Publications by authors named "Erwin Reiling"

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High protein intake causes gene-length-dependent transcriptional decline, shortens lifespan and accelerates ageing in progeroid DNA repair-deficient mice.
Ivar van Galen, Maria B Birkisdóttir, Rutger A Ozinga, Renata M C Brandt, Sander Barnhoorn, Erwin Reiling

NPJ Metab Health Dis· May 2025

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Corrigendum: The use of progeroid DNA repair-deficient mice for assessing anti-aging compounds, illustrating the benefits of nicotinamide riboside.
María B Birkisdóttir, Ivar van Galen, Renata M C Brandt, Sander Barnhoorn, Nicole van Vliet, Erwin Reiling

Front Aging· November 2022

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The use of progeroid DNA repair-deficient mice for assessing anti-aging compounds, illustrating the benefits of nicotinamide riboside.
María B Birkisdóttir, Ivar van Galen, Renata M C Brandt, Sander Barnhoorn, Nicole van Vliet, Erwin Reiling

Front Aging· October 2022

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Dietary restriction but not angiotensin II type 1 receptor blockade improves DNA damage-related vasodilator dysfunction in rapidly aging mice.
Haiyan Wu, Bibi S van Thiel, Paula K Bautista-Niño, Erwin Reiling, Matej Durik

Clin Sci (Lond)· August 2017

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The progeroid phenotype of Ku80 deficiency is dominant over DNA-PKCS deficiency.
Erwin Reiling, Martijn E T Dollé, Sameh A Youssef, Moonsook Lee, Bhawani Nagarajah

PLoS One· January 2015

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Deletion of individual Ku subunits in mice causes an NHEJ-independent phenotype potentially by altering apurinic/apyrimidinic site repair.
Yong Jun Choi, Han Li, Mi Young Son, Xiao-Hong Wang, Jamie L Fornsaglio, Erwin Reiling

PLoS One· November 2014

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Human TP53 polymorphism (rs1042522) modelled in mouse does not affect glucose metabolism and body composition.
Erwin Reiling, Ewoud N Speksnijder, Amanda C M Pronk, Sjoerd A A van den Berg, Silvia J W Neggers

Sci Rep· February 2014

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DNA damage in normally and prematurely aged mice.
Alexander Y Maslov, Shireen Ganapathi, Maaike Westerhof, Wilber Quispe-Tintaya, Ryan R White, Erwin Reiling

Aging Cell· June 2013

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Common variants in the type 2 diabetes KCNQ1 gene are associated with impairments in insulin secretion during hyperglycaemic glucose clamp.
Jana V van Vliet-Ostaptchouk, Timon W van Haeften, Gijs W D Landman, Erwin Reiling, Nanne Kleefstra

PLoS One· July 2012

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Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time.
Erwin Reiling, Valeriya Lyssenko, Jolanda M A Boer, Sandra Imholz, W Monique M Verschuren

Eur J Hum Genet· June 2012

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A common variant in TFB1M is associated with reduced insulin secretion and increased future risk of type 2 diabetes.
Thomas Koeck, Anders H Olsson, Marloes Dekker Nitert, Vladimir V Sharoyko, Claes Ladenvall, Erwin Reiling

Cell Metab· January 2011

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The association of mitochondrial content with prevalent and incident type 2 diabetes.
Erwin Reiling, Charlotte Ling, André G Uitterlinden, Esther Van't Riet, Laura M C Welschen

J Clin Endocrinol Metab· April 2010

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Combined risk allele score of eight type 2 diabetes genes is associated with reduced first-phase glucose-stimulated insulin secretion during hyperglycemic clamps.
Leen M 't Hart, Annemarie M Simonis-Bik, Giel Nijpels, Timon W van Haeften, Silke A Schäfer, Erwin Reiling

Diabetes· January 2010

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Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B affect different aspects of pancreatic beta-cell function.
Annemarie M Simonis-Bik, Giel Nijpels, Timon W van Haeften, Jeanine J Houwing-Duistermaat, Dorret I Boomsma, Erwin Reiling

Diabetes· January 2010

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Genetic association analysis of 13 nuclear-encoded mitochondrial candidate genes with type II diabetes mellitus: the DAMAGE study.
Erwin Reiling, Jana V van Vliet-Ostaptchouk, Esther van 't Riet, Timon W van Haeften, Pascal A Arp

Eur J Hum Genet· August 2009

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The HADHSC gene encoding short-chain L-3-hydroxyacyl-CoA dehydrogenase (SCHAD) and type 2 diabetes susceptibility: the DAMAGE study.
Els C van Hove, Torben Hansen, Jacqueline M Dekker, Erwin Reiling, Giel Nijpels

Diabetes· November 2006

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