Quantitative, Wide-Spectrum Kinase Profiling in Live Cells for Assessing the Effect of Cellular ATP on Target Engagement
Vasta, James D., Corona, Cesear R., Wilkinson, Jennifer, Zimprich, Chad A., Hartnett, James R., Ingold, Morgan R., Zimmerman, Kristopher, Machleidt, Thomas, Kirkland, Thomas A., Huwiler, Kristin G., Ohana, Rachel Friedman, Slater, Michael, Otto, Paul, Cong, Mei, Wells, Carrow I., Berger, Benedict-Tilman, Hanke, Thomas, Glas, Carina, Ding, Ke, Drewry, David H., Huber, Kilian V.M., Willson, Timothy M., Knapp, Stefan, Müller, Susanne, Meisenheimer, Poncho L., Fan, Frank, Wood, Keith V., Robers, Matthew B.
Published in Cell chemical biology (15.02.2018)
Published in Cell chemical biology (15.02.2018)
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Quantifying CDK inhibitor selectivity in live cells
Wells, Carrow I, Vasta, James D, Corona, Cesear R, Wilkinson, Jennifer, Zimprich, Chad A, Ingold, Morgan R, Pickett, Julie E, Drewry, David H, Pugh, Kathryn M, Schwinn, Marie K, Hwang, Byounghoon Brian, Zegzouti, Hicham, Huber, Kilian V M, Cong, Mei, Meisenheimer, Poncho L, Willson, Timothy M, Robers, Matthew B
Published in Nature communications (02.06.2020)
Published in Nature communications (02.06.2020)
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Tetrahydroquinoline-Capped Histone Deacetylase 6 Inhibitor SW-101 Ameliorates Pathological Phenotypes in a Charcot–Marie–Tooth Type 2A Mouse Model
Shen, Sida, Picci, Cristina, Ustinova, Kseniya, Benoy, Veronick, Kutil, Zsófia, Zhang, Guiping, Tavares, Maurício T, Pavlíček, Jiří, Zimprich, Chad A, Robers, Matthew B, Van Den Bosch, Ludo, Bařinka, Cyril, Langley, Brett, Kozikowski, Alan P
Published in Journal of medicinal chemistry (22.04.2021)
Published in Journal of medicinal chemistry (22.04.2021)
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The pathogenic LRRK2 R1441C mutation induces specific deficits modeling the prodromal phase of Parkinson's disease in the mouse
Giesert, F, Glasl, L, Zimprich, A, Ernst, L, Piccoli, G, Stautner, C, Zerle, J, Hölter, S.M, Vogt Weisenhorn, D.M, Wurst, W
Published in Neurobiology of disease (01.09.2017)
Published in Neurobiology of disease (01.09.2017)
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Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene
Krenn, M., Zulehner, G., Hotzy, C., Rath, J., Stogmann, E., Wagner, M., Haack, T. B., Strom, T. M., Zimprich, A., Zimprich, F.
Published in European journal of neurology (01.05.2017)
Published in European journal of neurology (01.05.2017)
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Journal Article
Brain Penetrable Histone Deacetylase 6 Inhibitor SW-100 Ameliorates Memory and Learning Impairments in a Mouse Model of Fragile X Syndrome
Kozikowski, Alan P, Shen, Sida, Pardo, Marta, Tavares, Maurício T, Szarics, Dora, Benoy, Veronick, Zimprich, Chad A, Kutil, Zsófia, Zhang, Guiping, Bařinka, Cyril, Robers, Matthew B, Van Den Bosch, Ludo, Eubanks, James H, Jope, Richard S
Published in ACS chemical neuroscience (20.03.2019)
Published in ACS chemical neuroscience (20.03.2019)
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Genotype‐guided diagnostic reassessment after exome sequencing in neuromuscular disorders: experiences with a two‐step approach
Krenn, M., Tomschik, M., Rath, J., Cetin, H., Grisold, A., Zulehner, G., Milenkovic, I., Stogmann, E., Zimprich, A., Strom, T. M., Meitinger, T., Wagner, M., Zimprich, F.
Published in European journal of neurology (01.01.2020)
Published in European journal of neurology (01.01.2020)
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Journal Article
Association of Body Mass Index and Parkinson Disease: A Bidirectional Mendelian Randomization Study
Domenighetti, Cloé, Sugier, Pierre-Emmanuel, Ashok Kumar Sreelatha, Ashwin, Schulte, Claudia, Grover, Sandeep, Portugal, Berta, Lee, Pei-Chen, May, Patrick, Bobbili, Dheeraj, Radivojkov Blagojevic, Milena, Lichtner, Peter, Singleton, Andrew B, Hernandez, Dena, Edsall, Connor, Mellick, George D, Zimprich, Alexander A, Pirker, Walter, Rogaeva, Ekaterina A, Lang, Anthony E, Koks, Sulev, Taba, Pille, Lesage, Suzanne, Brice, Alexis, Corvol, Jean-Christophe, Chartier-Harlin, Marie-Christine, Mutez, Eugenie, Brockmann, Kathrin, Deutschlander, Angela B, Hadjigeorgiou, Georgios M, Dardiotis, Efthimios, Stefanis, Leonidas, Simitsi, Athina Maria, Valente, Enza Maria, Petrucci, Simona, Straniero, Letizia, Zecchinelli, Anna L, Pezzoli, Gianni, Brighina, Laura, Ferrarese, Carlo, Annesi, Grazia, Quattrone, Andrea, Gagliardi, Monica, Matsuo, Hirotaka, Nakayama, Akiyoshi, Hattori, Nobutaka, Nishioka, Kenya, Chung, Sun Ju, Kim, Yun Joong, Kolber, Pierre, Van De Warrenburg, Bart P C, Bloem, Bastiaan R, Toft, Mathias, Pihlstrøm, Lasse, Correia Guedes, Leonor, Ferreira, Joaquim J, Bardien, Soraya, Carr, Jonathan, Tolosa, Eduardo, Ezquerra, Mario, Pastor, Pau, Diez-Fairen, Monica, Wirdefeldt, Karin, Pedersen, Nancy L, Ran, Caroline, Belin, Andrea C, Puschmann, Andreas, Hellberg, Clara, Clarke, Carl E, Morrison, Karen E, Tan, Manuela M, Krainc, Dimitri, Burbulla, Lena F, Farrer, Matthew, Kruger, Rejko, Gasser, Thomas, Sharma, Manu, Elbaz, Alexis
Published in Neurology (13.08.2024)
Published in Neurology (13.08.2024)
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The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNA
Cetin, H., Wöhrer, A., Rittelmeyer, I., Gencik, M., Zulehner, G., Zimprich, F., Ströbel, T., Zimprich, A.
