Browse by ["viewname_eprint_publisher" not defined]

B

Bygum, Anette and Fagerberg, Christina R. and Clemmensen, Ole J. and Fiebig, Britta and Hafner, Christian (2011) Systemic epidermal nevus with involvement of the oral mucosa due to FGFR3 mutation. BMC MEDICAL GENETICS, 12: 79. ISSN 1471-2350

D

Dirscherl, Konstantin and Karlstetter, Marcus and Ebert, Stefanie and Kraus, Dominik and Hlawatsch, Julia and Walczak, Yana and Moehle, Christoph and Fuchshofer, Rudolf and Langmann, Thomas (2012) Erratum to: Luteolin triggers global changes in the microglial transcriptome leading to a unique anti-inflammatory and neuroprotective phenotype (vol 7, pg 3, 2010). JOURNAL OF NEUROINFLAMMATION, 9: 118. ISSN 1742-2094

E

Engel, Christoph and Rhiem, Kerstin and Hahnen, Eric and Loibl, Sibylle and Weber, Karsten E. and Seiler, Sabine and Zachariae, Silke and Hauke, Jan and Wappenschmidt, Barbara and Waha, Anke and Bluemcke, Britta and Kiechle, Marion and Meindl, Alfons and Niederacher, Dieter and Bartram, Claus R. and Speiser, Dorothee and Schlegelberger, Brigitte and Arnold, Norbert and Wieacker, Peter and Leinert, Elena and Gehrig, Andrea and Briest, Susanne and Kast, Karin and Riess, Olaf and Emons, Guenter and Weber, Bernhard H. F. and Engel, Jutta and Schmutzler, Rita K. (2018) Prevalence of pathogenic BRCA1/2 germline mutations among 802 women with unilateral triple-negative breast cancer without family cancer history. BMC CANCER, 18: 265. ISSN 1471-2407

G

Girisha, Katta Mohan and Bidchol, Abdul Mueed and Graul-Neumann, Luitgard and Gupta, Ashish and Hehr, Ute and Lessel, Davor and Nader, Sean and Shah, Hitesh and Wickert, Julia and Kutsche, Kerstin (2016) Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients. BMC MEDICAL GENETICS, 17: 27. ISSN 1471-2350

Grassmann, Felix and Bergholz, Richard and Maendl, Julia and Jaegle, Herbert and Ruether, Klaus and Weber, Bernhard H. F. (2015) Common synonymous variants in ABCA4 are protective for chloroquine induced maculopathy (toxic maculopathy). BMC OPHTHALMOLOGY, 15: 18. ISSN 1471-2415

Grassmann, Felix and Kiel, Christina and Zimmermann, Martina E. and Gorski, Mathias and Grassmann, Veronika and Stark, Klaus and Heid, Iris M. and Weber, Bernhard H. F. (2017) Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits. GENOME MEDICINE, 9: 29. ISSN 1756-994X

Grunewald, Thomas G. P. and Herbst, Saskia M. and Heinze, Juergen and Burdach, Stefan (2011) Understanding tumor heterogeneity as functional compartments - superorganisms revisited. JOURNAL OF TRANSLATIONAL MEDICINE, 9: 79. ISSN 1479-5876

K

Karlstetter, Marcus and Lippe, Elena and Walczak, Yana and Moehle, Christoph and Aslanidis, Alexander and Mirza, Myriam and Langmann, Thomas (2011) Curcumin is a potent modulator of microglial gene expression and migration. JOURNAL OF NEUROINFLAMMATION, 8: 125. ISSN 1742-2094

M

Micklisch, Sven and Lin, Yuchen and Jacob, Saskia and Karlstetter, Marcus and Dannhausen, Katharina and Dasari, Prasad and von der Heide, Monika and Dahse, Hans-Martin and Schmoelz, Lisa and Grassmann, Felix and Alene, Medhanie and Fauser, Sascha and Neumann, Harald and Lorkowski, Stefan and Pauly, Diana and Weber, Bernhard H. and Joussen, Antonia M. and Langmann, Thomas and Zipfel, Peter F. and Skerka, Christine (2017) Age-related macular degeneration associated polymorphism rs10490924 in ARMS2 results in deficiency of a complement activator. JOURNAL OF NEUROINFLAMMATION, 14: 4. ISSN 1742-2094

Milenkovic, Vladimir M. and Brockmann, Marisa and Stoehr, Heidi and Weber, Bernhard H. F. and Strauss, Olaf (2010) Evolution and functional divergence of the anoctamin family of membrane proteins. BMC EVOLUTIONARY BIOLOGY, 10: 319. ISSN 1471-2148

V

Voigt, Claudia and Megarbane, Andre and Neveling, Kornelia and Czeschik, Johanna Christina and Albrecht, Beate and Callewaert, Bert and von Deimling, Florian and Hehr, Andreas and Smeland, Marie Falkenberg and Konig, Rainer and Kuechler, Alma and Marcelis, Carlo and Puiu, Maria and Reardon, Willie and Stensland, Hilde Monica Frostad Riise and Schweiger, Bernd and Steehouwer, Marloes and Teller, Christopher and Martin, Marcel and Rahmann, Sven and Hehr, Ute and Brunner, Han G. and Ludecke, Hermann-Josef and Wieczorek, Dagmar (2013) Oto-facial syndrome and esophageal atresia, intellectual disability and zygomatic anomalies - expanding the phenotypes associated with EFTUD2 mutations. ORPHANET JOURNAL OF RARE DISEASES, 8: 110. ISSN 1750-1172