Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jasmin Gries"'
Autor:
Matthias Döring, Jörn Walter, Nico Pfeifer, Karl Nordström, Pavlo Lutsik, Jasmin Gries, Gilles Gasparoni
Publikováno v:
BMC Bioinformatics
Highlights from the Third International Society for Computational Biology (ISCB) European Student Council Symposium 2014
Highlights from the Third International Society for Computational Biology (ISCB) European Student Council Symposium 2014
Background DNA methylation is an epigenetic modification known to play a prime role in gene silencing and is an important topic in epigenetic research. However, due to technology-dependent errors there are inconsistencies between methylation measurem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26b1bf5b3b47354fd90ea8c6064fa957
https://doi.org/10.1186/1471-2105-16-s3-a7
https://doi.org/10.1186/1471-2105-16-s3-a7
Autor:
Pavlo Lutsik, Jasmin Gries, Jörn Walter, Sascha Tierling, Iduna Fichtner, Maria Rivera Markelova, Christine Sers, Julia Arand, Dirk Schumacher
Publikováno v:
Epigenetics; Vol 8
The use of next generation sequencing has expanded our view on whole mammalian methylome patterns. In particular, it provides a genome-wide insight of local DNA methylation diversity at single nucleotide level and enables the examination of single ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77c9676d3d857884a146734f0a2dcb7f
https://pubmed.ncbi.nlm.nih.gov/23803588
https://pubmed.ncbi.nlm.nih.gov/23803588
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
Autor:
Eberhard Schwinger, Jörn Walter, Heribert Kentenich, Christina LoPorto, Marco Groth, Georg Griesinger, Gabriele Gillessen-Kaesbach, Karl Sperling, Pavlo Lutsik, Sascha Tierling, Isabelle Utz-Billing, N Y Souren, Jasmin Gries, Heidemarie Neitzel
Publikováno v:
Journal of Medical Genetics, 47(6), 371-6. BMJ Publishing Group
BACKGROUND Assisted reproductive technologies (ART) such as in vitro fertilisation (IVF) and intracytoplasmic sperm injection (ICSI) are believed to destabilise genomic imprints. An increased frequency of Beckwith-Wiedemann syndrome in children born
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eedb39bafe598c58e5d07bbf40ee1711
https://cris.maastrichtuniversity.nl/en/publications/3dd6052d-7446-4c45-80e0-1886c491a5a9
https://cris.maastrichtuniversity.nl/en/publications/3dd6052d-7446-4c45-80e0-1886c491a5a9