• No results found

A study into genes encoding longevity in humans Kuningas, M.

N/A
N/A
Protected

Academic year: 2021

Share "A study into genes encoding longevity in humans Kuningas, M."

Copied!
2
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

A study into genes encoding longevity in humans

Kuningas, M.

Citation

Kuningas, M. (2007, December 4). A study into genes encoding longevity in

humans. Retrieved from https://hdl.handle.net/1887/12474

Version: Corrected Publisher’s Version

License: Licence agreement concerning inclusion of doctoral

thesis in the Institutional Repository of the University

of Leiden

Downloaded from: https://hdl.handle.net/1887/12474

Note: To cite this publication please use the final published version (if

applicable).

(2)

Stellingen

behorende bij het proefschrift:

“A Study into Genes Encoding Longevity in Humans”

Maris Kuningas

The regulation of lifespan is complex and depends not only on multiple genetic-, epigenetic- 1. and environmental factors, but also on the interaction between them. (This thesis)

Stress-responsiveness determines susceptibility for disease and is highly variable among 2. humans. (This thesis)

Common genetic variants in the DNA repair genes do not influence ageing-trajectories and 3. survival in the population at large. (This thesis)

It is still uncertain to what extent the candidate genetic mechanisms identified in model 4. organisms explain variation in lifespan in human populations. (This thesis)

Genetically diverse populations provide the means to refine association signals detected in 5. relatively homogeneous populations characterized by extensive linkage disequilibrium (Nat

Genet. 2007 Feb;39(2):218-25)

The inability to replicate results stem frequently from between-study heterogeneity.

6. (Nat

Genet. 2001 Nov;29(3):306-9)

The genetic susceptibility to common diseases is largely due to alleles which have a rela- 7. tively moderate impact but high frequency in the population.

The analytical power arising from reference DNA sequences has jump-started what some 8. call the “biology century”. (Human Genome Project web-page)

It is difficult to find a more multidisciplinary field than research into ageing.

9.

Anyone can get old; all you have to do is live long enough.

10. (Groucho Marx)

Modesty is not a virtue in science.

11.

The experience of living in a foreign country makes you better understand your native 12. country.

Leiden, December 4, 2007

Referenties

GERELATEERDE DOCUMENTEN

waarschijnlijkheid van een normale vruchtbaarheid nam met meer dan een factor tien toe indien het aangeboren cytokine profiel werd gekarakteriseerd door hoge IL-1 (Th-2)

In case of humans, most information on the effect of genetic variation on longevity is being obtained by studying naturally occurring variants in candidate genes identified in

License: Licence agreement concerning inclusion of doctoral thesis in the Institutional Repository of the University of Leiden Downloaded.

This work was supported by an Innovative Orientated Research (IOP) grant from the Dutch Ministry of Economic Affairs (grant number IGE010114), by the Netherlands Genomics

The general objective of the thesis was to test the impact of the most prominent longevity candidate genes on the prevalence of age-related diseases and lifespan in a population-based

Here, we analyzed the effect of genetic variance in FOXO1a and FOXO3a on metabolic profile, age-related diseases, fertility, fecundity and mortality.. This study was carried out

The strong point of our study is that we selected genetic variants tagging all common hap- lotypes of the NR1H3 gene and associated them with a range of variables in inflammation and

An overall better performance on tests measuring attention, processing speed and memory, together with a lower prevalence of depressive symptoms were observed for carriers of