Genome-wide meta-analysis identifies new susceptibility loci for migraine von Anttila, V, Winsvold, BS, Gormley, P, Kurth, T, Bettella, F, McMahon, G, Kallela, M, Malik, R, De Vries, B, Terwindt, G, Medland, SE, Todt, U, McArdle, WL, Quaye, L, Koiranen, M, Ikram, MA, Lehtimaki, T, Stam, AH, Ligthart, L, Wedenoja, J, Dunham, I, Neale, BM, Palta, P, Hamalainen, E, Schuerks, M, Rose, LM, Buring, JE, Ridker, PM, Steinberg, S, Stefansson, H, Jakobsson, F, Lawlor, DA, Evans, DM, Ring, SM, Farkkila, M, Artto, V, Kaunisto, MA, Freilinger, T, Schoenen, J, Frants, RR, Pelzer, N, Weller, CM, Zielman, R, Heath, AC, Madden, PAF, Montgomery, GW, Martin, NG, Borck, G, Goebel, H, Heinze, A, Heinze-Kuhn, K, Williams, FMK, Hartikainen, A-L, Pouta, A, Van den Ende, J, Uitterlinden, AG, Hofman, A, Amin, N, Hottenga, J-J, Vink, JM, Heikkila, K, Alexander, M, Muller-Myhsok, B, Schreiber, S, Meitinger, T, Wichmann, HE, Aromaa, A, Eriksson, JG, Traynor, BJ, Trabzuni, D, Rossin, E, Lage, K, Jacobs, SBR, Gibbs, JR, Birney, E, Kaprio, J, Penninx, BW, Boomsma, DI, Van Duijn, C, Raitakari, O, Jarvelin, M-R, Zwart, J-A, Cherkas, L, Strachan, DP, Kubisch, C, Ferrari, MD, Van den Maagdenberg, AMJM, Dichgans, M, Wessman, M, Smith, GD, Stefansson, K, Daly, MJ, Nyholt, DR, Chasman, DI, Palotie, A

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V‐ATPase inhibition by archazolid leads to lysosomal dysfunction resulting in impaired cathepsin B activation in vivo von Kubisch, Rebekka, Fröhlich, Thomas, Arnold, Georg J., Schreiner, Laura, Schwarzenberg, Karin, Roidl, Andreas, Vollmar, Angelika M., Wagner, Ernst

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SignaLink3: a multi-layered resource to uncover tissue-specific signaling networks von Csabai, L, Fazekas, D, Kadlecsik, T, Szalay-Bekő, M, Bohár, B, Madgwick, M, Módos, D, Ölbei, M, Gul, L, Sudhakar, P, Kubisch, J, Oyeyemi, OJ, Liska, O, Ari, E, Hotzi, B, Billes, VA, Molnár, E, Földvári-Nagy, L, Csályi, K, Demeter, A, Pápai, N, Koltai, M, Varga, M, Lenti, K, Farkas, IJ, Türei, D, Csermely, P, Vellai, T, Korcsmáros, T

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Mutant Atp13a2 proteins involved in parkinsonism are degraded by ER-associated degradation and sensitize cells to ER-stress induced cell death von Ugolino, Janet, Fang, Shengyun, Kubisch, Christian, Monteiro, Mervyn J

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Clinical and genetic findings in a family with NMNAT1-associated Leber congenital amaurosis: case report and review of the literature von Hedergott, A., Volk, A. E., Herkenrath, P., Thiele, H., Fricke, J., Altmüller, J., Nürnberg, P., Kubisch, C., Neugebauer, A.

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Postmortem recovery and cryopreservation of spermatozoa from the vas deferens of rhesus macaques ( Macaca mulatta) von Goff, K., Liukkonen, J., Kubisch, H.M.

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Novel missense mutation in the caveolin-3 gene in a Belgian family with rippling muscle disease von Van den Bergh, P Y K, Gérard, J M, Elosegi, J A, Manto, M U, Kubisch, C, Schoser, B G H

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Glycosylation of silybin von Křen, Vladimír, Kubisch, Jiří, Sedmera, Petr, Halada, Petr, Přikrylová, Věra, Jegorov, Alexandr, Cvak, Ladislav, Gebhardt, Rolf, Ulrichová, Jitka, Šimánek, Vilím

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Pathophysiology of KCNQ Channels: Neonatal Epilepsy and Progressive Deafness von Jentsch, Thomas J., Schroeder, Bjoern C., Kubisch, Christian, Friedrich, Thomas, Stein, Valentin

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Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K + channels causes epilepsy von Jentsch, Thomas J, Schroeder, Björn C, Kubisch, Christian, Stein, Valentin

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New challenges for informed consent through whole genome array testing von Netzer, C, Klein, C, Kohlhase, J, Kubisch, C

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Christina Kubisch : inaudible, invisible 1974-2023 von Drugeon, Fanny

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Radiofrequency ablation after selective internal radiation therapy with Yttrium90 microspheres in metastatic liver disease—Is it feasible? von Hoffmann, R.T, Jakobs, T.F, Kubisch, C.H, Stemmler, H.J, Trumm, C, Tatsch, K, Helmberger, T.K, Reiser, M.F

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Effect of p-Substitution of Aryl α-D-Mannosides on Inhibiting Mannose-Sensitive Adhesion of Escherichia coli - Syntheses and Testing von Lindhorst, Thisbe K., Kötter, Sven, Kubisch, Jiří, Krallmann-Wenzel, Ulrike, Ehlers, Stefan, Křen, Vladimír

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Development and validation of a SNP-based assay for inferring the genetic ancestry of rhesus macaques (Macaca mulatta) von Kanthaswamy, Sree, Johnson, Zachary, Trask, Jessica Satkoski, Smith, David G., Ramakrishnan, Ranjani, Bahk, Jason, Ng, Jillian, Wiseman, Roger, Kubisch, H. Michael, Vallender, Eric J., Rogers, Jeffrey, Ferguson, Betsy

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Enzymatic Synthesis of P-Nitrophenyl β-Chitobioside von Kubisch, Jiří, Weignerová, Lenka, Kötter, Sven, Lindhorst, Thisbe K., Sedmera, Petr, Křen, Vladimír

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Werner syndrome. A prototypical form of segmental progeria. von Lessel, D, Oshima, J, Kubisch, C

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V-ATPase inhibition by archazolid leads to lysosomal dysfunction resulting in impaired cathepsin B activation in vivo: V-ATPase inhibition leads to impaired CTSB activation von Kubisch, Rebekka, Fröhlich, Thomas, Arnold, Georg J., Schreiner, Laura, von Schwarzenberg, Karin, Roidl, Andreas, Vollmar, Angelika M., Wagner, Ernst

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Werner-Syndrom von Lessel, D., Oshima, J., Kubisch, C.

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Werner-Syndrom. Eine prototypische Form der segmentalen Progerie von Lessel, D., Oshima, J., Kubisch, C.

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