Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Laura van Diepen"'
Publikováno v:
Molecular Microbiology. 106:876-890
Expression of phospholipid biosynthetic genes in yeast requires activator protein Ino2 which can bind to the UAS element inositol/choline-responsive element (ICRE) and trigger activation of target genes, using two separate transcriptional activation
Autor:
Harry Scherthan, Lars Riff Jensen, Andreas W. Kuss, Tim Kacprowski, Laura van Diepen, Robert Weissmann, Matthias Port, Michel Peper, Jennifer Esche
Publikováno v:
Health Physics
Ionizing radiation is known to induce genomic lesions, such as DNA double strand breaks, whose repair can lead to mutations that can modulate cellular and organismal fate. Soon after radiation exposure, cells induce transcriptional changes and altera
Autor:
Oliver von Bohlen und Halbach, Laura van Diepen, Jonathan Bertram, Jörg P. Pfannmöller, Dusan Bartsch, Bianca Hartmann, Leif Koschützke, Martin Lotze, Jennifer Esche, Andreas W. Kuss
Publikováno v:
Cell and Tissue Research. 366:1-11
SrGAP3 belongs to the family of Rho GTPase proteins. These proteins are thought to play essential roles in development and in the plasticity of the nervous system. SrGAP3-deficient mice have recently been created and approximately 10 % of these mice
Autor:
Ulf Diekmann, Malte Sgodda, Dirk Hoffmann, Axel Schambach, Nicolas M.B. Huber, Falk F. R. Buettner, Erdmann Rapp, Robert Weiβmann, Samanta Cajic, Christina T. Thiesler, Doris Steinemann, Laura van Diepen, Tobias Cantz, René Hennig, Christian Körner, Astrid Oberbeck, Christian Thiel, Andreas W. Kuss, Udo Reichl
Publikováno v:
Molecular & Cellular Proteomics : MCP
Molecular and Cellular Proteomics
Molecular and Cellular Proteomics
PMM2-CDG, formerly known as congenital disorder of glycosylation-Ia (CDG-Ia), is caused by mutations in the gene encoding phosphomannomutase 2 (PMM2). This disease is the most frequent form of inherited CDG-diseases affecting protein N-glycosylation
Autor:
Lars R. Jensen, Rita Gerardy-Schahn, Laura van Diepen, Axel Schambach, Oliver von Bohlen und Halbach, Andreas W. Kuss, Dirk Hoffmann, Doris Steinemann, Falk F. R. Buettner, Viola von Bohlen und Halbach, Christina T. Thiesler, Orly Elpeleg, Simon Edvardson
Publikováno v:
European journal of human genetics : EJHG. 26(12)
ST3GAL3 encodes the Golgi enzyme beta-galactoside-alpha-2,3-sialyltransferase-III that in humans forms, among others, the sialyl Lewis a (sLe(a)) epitope on proteins. Functionally deleterious variants in this gene were previously identified in patien
Publikováno v:
Molecular microbiology. 106(6)
Expression of phospholipid biosynthetic genes in yeast requires activator protein Ino2 which can bind to the UAS element inositol/choline-responsive element (ICRE) and trigger activation of target genes, using two separate transcriptional activation
Autor:
Robert Weißmann, Robert Zweigerdt, Laura van Diepen, Sarah A. Konze, Andreas W. Kuss, Falk F. R. Buettner, Andreas Pich, Anke Schröder, Hanna Möller, Ruth Olmer
The envisioned clinical and industrial use of human pluripotent stem cells and their derivatives has given major momentum to the establishment of suspension culture protocols that enable the mass production of cells. Understanding molecular changes a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3071fd4a6cea56eb13783222893f2a05
https://europepmc.org/articles/PMC3977196/
https://europepmc.org/articles/PMC3977196/