Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Tamara Hansmann"'
Autor:
Claudia Spix, Danuta Galetzka, Thomas Haaf, Brigitte Schneider-Rätzke, Nicolai Kohlschmidt, Marco Ludwig, O. Bartsch, Eva Weis, Vera Beyer, Nady El Hajj, Benjamin Irmscher, Tamara Hansmann, U. Zechner
Publikováno v:
Epigenetics
We describe monozygotic twins discordant for childhood leukemia and secondary thyroid carcinoma. We used bisulfite pyrosequencing to compare the constitutive promoter methylation of BRCA1 and several other tumor suppressor genes in primary fibroblast
Autor:
Thomas Haaf, Julia Heinzmann, Christine Wrenzycki, Tamara Hansmann, Doris Herrmann, Ulrich Zechner, Heiner Niemann
Publikováno v:
Molecular Reproduction and Development. 78:188-201
Assisted reproductive technologies are associated with an increased incidence of epigenetic aberrations, specifically in imprinted genes. Here, we used the bovine oocyte as a model to determine putative epigenetic mutations at three imprinted gene lo
Publikováno v:
Biosensors and Bioelectronics. 24:2119-2124
In this paper, the inhibition effect of aflatoxin B1 on different species of cholinesterases was investigated to unravel action mechanism. The inhibition curves of several cholinesterase mutants (obtained by spectrophotometric measurements of enzyme
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
Autor:
Christian Weissgerber, Ulrich Baulain, Thomas Haaf, Wilfried A. Kues, Julia Heinzmann, Brigitte Barg-Kues, Mike Diederich, Richard Reinhard, Heiner Niemann, Tamara Hansmann, Doris Herrmann, Patrick Aldag
Publikováno v:
Reproduction (Cambridge, England). 144(3)
The developmental capacity of oocytes from prepubertal cattle is reduced compared with their adult counterparts, and epigenetic mechanisms are thought to be involved herein. Here, we analyzed DNA methylation in three developmentally important, nonimp
Autor:
Thomas Haaf, Angelika Daser, Julia Heinzmann, Tom Trapphoff, Heiner Niemann, Ursula Eichenlaub-Ritter, Nady El Hajj, Tamara Hansmann, Kurt Reifenberg, Ulrich Zechner, Andreas May, Juliane Kuhtz, Matthias Linke
To detect rare epigenetic effects associated with assisted reproduction, it is necessary to monitor methylation patterns of developmentally important genes in a few germ cells and individual embryos. Bisulfite treatment degrades DNA and reduces its c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::986a096a53dd484af014c1b9a6031275
https://pub.uni-bielefeld.de/record/2440704
https://pub.uni-bielefeld.de/record/2440704
Autor:
Tamara Hansmann, Julia Heinzmann, Christine Wrenzycki, Heiner Niemann, U. Zechner, Thomas Haaf
Correct imprinting is crucial for normal fetal and placental development in mammals. Experimental evidence in animal models and epidemiological studies in humans suggest that assisted reproductive technologies (ARTs) can interfere with imprinted gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb30a0ae4356d3957bd8bea5559ebf90
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-199051
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-199051
Autor:
Christine Wrenzycki, Ulrich Zechner, Julia Heinzmann, Heiner Niemann, Thomas Haaf, Tamara Hansmann
Publikováno v:
Reproduction, Fertility and Development. 23:228
In cattle, in vitro maturation (IVM) of oocytes is an integral part of assisted reproduction technology. However, only 30% of in vitro matured bovine oocytes develop to the blastocyst stage after fertilization (compared with 60% for in vivo matured o
Autor:
Hansmann, Tamara, Pliushch, Galyna, Leubner, Monika, Kroll, Patricia, Endt, Daniela, Gehrig, Andrea, Preisler-Adams, Sabine, Wieacker, Peter, Haaf, Thomas
Publikováno v:
Human Molecular Genetics; Nov2012, Vol. 21 Issue 21, p4669-4679, 11p