Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nadine Wittstruck"'
Autor:
Maja C. Stöber, Rocío Chamorro González, Lotte Brückner, Thomas Conrad, Nadine Wittstruck, Annabell Szymansky, Angelika Eggert, Johannes H. Schulte, Richard P. Koche, Anton G. Henssen, Roland F. Schwarz, Kerstin Haase
Publikováno v:
Cell Reports, Vol 43, Iss 9, Pp 114711- (2024)
Summary: Neuroblastoma exhibits significant inter- and intra-tumor genetic heterogeneity and varying clinical outcomes. Extrachromosomal DNAs (ecDNAs) may drive this heterogeneity by independently segregating during cell division, leading to rapid on
Externí odkaz:
https://doaj.org/article/ab3a75bbde6043eaa8410044fc79d0e5
Autor:
Maja C Stöber, Rocío Chamorro González, Lotte Brückner, Thomas Conrad, Nadine Wittstruck, Annabell Szymansky, Angelika Eggert, Johannes H Schulte, Richard P Koche, Anton G Henssen, Roland F Schwarz, Kerstin Haase
Neuroblastoma is characterised by extensive inter- and intra-tumour genetic heterogeneity and varying clinical outcomes. One possible driver for this heterogeneity are extrachromosomal DNAs (ecDNA), which segregate independently to the daughter cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ae7ba7091ce1e02b5e326aabd499e03
https://doi.org/10.1101/2023.01.21.525014
https://doi.org/10.1101/2023.01.21.525014
Autor:
Yi Bei, Luca Bramé, Marieluise Kirchner, Raphaela Fritsche-Guenther, Sevrine Kunz, Animesh Bhattacharya, Julia Köppke, Jutta Proba, Nadine Wittstruck, Olga A. Sidorova, Rocío Chamorro González, Heathcliff Dorado Garcia, Lotte Brückner, Robin Xu, Mădălina Giurgiu, Elias Rodriguez-Fos, Richard Koche, Clemens Schmitt, Johannes H. Schulte, Angelika Eggert, Kerstin Haase, Jennifer Kirwan, Anja I.H. Hagemann, Philipp Mertins, Jan R. Dörr, Anton G. Henssen
SummaryAlthough DNA amplifications in cancers frequently harbor passenger genes alongside oncogenes, the functional consequence of such co-amplifications and their impact for therapy remains ill-defined. We discovered that passenger co-amplifications
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23cec1b64f1a5767ede4a61553464d2b
https://doi.org/10.1101/2022.09.08.506647
https://doi.org/10.1101/2022.09.08.506647
Autor:
Gerhard Fürstenberger, Katja Martina Eckl, Heiko Traupe, Peter Krieg, Wolfgang Küster, Hans Christian Hennies, Françoise André, Nadine Wittstruck
Publikováno v:
Human mutation. 26(4)
Autosomal-recessive congenital ichthyosis (ARCI) is a clinically and genetically heterogeneous group of severe hereditary keratinization disorders characterized by intense scaling of the whole integument, and differences in color and shape. It is oft
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cd84645377a8f196a820bc438151be4
https://pubmed.ncbi.nlm.nih.gov/16116617
https://pubmed.ncbi.nlm.nih.gov/16116617