Zobrazeno 1 - 10
of 19
pro vyhledávání: '"N Y Souren"'
Publikováno v:
International journal of cancerREFERENCES. 149(3)
Autor:
Hinrich Gronemeyer, N Y Souren
Publikováno v:
International Journal of Cancer. 148:2870-2871
Autor:
Jörn Walter, N Y Souren, Lisa Ann Gerdes, Tania Kümpfel, Thomas Klopstock, Reinhard Hohlfeld, Pavlo Lutsik
Publikováno v:
Human mutation 37(8), 765-775 (2016). doi:10.1002/humu.23003
We examined the debated link between mitochondrial DNA (mtDNA) variation and multiple sclerosis (MS) using 49 monozygotic (MZ) twin pairs clinically discordant for MS, which enables to associate de novo mtDNA variants, skewed heteroplasmy, and mtDNA
Autor:
Dieter Weichenhan, Gilles Gasparoni, Tania Kümpfel, Christoph Plass, Lisa Ann Gerdes, Pavlo Lutsik, Reinhard Hohlfeld, Abdulrahman Salhab, Eduardo Beltrán, Jörn Walter, N Y Souren
Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system with a modest concordance rate in monozygotic twins that strongly argues for involvement of epigenetic factors. We observe in 45 MS discordant monozygotic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60ed509700ab618968bfe7fd4aa98a37
https://doi.org/10.1101/381822
https://doi.org/10.1101/381822
Autor:
K. D. Zang, Jörn Walter, J Meng-Hentschel, D. Leitner, Sascha Tierling, N Y Souren, S. Reither, B Oehl-Jaschkowitz
Publikováno v:
Clinical Genetics, 79(6), 546-553. Wiley
Tierling S, Souren NY, Reither S, Zang KD, Meng-Hentschel J, Leitner D, Oehl-Jaschkowitz B, Walter J. DNA methylation studies on imprinted loci in a male monozygotic twin pair discordant for Beckwith–Wiedemann syndrome. Beckwith–Wiedemann syndrom
Autor:
Ruth J. F. Loos, Robert Vlietinck, Gaston Beunen, Hubert J.M. Smeets, N Y Souren, Anja Steyls, Maurice P. Zeegers, Marij Gielen, Aimee D C Paulussen, Catherine Derom, Alphons P. M. Stassen, Joep P.M. Geraedts, Robert Fagard
Publikováno v:
International Journal of Obesity, 32, 1233-1239. Nature Publishing Group
Children born small for gestational age are at increased risk of developing type 2 diabetes in adulthood. The satiety signal leptin that regulates food intake and energy expenditure might be a possible molecular link, as umbilical cord leptin levels
Autor:
Patrick J. Lindsey, N Y Souren, Robert Derom, Robert Vlietinck, Marij Gielen, Ruth J. F. Loos, Maurice P. Zeegers, Aimee D C Paulussen, Jan G. Nijhuis, Catherine Derom
Publikováno v:
Twin Research and Human Genetics, 11(2), 224-235. Australian Academic Press
The assessment of fetal growth is an essential component of good antenatal care, especially for twins. The aims of this study are to develop twin-specific intrauterine 'growth' charts, based on cross-sectional birthweight data, for monochorionic and
Autor:
N Y Souren, Alphons P. M. Stassen, Robert Vlietinck, Ruth J. F. Loos, Anja Steyls, Aimee D C Paulussen, Rob G J H Janssen, Jeroen Aerssens, Catherine Derom, Marij Gielen, Maurice P. Zeegers, Gaston Beunen, Robert Fagard
Publikováno v:
Twin Research and Human Genetics, 11(5), 505-16. Australian Academic Press
Insulin resistance and obesity are underlying causes of type 2 diabetes and therefore much interest is focused on the potential genes involved. A series of anthropometric and metabolic characteristic were measured in 240 MZ and 112 DZ twin pairs recr
Autor:
Robert Vlietinck, N Y Souren, Robert Fagard, Ruth J. F. Loos, Aimee D C Paulussen, Maurice P. Zeegers, Gaston Beunen, Marij Gielen, Catherine Derom
Publikováno v:
Diabetologia
Diabetologia, 50(10), 2107-2116. Springer, Cham
Diabetologia, 50(10), 2107-2116. Springer, Cham
Aims/hypothesis We determined the genetic contribution of 18 anthropometric and metabolic risk factors of type 2 diabetes using a young healthy twin population. Methods Traits were measured in 240 monozygotic (MZ) and 138 dizygotic (DZ) twin pairs ag
Autor:
Matthias Riemenschneider, Maurice P. Zeegers, Sascha Tierling, Gilles Gasparoni, N Y Souren, Jasmin Gries, Catherine Derom, Pavlo Lutsik, Jean-Pierre Fryns, Jörn Walter
Publikováno v:
Genome Biology, 14(5):44. BioMed Central Ltd
Genome Biology
Genome Biology
BACKGROUND: Low birth weight is associated with an increased adult metabolic disease risk. It is widely discussed that poor intra-uterine conditions could induce long-lasting epigenetic modifications, leading to systemic changes in regulation of meta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f09e8bed121c32aaa940fed9ab74bc1d
https://lirias.kuleuven.be/handle/123456789/401996
https://lirias.kuleuven.be/handle/123456789/401996