Association of genetic polymorphism of guanosintriphosphate of cyclohydrolases and catechol-O-methyltransferase with the frequency of the appearance of chronic pain after surgery von Gаbovich, B. E., Veske, A., Dаi, F., Kolesnikov, Yu. A.

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Retinal dystrophy of Swedish briard/briard-beagle dogs is due to a 4-bp deletion in RPE65 von Veske, A. (Universitats-Klinikum Hamburg-Eppendorf, Hamburg, Germany.), Nilsson, S.E.G, Narfstrom, K, Gal, A

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Plexin B3 is genetically associated with verbal performance and white matter volume in human brain von RUJESCU, D, MEISENZAHL, E. M, FINCKH, U, KREJCOVA, S, GIEGLING, I, ZETZSCHE, T, REISER, M, BORN, C. M, MÖLLER, H-J, VESKE, A, GAL, A

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Autosomal Recessive Non-Syndromic Deafness Locus (DFNB8) Maps on Chromosome 21Q22 in a Large Consanguineous Kindred from Pakistan von Veske, Andres, Oehlmann, Ralph, Younus, Farah, Mohyuddin, Aisha, Müller-Myhsok, Bertram, Qasim Mehdi, S., Gal, Andreas

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Constraining Black Hole Populations in Globular Clusters Using Microlensing: Application to Omega Centauri von Zaris, John, Veske, Do a, Samsing, Johan, Márka, Zsuzsa, Bartos, Imre, Márka, Szabolcs

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A human specific haplotype in Plexin B3 is associated with verbal performance and brain white matter volume von Rujescu, D, Meisenzahl, E M, Krejcova, S, Giegling, I, Zetzsche, T, Reiser, M, Born, C M, Möller, H-J, Veske, A, Gal, A, Finckh, U

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Primary Pulmonary Synovial Sarcoma : A Very Rare Presentation von Seyhan, Ekrem Cengiz, Sökücü, Sinem Nedime, Gunluoglu, Gulsah, Veske, Nurdan Simsek, Altın, Sedat

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Identification and characterization of mouse plexin B3 promoter von Tiismus, Liivi, Laht, Piret, Otsus, Maarja, Veske, Andres

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Plexin B3 promotes neurite outgrowth, interacts homophilically, and interacts with Rin von Hartwig, Christine, Veske, Andres, Krejcova, Sarka, Rosenberger, Georg, Finckh, Ulrich

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Microsatellite (CA)n polymorphism in intron 2 of the canine rod photoreceptor cGMP-phosphodiesterase α-subunit gene von Veske, A., Nilsson, S E G, Gal, A.

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Plexin B3 is genetically associated with verbal performance and white matter volume in human brain von Rujescu, D, Meisenzahl, E M, Krejcova, S, Giegling, I, Zetzsche, T, Reiser, M, Born, C M, Möller, H-J, Veske, A, Gal, A, Finckh, U

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Two novel mutations in the Norrie disease gene associated with the classical ocular phenotype von Caballero, M., Veske, A., Rodriguez, J. J., Lugo, N., Schroeder, B., Hesse, L., Gal, A.

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Microsatellite (TTCC)n polymorphism in intron 6 of the canine rod photoreceptor cGMP-gated cation channel alpha-subunit gene von Veske, A, Nilsson, S E, Gal, A

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Organization of the canine gene encoding the E isoform of retinal guanylate cyclase (cGC-E) and exclusion of its involvement in the inherited retinal dystrophy of the Swedish Briar... von Veske, Andres, Nilsson, Sven Erik G, Gal, Andreas

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Characterization of canine rod photoreceptor cGMP-gated cation channel α-subunit gene and exclusion of its involvement in the hereditary retinal dystrophy of Swedish Briards von Veske, Andres, Nilsson, Sven Erik G, Gal, Andreas

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Five novel mutations in the L1CAM gene in families with X linked hydrocephalus von Gu, S M, Orth, U, Veske, A, Enders, H, Klunder, K, Schlosser, M, Engel, W, Schwinger, E, Gal, A

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Isolation of canine retinal arrestin cDNA and exclusion of three candidate genes for Swedish Briard retinal dystrophy von Veske, Andres, Narfström, Kristina, Finckh, Ulrich, Sargan, David R., Nilsson, Sven Erik G., Gal, Andreas

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Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease von Finckh, Ulrich, Schröder, Jutta, Ressler, Bernadette, Veske, Andres, Gal, Andreas

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Detecting fundamental vector fields with LISA von Fell, Shaun, Heisenberg, Lavinia, Veske, Doğa

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Plasma cyclic AMP level in donors von Fedorov, N. A., Veske, M. A., Ermil'chenko, G. V., Malykhina, L. S.

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