Transplant-tolerance induction by CTLA-4Ig in liver-transplanted rats: a lesson for the treatment of autoimmune diseases?

por Fischer, U, Boas-Knoop, S, Neumann, U
Publicado 2003

Genome-wide copy number profiling to detect gene amplifications in neural progenitor cells

por Fischer, U., Keller, A., Backes, C., Meese, E.
Publicado 2014

Many cuts to ruin: a comprehensive update of caspase substrates

por Fischer, U, Jänicke, R U, Schulze-Osthoff, K
Publicado 2003

Proposal for an experiment on $K^{0}_{L}$ P -> $\lambda$ $\pi^{+}$

por Bamberger, A, Behrendt, H, Brundiers, H J, Fischer, U
Publicado 1974

Genome-wide copy number profiling of mouse neural stem cells during differentiation

por Fischer, U., Ludwig, N., Keller, A., Backes, C., Meese, E.
Publicado 2015

Damage production in Si by MeV carbon cluster irradiation

por Döbeli, M, Ender, R M, Fischer, U S, Suter, M, Synal, H A, Vetterli, D
Publicado 1994

Room temperature organic exciton–polariton condensate in a lattice

por Dusel, M., Betzold, S., Egorov, O. A., Klembt, S., Ohmer, J., Fischer, U., Höfling, S., Schneider, C.
Publicado 2020

A study of the reactions $\overline{K}$0p --> LAMBDA.pi+(backward) and $\overline{K}$0p --> SIGMA0pi+(backward) for kaon momenta between 1 and 8 GeV/c

por Bamberger, Andreas, Brüning, H, Brundiers, H J, Fischer, U, Hartung, R W, Maier, R S, Runge, K, Schäfer, K G, Weber, H C
Publicado 1980

Availability of secondary prevention services after stroke in Europe: An ESO/SAFE survey of national scientific societies and stroke experts

por Webb, A, Heldner, MR, Aguiar de Sousa, D, Sandset, EC, Randall, G, Bejot, Y, van der Worp, B, Caso, V, Fischer, U
Publicado 2018

Submonolayer Quantum Dots for High Speed Surface Emitting Lasers

por Ledentsov, NN, Bimberg, D, Hopfer, F, Mutig, A, Shchukin, VA, Savel’ev, AV, Fiol, G, Stock, E, Eisele, H, Dähne, M, Gerthsen, D, Fischer, U, Litvinov, D, Rosenauer, A, Mikhrin, SS, Kovsh, AR, Zakharov, ND, Werner, P
Publicado 2007

Free propagation phase-contrast breast CT provides higher image quality than cone-beam breast-CT at low radiation doses: a feasibility study on human mastectomies

por Pacilè, S., Dullin, C., Baran, P., Tonutti, M., Perske, C., Fischer, U., Albers, J., Arfelli, F., Dreossi, D., Pavlov, K., Maksimenko, A., Mayo, S. C., Nesterets, Y. I., Taba, S. Tavakoli, Lewis, S., Brennan, P. C., Gureyev, T. E., Tromba, G., Wienbeck, S.
Publicado 2019

Neutrons for Science (NFS) at SPIRAL-2

por Ridikas, D, Plompen, A, Ledoux, X, Heil, M, Rudolf, G, Thomas, J B, Gunsing, F, Käppeler, F K, Bem, P, Diegele, E, Fischer, U, Mittig, W, Morse, E C, Oberstedt, S, Reifarth, S, Sorlin, O, Vieira, D, Villari, A C C
Publicado 2005

A hydrogen high pressure proportional drift detector

por Arefev, A, Babaev, A, Bamberger, Andreas, Brundiers, H J, Eliseev, G, Fischer, U, Friedrich, D, Galaktionov, Yu, Gorodkov, Yu V, Hartung, R W, Heck, W, Kamyshkov, Yu A, Lubimov, V, Maier, R S, Plyaskin, V, Pozhidaev, V, Runge, K, Schaile, O, Shevchenko, V, Thomauske, B, Vlasov, M K, Weber, C
Publicado 1983

