Endothelial progenitor cell culture and differentiation in vitro: a methodological comparison using human umbilical cord blood von EGGERMANN, Juliane, KLICHE, Stefanie, JARMY, Gergely, HOFFMANN, Karin, MAYR-BEYRLE, Ulrike, DEBATIN, Klaus-Michael, WALTENBERGER, Johannes, BELTINGER, Christian

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Diabetes mellitus impairs CD133+ progenitor cell function after myocardial infarction von Vöö, S., Dunaeva, M., Eggermann, J., Stadler, N., Waltenberger, J.

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Sphingosylphosphorylcholine regulates keratin network architecture and visco-elastic properties of human cancer cells von Beil, Michael, Micoulet, Alexandre, von Wichert, Götz, Paschke, Stephan, Walther, Paul, Omary, M. Bishr, Van Veldhoven, Paul P., Gern, Ulrike, Wolff-Hieber, Elke, Eggermann, Juliane, Waltenberger, Johannes, Adler, Guido, Spatz, Joachim, Seufferlein, Thomas

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Stress-Hormone Levels of Wolves in Relation to Breeding Season, Pack Size, Human Activity, and Prey Density von Eggermann, Julia, Theuerkauf, Jörn, Pirga, Bartosz, Milanowski, Artur, Gula, Roman

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Human impact on wolf activity in the Bieszczady Mountains, SE Poland von Theuerkauf, Jörn, Gula, Roman, Pirga, Bartosz, Tsunoda, Hiroshi, Eggermann, Julia, Brzezowska, Barbara, Rouys, Sophie, Radler, Stephan

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Oxygen pneumonitis in man., Light- and electron-microscopic morphometric studies von Kapanci, Y, Tosco, R, Eggermann, J, Gould, V E

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EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome von Eggermann, Katja, Bliek, Jet, Brioude, Frédéric, Algar, Elizabeth, Buiting, Karin, Russo, Silvia, Tümer, Zeynep, Monk, David, Moore, Gudrun, Antoniadi, Thalia, Macdonald, Fiona, Netchine, Irène, Lombardi, Paolo, Soellner, Lukas, Begemann, Matthias, Prawitt, Dirk, Maher, Eamonn R, Mannens, Marcel, Riccio, Andrea, Weksberg, Rosanna, Lapunzina, Pablo, Grønskov, Karen, Mackay, Deborah Jg, Eggermann, Thomas

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Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement von Brioude, Frédéric, Kalish, Jennifer M., Mussa, Alessandro, Foster, Alison C., Bliek, Jet, Ferrero, Giovanni Battista, Boonen, Susanne E., Cole, Trevor, Baker, Robert, Bertoletti, Monica, Cocchi, Guido, Coze, Carole, De Pellegrin, Maurizio, Hussain, Khalid, Ibrahim, Abdulla, Kilby, Mark D., Krajewska-Walasek, Malgorzata, Kratz, Christian P., Ladusans, Edmund J., Lapunzina, Pablo, Le Bouc, Yves, Maas, Saskia M., Macdonald, Fiona, Õunap, Katrin, Peruzzi, Licia, Rossignol, Sylvie, Russo, Silvia, Shipster, Caroleen, Skórka, Agata, Tatton-Brown, Katrina, Tenorio, Jair, Tortora, Chiara, Grønskov, Karen, Netchine, Irène, Hennekam, Raoul C., Prawitt, Dirk, Tümer, Zeynep, Eggermann, Thomas, Mackay, Deborah J. G., Riccio, Andrea, Maher, Eamonn R.

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Recent Advances in Imprinting Disorders von Soellner, L., Begemann, M., Mackay, D.J.G., Grønskov, K., Tümer, Z., Maher, E.R., Temple, I.K., Monk, D., Riccio, A., Linglart, A., Netchine, I., Eggermann, T.

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Demonstration of the extracellular alveolar lining layer (surfactant) in human lungs: An ultrastructural study von Kapanci, Y., Tosco, R., Eggermann, J.

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Genomic imprinting disorders: lessons on how genome, epigenome and environment interact von Monk, David, Mackay, Deborah J. G., Eggermann, Thomas, Maher, Eamonn R., Riccio, Andrea

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Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients von Rudnik-Schöneborn, S., Tölle, D., Senderek, J., Eggermann, K., Elbracht, M., Kornak, U., von der Hagen, M., Kirschner, J., Leube, B., Müller-Felber, W., Schara, U., von Au, K., Wieczorek, D., Bußmann, C., Zerres, K.

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NSD1 duplication in Silver–Russell syndrome (SRS): molecular karyotyping in patients with SRS features von Sachwitz, J., Meyer, R., Fekete, G., Spranger, S., Matulevičienė, A., Kučinskas, V., Bach, A., Luczay, A., Brüchle, N.O., Eggermann, K., Zerres, K., Elbracht, M., Eggermann, T.

