DDOST, PRKCSH and LGALS3, which encode AGE-receptors 1, 2 and 3, respectively, are not associated with diabetic nephropathy in type 1 diabetes von Hoverfelt, A, Sallinen, R, Söderlund, J. M, Forsblom, C, Pettersson-Fernholm, K, Parkkonen, M, Groop, P.-H, Wessman, M

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Powering aircraft with 100 % sustainable aviation fuel reduces ice crystals in contrails von Märkl, Raphael Satoru, Voigt, Christiane, Sauer, Daniel, Dischl, Rebecca Katharina, Kaufmann, Stefan, Harlaß, Theresa, Hahn, Valerian, Roiger, Anke, Weiß-Rehm, Cornelius, Burkhardt, Ulrike, Schumann, Ulrich, Marsing, Andreas, Scheibe, Monika, Dörnbrack, Andreas, Renard, Charles, Gauthier, Maxime, Swann, Peter, Madden, Paul, Luff, Darren, Sallinen, Reetu, Schripp, Tobias, Le Clercq, Patrick

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Measurement report: In-flight and ground-based measurements of nitrogen oxide emissions from latest-generation jet engines and 100 % sustainable aviation fuel von Harlass, Theresa, Dischl, Rebecca, Kaufmann, Stefan, Märkl, Raphael, Sauer, Daniel, Scheibe, Monika, Stock, Paul, Bräuer, Tiziana, Dörnbrack, Andreas, Roiger, Anke, Schlager, Hans, Schumann, Ulrich, Pühl, Magdalena, Schripp, Tobias, Grein, Tobias, Bondorf, Linda, Renard, Charles, Gauthier, Maxime, Johnson, Mark, Luff, Darren, Madden, Paul, Swann, Peter, Ahrens, Denise, Sallinen, Reetu, Voigt, Christiane

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Measurements of particle emissions of an A350-941 burning 100 % sustainable aviation fuels in cruise von Dischl, Rebecca, Sauer, Daniel, Voigt, Christiane, Harlaß, Theresa, Sakellariou, Felicitas, Märkl, Raphael, Schumann, Ulrich, Scheibe, Monika, Kaufmann, Stefan, Roiger, Anke, Dörnbrack, Andreas, Renard, Charles, Gauthier, Maxime, Swann, Peter, Madden, Paul, Luff, Darren, Johnson, Mark, Ahrens, Denise, Sallinen, Reetu, Schripp, Tobias, Eckel, Georg, Bauder, Uwe, Le Clercq, Patrick

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New methods for molecular diagnosis and demonstration of the (CCTG) n mutation in myotonic dystrophy type 2 (DM2) von Sallinen, R, Vihola, A, Bachinski, L.L, Huoponen, K, Haapasalo, H, Hackman, P, Zhang, S, Sirito, M, Kalimo, H, Meola, G, Horelli-Kuitunen, N, Wessman, M, Krahe, R, Udd, B

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Genetic Risk Score for Serum 25-Hydroxyvitamin D Concentration Helps to Guide Personalized Vitamin D Supplementation in Healthy Finnish Adults von Sallinen, Riitta J, Dethlefsen, Olga, Ruotsalainen, Sanni, Mills, Robert D, Miettinen, Timo A, Jääskeläinen, Tuija E, Lundqvist, Annamari, Kyllönen, Eero, Kröger, Heikki, Karppinen, Jaro I, Lamberg-Allardt, Christel, Viljakainen, Heli, Kaunisto, Mari A, Kallioniemi, Olli

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Confirmation of the Type 2 Myotonic Dystrophy (CCTG) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Sin... von Bachinski, Linda L., Udd, Bjarne, Meola, Giovanni, Sansone, Valeria, Bassez, Guillaume, Eymard, Bruno, Thornton, Charles A., Moxley, Richard T., Harper, Peter S., Rogers, Mark T., Jurkat-Rott, Karin, Lehmann-Horn, Frank, Wieser, Thomas, Gamez, Josep, Navarro, Carmen, Bottani, Armand, Kohler, Andre, Shriver, Mark D., Sallinen, Riitta, Wessman, Maija, Zhang, Shanxiang, Wright, Fred A., Krahe, Ralf

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Chromosomal localization of SLC12A5/Slc12a5, the human and mouse genes for the neuron-specific K+-Cl– cotransporter (KCC2) defines a new region of conserved homology von Sallinen, R., Tornberg, J., Putkiranta, M., Horelli-Kuitunen, N., Airaksinen, M.S., Wessman, M.

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Novel splice site CACNA1A mutation causing episodic ataxia type 2 von KAUNISTO, M. A, HARNO, H, FÄRKKILÄ, M, WESSMAN, M, KALLELA, M, SOMER, H, SALLINEN, R, HÄMÄLÄINEN, E, MIETTINEN, P. J, VESA, J, ORPANA, A, PALOTIE, A

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Chromosomal localization of SLC12A5/Slc12a5, the human and mouse genes for the neuron-specific K+-Cl– cotransporter (KCC2) defines a new region of conserved homology von Sallinen, R., Tornberg, J., Putkiranta, M., Horelli-Kuitunen, N., Airaksinen, M.S., Wessman, M.

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Novel splice site CACNA1A mutation causing episodic ataxia type 2 von Kaunisto, M A, Harno, H, Kallela, M, Somer, H, Sallinen, R, Hämäläinen, E, Miettinen, P J, Vesa, J, Orpana, A, Palotie, A, Färkkilä, M, Wessman, M

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Erratum von Sallinen, R, Tornberg, J, Putkiranta, M, Horelli-Kuitunen, N

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Chromosomal localization of SLC12A5/Slc12a5, the human and mouse genes for the neuron-specific K+-CI- cotransporter (KCC2) defines a new region of conserved homology von Sallinen, R, Tornberg, J, Putkiranta, M, Horelli-Kuitunen, N

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Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL von Pajukanta, P, Bodnar, J S, Sallinen, R, Chu, M, Airaksinen, T, Xiao, Q, Castellani, L W, Sheth, S S, Wessman, M, Palotie, A, Sinsheimer, J S, Demant, P, Lusis, A J, Peltonen, L

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Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization von Sallinen, R, Kuang, W, Engvall, E, Palotie, A

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Assignment 1 of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4–B1 by fluorescence in situ hybridization von Sallinen, R., Kuang, W., Engvall, E., Palotie, A., Wessman, M., Horelli-Kuitunen, N.

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Physical mapping of mouse collagen genes on chromosome 10 by high-resolution FISH von Sallinen, R, Latvanlehto, A, Kvist, A P, Rehn, M, Eerola, I, Chu, M L, Bonaldo, P, Saitta, B, Bressan, G M, Pihlajaniemi, T, Vuorio, E, Palotie, A, Wessman, M, Horelli-Kuitunen, N

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Chromosomal localization of SLC12A5/Slc12a5, the human and mouse genes for the neuron-specific K super(+)-Cl super(-) cotransporter (KCC2) defines a new region of conserved homolog... von Sallinen, R, Tornberg, J, Putkiranta, M, Horelli-Kuitunen, N, Airaksinen, MS, Wessman, M

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Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridization von SALLINEN, R, KUANG, W, ENGVALL, E, PALOTIE, A, WESSMAN, M, HORELLI-KUITUNEN, N

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Bolometer operating at the threshold for circuit quantum electrodynamics von Kokkoniemi, R., Girard, J.-P., Hazra, D., Laitinen, A., Govenius, J., Lake, R. E., Sallinen, I., Vesterinen, V., Partanen, M., Tan, J. Y., Chan, K. W., Tan, K. Y., Hakonen, P., Möttönen, M.

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