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小鼠模型与衰老:长寿和早衰。

Mouse models and aging: longevity and progeria.

作者信息

Liao Chen-Yu, Kennedy Brian K

机构信息

Buck Institute for Research on Aging, Novato, California, USA.

Buck Institute for Research on Aging, Novato, California, USA.

出版信息

Curr Top Dev Biol. 2014;109:249-85. doi: 10.1016/B978-0-12-397920-9.00003-2.

Abstract

Aging is a complex, multifactorial process that is likely influenced by the activities of a range of biological pathways. Genetic approaches to identify genes modulating longevity have been highly successful and recent efforts have extended these studies to mammalian aging. A variety of genetic models have been reported to have enhanced lifespan and, similarly, many genetic interventions lead to progeroid phenotypes. Here, we detail and evaluate both sets of models, focusing on the insights they provide about the molecular processes modulating aging and the extent to which mutations conferring progeroid pathologies really phenocopy accelerated aging.

摘要

衰老 是一个复杂的多因素过程,可能受到一系列生物途径活动的影响。通过遗传学方法来识别调控寿命的基因已取得了巨大成功,最近的研究已将这些研究扩展到哺乳动物衰老领域。据报道,多种遗传模型具有延长的寿命,同样,许多基因干预会导致早衰表型。在这里,我们详细介绍并评估这两组模型,重点关注它们对调节衰老的分子过程所提供的见解,以及导致早衰病理的突变在多大程度上真正模拟了加速衰老。

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