Transgenic Mouse Studies to Understand the Regulation, Expression and Function of the Testis-Specific Protein Y-Encoded (TSPY) Gene

di Schubert, Stephanie, Schmidtke, Jörg
Pubblicazione 2010

Assessing the Stochastic Intermittency of Single Quantum Dot Luminescence for Robust Quantification of Biomoleculs

di Palacios, Manuel. A., Lacy, Michael M., Schubert, Stephanie M., Manesse, Mael, Walt, David R.
Pubblicazione 2013

Expression of a Y-located human proto-oncogene TSPY in a transgenic mouse model of prostate cancer

di Kido, Tatsuo, Schubert, Stephanie, Hatakeyama, Shingo, Ohyama, Chikara, Schmidtke, Jörg, Lau, Yun-Fai Chris
Pubblicazione 2014

The missing heritability of familial colorectal cancer

di Schubert, Stephanie A, Morreau, Hans, de Miranda, Noel F C C, van Wezel, Tom
Pubblicato in Mutagenesis (2020)

Acid-Degradable Cationic Dextran Particles for the Delivery of siRNA Therapeutics

di Cohen, Jessica L., Schubert, Stephanie, Wich, Peter R., Cui, Lina, Cohen, Joel A., Mynar, Justin L., Fréchet, Jean M. J.
Pubblicazione 2011

Hspa4l-Deficient Mice Display Increased Incidence of Male Infertility and Hydronephrosis Development

di Held, Torsten , Paprotta, Ilona, Khulan, Janchiv, Hemmerlein, Bernhardt, Binder, Lutz, Wolf, Stephan, Schubert, Stephanie, Meinhardt, Andreas, Engel, Wolfgang, Adham, Ibrahim M.
Pubblicazione 2006

A Mutation in Myo15 Leads to Usher-Like Symptoms in LEW/Ztm-ci2 Rats

di Held, Nadine, Smits, Bart M. G., Gockeln, Roland, Schubert, Stephanie, Nave, Heike, Northrup, Emily, Cuppen, Edwin, Hedrich, Hans J., Wedekind, Dirk
Pubblicazione 2011

Ultra-sensitive protein detection via Single Molecule Arrays towards early stage cancer monitoring

di Schubert, Stephanie M., Arendt, Lisa M., Zhou, Wenhui, Baig, Shazia, Walter, Stephanie R., Buchsbaum, Rachel J., Kuperwasser, Charlotte, Walt, David R.
Pubblicato in Sci Rep (2015)

Reduction of Spermatogenesis but Not Fertility in Creb3l4-Deficient Mice

di Adham, Ibrahim M., Eck, Thomas J., Mierau, Kerstin, Müller, Nicole, Sallam, Mahmoud A., Paprotta, Ilona, Schubert, Stephanie, Hoyer-Fender, Sigrid, Engel, Wolfgang
Pubblicazione 2005

From a variant of unknown significance to pathogenic: Reclassification of a large novel duplication in BRCA2 by high‐throughput sequencing

di van Luttikhuizen, Jana Lisa, Bublitz, Janin, Schubert, Stephanie, Schmidt, Gunnar, Hofmann, Winfried, Morlot, Susanne, Buurman, Reena, Auber, Bernd, Schlegelberger, Brigitte, Steinemann, Doris
Pubblicato in Mol Genet Genomic Med (2019)

GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families

di Schubert, Stephanie, Ripperger, Tim, Rood, Melanie, Petkidis, Anthony, Hofmann, Winfried, Frye-Boukhriss, Hildegard, Tauscher, Marcel, Auber, Bernd, Hille-Betz, Ursula, Illig, Thomas, Schlegelberger, Brigitte, Steinemann, Doris
Pubblicato in Genes Cancer (2017)

Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer

di Schubert, Stephanie A., Ruano, Dina, Tiersma, Yvonne, Drost, Mark, de Wind, Niels, Nielsen, Maartje, van Hest, Liselotte P., Morreau, Hans, de Miranda, Noel F. C. C., van Wezel, Tom
Pubblicato in Genes Chromosomes Cancer (2020)

