Requirement of Human Renal Water Channel Aquaporin-2 for Vasopressin-Dependent Concentration of Urine
Peter M. T. Deen, Marian A. J. Verdijk, Nine V. A. M. Knoers, Wieringa, Bé, Leo A. H. Monnens, van Os, Carel H., van Oost, Bernard A.
Published in Science (American Association for the Advancement of Science) (01.04.1994)
Published in Science (American Association for the Advancement of Science) (01.04.1994)
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High‐resolution genetic mapping of mammalian motor activity levels in mice
Kas, M. J. H., De Mooij‐van Malsen, J. G., De Krom, M., Van Gassen, K. L. I., Van Lith, H. A., Olivier, B., Oppelaar, H., Hendriks, J., De Wit, M., Groot Koerkamp, M. J. A., Holstege, F. C. P., Van Oost, B. A., De Graan, P. N. E.
Published in Genes, brain and behavior (01.02.2009)
Published in Genes, brain and behavior (01.02.2009)
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A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome
De Coo, I. F. M., Renier, W. O., Ruitenbeek, W., Ter Laak, H. J., Bakker, M., Schägger, H., Van Oost, B. A., Smeets, H. J. M.
Published in Annals of neurology (01.01.1999)
Published in Annals of neurology (01.01.1999)
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Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease
Kluijtmans, L A, van den Heuvel, L P, Boers, G H, Frosst, P, Stevens, E M, van Oost, B A, den Heijer, M, Trijbels, F J, Rozen, R, Blom, H J
Published in American journal of human genetics (01.01.1996)
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Published in American journal of human genetics (01.01.1996)
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X-linked borderline mental retardation with prominent behavioral disturbance : phenotype, genetic localization, and evidence for disturbed monoamine metabolism
BRUNNER, H. G, NELEN, M. R, VAN ZANDVOORT, P, ABELING, N. G. G. M, VAN GENNIP, A. H, WOLTERS, E. C, KUIPER, M. A, ROPERS, H. H, VAN OOST, B. A
Published in American journal of human genetics (01.06.1993)
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Published in American journal of human genetics (01.06.1993)
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Evaluation of the Serotonergic Genes htr1A, htr1B, htr2A, and slc6A4 in Aggressive Behavior of Golden Retriever Dogs
van den Berg, L., Vos-Loohuis, M., Schilder, M. B. H., van Oost, B. A., Hazewinkel, H. A. W., Wade, C. M., Karlsson, E. K., Lindblad-Toh, K., Liinamo, A. E., Leegwater, P. A. J.
Published in Behavior genetics (01.01.2008)
Published in Behavior genetics (01.01.2008)
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Structure and Variation of Three Canine Genes Involved in Serotonin Binding and Transport: The Serotonin Receptor 1A Gene (htr1A), Serotonin Receptor 2A Gene (htr2A), and Serotonin Transporter Gene (slc6A4)
Berg, L. van den, Kwant, L, Hestand, M. S, Oost, B. A. van, Leegwater, P. A. J
Published in The Journal of heredity (2005)
Published in The Journal of heredity (2005)
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Characterization of the COMMD1 (MURR1) mutation causing copper toxicosis in Bedlington terriers
Forman, O.P, Boursnell, M.E.G, Dunmore, B.J, Stendall, N, Sluis, B. van de, Fretwell, N, Jones, C, Wijmenga, C, Rothuizen, J, Oost, B.A. van
Published in Animal genetics (01.12.2005)
Published in Animal genetics (01.12.2005)
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Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene
VAN LIEBURG, A. F, VERDIJK, M. A. J, KNOERS, V. V. A. M, VAN ESSEN, A. J, PROESMANS, W, MALLMANN, R, MONNENS, L. A. H, VAN OOST, B. A, VAN OS, C. H, DEEN, P. M. T
Published in American journal of human genetics (01.10.1994)
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Published in American journal of human genetics (01.10.1994)
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Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia
De Vries, D D, Went, L N, Bruyn, G W, Scholte, H R, Hofstra, R M, Bolhuis, P A, van Oost, B A
Published in American journal of human genetics (01.04.1996)
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Published in American journal of human genetics (01.04.1996)
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Genetic Mapping of the Copper Toxicosis Locus in Bedlington Terriers to Dog Chromosome 10, in a Region Syntenic to Human Chromosome Region 2p13–p16
van de Sluis, Bart J. A., Breen, Matthew, Nanji, Manoj, van Wolferen, Monique, de Jong, Pieter, Binns, Matthew M., Pearson, Peter L., Kuipers, Jeroen, Rothuizen, Jan, Cox, Diane W., Wijmenga, Cisca, van Oost, Bernard A.
Published in Human molecular genetics (01.03.1999)
Published in Human molecular genetics (01.03.1999)
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