Review of How Genetic Research on Segmental Progeroid Syndromes Has Documented Genomic Instability as a Hallmark of Aging But Let Us Now Pursue Antigeroid Syndromes!

Author:

Martin George M1,Hisama Fuki M2,Oshima Junko1

Affiliation:

1. Department of Laboratory Medicine and Pathology, University of Washington, Seattle

2. Division of Medical Genetics, Department of Medicine, University of Washington, Seattle

Abstract

Abstract The purpose of this early contribution to the new Fellows Forum of this pioneering journal for what is now called Geroscience is to provide an example of how the author’s interest in using the emerging tools of human genetics has led to strong support for one of the hallmarks of aging—Genomic Instability. We shall also briefly review our emerging interests in the genetic analysis of what we have called Antigeroid Syndromes. While there has been significant progress in that direction via genetic studies of centenarians, the search for genetic pathways that make individuals unusually resistant or resilient to the ravages of specific geriatric disorders has been comparatively neglected. We refer to these disorders as Unimodal Antigeroid Syndromes. It is our hope that our young colleagues will consider research efforts in that direction.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Aging

Reference66 articles.

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2. Positional cloning of the Werner’s syndrome gene;Yu;Science.,1996

3. How research on human progeroid and antigeroid syndromes can contribute to the longevity dividend initiative;Hisama;Cold Spring Harb Perspect Med.,2016

4. Werner syndrome: clinical features, pathogenesis and potential therapeutic interventions;Oshima;Ageing Res Rev.,2017

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