Human catechol O-methyltransferase genetic variation: gene resequencing and functional characterization of variant allozymes von Shield, A J, Thomae, B A, Eckloff, B W, Wieben, E D, Weinshilboum, R M

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Genetic diversity and function in the human cytosolic sulfotransferases von Hildebrandt, M A T, Carrington, D P, Thomae, B A, Eckloff, B W, Schaid, D J, Yee, V C, Weinshilboum, R M, Wieben, E D

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Human sulfotransferase SULT2A1 pharmacogenetics: genotype-to-phenotype studies von Thomae, B A, Eckloff, B W, Freimuth, R R, Wieben, E D, Weinshilboum, R M

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The Risk of Pretransplant Blood Transfusion for Primary Graft Dysfunction After Lung Transplant von Kaihou, Taisuke, Toyoda, Takahide, Cerier, Emily, Yagi, Yuriko, Manerikar, Adwaiy, Thomae, Benjamin Louis, Kandula, Viswajit, Bharat, Ankit, Kurihara, Chitaru

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Human Arsenic Methyltransferase (AS3MT) Pharmacogenetics: GENE RESEQUENCING AND FUNCTIONAL GENOMICS STUDIES von Wood, Thomas C, Salavagionne, Oreste E, Mukherjee, Baidehi, Wang, Liewei, Klumpp, Annette F, Thomae, Bianca A, Eckloff, Bruce W, Schaid, Daniel J, Wieben, Eric D, Weinshilboum, Richard M

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Human estrogen sulfotransferase (SULT1E1) pharmacogenomics: gene resequencing and functional genomics von Adjei, Araba A, Thomae, Bianca A, Prondzinski, Janel L, Eckloff, Bruce W, Wieben, Eric D, Weinshilboum, Richard M

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Human catecholamine sulfotransferase (SULT1A3) pharmacogenetics: functional genetic polymorphism von Thomae, Bianca A., Rifki, Oktay F., Theobald, Michelle A., Eckloff, Bruce W., Wieben, Eric D., Weinshilboum, Richard M.

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Human phenylethanolamine N-methyltransferase (PNMT) pharmacogenetics: gene resequencing and functional genomic studies von Ji, Y., Salavaggione, O. E., Adjei, A. A., Thomae, B. A., Eckloff, B., Wieben, E. D., Weinshilboum, R. M.

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Pharmacogenetics of human 3′-phosphoadenosine 5′-phosphosulfate synthetase 1 (PAPSS1): gene resequencing, sequence variation, and functional genomics von Xu, Zhen-Hua, Thomae, Bianca A., Eckloff, Bruce W., Wieben, Eric D., Weinshilboum, Richard M.

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Human sulfotransferase SULT2A1 pharmacogenetics: genotype-to-phenotype studies von Thomae, BA, Eckloff, B W, Freimuth, R R, Wieben, ED, Weinshilboum, R M

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Disputatio moralis de voluntate quam ... sub praesidio ... M. Israelis Bringii, ... pro gradu in philosophia consequendo, publicæ disquisitioni submittit Samuel Thomae B. Vest-Mont... von Bringius, Israel

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Characterizing stress processes by linking big five personality states, traits, and day-to-day stressors von Ringwald, Whitney R, Nielsen, Sienna R, Mostajabi, Janan, Vize, Colin E, van den Berg, Tessa, Manuck, Stephen B, Marsland, Anna L, Wright, Aidan G.C

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Structure of the RNA Helicase MLE Reveals the Molecular Mechanisms for Uridine Specificity and RNA-ATP Coupling von Prabu, J. Rajan, Müller, Marisa, Thomae, Andreas W., Schüssler, Steffen, Bonneau, Fabien, Becker, Peter B., Conti, Elena

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Isagoge historico-theologica ad theologiam vniversam singvlasqve eivs partes, novis svpplementis avctior von Johann Franz Budde, jn20000601060

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Two-step mechanism for selective incorporation of lncRNA into a chromatin modifier von Müller, Marisa, Schauer, Tamas, Krause, Silke, Villa, Raffaella, Thomae, Andreas W, Becker, Peter B

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Histone Methylation by PRC2 Is Inhibited by Active Chromatin Marks von Schmitges, Frank W., Prusty, Archana B., Faty, Mahamadou, Stützer, Alexandra, Lingaraju, Gondichatnahalli M., Aiwazian, Jonathan, Sack, Ragna, Hess, Daniel, Li, Ling, Zhou, Shaolian, Bunker, Richard D., Wirth, Urs, Bouwmeester, Tewis, Bauer, Andreas, Ly-Hartig, Nga, Zhao, Kehao, Chan, Homan, Gu, Justin, Gut, Heinz, Fischle, Wolfgang, Müller, Jürg, Thomä, Nicolas H.

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Structural basis of RNA-induced autoregulation of the DExH-type RNA helicase maleless von Jagtap, Pravin Kumar Ankush, Müller, Marisa, Kiss, Anna E, Thomae, Andreas W, Lapouge, Karine, Beck, Martin, Becker, Peter B, Hennig, Janosch

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(1278) - Isolated Right Heart Stress-Induced Cardiomyopathy After Lung Transplant von Thomae, B., Kaiho, T., Bharat, A., Kurihara, C.

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(562) - COVID-19-Associated ARDS: Not a Risk Factor for Chronic Allograft Dysfunction in Lung Transplant Patients von Thomae, B., Kaiho, T., Bharat, A., Buddinger, G., Kurihara, C.

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The histone variant H2A.Bbd is enriched at sites of DNA synthesis von Sansoni, Viola, Casas-Delucchi, Corella S, Rajan, Malini, Schmidt, Andreas, Bönisch, Clemens, Thomae, Andreas W, Staege, Martin S, Hake, Sandra B, Cardoso, M Cristina, Imhof, Axel

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