Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Jessica M.E. van den Oever"'
Autor:
Egbert Bakker, Elles M. J. Boon, Inge B. Mathijssen, Jessica M.E. van den Oever, Martine J. van Belzen, N. D. Muntjewerff, Ilse Feenstra, Emilia K. Bijlsma
Publikováno v:
Prenatal Diagnosis. 35:945-949
OBJECTIVE: With a shift towards noninvasive testing, we have explored and validated the use of noninvasive prenatal diagnosis (NIPD) for Huntington disease (HD). METHODS: Fifteen couples have been included, assessing a total of n = 20 pregnancies. Fe
Autor:
Nicole A. Datson, E. Ronald de Kloet, Oksana B. Korobko, Ana Maria Magarinos, Jessica M.E. van den Oever, Bruce S. McEwen
Publikováno v:
Endocrinology, 154(9), 3261-3272
Chronic stress is a risk factor for several neuropsychiatric diseases, such as depression and psychosis. In response to stress glucocorticoids (GCs) are secreted that bind to mineralocorticoid and glucocorticoid receptors, ligand-activated transcript
Autor:
Erik A.L. Biessen, Martin Lipp, Theo J.C. Van Berkel, Gijs H.M. van Puijvelde, W. E. Fibbe, Kirsten Canté-Barrett, Cathrine Husberg, Jessica M.E. van den Oever, Arne Yndestad, Saskia C. A. de Jager, Ilze Bot, Peter J. van Santbrink, Johan Kuiper, Pål Aukrust, Jaap Jan Zwaginga
Publikováno v:
Transplantation. 88:631-639
Background. The development of graft versus host disease (GvHD) is one of the major challenges of bone marrow transplantations (BMTs). Although clinical symptoms of GvHD share many features with auto immune diseases, the underlying mechanisms remain
Autor:
Ivonne J. H. M. van Minderhout, Nicolette S. den Hollander, Egbert Bakker, Jessica M.E. van den Oever, Elles M. J. Boon, Nienke van der Stoep, Cornelis L. Harteveld
Publikováno v:
Journal of Molecular Diagnostics, 17(5), 590-596. Association of Molecular Pathology
Van Den Oever, J M E, Van Minderhout, I J H M, Harteveld, C L, Den Hollander, N S, Bakker, E, Van Der Stoep, N & Boon, E M J 2015, ' A novel targeted approach for noninvasive detection of paternally inherited mutations in maternal plasma ', Journal of Molecular Diagnostics, vol. 17, no. 5, pp. 590-596 . https://doi.org/10.1016/j.jmoldx.2015.05.006
The Journal of Molecular Diagnostics, 17(5), 590-596
Van Den Oever, J M E, Van Minderhout, I J H M, Harteveld, C L, Den Hollander, N S, Bakker, E, Van Der Stoep, N & Boon, E M J 2015, ' A novel targeted approach for noninvasive detection of paternally inherited mutations in maternal plasma ', Journal of Molecular Diagnostics, vol. 17, no. 5, pp. 590-596 . https://doi.org/10.1016/j.jmoldx.2015.05.006
The Journal of Molecular Diagnostics, 17(5), 590-596
The challenge in noninvasive prenatal diagnosis for monogenic disorders lies in the detection of low levels of fetal variants in the excess of maternal cell-free plasma DNA. Next-generation sequencing, which is the main method used for noninvasive pr
Autor:
E. Joanne Verweij, Elles M. J. Boon, Sahila Balkassmi, Tim Segboer, Egbert Bakker, Jessica M.E. van den Oever, Pieter A. van der Velden, Dick Oepkes
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e84051 (2013)
PLoS ONE; Vol 8
PLoS ONE, 8(12)
Van Den Oever, J M E, Balkassmi, S, Segboer, T, Verweij, E J, Van Der Velden, P A, Oepkes, D, Bakker, E & Boon, E M J 2013, ' Mrassf1a-Pap, a novel methylation-based assay for the detection of cell-free fetal DNA in maternal plasma ', PLoS ONE, vol. 8, no. 12, e84051 . https://doi.org/10.1371/journal.pone.0084051
PLoS ONE, 8(12):e84051. Public Library of Science
PLoS ONE
PLoS ONE; Vol 8
PLoS ONE, 8(12)
Van Den Oever, J M E, Balkassmi, S, Segboer, T, Verweij, E J, Van Der Velden, P A, Oepkes, D, Bakker, E & Boon, E M J 2013, ' Mrassf1a-Pap, a novel methylation-based assay for the detection of cell-free fetal DNA in maternal plasma ', PLoS ONE, vol. 8, no. 12, e84051 . https://doi.org/10.1371/journal.pone.0084051
PLoS ONE, 8(12):e84051. Public Library of Science
PLoS ONE
Objectives: RASSF1A has been described to be differentially methylated between fetal and maternal DNA and can therefore be used as a universal sex-independent marker to confirm the presence of fetal sequences in maternal plasma. However, this require
Autor:
J. Annelies E. Polman, E. Ronald de Kloet, Niels Speksnijder, Bruce S. McEwen, Nicole A. Datson, Oksana B. Korobko, Jessica M.E. van den Oever, Richard G. Hunter
Publikováno v:
Endocrinology, 153(9), 4317-4327. ENDOCRINE SOC
Glucocorticoid (GC) hormones, released by the adrenals in response to stress, are key regulators of neuronal plasticity. In the brain, the hippocampus is a major target of GC, with abundant expression of the GC receptor. GC differentially affect the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e8eb558f8f2b3af1ee47b46f2fbf949
https://hdl.handle.net/1887/3277745
https://hdl.handle.net/1887/3277745
Autor:
Maarten van Iterson, Jessica M.E. van den Oever, Egbert Bakker, E. Joanne Verweij, Mariëtte J.V. Hoffer, Jan M. M. van Lith, Elles M. J. Boon, Phebe N. Adama van Scheltema, Sahila Balkassmi, Johan T. den Dunnen, Dick Oepkes
Publikováno v:
Clinical chemistry, 58(4), 699-706. American Association for Clinical Chemistry Inc.