Published in Clinical genetics (01.10.2016)
Published in Clinical genetics (01.10.2016)
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Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy
Zimprich, F, Sunder-Plassmann, R, Stogmann, E, Gleiss, A, Dal-Bianco, A, Zimprich, A, Plumer, S, Baumgartner, C, Mannhalter, C
Published in Neurology (28.09.2004)
Published in Neurology (28.09.2004)
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Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His
van der Zee, J, Pirici, D, Van Langenhove, T, Engelborghs, S, Vandenberghe, R, Hoffmann, M, Pusswald, G, Van den Broeck, M, Peeters, K, Mattheijssens, M, Martin, J-J, De Deyn, P P, Cruts, M, Haubenberger, D, Kumar-Singh, S, Zimprich, A, Van Broeckhoven, C
Published in Neurology (25.08.2009)
Published in Neurology (25.08.2009)
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Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
Wszolek, Z K, Pfeiffer, R F, Tsuboi, Y, Uitti, R J, McComb, R D, Stoessl, A J, Strongosky, A J, Zimprich, A, Müller-Myhsok, B, Farrer, M J, Gasser, T, Calne, D B, Dickson, D W
Published in Neurology (11.05.2004)
Published in Neurology (11.05.2004)
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Journal Article
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene
Haubenberger, D, Bittner, R E, Rauch-Shorny, S, Zimprich, F, Mannhalter, C, Wagner, L, Mineva, I, Vass, K, Auff, E, Zimprich, A
Published in Neurology (25.10.2005)
Published in Neurology (25.10.2005)
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A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa
Asmus, F, Horber, V, Pohlenz, J, Schwabe, D, Zimprich, A, Munz, M, Schöning, M, Gasser, T
Published in Neurology (14.06.2005)
Published in Neurology (14.06.2005)
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Replication of restless legs syndrome loci in three European populations
Kemlink, D, Polo, O, Frauscher, B, Gschliesser, V, Högl, B, Poewe, W, Vodicka, P, Vavrova, J, Sonka, K, Nevsimalova, S, Schormair, B, Lichtner, P, Silander, K, Peltonen, L, Gieger, C, Wichmann, H E, Zimprich, A, Roeske, D, Müller-Myhsok, B, Meitinger, T, Winkelmann, J
Published in Journal of medical genetics (01.05.2009)
Published in Journal of medical genetics (01.05.2009)
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A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures
Schlachter, K, Gruber-Sedlmayr, U, Stogmann, E, Lausecker, M, Hotzy, C, Balzar, J, Schuh, E, Baumgartner, C, Mueller, J C, Illig, T, Wichmann, H E, Lichtner, P, Meitinger, T, Strom, T M, Zimprich, A, Zimprich, F
Published in Neurology (17.03.2009)
Published in Neurology (17.03.2009)
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Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis
Greisenegger, EK, Novak, N, Maintz, L, Bieber, T, Zimprich, F, Haubenberger, D, Gleiss, A, Stingl, G, Kopp, T, Zimprich, A
Published in Journal of the European Academy of Dermatology and Venereology (01.05.2010)
Published in Journal of the European Academy of Dermatology and Venereology (01.05.2010)
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Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations
Stogmann, E, Lichtner, P, Baumgartner, C, Bonelli, S, Assem-Hilger, E, Leutmezer, F, Schmied, M, Hotzy, C, Strom, T M, Meitinger, T, Zimprich, F, Zimprich, A
Published in Neurology (12.12.2006)
Published in Neurology (12.12.2006)
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KRAS is vulnerable to reversible switch-II pocket engagement in cells
Vasta, James D, Peacock, D Matthew, Zheng, Qinheng, Walker, Joel A, Zhang, Ziyang, Zimprich, Chad A, Thomas, Morgan R, Beck, Michael T, Binkowski, Brock F, Corona, Cesear R, Robers, Matthew B, Shokat, Kevan M
Published in Nature chemical biology (01.06.2022)
Published in Nature chemical biology (01.06.2022)
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Journal Article
Discovery of a New Isoxazole-3-hydroxamate-Based Histone Deacetylase 6 Inhibitor SS-208 with Antitumor Activity in Syngeneic Melanoma Mouse Models
Shen, Sida, Hadley, Melissa, Ustinova, Kseniya, Pavlicek, Jiri, Knox, Tessa, Noonepalle, Satish, Tavares, Mauricio T, Zimprich, Chad A, Zhang, Guiping, Robers, Matthew B, Bařinka, Cyril, Kozikowski, Alan P, Villagra, Alejandro
Published in Journal of medicinal chemistry (26.09.2019)
Published in Journal of medicinal chemistry (26.09.2019)
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