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pro vyhledávání: '"R. van 't Slot"'
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Autor:
Arnaud Zaldumbide, V M de Jong, B. P. C. Koeleman, A. R. Van Der Slik, Bart O. Roep, R. van 't Slot, Sandra Laban
Publikováno v:
Genes and Immunity, 17(6), 342-348
Autoreactive CD8(+) T cells recognizing autoantigens expressed by pancreatic islets lead to the destruction of insulin-producing beta cells in type 1 diabetes (T1D), but these T cells also occur in healthy subjects. We tested the hypothesis that unco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d058e058b7f4093954b13d85e3063a1
http://hdl.handle.net/1887/112082
http://hdl.handle.net/1887/112082
Autor:
Ron Hochstenbach, R. Raemakers, J.J. van der Smagt, R. van ’t Slot, P.J. Krijtenburg, M.E. van Gijn, Marc J. Eleveld, Ivo Renkens, Martin Poot
Publikováno v:
Molecular Syndromology. 3:274-283
In a 24-year-old man with mild intellectual disability, congenital heart defects and obesity, we identified up to 4 small supernumerary marker chromosomes (sSMCs) in blood metaphases. The ring-shaped sSMCs were derived from chromosomes 11, 12 and X a
Autor:
Edith J. M. Feskens, Christine L. E. Siezen, Cisca Wijmenga, S. W. van den Berg, Jolanda M. A. Boer, W.M.M. Verschuren, B. Hoebee, Sandra Imholz, Martijn E.T. Dollé, C. Strien, R. van 't Slot
Publikováno v:
International Journal of Obesity 33 (2009) 10
International Journal of Obesity, 33(10), 1143-1152
International Journal of Obesity, 33(10), 1143-1152. Nature Publishing Group
International Journal of Obesity, 33(10), 1143-1152
International Journal of Obesity, 33(10), 1143-1152. Nature Publishing Group
Background: As nuclear receptors and transcription factors have an important regulatory function in adipocyte differentiation and fat storage, genetic variation in these key regulators and downstream pathways may be involved in the onset of obesity.O
Autor:
Ynte M. Ruigrok, R. van 't Slot, Robert H. Geelkerken, C. G. F. de Kovel, Alexandra Zhernakova, Diederik E. Grobbee, S M van Sterkenburg, J D Blankensteijn, Annette F. Baas, Steef Kranendonk, Jelena Medic, Cisca Wijmenga, A.P.M. Boll
Publikováno v:
European Journal of Human Genetics, 18(2), 240-244. Nature Publishing Group
Baas, A F, Medic, J, van't Slot, R, de Kovel, C G, Zhernakova, A, Geelkerken, R H, Kranendonk, S E, van Sterkenburg, S M, Grobbee, D E, Boll, A P, Wijmenga, C, Blankensteijn, J D & Ruigrok, Y M 2010, ' Association of the TGF-beta receptor genes with abdominal aortic aneurysm ', European Journal of Human Genetics, vol. 18, no. 2, pp. 240-244 . https://doi.org/10.1038/ejhg.2009.141
Baas, A F, Medic, J, van't Slot, R, de Kovel, C G, Zhernakova, A, Geelkerken, R H, Kranendonk, S E, van Sterkenburg, S M, Grobbee, D E, Boll, A P, Wijmenga, C, Blankensteijn, J D & Ruigrok, Y M 2010, ' Association of the TGF-beta receptor genes with abdominal aortic aneurysm ', European Journal of Human Genetics, vol. 18, no. 2, pp. 240-244 . https://doi.org/10.1038/ejhg.2009.141
Abdominal aortic aneurysm (AAA) is a multifactorial condition. The transforming growth factor beta (TGF-beta) pathway regulates vascular remodeling and mutations in its receptor genes, TGFBR1 and TGFBR2, cause syndromes with thoracic aortic aneurysm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f104ef175cf6ea8506b00ddb3ca122c4
https://research.rug.nl/en/publications/714bf996-78d0-4897-ad2d-0df98592436b
https://research.rug.nl/en/publications/714bf996-78d0-4897-ad2d-0df98592436b
Autor:
Peter L. Pearson, Steven C. Bakker, W.B. Gunning, Alienke J. Monsuur, E. M. van der Meulen, Jan K. Buitelaar, R.B. Minderaa, R. van 't Slot, Richard J. Sinke, Lodewijk A. Sandkuijl, David L. Pauls
Publikováno v:
American Journal of Human Genetics, 72, 5, pp. 1251-60
American Journal of Human Genetics, 72, 1251-60
American Journal of Human Genetics, 72(5), 1251-1260. CELL PRESS
American Journal of Human Genetics, 72, 1251-60
American Journal of Human Genetics, 72(5), 1251-1260. CELL PRESS
Item does not contain fulltext A genome scan was performed on 164 Dutch affected sib pairs (ASPs) with attention-deficit/hyperactivity disorder (ADHD). All subjects were white and of Dutch descent and were phenotyped according to criteria set out in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bc91fb9fb351241a2ba85c8acd0dd86
https://europepmc.org/articles/PMC1180276/
https://europepmc.org/articles/PMC1180276/
Autor:
Madelon C. Vonk, Javier Martín, Patricia Carreira, Lorenzo Beretta, Jun Ying, Nicolas Hunzelmann, Annet Italiaander, Carmen Fonseca, Alexandre E. Voskuyl, Christopher I. Amos, María Teruel, Sandeep K. Agarwal, Monique Hinchcliff, P. García de la Peña, John Varga, Behrooz Z. Alizadeh, C.P. Simeon, Christopher P. Denton, Annika Nordin, Roger Hesselstrand, Annette Lee, Annemie J. Schuerwegh, Anna-Maria Hoffmann-Vold, Meng May Chee, Paul G. Shiels, Norberto Ortego-Centeno, Frank C. Arnett, Shervin Assassi, Jane Worthington, Benedicte A. Lie, E. De Baere, Miguel A. González-Gay, V. Fonollosa, Alexander Kreuter, Plcm van Riel, Lina-Marcela Diaz-Gallo, M. J. H. Coenen, Francisco J. García-Hernández, Rene Westhovens, Filemon K. Tan, Leonid Padyukov, R. van 't Slot, G. Riemekasten, Vanessa Smith, María Francisca González-Escribano, Roel A. Ophoff, Marie Vanthuyne, Ariane L. Herrick, Torsten Witte, B. P. C. Koeleman, Peter K. Gregersen, Olga Y. Gorlova, Jasper C A Broen, Trdj Radstake, Raffaella Scorza, Pravitt Gourh, F De Keyser, Blanca Rueda, J.M. van Laar, Rajan Madhok, Paolo Airò, Fredric Houssiau, Claudio Lunardi, J M Martin, Maureen D. Mayes
Publikováno v:
Journal of Translational Medicine
Europe PubMed Central
Europe PubMed Central
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Akademický článek
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