Zobrazeno 1 - 10
of 2 113
pro vyhledávání: '"Reijnders M"'
Autor:
Debernardi, N., Reijnders, M. P., Engelen, W. J., Clevis, T. T. J., Mutsaers, P. H. A., Luiten, O. J., Vredenbregt, E. J. D.
Publikováno v:
J.Appl.Phys.110:024501,2011
We report on a measurement of the characteristic temperature of an ultracold rubidium ion source, in which a cloud of laser-cooled atoms is converted to ions by photo-ionization. Extracted ion pulses are focused on a detector with a pulsed-field tech
Externí odkaz:
http://arxiv.org/abs/1011.2369
Autor:
Johannesen, K.M., Gardella, E., Gjerulfsen, C.E., Bayat, A., Rouhl, R.P.W., Reijnders, M., Whalen, S., Keren, B., Buratti, J., Courtin, T., Wierenga, K.J., Isidor, B., Piton, A., Faivre, L., Garde, A., Moutton, S., Tran-Mau-Them, F., Denomme-Pichon, A.S., Coubes, C., Larson, A., Esser, M.J., Appendino, J.P., Al-Hertani, W., Gamboni, B., Mampel, A., Mayorga, L., Orsini, A., Bonuccelli, A., Suppiej, A., Van-Gils, J., Vogt, J., Damioli, S., Giordano, L., Moortgat, S., Wirrell, E., Hicks, S., Kini, U., Noble, N., Stewart, H., Asakar, S., Cohen, J.S., Naidu, S.R., Collier, A., Brilstra, E.H., Li, M.H., Brew, C., Bigoni, S., Ognibene, D., Ballardini, E., Ruivenkamp, C.
Publikováno v:
Neurology. Genetics, 7(6):e613. LIPPINCOTT WILLIAMS & WILKINS
Background and ObjectivesPurine-rich element-binding protein A (PURA) gene encodes Pur-alpha, a conserved protein essential for normal postnatal brain development. Recently, a PURA syndrome characterized by intellectual disability, hypotonia, epileps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::8806df5dde1854795a986b7fd137056e
https://cris.maastrichtuniversity.nl/en/publications/4020e32d-88c6-40a2-970d-ba1b2809b360
https://cris.maastrichtuniversity.nl/en/publications/4020e32d-88c6-40a2-970d-ba1b2809b360
Autor:
Kennedy, J., Goudie, D., Blair, E., Chandler, K., Joss, S., McKay, V., Green, A., Armstrong, R., Lees, M., Kamien, B., Hopper, B., Tan, T.Y., Yap, P., Stark, Z., Okamoto, N., Miyake, N., Matsumoto, N., Macnamara, E., Murphy, J.L., McCormick, E., Hakonarson, H., Falk, M.J., Li, D., Blackburn, P., Klee, E., Babovic-Vuksanovic, D., Schelley, S., Hudgins, L., Kant, S., Isidor, B., Cogne, B., Bradbury, K., Williams, M., Patel, C., Heussler, H., Duff-Farrier, C., Lakeman, P., Scurr, I., Kini, U., Elting, M., Reijnders, M., Schuurs-Hoeijmakers, J., Wafik, M., Blomhoff, A., Ruivenkamp, C.A.L., Nibbeling, E., Dingemans, A.J.M., Douine, E.D., Nelson, S.F., Hempel, M., Bierhals, T., Lessel, D., Johannsen, J., Arboleda, V.A., Newbury-Ecob, R., DDD Study
Publikováno v:
Genetics in Medicine, 22(11), 1920-1920. NATURE PUBLISHING GROUP
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b215076ffb7ac5e70c346089be959f25
https://doi.org/10.1038/s41436-020-00944-7
https://doi.org/10.1038/s41436-020-00944-7
Autor:
Prins, J. T. H., Van Lieshout, E. M. M., Reijnders, M. R. L., Verhofstad, M. H. J., Wijffels, M. M. E.
Publikováno v:
Osteoporosis International; Feb2020, Vol. 31 Issue 2, p225-231, 7p, 2 Diagrams, 2 Charts, 1 Graph
Autor:
Debernardi, N., Reijnders, M. P., Engelen, W. J., Clevis, T. T. J., Mutsaers, P. H. A., Luiten, O. J., Vredenbregt, E. J. D.
Publikováno v:
Journal of Applied Physics; Jul2011, Vol. 110 Issue 2, p024501, 7p
Autor:
Reijnders, M. P., Debernardi, N., van der Geer, S. B., Mutsaers, P. H. A., Vredenbregt, E. J. D., Luiten, O. J.
Publikováno v:
Journal of Applied Physics; Feb2011, Vol. 109 Issue 3, p033302, 14p, 5 Diagrams, 12 Graphs
Autor:
van der Geer, S. B., Reijnders, M. P., de Loos, M. J., Vredenbregt, E. J. D., Mutsaers, P. H. A., Luiten, O. J.
Publikováno v:
Journal of Applied Physics; Nov2007, Vol. 102 Issue 9, p094312, 7p, 1 Diagram, 3 Graphs
Autor:
Jean-Marcais, N., Olson, H. E., Yang, E., Heron, D., Tatton-Brown, K., van der Zwaag, P. A., Bijlsma, E. K., Krock, B. L., Backer, E., Kamsteeg, E., Sinnema, M., Reijnders, M. R. F., Bearden, D., Lunsing, R. J., Burglen, L., Lesca, G., Smith, L. A., Sheidley, B., Pearl, P. L., El Achkar, C. Moufawad, Poduri, A., Skraban, C. M., Nesbitt, A. I., van de Putte, D. E. Fransen, Ruivenkamp, C. A. L., Rump, P., Sabatier, I., Sweetser, D. A., Waxler, J. L., Tarpinian, J., Wierenga, K. J., Donadieu, J., Narayanan, V., Ramsey, K. M., Nava, C., Lelieveld, S. H., Schuurs-Hoeijmakers, J., Brunner, H. G., Keren, B., Mau-Them, F. Tran, Thevenon, J., Faivre, L., Thomas, G., Thauvin-Robinet, C.
Publikováno v:
European Journal of Human Genetics, 27, 853-854. Nature Publishing Group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::d0114cea4f687e72dbc0ec2faa82754e
https://research.rug.nl/en/publications/0b4fba38-3f4b-40f5-9cd4-f1696ea47a29
https://research.rug.nl/en/publications/0b4fba38-3f4b-40f5-9cd4-f1696ea47a29
Autor:
Reijnders, M, Miller, K, Alvi, M, Calpena, E, Koelling, N, McGowan, S, Twigg, S, Nellaker, C, Wilkie, A, al., E
Publikováno v:
American Journal of Human Genetics. 102(6)
Next-generation sequencing is a powerful tool for the discovery of genes related to neurodevelopmental disorders (NDDs). Here, we report the identification of a distinct syndrome due to de novo or inherited heterozygous mutations in Tousled-like kina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::34a64964ef8b21d2b6f2cf1518b85eba
http://ora.ox.ac.uk/objects/uuid:
http://ora.ox.ac.uk/objects/uuid:
Publikováno v:
Epidemiology & Psychiatric Science; Feb2019, Vol. 28 Issue 1, p21-30, 10p