Zobrazeno 1 - 10
of 226
pro vyhledávání: '"van Oost, B."'
Publikováno v:
In The Journal of nutrition, health and aging August 2020 24(8):821-826
Autor:
Vos-Loohuis, M, van Oost, B A, Dangel, C, Langbein-Detsch, I, Leegwater, P A, CSCA AVM, dCSCA AVR, dCSCA RMSC-1
Publikováno v:
Animal Genetics, 48(4), 493. Wiley-Blackwell
Von Willebrand disease (VWD), caused by deficiency of the von Willebrand factor (VWF), is the most common bleeding disorder in humans and dogs. The complete cDNA encoding VWF of a German Wirehaired Pointer with type 2 VWD was sequenced, and we found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b62f5149d7602f5aea56831dfb54a82b
https://doi.org/10.1111/age.12544
https://doi.org/10.1111/age.12544
Publikováno v:
Science, 1993 Oct . 262(5133), 578-580.
Externí odkaz:
https://www.jstor.org/stable/2882585
Von Willebrand disease (VWD), caused by deficiency of the von Willebrand factor (VWF), is the most common bleeding disorder in humans and dogs. The complete cDNA encoding VWF of a German Wirehaired Pointer with type 2 VWD was sequenced, and we found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______101::5e26e783a3fbbbb752817cfd35c5065d
https://dspace.library.uu.nl/handle/1874/360915
https://dspace.library.uu.nl/handle/1874/360915
Autor:
van Oost, B.
Publikováno v:
Krisis, 2, 48-50. Stichting Krisis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::a58f6d3bcfc9666bc07f8e06d5415461
https://cris.maastrichtuniversity.nl/en/publications/5330caa7-ad0e-42b3-96db-9c754f552be6
https://cris.maastrichtuniversity.nl/en/publications/5330caa7-ad0e-42b3-96db-9c754f552be6
Publikováno v:
In European Research in Telemedicine/La Recherche Européenne en Télémédecine April 2017 6(1):35-35
Autor:
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.
Mild hyperhomocysteinemia is an established risk factor for cardiovascular disease. Genetic aberrations in the cystathionine beta-synthase (CBS) and methylenetetrahydrofolate reductase (MTHFR) genes may account for reduced enzyme activities and eleva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::407408edf3fb4b9a05bb2fc4a099609f
https://europepmc.org/articles/PMC1914961/
https://europepmc.org/articles/PMC1914961/
Autor:
van Lieburg, A. F., Verdijk, M. A., Knoers, V. V., van Essen, A. J., Proesmans, W., Mallmann, R., Monnens, L. A., van Oost, B. A., van Os, C. H., Deen, P. M.
Mutations in the X-chromosomal V2 receptor gene are known to cause nephrogenic diabetes insipidus (NDI). Besides the X-linked form, an autosomal mode of inheritance has been described. Recently, mutations in the autosomal gene coding for water-channe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d31951cf19bced768de2e6905cb2b3cf
https://europepmc.org/articles/PMC1918308/
https://europepmc.org/articles/PMC1918308/
Autor:
Brunner, H. G., Nelen, M. R., van Zandvoort, P., Abeling, N. G., van Gennip, A. H., Wolters, E. C., Kuiper, M. A., Ropers, H. H., van Oost, B. A.
Publikováno v:
American journal of human genetics, 52(6), 1032-1039. Cell Press
We have identified a large Dutch kindred with a new form of X-linked nondysmorphic mild mental retardation. All affected males in this family show very characteristic abnormal behavior, in particular aggressive and sometimes violent behavior. Other t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0bae68fee882ce0c94f0f3725c1a52a2
https://europepmc.org/articles/PMC1682278/
https://europepmc.org/articles/PMC1682278/