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[1]G. Desalegn, O. Pabst,
"Inflammation triggers immediate rather than progressive changes in monocyte differentiation in the small intestine", Nature Communications, vol. 10, 2019, pp. 3229.
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[2]M. Ugur, A. Kaminski and O. Pabst,
"Lymph node γδ and αβ CD8+ T cells share migratory properties", Scientific reports, vol. 8, no. 1, 2018, pp. 8986.
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[3]M. K. Sethi, F. Thol, M. Stadler, M. Heuser, A. Ganser, C. Koenecke, O. Pabst,
"VH1 Family Immunoglobulin Repertoire Sequencing after Allogeneic Hematopoietic Stem Cell Transplantation", PLoS one, vol. 12, no. 1, 2017, pp. e0168096.
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[4]C. Lindner, I. Thomsen, B. Wahl, M. Ugur, M. K. Sethi, M. Friedrichsen, A. Smoczek, S. Ott, U. Baumann, S. Suerbaum, S. Schreiber, A. Bleich, V. Gaboriau-Routhiau, N. Cerf-Bensussan, H. Hazanov, R. Mehr, P. Boysen, P. Rosenstiel, O. Pabst,
"Diversification of memory B cells drives the continuous adaptation of secretory antibodies to gut microbiota", Nature immunology, vol. 16, no. 8, 2015, pp. 880–888.
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[5]M. Ugur, O. Schulz, M. B. Menon, A. Krueger, O. Pabst,
"Resident CD4+ T cells accumulate in lymphoid organs after prolonged antigen exposure", Nature Communications, vol. 5, 2014, pp. 4821.
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[6]O. Schulz, M. Ugur, M. Friedrichsen, K. Radulovic, J. Niess, S. Jalkanen, A. Krueger, O. Pabst,
"Hypertrophy of infected Peyer's patches arises from global, interferon-receptor, and CD69-independent shutdown of lymphocyte egress", Mucosal immunology, vol. 7, no. 4, 2014, pp. 892–904.
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[7]C. Lindner, B. Wahl, L. Föhse, S. Suerbaum, A. J. Macpherson, I. Prinz, O. Pabst,
"Age, microbiota, and T cells shape diverse individual IgA repertoires in the intestine", Journal of experimental medicine, vol. 209, no. 2, 2012, pp. 365–377.
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[8]U. Hadis, B. Wahl, O. Schulz, M. Hardtke-Wolenski, A. Schippers, N. Wagner, W. Müller, T. Sparwasser, R. Förster, O. Pabst,
"Intestinal Tolerance Requires Gut Homing and Expansion of FoxP3(+) Regulatory T Cells in the Lamina Propria", Immunity, vol. 34, no. 2, 2011, pp. 237–246.
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[9]O. Schulz, E. Jaensson, E. K. Persson, X. Liu, T. Worbs, W. W. Agace, O. Pabst,
"Intestinal CD103+, but not CX3CR1+, antigen sampling cells migrate in lymph and serve classical dendritic cell functions", Journal of experimental medicine, vol. 206, no. 13, 2009, pp. 3101–3114.
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[10]S. I. Hammerschmidt, M. Ahrendt, U. Bode, B. Wahl, E. Kremmer, R. Förster, O. Pabst,
"Stromal mesenteric lymph node cells are essential for the generation of gut-homing T cells in vivo", Journal of experimental medicine, vol. 205, no. 11, 2008, pp. 2483–2490.
[bibtex] [url] [doi]