Formulation of Liver-Specific PLGA-DY-635 Nanoparticles Loaded with the Protein Kinase C Inhibitor Bisindolylmaleimide I

di Shkodra, Blerina, Press, Adrian T., Vollrath, Antje, Nischang, Ivo, Schubert, Stephanie, Hoeppener, Stephanie, Haas, Dorothee, Enzensperger, Christoph, Lehmann, Marc, Babic, Petra, Benecke, Kay Jovana, Traeger, Anja, Bauer, Michael, Schubert, Ulrich S.
Pubblicato in Pharmaceutics (2020)

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity

di Penkert, Judith, Schmidt, Gunnar, Hofmann, Winfried, Schubert, Stephanie, Schieck, Maximilian, Auber, Bernd, Ripperger, Tim, Hackmann, Karl, Sturm, Marc, Prokisch, Holger, Hille-Betz, Ursula, Mark, Dorothea, Illig, Thomas, Schlegelberger, Brigitte, Steinemann, Doris
Pubblicato in Breast Cancer Res (2018)

Encapsulation of the dual FLAP/mPEGS-1 inhibitor BRP-187 into acetalated dextran and PLGA nanoparticles improves its cellular bioactivity

di Shkodra, Blerina, Kretzer, Christian, Jordan, Paul M., Klemm, Paul, Koeberle, Andreas, Pretzel, David, Banoglu, Erden, Lorkowski, Stefan, Wallert, Maria, Höppener, Stephanie, Stumpf, Steffi, Vollrath, Antje, Schubert, Stephanie, Werz, Oliver, Schubert, Ulrich S.
Pubblicato in J Nanobiotechnology (2020)

Germline biallelic Mcm8 variants are associated with early-onset Lynch-like syndrome

di Golubicki, Mariano, Bonjoch, Laia, Acuña-Ochoa, José G., Díaz-Gay, Marcos, Muñoz, Jenifer, Cuatrecasas, Miriam, Ocaña, Teresa, Iseas, Soledad, Mendez, Guillermo, Cisterna, Daniel, Schubert, Stephanie A., Nielsen, Maartje, van Wezel, Tom, Goldberg, Yael, Pikarsky, Eli, Robbio, Juan, Roca, Enrique, Castells, Antoni, Balaguer, Francesc, Antelo, Marina, Castellví-Bel, Sergi
Pubblicato in JCI Insight (2020)

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

di Schubert, Stephanie A, Ruano, Dina, Elsayed, Fadwa A, Boot, Arnoud, Crobach, Stijn, Sarasqueta, Arantza Farina, Wolffenbuttel, Bruce, van der Klauw, Melanie M, Oosting, Jan, Tops, Carli M, van Eijk, Ronald, Vasen, Hans FA, Vossen, Rolf HAM, Nielsen, Maartje, Castellví-Bel, Sergi, Ruiz-Ponte, Clara, Tomlinson, Ian, Dunlop, Malcolm G, Vodicka, Pavel, Wijnen, Juul T, Hes, Frederik J, Morreau, Hans, de Miranda, Noel FCC, Sijmons, Rolf H, van Wezel, Tom
Pubblicato in Br J Cancer (2017)

Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia

di Schubert, Stephanie A, Ruano, Dina, Elsayed, Fadwa A, Boot, Arnoud, Crobach, Stijn, Sarasqueta, Arantza Farina, Wolffenbuttel, Bruce, van der Klauw, Melanie M, Oosting, Jan, Tops, Carli M, van Eijk, Ronald, Vasen, Hans FA, Vossen, Rolf HAM, Nielsen, Maartje, Castellví-Bel, Sergi, Ruiz-Ponte, Clara, Tomlinson, Ian, Dunlop, Malcolm G, Vodicka, Pavel, Wijnen, Juul T, Hes, Frederik J, Morreau, Hans, de Miranda, Noel FCC, Sijmons, Rolf H, van Wezel, Tom
Pubblicato in Br J Cancer (2018)