Microglial recruitment of IL-1β-producing monocytes to brain endothelium causes stress-induced anxiety von McKim, D B, Weber, M D, Niraula, A, Sawicki, C M, Liu, X, Jarrett, B L, Ramirez-Chan, K, Wang, Y, Roeth, R M, Sucaldito, A D, Sobol, C G, Quan, N, Sheridan, J F, Godbout, J P

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Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm control von Hoffmann, S., Schmitteckert, S., Raedecke, K., Rheinert, D., Diebold, S., Roeth, R., Weiss, B., Granzow, M., Niesler, B., Griesbeck, A., Eckstein, V., Zimmermann, W.-H., Just, S., Rappold, G.A.

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Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency von Rappold, Gudrun, Blum, Werner F, Shavrikova, Elena P, Crowe, Brenda J, Roeth, Ralph, Quigley, Charmian A, Ross, Judith L, Niesler, Beate

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Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain von Chen, J, Wildhardt, G, Zhong, Z, Röth, R, Weiss, B, Steinberger, D, Decker, J, Blum, W F, Rappold, G

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Site‐specific gene expression analysis from archived human intestine samples combining laser‐capture microdissection and multiplexed color‐coded probes von Braun, A., Martinez, C., Schmitteckert, S., Röth, R., Lasitschka, F., Niesler, B.

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Natural compounds boldine and menthol are antagonists of human 5‐HT3 receptors: implications for treating gastrointestinal disorders von Walstab, J., Wohlfarth, C., Hovius, R., Schmitteckert, S., Röth, R., Lasitschka, F., Wink, M., Bönisch, H., Niesler, B.

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Microglial recruitment of IL-1[beta]-producing monocytes to brain endothelium causes stress-induced anxiety von McKim, D B, Weber, M D, Niraula, A, Sawicki, C M, Liu, X, Jarrett, B L, Ramirez-Chan, K, Wang, Y, Roeth, R M, Sucaldito, A D, Sobol, C G, Quan, N, Sheridan, J F, Godbout, J P

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Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability von Tyson, C., Dawson, A.J., Bal, S., Tomiuk, M., Anderson, T., Tucker, D., Riordan, D., Chudoba, I., Morash, B., Mhanni, A., Chudley, A.E., McGillivray, B., Parslow, M., Rappold, G., Roeth, R., Fawcett, C., Qiao, Y., Harvard, C., Rajcan‐Separovic, E.

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Missense mutations and gene interruption in PROSIT240, a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries) von MUNCKE, Nadja, JUNG, Christine, RAPPOLD, Gudrun, RÜDIGER, Heinz, ULMER, Herbert, ROETH, Ralph, HUBERT, Annette, GOLDMUNTZ, Elizabeth, DRISCOLL, Deborah, GOODSHIP, Judith, SCHÖN, Karin

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Novel insights into a reputably irreversible process: combined mRNA and miRNA profiling of tissue from vesicourethral anastomotic stenosis after radical prostatectomy von Worst, T. S., Daskalova, K., Steidler, A., Berner-Leischner, K., Röth, R., Niesler, B., Weis, C.-A., Kriegmair, M. C., Erben, P., Pfalzgraf, D.

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Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study von Hammer, C, Cichon, S, Mühleisen, T W, Haenisch, B, Degenhardt, F, Mattheisen, M, Breuer, R, Witt, S H, Strohmaier, J, Oruc, L, Rivas, F, Babadjanova, G, Grigoroiu-Serbanescu, M, Hauser, J, Röth, R, Rappold, G, Rietschel, M, Nöthen, M M, Niesler, B

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Aged monkeys as a partial model for Parkinson's disease von Hurley, P.J., Elsworth, J.D., Whittaker, M.C., Roth, R.H., Redmond, D.E.

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Identification of a Major Recombination Hotspot in Patients with Short Stature and SHOX Deficiency von Schneider, Katja U., Sabherwal, Nitin, Jantz, Karin, Röth, Ralph, Muncke, Nadja, Blum, Werner F., Cutler, Gordon B., Rappold, Gudrun

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Identification of novel genes including NAV2 associated with isolated tall stature von Weiss, B., Ott, T., Vick, P., Lui, J.C., Roeth, R., Vogel, S., Waldmüller, S., Hoffmann, S., Baron, J., Wit, J.M., Rappold, G.A.

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Impaired miRNA Regulation as Molecular Cause of Altered 5-HT4 Receptor Signalling in Irritable Bowel Syndrome von Wohlfarth, C, Hartle, JDC, Assadi, G, Houghton, LA, Pohner, S, Becker, PP, Fischer, C, Monnikes, H, Mayer, EA, Sayuk, GS, Boeckxstaens, GE, Wouters, MM, Simren, M, Lindberg, G, Ohlsson, B, Schmidt, PT, Dlugosz, A, Agreus, L, Andreasson, A, D'Amato, M, Burwinkel, B, Roeth, R, Lasitschka, F, Rappold, G, Niesler, B

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Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA) von Muncke, Nadja, Niesler, Beate, Roeth, Ralph, Schön, Karin, Rüdiger, Heinz-Juergen, Goldmuntz, Elizabeth, Goodship, Judith, Rappold, Gudrun

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Severe long-term 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonism in the vervet monkey ( Cercopithecus aethiops sabaeus) von Taylor, J.R, Elsworth, J.D, Roth, R.H, Sladek, J.R, Redmond, D.E

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Evidence that non-syndromic familial tall stature has an oligogenic origin including ciliary genes von Weiss, B., Eberle, B., Roeth, R., Bruin, C. de, Lui, J.L.C., Paramasivam, N., Hinderhofer, K., Duyvenvoorde, H.A. van, Baron, J., Wit, J.M., Rappold, G.A.

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Akt Modulates STAT3-mediated Gene Expression through a FKHR (FOXO1a)-dependent Mechanism von Kortylewski, M, Feld, F, Krueger, K, Bahrenberg, G, Roth, R A, Joost, H, Heinrich, P C, Behrmann, I, Barthel, A

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Taping – Step by Step von Roth, R.

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