The interplay between genotype, metabolic state and cofactor treatment governs phenylalanine hydroxylase function and drug response von STAUDIGL, Michael, GERSTING, Soren W, DANECKA, Marta K, MESSING, Dunja D, WOIDY, Mathias, PINKAS, Daniel, KEMTER, Kristina F, BLAU, Nenad, MUNTAU, Ania C

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The interplay between genotype, metabolic state and cofactor treatment governs phenylalanine hydroxylase function and drug response von Staudigl, M, Gersting, S W, Danecka, M K, Messing, D D, Woidy, M, Pinkas, D, Kemter, K F, Blau, N, Muntau, A C

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Loss of Function in Phenylketonuria is Caused by Impaired Molecular Motions and Conformational Instability von Gersting, S W, Kemter, K F, Staudigl, M, Messing, D D, Danecka, M K, Lagler, F B, Sommerhoff, C P, Roscher, A A, Muntau, A C

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FLAT WARP KNITTING MACHINE, ESPECIALLY SEWING-KNITTING MACHINE von WOLFGANG H. DORING, HANS-DIETER HENTSCHEL, HEINZ K. F. KEMTER, ALFRED H. SCHMIDT, WERNER F. H. MICKENAUTSCH, PAUL B. FRENZEL

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Loss of Function in Phenylketonuria Is Caused by Impaired Molecular Motions and Conformational Instability von Gersting, Søren W., Kemter, Kristina F., Staudigl, Michael, Messing, Dunja D., Danecka, Marta K., Lagler, Florian B., Sommerhoff, Christian P., Roscher, Adelbert A., Muntau, Ania C.

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Activation of Phenylalanine Hydroxylase Induces Positive Cooperativity toward the Natural Cofactor von Gersting, Søren W., Staudigl, Michael, Truger, Marietta S., Messing, Dunja D., Danecka, Marta K., Sommerhoff, Christian P., Kemter, Kristina F., Muntau, Ania C.

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Pahenu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivo von Gersting, Søren W., Lagler, Florian B., Eichinger, Anna, Kemter, Kristina F., Danecka, Marta K., Messing, Dunja D., Staudigl, Michael, Domdey, Katharina A., Zsifkovits, Clemens, Fingerhut, Ralph, Glossmann, Hartmut, Roscher, Adelbert A., Muntau, Ania C.

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CELL SIGNALLING AND APOPTOSIS von Shiohira, S., Yoshida, T., Sugiura, H., Nishida, M., Nitta, K., Tsuchiya, K., Grampp, S., Goppelt-Strube, M., Eckardt, K. U., Schodel, J., Kang, S. W., Kim, Y., Seo, S.-K., Kim, T., Ong, S., Yang, W. S., Han, N. J., Lee, J. M., Baek, C. H., Park, S.-K., Kemter, E., Aigner, B., Wanke, R., Troyano Suarez, N., Olmos Centenero, G., Mora, I., Griera, M., Cano, J. L., Martin, P., Zamora, J., Ruiz-Torres, M. P., Falke, L. L., Leask, A., Lyons, K., Nguyen, T. Q., Goldschmeding, R., Park, S. K., Kim, D., Lee, A. S., Jung, Y. J., Yang, K. H., Lee, S., Kim, W., Kang, K. P., Garcia-Jerez, A., Luengo-Rodriguez, A., Ramirez-Chamond, R., Carracedo, J., Medrano-Andres, D., Rodriguez-Puyol, D., Calleros, L., Kim, H. W., Lee, S. K., Chang, J. W., Seo, J. W., Lee, C.-T., Chou, C.-A., Lee, Y.-T., Ng, H.-Y., Sanchez-Nino, M. D., Fernandez-Fernandez, B., Perez-Gomez, M. V., Poveda, J., Sanz, A. B., Cannata-Ortiz, P., Egido, J., Selgas, R., Ortiz, A., Ma, S. K., Kim, I. J., Kim, C. S., Bae, E. H., Kim, S. W., Kokeny, G., Boo'Si, M., Fazekas, K., Rosivall, L., Mozes, M. M., Mijuskovic, M., Ulrich, C., Berger, H., Trojanowicz, B., Kohler, F., Wolf, A., Seibert, E., Fiedler, R., Markau, S., Glomb, M., Girndt, M., Lajdova, I., Spustova, V., Oksa, A., Chorvat, D., Marcek Chorvatova, A., Choi, S. O., Kim, J. S., Han, B. G., Yang, J. W., Liu, S., Lv, J.

