Hakutulokset - Hahnen, Eric

Peroxisome Proliferator-Activated Receptors (PPARs) as Potential Inducers of Antineoplastic Effects in CNS Tumors Tekijä Tatenhorst, Lars, Hahnen, Eric, Heneka, Michael T.

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A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy Tekijä Lorson, Christian L., Hahnen, Eric, Androphy, Elliot J., Wirth, Brunhilde

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Germline Mutations in Triple-Negative Breast Cancer Tekijä Hahnen, Eric, Hauke, Jan, Engel, Christoph, Neidhardt, Guido, Rhiem, Kerstin, Schmutzler, Rita K.

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Performance of in silico prediction tools for the classification of rare BRCA1/2 missense variants in clinical diagnostics Tekijä Ernst, Corinna, Hahnen, Eric, Engel, Christoph, Nothnagel, Michael, Weber, Jonas, Schmutzler, Rita K., Hauke, Jan

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Non-small cell neuroendocrine carcinoma of the ovary in a BRCA2-germline mutation carrier: A case report and brief review of the literature Tekijä Herold, Natalie, Wappenschmidt, Barbara, Markiefka, Birgid, Keupp, Katharina, Kröber, Sandra, Hahnen, Eric, Schmutzler, Rita, Rhiem, Kerstin

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PPAR Gamma Activators: Off-Target Against Glioma Cell Migration and Brain Invasion Tekijä Seufert, Sebastian, Coras, Roland, Tränkle, Christian, Zlotos, Darius P., Blümcke, Ingmar, Tatenhorst, Lars, Heneka, Michael T., Hahnen, Eric

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Survival motor neuron gene 2 silencing by DNA methylation correlates with spinal muscular atrophy disease severity and can be bypassed by histone deacetylase inhibition Tekijä Hauke, Jan, Riessland, Markus, Lunke, Sebastian, Eyüpoglu, Ilker Y., Blümcke, Ingmar, El-Osta, Assam, Wirth, Brunhilde, Hahnen, Eric

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Analysis of 30 Putative BRCA1 Splicing Mutations in Hereditary Breast and Ovarian Cancer Families Identifies Exonic Splice Site Mutations That Escape In Silico Prediction Tekijä Wappenschmidt, Barbara, Becker, Alexandra A., Hauke, Jan, Weber, Ute, Engert, Stefanie, Köhler, Juliane, Kast, Karin, Arnold, Norbert, Rhiem, Kerstin, Hahnen, Eric, Meindl, Alfons, Schmutzler, Rita K.

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Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia‐like phenotype, and no chromosome fragility Tekijä Keupp, Katharina, Hampp, Stephanie, Hübbel, Annette, Maringa, Monika, Kostezka, Sarah, Rhiem, Kerstin, Waha, Anke, Wappenschmidt, Barbara, Pujol, Roser, Surrallés, Jordi, Schmutzler, Rita K., Wiesmüller, Lisa, Hahnen, Eric

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Spontaneous In Vitro Transformation of Adult Neural Precursors into Stem‐Like Cancer Cells Tekijä Siebzehnrubl, Florian A., Jeske, Ina, Müller, Dorit, Buslei, Rolf, Coras, Roland, Hahnen, Eric, Huttner, Hagen B., Corbeil, Denis, Kaesbauer, Johanna, Appl, Thomas, Von Hörsten, Stephan, Blümcke, Ingmar

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Deep sequencing reveals increased DNA methylation in chronic rat epilepsy Tekijä Kobow, Katja, Kaspi, Antony, Harikrishnan, K. N., Kiese, Katharina, Ziemann, Mark, Khurana, Ishant, Fritzsche, Ina, Hauke, Jan, Hahnen, Eric, Coras, Roland, Mühlebner, Angelika, El-Osta, Assam, Blümcke, Ingmar

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RAD51C deletion screening identifies a recurrent gross deletion in breast cancer and ovarian cancer families Tekijä Schnurbein, Gioia, Hauke, Jan, Wappenschmidt, Barbara, Weber-Lassalle, Nana, Engert, Stefanie, Hellebrand, Heide, Garbes, Lutz, Becker, Alexandra, Neidhardt, Guido, Rhiem, Kerstin, Meindl, Alfons, Schmutzler, Rita K, Hahnen, Eric

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Performance of In Silico Prediction Tools for the Detection of Germline Copy Number Variations in Cancer Predisposition Genes in 4208 Female Index Patients with Familial Breast and... Tekijä Lepkes, Louisa, Kayali, Mohamad, Blümcke, Britta, Weber, Jonas, Suszynska, Malwina, Schmidt, Sandra, Borde, Julika, Klonowska, Katarzyna, Wappenschmidt, Barbara, Hauke, Jan, Kozlowski, Piotr, Schmutzler, Rita K., Hahnen, Eric, Ernst, Corinna

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A Novel Large In-Frame Deletion within the CACNA1F Gene Associates with a Cone-Rod Dystrophy 3-Like Phenotype Tekijä Hauke, Jan, Schild, Andrea, Neugebauer, Antje, Lappa, Alexandra, Fricke, Julia, Fauser, Sascha, Rösler, Stefanie, Pannes, Andrea, Zarrinnam, Dirk, Altmüller, Janine, Motameny, Susanne, Nürnberg, Gudrun, Nürnberg, Peter, Hahnen, Eric, Beck, Bodo B.