Measurement of np elastic scattering at high energies and very small momentum transfers

por Arefev, A, Babaev, A, Bamberger, Andreas, Brundiers, H J, Eliseev, G, Fischer, U, Friedrich, D, Galaktionov, Yu, Gorodkov, Yu V, Hartung, R W, Heck, W, Kamyshkov, Yu A, Lubimov, V, Maier, R S, Plyaskin, V, Pozhidaev, V, Runge, K, Schaile, O, Shevchenko, V, Thomauske, B, Vlasov, M K, Weber, C
Publicado 1983

In utero gene therapy rescues microcephaly caused by Pqbp1-hypofunction in neural stem progenitor cells

por Ito, H, Shiwaku, H, Yoshida, C, Homma, H, Luo, H, Chen, X, Fujita, K, Musante, L, Fischer, U, Frints, S G M, Romano, C, Ikeuchi, Y, Shimamura, T, Imoto, S, Miyano, S, Muramatsu, S-i, Kawauchi, T, Hoshino, M, Sudol, M, Arumughan, A, Wanker, E E, Rich, T, Schwartz, C, Matsuzaki, F, Bonni, A, Kalscheuer, V M, Okazawa, H
Publicado 2015

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

por Palmer, E E, Stuhlmann, T, Weinert, S, Haan, E, Van Esch, H, Holvoet, M, Boyle, J, Leffler, M, Raynaud, M, Moraine, C, van Bokhoven, H, Kleefstra, T, Kahrizi, K, Najmabadi, H, Ropers, H-H, Delgado, M R, Sirsi, D, Golla, S, Sommer, A, Pietryga, M P, Chung, W K, Wynn, J, Rohena, L, Bernardo, E, Hamlin, D, Faux, B M, Grange, D K, Manwaring, L, Tolmie, J, Joss, S, Cobben, J M, Duijkers, F A M, Goehringer, J M, Challman, T D, Hennig, F, Fischer, U, Grimme, A, Suckow, V, Musante, L, Nicholl, J, Shaw, M, Lodh, S P, Niu, Z, Rosenfeld, J A, Stankiewicz, P, Jentsch, T J, Gecz, J, Field, M, Kalscheuer, V M
Publicado 2018

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

por Hu, H, Haas, S A, Chelly, J, Van Esch, H, Raynaud, M, de Brouwer, A P M, Weinert, S, Froyen, G, Frints, S G M, Laumonnier, F, Zemojtel, T, Love, M I, Richard, H, Emde, A-K, Bienek, M, Jensen, C, Hambrock, M, Fischer, U, Langnick, C, Feldkamp, M, Wissink-Lindhout, W, Lebrun, N, Castelnau, L, Rucci, J, Montjean, R, Dorseuil, O, Billuart, P, Stuhlmann, T, Shaw, M, Corbett, M A, Gardner, A, Willis-Owen, S, Tan, C, Friend, K L, Belet, S, van Roozendaal, K E P, Jimenez-Pocquet, M, Moizard, M-P, Ronce, N, Sun, R, O'Keeffe, S, Chenna, R, van Bömmel, A, Göke, J, Hackett, A, Field, M, Christie, L, Boyle, J, Haan, E, Nelson, J, Turner, G, Baynam, G, Gillessen-Kaesbach, G, Müller, U, Steinberger, D, Budny, B, Badura-Stronka, M, Latos-Bieleńska, A, Ousager, L B, Wieacker, P, Rodríguez Criado, G, Bondeson, M-L, Annerén, G, Dufke, A, Cohen, M, Van Maldergem, L, Vincent-Delorme, C, Echenne, B, Simon-Bouy, B, Kleefstra, T, Willemsen, M, Fryns, J-P, Devriendt, K, Ullmann, R, Vingron, M, Wrogemann, K, Wienker, T F, Tzschach, A, van Bokhoven, H, Gecz, J, Jentsch, T J, Chen, W, Ropers, H-H, Kalscheuer, V M
Publicado 2016