Zobrazeno 1 - 10
of 89
pro vyhledávání: '"M. van Puijenbroek"'
Autor:
J. Suomalainen, N. Anders, J. Franke, H. Bartholomeus, C. Nolet, M. van Puijenbroek, H. Kramer, S. Keesstra, S. Mücher, L. Kooistra
Publikováno v:
The International Archives of the Photogrammetry, Remote Sensing and Spatial Information Sciences, Vol XL-1-W4, Pp 261-262 (2015)
The WUR Unmanned Aerial Remote Sensing Facility (UARSF) (www.wageningenur.nl/uarsf ) is a co-operation organization of different groups within Wageningen University and Research Centre to use UAVs in remote sensing applications. The facility was foun
Externí odkaz:
https://doaj.org/article/e61b9e98c98347628304e494d57b191b
Autor:
Edward R. Jones, Marc F.P. Bierkens, Peter J. T. M. van Puijenbroek, Michelle T. H. van Vliet
Human activities greatly impact surface water quality due to the emission of various pollutants associated with different water use sectors (e.g. irrigation, livestock, domestic, energy and manufacturing)1,2. In-stream concentrations are also strongl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5311e80df88d6357d40c43140f348ede
https://doi.org/10.5194/egusphere-egu23-1161
https://doi.org/10.5194/egusphere-egu23-1161
Autor:
Gert Jan Fleuren, T. van Wezel, Bin Tean Teh, Carola J. Haven, Hans Morreau, Min-Han Tan, M. van Puijenbroek
Publikováno v:
Clinical Endocrinology. 67:370-376
Summary Objective Parathyroid carcinoma remains difficult to diagnose. Recently, it has been shown that mutations in the HRPT2 gene (encoding parafibromin) are associated with the development of parathyroid carcinoma. Although MEN1 is not typically t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1992c70b4bf003b81d8e251103e23f12
https://doi.org/10.1111/j.1365-2265.2007.02894.x
https://doi.org/10.1111/j.1365-2265.2007.02894.x
Autor:
A Sanchez de Abajo, Hans Morreau, Trinidad Caldés, Javier Godino, Eduardo Díaz-Rubio, M. van Puijenbroek, M. De La Hoya
Publikováno v:
Oncogene. 25:2124-2130
hMLH1 and hMSH2 can be considered tumor suppressor genes, as both alleles must be inactivated in order to lose the mismatch repair (MMR) function. In this regard, it has been proposed that LOH at MMR loci is a common Knudson's second-hit mechanism in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::057a3591022f5f9650bc770447611845
https://doi.org/10.1038/sj.onc.1209233
https://doi.org/10.1038/sj.onc.1209233
Autor:
A F, Bouwman, A H W, Beusen, J, Griffioen, J W, Van Groenigen, M M, Hefting, O, Oenema, P J T M, Van Puijenbroek, S, Seitzinger, C P, Slomp, E, Stehfest
Publikováno v:
Philosophical transactions of the Royal Society of London. Series B, Biological sciences. 368(1621)
Soil nitrogen (N) budgets are used in a global, distributed flow-path model with 0.5° × 0.5° resolution, representing denitrification and N2O emissions from soils, groundwater and riparian zones for the period 1900-2000 and scenarios for the perio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a76c23de37ac961b93a3472721e18b84
https://pubmed.ncbi.nlm.nih.gov/23713114
https://pubmed.ncbi.nlm.nih.gov/23713114
Autor:
T. van Wezel, Giusi Irma Forte, Juul T. Wijnen, Jan Oosting, W.E. Corver, R. van Eijk, Anneke Middeldorp, Hans Morreau, M. van Puijenbroek, Trinidad Caldés, Dina Ruano, M.P. van Nieuwenhuizen
Publikováno v:
International Journal of Cancer, 130(4), 837-46
Many hereditary nonpolyposis colorectal cancers (CRCs) cannot be explained by Lynch syndrome. Other high penetrance genetic risk factors are likely to play a role in these mismatch repair (MMR)-proficient CRC families. Because genomic profiles of CRC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::457ef6541188d2ad99570e5707d27597