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Clonal Hematopoiesis–Associated Gene Mutations in a Clinical Cohort of 448 Patients With Ovarian Cancer Tekijä Weber-Lassalle, Konstantin, Ernst, Corinna, Reuss, Alexander, Möllenhoff, Kathrin, Baumann, Klaus, Jackisch, Christian, Hauke, Jan, Dietrich, Dimo, Borde, Julika, Park-Simon, Tjoung-Won, Hanker, Lars, Prieske, Katharina, Schmidt, Sandra, Weber-Lassalle, Nana, Pohl-Rescigno, Esther, Kommoss, Stefan, Marmé, Frederik, Heitz, Florian, Stingl, Julia C, Schmutzler, Rita K, Harter, Philipp, Hahnen, Eric

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Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers Tekijä Borde, Julika, Laitman, Yael, Blümcke, Britta, Niederacher, Dieter, Weber-Lassalle, Konstantin, Sutter, Christian, Rump, Andreas, Arnold, Norbert, Wang-Gohrke, Shan, Horváth, Judit, Gehrig, Andrea, Schmidt, Gunnar, Dutrannoy, Véronique, Ramser, Juliane, Hentschel, Julia, Meindl, Alfons, Schroeder, Christopher, Wappenschmidt, Barbara, Engel, Christoph, Kuchenbaecker, Karoline, Schmutzler, Rita K., Friedman, Eitan, Hahnen, Eric, Ernst, Corinna

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Consensus Recommendations of the German Consortium for Hereditary Breast and Ovarian Cancer Tekijä Rhiem, Kerstin, Auber, Bernd, Briest, Susanne, Dikow, Nicola, Ditsch, Nina, Dragicevic, Neda, Grill, Sabine, Hahnen, Eric, Horvath, Judit, Jaeger, Bernadette, Kast, Karin, Kiechle, Marion, Leinert, Elena, Morlot, Susanne, Püsken, Michael, Schäfer, Dieter, Schott, Sarah, Schroeder, Christopher, Siebers-Renelt, Ulrike, Solbach, Christine, Weber-Lassalle, Nana, Witzel, Isabell, Zeder-Göß, Christine, Schmutzler, Rita K.

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Association of Germline Variant Status With Therapy Response in High-risk Early-Stage Breast Cancer: A Secondary Analysis of the GeparOcto Randomized Clinical Trial Tekijä Pohl-Rescigno, Esther, Hauke, Jan, Loibl, Sibylle, Möbus, Volker, Denkert, Carsten, Fasching, Peter A., Kayali, Mohamad, Ernst, Corinna, Weber-Lassalle, Nana, Hanusch, Claus, Tesch, Hans, Müller, Volkmar, Altmüller, Janine, Thiele, Holger, Untch, Michael, Lübbe, Kristina, Nürnberg, Peter, Rhiem, Kerstin, Furlanetto, Jenny, Lederer, Bianca, Jackisch, Christian, Nekljudova, Valentina, Schmutzler, Rita K., Schneeweiss, Andreas, Hahnen, Eric

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Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883) Tekijä Hauke, Jan, Harter, Philipp, Ernst, Corinna, Burges, Alexander, Schmidt, Sandra, Reuss, Alexander, Borde, Julika, De Gregorio, Nikolaus, Dietrich, Dimo, El-Balat, Ahmed, Kayali, Mohamad, Gevensleben, Heidrun, Hilpert, Felix, Altmüller, Janine, Heimbach, André, Meier, Werner, Schoemig-Markiefka, Birgid, Thiele, Holger, Kimmig, Rainer, Nürnberg, Peter, Kast, Karin, Richters, Lisa, Sehouli, Jalid, Schmutzler, Rita K, Hahnen, Eric

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Prevalence of Cancer Predisposition Germline Variants in Male Breast Cancer Patients: Results of the German Consortium for Hereditary Breast and Ovarian Cancer Tekijä Rolfes, Muriel, Borde, Julika, Möllenhoff, Kathrin, Kayali, Mohamad, Ernst, Corinna, Gehrig, Andrea, Sutter, Christian, Ramser, Juliane, Niederacher, Dieter, Horváth, Judit, Arnold, Norbert, Meindl, Alfons, Auber, Bernd, Rump, Andreas, Wang-Gohrke, Shan, Ritter, Julia, Hentschel, Julia, Thiele, Holger, Altmüller, Janine, Nürnberg, Peter, Rhiem, Kerstin, Engel, Christoph, Wappenschmidt, Barbara, Schmutzler, Rita K., Hahnen, Eric, Hauke, Jan

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