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Genetic diseases and molecular genetics von Legendre, C., Cohen, D., Delmas, Y., Feldkamp, T., Fouque, D., Furman, R., Gaber, O., Greenbaum, L., Goodship, T., Haller, H., Herthelius, M., Hourmant, M., Licht, C., Moulin, B., Sheerin, N., Trivelli, A., Bedrosian, C. L., Loirat, C., Babu, S., Jungraithmayr, T., Lebranchu, Y., Riedl, M., Gaber, A. O., Bedrosian, C., Muus, P., Douglas, K., Remuzzi, G., Kourouklaris, A., Ioannou, K., Athanasiou, I., Demetriou, K., Panagidou, A., Zavros, M., Rodriguez C, N. Y., Blasco, M., Arcal, C., Quintana, L. F., Rodriguez de Cordoba, S., Campistol, J. M., Bachmann, N., Eisenberger, T., Decker, C., Bolz, H. J., Bergmann, C., Pesce, F., Cox, S. N., Serino, G., De Palma, G., Sallustio, F. P., Schena, F., Falchi, M., Pieri, M., Stefanou, C., Zaravinos, A., Erguler, K., Lapathitis, G., Dweep, H., Sticht, C., Anastasiadou, N., Zouvani, I., Voskarides, K., Gretz, N., Deltas, C. C., Ruiz, A., Bonny, O., Sallustio, F., Curci, C., Cox, S., Kemter, E., Sklenak, S., Aigner, B., Wanke, R., Kitzler, T. M., Moskowitz, J. L., Piret, S. E., Lhotta, K., Tashman, A., Velez, E., Thakker, R. V., Kotanko, P., Leierer, J., Rudnicki, M., Perco, P., Koppelstaetter, C., Mayer, G., Sa, M. J. N., Alves, S., Storey, H., Flinter, F., Willems, P. J., Carvalho, F., Oliveira, J., Arsali, M., Papazachariou, L., Demosthenous, P., Lazarou, A., Hadjigavriel, M., Stavrou, C., Yioukkas, L., Deltas, C.

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Pah enu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivo von Gersting, Søren W., Lagler, Florian B., Eichinger, Anna, Kemter, Kristina F., Danecka, Marta K., Messing, Dunja D., Staudigl, Michael, Domdey, Katharina A., Zsifkovits, Clemens, Fingerhut, Ralph, Glossmann, Hartmut, Roscher, Adelbert A., Muntau, Ania C.

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Pah super(e)nu1is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivo von Gersting, Soeren W, Lagler, Florian B, Eichinger, Anna, Kemter, Kristina F, Danecka, Marta K, Messing, Dunja D, Staudigl, Michael, Domdey, Katharina A, Zsifkovits, Clemens, Fingerhut, Ralph, Glossmann, Hartmut, Roscher, Adelbert A, Muntau, Ania C

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Pah enu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivo von Gersting, Søren W, Lagler, Florian B, Eichinger, Anna, Kemter, Kristina F, Danecka, Marta K, Messing, Dunja D, Staudigl, Michael, Domdey, Katharina A, Zsifkovits, Clemens, Fingerhut, Ralph, Glossmann, Hartmut, Roscher, Adelbert A, Muntau, Ania C

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The Intraflavin Hydrogen Bond in Human Electron Transfer Flavoprotein Modulates Redox Potentials and May Participate in Electron Transfer von Dwyer, Timothy M, Mortl, Simone, Kemter, Kristina, Bacher, Adelbert, Fauq, Abdul, Frerman, Frank E

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super(13) C-, super(15) N- and super(31) P-NMR studies of oxidized and reduced low molecular mass thioredoxin reductase and some mutant proteins von Eisenreich, W, Kemter, K, Bacher, A, Mulrooney, S B, Williams, CH, Mueller, F

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