Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Galyna Pliushch"'
Autor:
Thomas Haaf, Nady El Hajj, Megan Mitchell, Nicole O. McPherson, Pamela L. Strissel, Ralf Dittrich, Galyna Pliushch, Reiner Strick, Ramya Potabattula, Michelle Lane
Publikováno v:
Molecular Reproduction and Development. 84:316-328
Gene expression and/or epigenetic deregulation may have consequences for sperm and blastocysts, as well as for the placenta, together potentially contributing to problems observed in offspring. We previously demonstrated specific perturbations of fer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcdb92195244b00e6fc829371a5a703a
https://doi.org/10.1002/mrd.22784
https://doi.org/10.1002/mrd.22784
Autor:
Megan, Mitchell, Reiner, Strick, Pamela L, Strissel, Ralf, Dittrich, Nicole O, McPherson, Michelle, Lane, Galyna, Pliushch, Ramya, Potabattula, Thomas, Haaf, Nady, El Hajj
Publikováno v:
Molecular Reproduction and Development
Gene expression and/or epigenetic deregulation may have consequences for sperm and blastocysts, as well as for the placenta, together potentially contributing to problems observed in offspring. We previously demonstrated specific perturbations of fer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::708610bee66a1bd08c511943ae857d84
Autor:
Thomas Haaf, Marcus Dittrich, Harald Lehnen, Michael Korenkov, Tobias Müller, Melanie Aretz, Nady El Hajj, Galyna Pliushch, U. Zechner, Eberhard Schneider
Publikováno v:
Diabetes
Epigenetic processes are primary candidates when searching for mechanisms that can stably modulate gene expression and metabolic pathways according to early life conditions. To test the effects of gestational diabetes mellitus (GDM) on the epigenome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::620df5dc32ad60a00c12a0ae9fed5731
https://doi.org/10.2337/db12-0289
https://doi.org/10.2337/db12-0289
Autor:
A. M. Müller, Daniela Weise, Ulrich Zechner, Larissa Seidmann, Nady El Hajj, Achim Tresch, Thomas Haaf, Eberhard Schneider, Wiltrud Coerdt, Galyna Pliushch
Publikováno v:
The American Journal of Pathology. 176:1084-1090
Imprinted genes play an important role in fetal and placental development. Using quantitative bisulfite pyrosequencing assays, we determined the DNA methylation levels at two paternally methylated (H19 and MEG3) and four maternally methylated (LIT1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::793e2870682c11092a45365583698a2b
https://doi.org/10.2353/ajpath.2010.090764
https://doi.org/10.2353/ajpath.2010.090764
Autor:
Ulrich Zechner, Gavin Kelsey, Danuta Galetzka, Sylvia Bähring, Friedrich C. Luft, Galyna Pliushch, Peter Nürnberg, Thomas Haaf, Nico Ruf
Publikováno v:
Human Molecular Genetics. 16:2591-2599
Genomic imprinting is the epigenetic marking of gene subsets resulting in monoallelic or predominant expression of one of the two parental alleles according to their parental origin. We describe the systematic experimental verification of a prioritiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::052c1d35b00029010e053764a1fea707
https://doi.org/10.1093/hmg/ddm216
https://doi.org/10.1093/hmg/ddm216
Autor:
Tamara Schneider, Thomas Haaf, Thomas Strowitzki, Galyna Pliushch, Eberhard Schneider, Nady El Hajj, Sabine Rösner
Publikováno v:
Fertility and sterility. 103(3)
Objective To study the possible transmission, to the next generation, of epigenetic defects associated with in vitro maturation (IVM) of human oocytes. Design Case–control study using epigenetic data. Setting Two collaborating university department
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05270df0a34591116b47d84eaa3de9b9
https://pubmed.ncbi.nlm.nih.gov/25572872
https://pubmed.ncbi.nlm.nih.gov/25572872
Autor:
Thomas Haaf, Sabine Preisler-Adams, Monika Leubner, Galyna Pliushch, Andrea Gehrig, Patricia Kroll, Daniela Endt, Peter Wieacker, Tamara Hansmann
Publikováno v:
Human Molecular Genetics
Genetic defects in breast cancer (BC) susceptibility genes, most importantly BRCA1 and BRCA2, account for ∼40% of hereditary BC and ovarian cancer (OC). Little is known about the contribution of constitutive (soma-wide) epimutations to the remainin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f7c23b1af804d1c794895a39ce36e74
https://pubmed.ncbi.nlm.nih.gov/22843497
https://pubmed.ncbi.nlm.nih.gov/22843497
Autor:
U. Zechner, Nady El Hajj, Melanie Aretz, Harald Lehnen, Eberhard Schneider, Michael Korenkov, Tobias Müller, Galyna Pliushch, Marcus Dittrich, Thomas Haaf
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 216
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2aea18bcc1314eb748df5200bab78294
https://doi.org/10.1055/s-0032-1309143
https://doi.org/10.1055/s-0032-1309143
Autor:
A. M. Müller, Nady El Hajj, Thomas Riepert, Ulrich Zechner, Danuta Galetzka, Katrin Frauenknecht, Eberhard Schneider, Galyna Pliushch, Martin Schorsch, Thomas Haaf, Wiltrud Coerdt, Alexander Puhl, Achim Tresch
Publikováno v:
Nucleic Acids Research
DNA methylation is an epigenetic modification that plays an important role in gene regulation. It can be influenced by stochastic events, environmental factors and developmental programs. However, little is known about the natural variation of gene-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a461e720e6b0adf9fa73475df9707355
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/6242
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/6242
Autor:
Yoel Shufaro, Wiltrud Coerdt, Eberhard Schneider, Achim Tresch, Larissa Seidmann, Thomas Haaf, A. M. Müller, Ulrich Zechner, Nady El Hajj, Galyna Pliushch
Publikováno v:
Molecular human reproduction. 16(9)
To study possible effects of assisted reproductive technologies (ART) on epigenetic reprogramming, we have analyzed the DNA methylation levels of differentially methylated regions (DMRs) of seven imprinted genes (H19, MEG3, LIT1, MEST, NESP55, PEG3 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c7237efb8e6b228786337ef7ba3fdd7
https://pubmed.ncbi.nlm.nih.gov/20007506
https://pubmed.ncbi.nlm.nih.gov/20007506