Einträge von Groesser, Leopold auf dem Publikationsserver

Twigg, Stephen R. F. , Hufnagel, Robert B., Miller, Kerry A., Zhou, Yan, McGowan, Simon J. , Taylor, John, Craft, Jude, Taylor, Jenny C., Santoro, Stephanie L., Huang, Taosheng, Hopkin, Robert J., Brady, Angela F., Clayton-Smith, Jill, Clericuzio, Carol L., Grange, Dorothy K., Groesser, Leopold, Hafner, Christian, Horn, Denise, Temple, I. Karen, Dobyns, William B. , Curry, Cynthia J., Jones, Marilyn C. und Wilkie, Andrew O. M. (2016) A Recurrent Mosaic Mutation in SMO , Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome. The American Journal of Human Genetics 98 (6), S. 1256-1265. Volltext nicht vorhanden.

Groesser, Leopold, Peterhof, Eva, Evert, Matthias, Landthaler, Michael, Berneburg, Mark und Hafner, Christian (2016) BRAF and RAS Mutations in Sporadic and Secondary Pyogenic Granuloma. Journal of Investigative Dermatology 136 (2), S. 481-486. Volltext nicht vorhanden.

Thomas, Anna C., Zeng, Zhiqiang, Rivière, Jean-Baptiste, O’Shaughnessy, Ryan , Al-Olabi, Lara, St.-Onge, Judith, Atherton, David J., Aubert, Hélène, Bagazgoitia, Lorea, Barbarot, Sébastien , Bourrat, Emmanuelle, Chiaverini, Christine, Chong, W. Kling, Duffourd, Yannis, Glover, Mary, Groesser, Leopold, Hadj-Rabia, Smail , Hamm, Henning, Happle, Rudolf, Mushtaq, Imran, Lacour, Jean-Philippe , Waelchli, Regula, Wobser, Marion, Vabres, Pierre , Patton, E. Elizabeth und Kinsler, Veronica A. (2016) Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis. Journal of Investigative Dermatology 136 (4), S. 770-778. Volltext nicht vorhanden.

Shen, Anne-Sophie, Peterhof, Eva, Kind, Peter, Rütten, Arno, Zelger, Bernhard, Landthaler, Michael, Berneburg, Mark, Hafner, Christian und Groesser, Leopold (2015) Activating mutations in the RAS/mitogen-activated protein kinase signaling pathway in sporadic trichoblastoma and syringocystadenoma papilliferum. Human Pathology 46 (2), S. 272-276. Volltext nicht vorhanden.

Kohl, Elisabeth, Meierhöfer, Julia, Koller, Michael, Zeman, Florian, Groesser, Leopold, Karrer, Sigrid, Hohenleutner, Ulrich, Landthaler, Michael und Hohenleutner, Silvia (2015) Fractional carbon dioxide laser resurfacing of rhytides and photoaged skin – A prospective clinical study on patient expectation and satisfaction. Lasers in Surgery and Medicine 47 (2), S. 111-119. Volltext nicht vorhanden.

Hassel, Jessica C., Groesser, Leopold, Herschberger, Eva, Weichert, Wilko und Hafner, Christian (2015) RAS Mutations in Benign Epithelial Tumors Associated with BRAF Inhibitor Treatment of Melanoma. Journal of Investigative Dermatology 135 (2), S. 636-639. Volltext nicht vorhanden.

Georgieva, Ivelina A., Mauerer, Andreas, Groesser, Leopold, Herschberger, Eva, Aslanidis, Charalampos, Dietmaier, Wolfgang, Landthaler, Michael und Hafner, Christian (2014) Low Incidence of Oncogenic EGFR, HRAS, and KRAS Mutations in Seborrheic Keratosis. The American Journal of Dermatopathology 36 (8), S. 635-642. Volltext nicht vorhanden.

Schrama, David, Groesser, Leopold, Ugurel, Selma, Hafner, Christian, Pastrana, Diana V., Buck, Christopher B. , Cerroni, Lorenzo, Theiler, Anna und Becker, Jürgen C. (2014) Presence of Human Polyomavirus 6 in Mutation-Specific BRAF Inhibitor–Induced Epithelial Proliferations. JAMA Dermatology 150 (11), S. 1180. Volltext nicht vorhanden.

Groesser, Leopold, Herschberger, Eva, Sagrera, Ana, Shwayder, Tor, Flux, Katharina, Ehmann, Laura, Wollenberg, Andreas, Torrelo, Antonio, Bagazgoitia, Lorea, Diaz-Ley, Blanca, Tinschert, Sigrid, Oschlies, Ilske, Singer, Sebastian, Mickler, Marion, Toll, Agusti, Landthaler, Michael, Real, Francisco X. und Hafner, Christian (2013) Phacomatosis Pigmentokeratotica Is Caused by a Postzygotic HRAS Mutation in a Multipotent Progenitor Cell. Journal of Investigative Dermatology 133 (8), S. 1998-2003. Volltext nicht vorhanden.

Groesser, Leopold, Herschberger, Eva, Ruetten, Arno, Ruivenkamp, Claudia, Lopriore, Enrico, Zutt, Markus, Langmann, Thomas, Singer, Sebastian, Klingseisen, Laura, Schneider-Brachert, Wulf, Toll, Agusti, Real, Francisco X, Landthaler, Michael und Hafner, Christian (2012) Postzygotic HRAS and KRAS mutations cause nevus sebaceous and Schimmelpenning syndrome. Nature Genetics 44 (7), S. 783-787. Volltext nicht vorhanden.