http://hdl.handle.net/1887/118605
http://hdl.handle.net/1887/118605
Autor:
M. van Puijenbroek, Hans Morreau, C. Tops, Juul T. Wijnen, N. ter Haar, Ekaterina S. Jordanova, R. van Eijk, Jan Oosting, E. H. Lips, Maartje Nielsen, Anneke Middeldorp, Frederik J. Hes, Wim E. Corver, Hans F. A. Vasen, T. van Wezel
Genetic instability is known to drive colorectal carcinogenesis. Generally, a distinction is made between two types of genetic instability: chromosomal instability (CIN) and microsatellite instability (MIN or MSI). Most CIN tumours are aneuploid, whe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfec242297ed330c91e33d845a06a4dc
https://biblio.vub.ac.be/vubir/high-frequency-of-copyneutral-loh-in-mutyhassociated-polyposis-carcinomas(8d233bb4-de12-4a0a-9e32-bda3d8630306).html
https://biblio.vub.ac.be/vubir/high-frequency-of-copyneutral-loh-in-mutyhassociated-polyposis-carcinomas(8d233bb4-de12-4a0a-9e32-bda3d8630306).html
Autor:
Frederik J. Hes, C J Dommering, Senno Verhoef, A Wagner, M. van Puijenbroek, Jan-Werner Poley, Maartje Nielsen, Hans Morreau, Marjan M. Weiss, Ernst J. Kuipers, G T Burger, Hans F. A. Vasen
Publikováno v:
Nielsen, M, Poley, J W, Verhoef, S, Van Puijenbroek, M, Weiss, M M, Burger, G T, Dommering, C J, Vasen, H F A, Kuipers, E J, Wagner, A, Morreau, H & Hes, F J 2006, ' Duodenal carcinoma in MUTYH-associated polyposis ', Journal of Clinical Pathology, vol. 59, no. 11, pp. 1212-1215 . https://doi.org/10.1136/jcp.2005.031757
Journal of Clinical Pathology, 59(11), 1212-1215. BMJ Publishing Group
Journal of Clinical Pathology, 59(11), 1212-1215. BMJ Publishing Group
Bi-allelic germline mutations in the MUTYH gene give rise to multiple adenomas and an increased incidence of colorectal cancer. In addition, duodenal adenomas and other extracolonic manifestations have been described in MUTYH-associated polyposis (MA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12932d581ded7ee3242b4ccc7a1db29f
https://research.vumc.nl/en/publications/d88042db-28a7-4725-b974-668f718cb773
https://research.vumc.nl/en/publications/d88042db-28a7-4725-b974-668f718cb773
Autor:
C. Tops, A. E. de Jong, Yvonne M.C. Hendriks, A H J T Bröcker-Vriends, J. Th. Wijnen, Hans F. A. Vasen, M. van Puijenbroek, Hans Morreau
Publikováno v:
Disease markers
Disease Markers, Vol 20, Iss 4-5, Pp 207-213 (2004)
Disease Markers, Vol 20, Iss 4-5, Pp 207-213 (2004)
Hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) is a dominantly inherited syndrome characterized by the development of colorectal cancer, endometrial cancer and other cancers and the presence of microsatellite instability (MSI) in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61048687168f86b9b49a8347a4b41a03
https://pubmed.ncbi.nlm.nih.gov/15528786
https://pubmed.ncbi.nlm.nih.gov/15528786
Autor:
Rogier A. Oldenburg, Hanne Meijers-Heijboer, Gerrit Griffioen, A. M. W. Van Den Ouweland, Hans Morreau, Peter Devilee, M. van Puijenbroek, Egbert Bakker, C. J. Cornelisse, Hans F. A. Vasen, W. H. de Vos tot Nederveen Cappel
Publikováno v:
Journal of Medical Genetics, 41, 1-4. BMJ Publishing Group
Journal of medical genetics, 41(3). BMJ Publishing Group
Journal of medical genetics, 41(3). BMJ Publishing Group
Familial atypical multiple mole melanoma (FAMMM; OMIM #155601) is characterised by the familial occurrence of melanoma of the skin in combination with multiple atypical precursor naevi.1–4 The disease is inherited as an autosomal dominant trait, wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31d3a1368582d86b3670298c86969265
https://pure.eur.nl/en/publications/3bbc8514-40b0-4b79-8ae1-f8e6f631e954
https://pure.eur.nl/en/publications/3bbc8514-40b0-4b79-8ae1-f8e6f631e954