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Development and characterization of a human embryonic stem cell-derived 3D neural tissue model for neurotoxicity testing von Sandström, J, Eggermann, E, Charvet, I, Roux, A, Toni, N, Greggio, C, Broyer, A, Monnet-Tschudi, F, Stoppini, L

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Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling von Eggermann, Thomas, Brioude, Frédéric, Russo, Silvia, Lombardi, Maria P, Bliek, Jet, Maher, Eamonn R, Larizza, Lidia, Prawitt, Dirk, Netchine, Irène, Gonzales, Marie, Grønskov, Karen, Tümer, Zeynep, Monk, David, Mannens, Marcel, Chrzanowska, Krystyna, Walasek, Malgorzata K, Begemann, Matthias, Soellner, Lukas, Eggermann, Katja, Tenorio, Jair, Nevado, Julián, Moore, Gudrun E, Mackay, Deborah Jg, Temple, Karen, Gillessen-Kaesbach, Gabriele, Ogata, Tsutomu, Weksberg, Rosanna, Algar, Elizabeth, Lapunzina, Pablo

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Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies von Lischka, Annette, Eggermann, Katja, Record, Christopher J, Dohrn, Maike F, Laššuthová, Petra, Kraft, Florian, Begemann, Matthias, Dey, Daniela, Eggermann, Thomas, Beijer, Danique, Šoukalová, Jana, Laura, Matilde, Rossor, Alexander M, Mazanec, Radim, Van Lent, Jonas, Tomaselli, Pedro J, Ungelenk, Martin, Debus, Karlien Y, Feely, Shawna M E, Gläser, Dieter, Jagadeesh, Sujatha, Martin, Madelena, Govindaraj, Geeta M, Singhi, Pratibha, Baineni, Revanth, Biswal, Niranjan, Ibarra-Ramírez, Marisol, Bonduelle, Maryse, Gess, Burkhard, Hornemann, T

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Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure von Mulchandani, Surabhi, Bhoj, Elizabeth J., Luo, Minjie, Powell-Hamilton, Nina, Jenny, Kim, Gripp, Karen W., Elbracht, Miriam, Eggermann, Thomas, Turner, Claire L.S., Temple, I. Karen, Mackay, Deborah J.G., Dubbs, Holly, Stevenson, David A., Slattery, Leah, Zackai, Elaine H., Spinner, Nancy B., Krantz, Ian D., Conlin, Laura K.

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Functional connectivity signatures of NMDAR dysfunction in schizophrenia—integrating findings from imaging genetics and pharmaco-fMRI von Gaebler, Arnim J., Fakour, Nilüfer, Stöhr, Felix, Zweerings, Jana, Taebi, Arezoo, Suslova, Mariia, Dukart, Juergen, Hipp, Joerg F., Adhikari, Bhim M., Kochunov, Peter, Muthukumaraswamy, Suresh D., Forsyth, Anna, Eggermann, Thomas, Kraft, Florian, Kurth, Ingo, Paulzen, Michael, Gründer, Gerhard, Schneider, Frank, Mathiak, Klaus

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PKHD1, the Polycystic Kidney and Hepatic Disease 1 Gene, Encodes a Novel Large Protein Containing Multiple Immunoglobulin-Like Plexin-Transcription–Factor Domains and Parallel Beta... von Onuchic, Luiz F., Furu, Laszlo, Nagasawa, Yasuyuki, Hou, Xiaoying, Eggermann, Thomas, Ren, Zhiyong, Bergmann, Carsten, Senderek, Jan, Esquivel, Ernie, Zeltner, Raoul, Rudnik-Schöneborn, Sabine, Mrug, Michael, Sweeney, William, Avner, Ellis D., Zerres, Klaus, Guay-Woodford, Lisa M., Somlo, Stefan, Germino, Gregory G.

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Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations von Okada, Yukinori, Sim, Xueling, Go, Min Jin, Wu, Jer-Yuarn, Gu, Dongfeng, Takeuchi, Fumihiko, Takahashi, Atsushi, Maeda, Shiro, Tsunoda, Tatsuhiko, Chen, Peng, Lim, Su-Chi, Wong, Tien-Yin, Liu, Jianjun, Young, Terri L, Aung, Tin, Seielstad, Mark, Teo, Yik-Ying, Kim, Young Jin, Lee, Jong-Young, Han, Bok-Ghee, Kang, Daehee, Chen, Chien-Hsiun, Tsai, Fuu-Jen, Chang, Li-Ching, Fann, S-J Cathy, Mei, Hao, Rao, Dabeeru C, Hixson, James E, Chen, Shufeng, Katsuya, Tomohiro, Isono, Masato, Ogihara, Toshio, Chambers, John C, Zhang, Weihua, Kooner, Jaspal S, Albrecht, Eva, Yamamoto, Kazuhiko, Kubo, Michiaki, Nakamura, Yusuke, Kamatani, Naoyuki, Kato, Norihiro, He, Jiang, Chen, Yuan-Tsong, Cho, Yoon Shin, Tai, E-Shyong, Tanaka, Toshihiro

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