | Europe | |
dc.subject | female | |
dc.subject | genetic variability | |
dc.subject | genotype | |
dc.subject | heart arrhythmia | |
dc.subject | heart death | |
dc.subject | heart disease | |
dc.subject | heart function | |
dc.subject | heart muscle cell | |
dc.subject | heart muscle contractility | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | in vitro study | |
dc.subject | lifespan | |
dc.subject | mouse | |
dc.subject | nonhuman | |
dc.subject | nucleotide sequence | |
dc.subject | phenotypic variation | |
dc.subject | premature aging | |
dc.subject | prevalence | |
dc.subject | risk assessment | |
dc.subject | senescence | |
dc.subject | aging | |
dc.subject | animal | |
dc.subject | C57BL mouse | |
dc.subject | cell aging | |
dc.subject | death | |
dc.subject | echocardiography | |
dc.subject | genetics | |
dc.subject | heart contraction | |
dc.subject | heart disease | |
dc.subject | methodology | |
dc.subject | pathology | |
dc.subject | phenotype | |
dc.subject | physiology | |
dc.subject | risk | |
dc.subject | syndrome | |
dc.subject | Aging | |
dc.subject | Animals | |
dc.subject | Ankyrins | |
dc.subject | Cell Aging | |
dc.subject | Death | |
dc.subject | Echocardiography | |
dc.subject | Heart Diseases | |
dc.subject | Humans | |
dc.subject | Mice | |
dc.subject | Mice, Inbred C57BL | |
dc.subject | Myocardial Contraction | |
dc.subject | Phenotype | |
dc.subject | Risk | |
dc.subject | Syndrome | |
dc.type | Article | |
dc.contributor.department | DUKE-NUS MEDICAL SCHOOL | |
dc.description.doi | 10.1371/journal.pone.0001051 | |
dc.description.sourcetitle | PLoS ONE | |
dc.description.volume | 2 | |
dc.description.issue | 10 | |
dc.description.page | e1051 | |
Appears in Collections: | Staff Publications Elements |
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