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

Por Schubert, Stephanie, Schmidtke, Jörg
Publicado em 2010

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

Por Palacios, Manuel. A., Lacy, Michael M., Schubert, Stephanie M., Manesse, Mael, Walt, David R.
Publicado em 2013

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

Por Kido, Tatsuo, Schubert, Stephanie, Hatakeyama, Shingo, Ohyama, Chikara, Schmidtke, Jörg, Lau, Yun-Fai Chris
Publicado em 2014

The missing heritability of familial colorectal cancer

Por Schubert, Stephanie A, Morreau, Hans, de Miranda, Noel F C C, van Wezel, Tom
Publicado no Mutagenesis (2020)

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

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

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

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

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

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

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

Por Schubert, Stephanie M., Arendt, Lisa M., Zhou, Wenhui, Baig, Shazia, Walter, Stephanie R., Buchsbaum, Rachel J., Kuperwasser, Charlotte, Walt, David R.
Publicado no Sci Rep (2015)

Reduction of Spermatogenesis but Not Fertility in Creb3l4-Deficient Mice

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

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

Por van Luttikhuizen, Jana Lisa, Bublitz, Janin, Schubert, Stephanie, Schmidt, Gunnar, Hofmann, Winfried, Morlot, Susanne, Buurman, Reena, Auber, Bernd, Schlegelberger, Brigitte, Steinemann, Doris
Publicado no Mol Genet Genomic Med (2019)

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

Por 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
Publicado no Genes Cancer (2017)

Digenic inheritance of MSH6 and MUTYH variants in familial colorectal cancer

Por 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
Publicado no Genes Chromosomes Cancer (2020)

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

Por 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.
Publicado no Pharmaceutics (2020)

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

Por 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
Publicado no Breast Cancer Res (2018)

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

Por 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.
Publicado no J Nanobiotechnology (2020)

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

Por 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
Publicado no JCI Insight (2020)

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

Por 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
Publicado no Br J Cancer (2017)

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

Por 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
Publicado no Br J Cancer (2018)