Clinical Chemistry, 58(4), 699-706
Van Den Oever, J M E, Balkassmi, S, Verweij, E J, Van Iterson, M, Van Scheltema, P N A, Oepkes, D, Van Lith, J M M, Hoffer, M J V, Den Dunnen, J T, Bakker, E & Boon, E M J 2012, ' Single molecule sequencing of free DNA from maternal plasma for noninvasive trisomy 21 detection ', Clinical Chemistry, vol. 58, no. 4, pp. 699-706 . https://doi.org/10.1373/clinchem.2011.174698
Clinical Chemistry, 58(4), 699-706
Van Den Oever, J M E, Balkassmi, S, Verweij, E J, Van Iterson, M, Van Scheltema, P N A, Oepkes, D, Van Lith, J M M, Hoffer, M J V, Den Dunnen, J T, Bakker, E & Boon, E M J 2012, ' Single molecule sequencing of free DNA from maternal plasma for noninvasive trisomy 21 detection ', Clinical Chemistry, vol. 58, no. 4, pp. 699-706 . https://doi.org/10.1373/clinchem.2011.174698
BACKGROUND Noninvasive fetal aneuploidy detection by use of free DNA from maternal plasma has recently been shown to be achievable by whole genome shotgun sequencing. The high-throughput next-generation sequencing platforms previously tested use a PC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4392ee3bd745d030765c1f1b4f7d0d7b
https://hdl.handle.net/1887/96816
https://hdl.handle.net/1887/96816
Autor:
Phebe N. Adama van Scheltema, Elles M. J. Boon, E. J. (Joanne) Verweij, Dick Oepkes, Marjon A. de Boer, Jessica M.E. van den Oever
Publikováno v:
American Journal of Obstetrics and Gynecology. 206:S313
Publikováno v:
Blood. 112:2414-2414
It is widely accepted that Mesenchymal Stem Cells (MSCs) exhibit immunosuppressive capacities in vitro and in vivo. In an effort to understand the mechanism of suppression, co-cultures of MSCs with several types of immune cells have been studied. MSC
Autor:
Phebe N. Adama van Scheltema, R.F. Suijkerbuijk, Lennart Johansson, Sahila Balkassmi, Jessica M.E. van den Oever, Richard J. Sinke, Egbert Bakker, Birgit Sikkema-Raddatz, Mariëtte J.V. Hoffer, Elles M. J. Boon
Publikováno v:
Jessica, M E V D O, Balkassmi, S, Johansson, L F, Van Scheltema, P N A, Suijkerbuijk, R F, Hoffer, M J V, Sinke, R J, Bakker, E, Sikkema-Raddatz, B & Boon, E M J 2013, ' Successful noninvasive trisomy 18 detection using single molecule sequencing ', Clinical Chemistry, vol. 59, no. 4, pp. 705-709 . https://doi.org/10.1373/clinchem.2012.196212
Clinical Chemistry
Clinical Chemistry, 59(4), 705-709
Clinical Chemistry, 59(4), 705-709. AMER ASSOC CLINICAL CHEMISTRY
Clinical Chemistry
Clinical Chemistry, 59(4), 705-709
Clinical Chemistry, 59(4), 705-709. AMER ASSOC CLINICAL CHEMISTRY
BACKGROUND Noninvasive trisomy 21 detection performed by use of massively parallel sequencing is achievable with high diagnostic sensitivity and low false-positive rates. Detection of fetal trisomy 18 and 13 has been reported as well but seems to be