Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Brigitte Schneider-Rätzke"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f123e0d23c9e16cbc4e7ac0419afb1ed
http://europepmc.org/articles/PMC3329502
http://europepmc.org/articles/PMC3329502
Autor:
Julia K. Bickmann, Jürgen J. Wenzel, Heidi Rossmann, Karl J. Lackner, Carolin Neukirch, Thomas J. Musholt, Christian Fottner, Peter Lohse, Matthias M. Weber, Timo Minnemann, Stefan Neuwirth, Brigitte Schneider-Rätzke
Publikováno v:
Clinical chemistry. 55(7)
Background: Reliable PCR amplification of DNA fragments is the prerequisite for most genetic assays. We investigated the impact of G-quadruplex– or i-motif–like sequences on the reliability of PCR-based genetic analyses. Methods: We found the seq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f72116e61ab2d0271797844e0045d54
https://pubmed.ncbi.nlm.nih.gov/19406917
https://pubmed.ncbi.nlm.nih.gov/19406917
Autor:
Ruxandra Farcas, Thomas Haaf, Oliver Bartsch, Gabriele Frey-Mahn, Brigitte Schneider-Rätzke, Ulrike Napiontek, Uwe Wolfrum, Nicolai Kohlschmidt, Vera Beyer, Bärbel Grossmann, Annerose Keilmann, Tina Märker, Katharina Bauss, Eberhard Schneider, Angelika Daser, Ulrich Zechner
Publikováno v:
Human molecular genetics. 18(4)
A homozygous reciprocal translocation, 46,XY,t(10;11),t(10;11), was detected in a boy with non-syndromic congenital sensorineural hearing impairment. Both parents and their four other children were heterozygous translocation carriers, 46,XX,t(10;11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e38b7c6ff760b1b2a2907e1d777bc6c
https://pubmed.ncbi.nlm.nih.gov/19028668
https://pubmed.ncbi.nlm.nih.gov/19028668
Autor:
Bernd Reitter, Brigitte Schneider-Rätzke, Eberhard Merz, Hans H. Goebel, Jouni Vesa, Timm O. Goecke
Publikováno v:
Braindevelopment. 17(2)
Based on two unrelated index patients afflicted with INCL, fetal chorion tissues were studied from subsequent pregnancies of the two respective mothers resulting in the prenatal diagnosis of INCL in two of the three pregnancies. Documentation of INCL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16cf3bc86d268a6053eefb3b09513ad1
https://pubmed.ncbi.nlm.nih.gov/7625554
https://pubmed.ncbi.nlm.nih.gov/7625554
Autor:
Manuela Marron, Danuta Galetzka, Claudia-Martina Messow, Nicolai Kohlschmitd, Claudia Spix, Thomas Haaf, Anja Victor, Brigitte Schneider-Rätzke, Eva Weis
Publikováno v:
Cancer Research. 72:5504-5504
Treatment of the primary neoplasm with radiotherapy or chemotherapy is an established risk factor for second neoplasms (SNs) after childhood cancer. As only a small percentage of the treated children suffer from SN, other shared risk factors must be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e16738a345c02877796d074a5f638f96
https://doi.org/10.1158/1538-7445.am2012-5504
https://doi.org/10.1158/1538-7445.am2012-5504