Search Results - Uebe, Steffen

Identifikation und Charakterisierung neuer genetischer Risikofaktoren für komplexe Erkrankungen

by Uebe, Steffen

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Tumor microenvironment‐dependent epigenetic imprinting in the vasculature predicts colon cancer outcome

by Naschberger, Elisabeth, Fuchs, Maximilian, Dickel, Nicholas, Kunz, Meik, Popp, Bernt, Anchang, Charles Gwellem, Demmler, Richard, Lyu, Yanmin, Uebe, Steffen, Ekici, Arif Bülent, Geppert, Carol Immanuel, Hartmann, Arndt, Flierl, Christian, Petter, Katja, Gass, Tobias, Völkl, Simon, Scharl, Michael, Ramming, Andreas, Günther, Claudia, Merkel, Susanne, Schellerer, Vera Simone, Stürzl, Michael

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Network- and systems-based re-engineering of dendritic cells with non-coding RNAs for cancer immunotherapy

by Lai, Xin, Dreyer, Florian S., Cantone, Martina, Eberhardt, Martin, Gerer, Kerstin F., Jaitly, Tanushree, Uebe, Steffen, Lischer, Christopher, Ekici, Arif, Wittmann, Jürgen, Jäck, Hans-Martin 1955-, Schaft, Niels, Dörrie, Jan, Vera, Julio

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Integrative bioinformatics analysis characterizing the role of EDC3 in mRNA decay and its association to intellectual disability

by Scheller, Ute, Pfisterer, Kathrin, Uebe, Steffen, Ekici, Arif B., Reis, André 1960-, Jamra, Rami, Ferrazzi, Fulvia

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High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder

by Grünblatt, Edna, Oneda, Beatrice, Ekici, Arif B., Ball, Juliane, Geissler, Julia, Uebe, Steffen, Romanos, Marcel 1975-, Rauch, Anita, Walitza, Susanne

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Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria

by Hoyer, Juliane, Vasileiou, Georgia, Uebe, Steffen, Wunderle, Marius, Kraus, Cornelia, Fasching, Peter A., Thiel, Christian T., Hartmann, Arndt, Beckmann, Matthias W., Lux, Michael P., Reis, André

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DNA methylation mediates genotype and smoking interaction in the development of anti-citrullinated peptide antibody-positive rheumatoid arthritis

by Meng, Weida, Zhu, Zaihua, Jiang, Xia, Too, Chun Lai, Uebe, Steffen, Jagodic, Maja, Kockum, Ingrid, Murad, Shahnaz, Ferrucci, Luigi, Alfredsson, Lars, Zou, Hejian, Klareskog, Lars, Feinberg, Andrew P., Ekström, Tomas J., Padyukov, Leonid, Liu, Yun

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Mutations in DCPS and EDC3 in autosomal recessive intellectual disability indicate a crucial role for mRNA decapping in neurodevelopment

by Ahmed, Iltaf, Buchert, Rebecca, Zhou, Mi, Jiao, Xinfu, Mittal, Kirti, Sheikh, Taimoor I., Scheller, Ute, Vasli, Nasim, Rafiq, Muhammad Arshad, Brohi, M. Qasim, Mikhailov, Anna, Ayaz, Muhammad, Bhatti, Attya, Sticht, Heinrich, Nasr, Tanveer, Carter, Melissa T., Uebe, Steffen, Reis, Andre, Ayub, Muhammad, John, Peter, Kiledjian, Megerditch, Vincent, John B., Jamra, Rami Abou

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Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma

by Mauri, Lucia, Uebe, Steffen, Sticht, Heinrich, Vossmerbaeumer, Urs, Weisschuh, Nicole, Manfredini, Emanuela, Maselli, Edoardo, Patrosso, Mariacristina, Weinreb, Robert N., Penco, Silvana, Reis, Andre, Pasutto, Francesca

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PTPN22 is associated with susceptibility to psoriatic arthritis but not psoriasis: evidence for a further PsA-specific risk locus

by Bowes, John, Loehr, Sabine, Budu-Aggrey, Ashley, Uebe, Steffen, Bruce, Ian N., Feletar, Marie, Marzo-Ortega, Helena, Helliwell, Philip, Ryan, Anthony W., Kane, David, Korendowych, Eleanor, Alenius, Gerd-Marie, Giardina, Emiliano, Packham, Jonathan, McManus, Ross, FitzGerald, Oliver, Brown, Matthew A., Behrens, Frank, Burkhardt, Harald, McHugh, Neil, Huffmeier, Ulrike, Ho, Pauline, Reis, Andre, Barton, Anne

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The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy

by Hebebrand, Moritz, Hüffmeier, Ulrike, Trollmann, Regina, Hehr, Ute, Uebe, Steffen, Ekici, Arif B., Kraus, Cornelia, Krumbiegel, Mandy, Reis, André, Thiel, Christian T., Popp, Bernt

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Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability

by Popp, Bernt, Agaimy, Abbas, Kraus, Cornelia, Knaup, Karl X., Ekici, Arif B., Uebe, Steffen, Reis, André, Wiesener, Michael, Zweier, Christiane

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Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients

by Uebe, Steffen, Ehrlicher, Maria, Ekici, Arif Bülent, Behrens, Frank, Böhm, Beate, Homuth, Georg, Schurmann, Claudia, Völker, Uwe, Jünger, Michael, Nauck, Matthias, Völzke, Henry 1967-, Traupe, Heiko, Krawczak, Michael, Burkhardt, Harald, Reis, Andre, Hüffmeier, Ulrike

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Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus

by Hauser, Michael A., Aboobakar, Inas F., Liu, Yutao, Miura, Shiroh, Whigham, Benjamin T., Challa, Pratap, Wheeler, Joshua, Williams, Andrew, Santiago-Turla, Cecelia, Qin, Xuejun, Rautenbach, Robyn M., Ziskind, Ari, Ramsay, Michèle, Uebe, Steffen, Song, Lingyun, Safi, Alexias, Vithana, Eranga N., Mizoguchi, Takanori, Nakano, Satoko, Kubota, Toshiaki, Hayashi, Ken, Manabe, Shin-ichi, Kazama, Shigeyasu, Mori, Yosai, Miyata, Kazunori

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