Differences among black smoke, PM(10), and PM(1.0) levels at Urban Measurement Sites.

von Roemer, W H, van Wijnen, J H
Veröffentlicht 2001

Vector-Alu PCR: a rapid step in mapping cosmids and YACs.

von Breukel, C, Wijnen, J, Tops, C, vd Klift, H, Dauwerse, H, Khan, P M
Veröffentlicht 1990

Exposure to polycyclic aromatic hydrocarbons among Dutch children.

von van Wijnen, J H, Slob, R, Jongmans-Liedekerken, G, van de Weerdt, R H, Woudenberg, F
Veröffentlicht 1996

Electrotypes and formal genetics of red cell glutathione peroxidase (GPX1) in the Djuka of Surinam.

von Meera Khan, P, Verma, C, Wijnen, L M, Wijnen, J T, Prins, H K, Nijenhuis, L E
Veröffentlicht 1986

Acute effects of urban air pollution on respiratory health of children with and without chronic respiratory symptoms

von van der Zee, S., Hoek, G., Boezen, H. M., Schouten, J. P., van Wijnen, J. H., Brunekreef, B.
Veröffentlicht 1999

Monitoring of Waterborne Pathogens in Surface Waters in Amsterdam, The Netherlands, and the Potential Health Risk Associated with Exposure to Cryptosporidium and Giardia in These W...

von Schets, F. M., van Wijnen, J. H., Schijven, J. F., Schoon, H., de Roda Husman, A. M.
Veröffentlicht 2008

CA repeat polymorphism from YAC JW25 at the D5S318 locus, distal to adenomatous polyposis coli (APC)

von Wijnen, J., Tops, C., Breukel, C., Van Leeuwen, C., Goverde, A., Van Der Klift, H., Fodde, R., Khan, P.Meera
Veröffentlicht 1991

Severe combined immune deficiency due to a homozygous 3.2-kb deletion spanning the promoter and first exon of the adenosine deaminase gene.

von Berkvens, T M, Gerritsen, E J, Oldenburg, M, Breukel, C, Wijnen, J T, van Ormondt, H, Vossen, J M, van der Eb, A J, Meera Khan, P
Veröffentlicht 1987

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.

von Wijnen, J, Khan, P M, Vasen, H, van der Klift, H, Mulder, A, van Leeuwen-Cornelisse, I, Bakker, B, Losekoot, M, Møller, P, Fodde, R
Veröffentlicht 1997

Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation

von Wagner, A, Tops, C, Wijnen, J, Zwinderman, K, van der Meer, C, Kets, M, Niermeijer, M, Klijn, J, Tibben, A, Vasen, H, Meijers-Heijboer, H
Veröffentlicht 2002

Identification of HNPCC by Molecular Analysis of Colorectal and Endometrial Tumors

von Vasen, H. F. A., Hendriks, Y., de Jong, A. E., van Puijenbroek, M., Tops, C., Bröcker-Vriends, A. H. J. T., Wijnen, J. Th., Morreau, H.
Veröffentlicht 2004

Silencing of the glycerophosphocholine phosphodiesterase GDPD5 alters the phospholipid metabolite profile in a breast cancer model in vivo as monitored by (31)P Magnetic Resonance...

von Wijnen, J.P., Jiang, L., Greenwood, T.R., Cheng, M., Döpkens, M., Cao, M.D., Bhujwalla, Z.M., Krishnamachary, B., Klomp, D.W.J., Glunde, K.
Veröffentlicht 2014

Acute stress effects on GABA and glutamate levels in the prefrontal cortex: A 7T (1)H magnetic resonance spectroscopy study

von Houtepen, L.C., Schür, R.R., Wijnen, J.P., Boer, V.O., Boks, M.P.M., Kahn, R.S., Joëls, M., Klomp, D.W., Vinkers, C.H.
Veröffentlicht in Neuroimage Clin (2017)

Possible relevance of pigeons as an indicator species for monitoring air pollution.

von Schilderman, P A, Hoogewerff, J A, van Schooten, F J, Maas, L M, Moonen, E J, van Os, B J, van Wijnen, J H, Kleinjans, J C
Veröffentlicht 1997

RNA-based mutation screening in hereditary nonpolyposis colorectal cancer.

von Kohonen-Corish, M., Ross, V. L., Doe, W. F., Kool, D. A., Edkins, E., Faragher, I., Wijnen, J., Khan, P. M., Macrae, F., St John, D. J.
Veröffentlicht 1996

An MLH1 haplotype is over-represented on chromosomes carrying an HNPCC predisposing mutation in MLH1

von Hutter, P, Wijnen, J, Rey-Berthod, C, Thiffault, I, Verkuijlen, P, Farber, D, Hamel, N, Bapat, B, Thibodeau, S, Burn, J, Wu, J, MacNamara, E, Heinimann, K, Chong, G, Foulkes, W
Veröffentlicht 2002

Multi-center reproducibility of neurochemical profiles in the human brain at 7 Tesla

von van de Bank, B.L., Emir, U.E., Boer, V.O., van Asten, J.J.A., Maas, M.C., Wijnen, J. P., Kan, H.E., Oz, G., Klomp, D.W.J., Scheenen, T.W.J.
Veröffentlicht in NMR Biomed (2015)

Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers

von Ghorbanoghli, Z., Nieuwenhuis, M. H., Houwing-Duistermaat, J. J., Jagmohan-Changur, S., Hes, F. J., Tops, C. M., Wagner, A., Aalfs, C. M., Verhoef, S., Gómez García, E. B., Sijmons, R. H., Menko, F. H., Letteboer, T. G., Hoogerbrugge, N., van Wezel, T., Vasen, H. F. A., Wijnen, J. T.
Veröffentlicht in Fam Cancer (2016)

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

von Wagner, A, Hendriks, Y, Meijers-Heijboer, E, de Leeuw, W J F, Morreau, H, Hofstra, R, Tops, C, Bik, E, Brocker-Vriends, A, van der Meer, C, Lindhout, D, Vasen, H, Breuning, M, Cornelisse, C, van Krimpen, C, Niermeijer, M, Zwinderman, A, Wijnen, J, Fodde, R
Veröffentlicht 2001

Guidelines for the clinical management of Lynch syndrome (hereditary non‐polyposis cancer)

von Vasen, H F A, Möslein, G, Alonso, A, Bernstein, I, Bertario, L, Blanco, I, Burn, J, Capella, G, Engel, C, Frayling, I, Friedl, W, Hes, F J, Hodgson, S, Mecklin, J‐P, Møller, P, Nagengast, F, Parc, Y, Renkonen‐Sinisalo, L, Sampson, J R, Stormorken, A, Wijnen, J
Veröffentlicht 2007