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Browsing publications by Dr Gabriele Saretzki

Newcastle AuthorsTitleYearFull text
Dr Danny Chan
Dr Carmen Martin-Ruiz
Dr Gabriele Saretzki
Dr R Neely
Dr Vijay Kunadian
et al.		The association of telomere length and telomerase activity with adverse outcomes in older patients with non-ST-elevation acute coronary syndrome2020
Dr Carmen Martin-Ruiz
Dr Alison Yarnall
Dr John Boucher
Dr Rachael Lawson
Claire Kolenda
et al.		Senescence and inflammatory markers for predicting clinical progression in Parkinson's disease-the ICICLE-PD study2019
Dr Mikolaj Ogrodnik
Dr Olena Kucheryavenko
Julien Glibert
Dr Satomi Miwa
Abbas Ishaq
et al.		The bystander effect contributes to the accumulation of senescent cells in vivo2019
Abbas Ishaq
Julia Schroder
Miss Edwards
Professor Thomas von Zglinicki
Dr Gabriele Saretzki
et al.		Dietary restriction ameliorates age-related increase in DNA damage, senescence and inflammation in mouse adipose tissuey2018
Dario Melguizo Sanchis
Dr Yaobo Xu
Dheraj Taheem
Dr Min Yu
Dr Katarzyna Tilgner
et al.		iPSC modelling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors2018
Abbas Ishaq
Damien Dufour
Dr Kerry Cameron
Professor Thomas von Zglinicki
Dr Gabriele Saretzki
et al.		Metabolic memory of dietary restriction ameliorates DNA damage and adipocyte size in mouse visceral adipose tissue2018
Dr Gavin Richardson
Dr Karim Bennaceur
Emily Dookun
Lilia Draganova
Dr Gabriele Saretzki
et al.		Telomerase Mediates Lymphocyte Proliferation but Not the Atherosclerosis-Suppressive Potential of Regulatory T-Cells2018
Dr Gabriele Saretzki
Telomeres, Telomerase and Ageing2018
Dr Dean Hallam
Dr Joseph Collin
Dr Sanja Bojic
Dr Valeria Chichagova
Adriana Buskin
et al.		An iPSC patient specific model of CFH (Y402H) polymorphism displays characteristic features of AMD and indicates a beneficial role for UV light exposure2017
Dr Valeria Chichagova
Dr Dean Hallam
Dr Joseph Collin
Adriana Buskin
Dr Gabriele Saretzki
et al.		Human iPSC disease modelling reveals functional and structural defects in retinal pigment epithelial cells harbouring the m.3243A>G mitochondrial DNA mutation2017
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