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Meijers, C.

(Carel Meijers)


cancer breast cancer breast family mutation syndrome brca 1 brca 2 mutations variant protein chek 2*1100delc patient genet chimeric gata 6 individual expression region transcript sequence endoderm embryo morphogenesi disease 6-/- control hirschsprung disease mouse development genetic hirschsprung 2*1100delc marker probe epithelial cell differentiation factor chek 2 men 2 b gata 6 mrna transcription study chimeric lungs digeorge syndrome analysis wild-type netherland phenotype domain kiaa 1279 hybridization epithelial thyroid differentiation genomic frequency susceptibility stage breast cancer risk subject 2.3 kb transcript digeorge chromosome result feature goldberg-shprintzen syndrome ednrb medullary thyroid carcinoma heart adult function deletion lung buds table exon 3 r 117g retardation 4.4 kb transcript specification research microcephaly




7 Most Recent Publications

Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systems (Article)
Brooks, A.S. Breedveld, G.J. Meijers, C. Coo, R.F. de Oostra, B.A. Matera, I. Bertoli Avella, A.M. Burzynski, G.M. Graaff, E. de Tibboel, D. Osinga, J. Boven, L.G. Hurst, J.A. Willems, P.J. Hofstra, R.M. Mancini, G.M.S. Lequin, M.H.
2005-01-01
Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility (Article)
Schutte, A.E.M. Meijers-Heijboer, E.J. Nathanson, K.L. Futreal, P.A. Stratton, M.R. Seal, S. Barfoot, R. Ouweland, A.M.W. van den Klijn, J.G.M. Easton, D.F. Wasielewski, M. Evans, D.G. Eccles, D. Weber, B.L. Rahman, N. Meijers, C. Lohman, F.
2003-01-01
Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations (Article)
Meijers-Heijboer, E.J. Snoo, A. de Schutte, M. McGuffog, L. Thompson, D. Easton, D.F. Sodha, N. Seal, S. Barfoot, R. Mangion, J. Chang-Claude, J. Eccles, D. Oldenburg, R. Eeles, R. Evans, D.G. Houlston, R. Murday, V. Narod, S. Peretz, T. Peto, J. Phelan, C. Zhang, H.X. Szabo, C. Hollestelle, A. Devilee, P. Goldgar, D. Futreal, P.A. Nathanson, K.L. Weber, B.L. Rahman, N. Stratton, M.R. Ouweland, A.M.W. van den Klijn, J.G.M. Wasielewski, M. Houben, M. Elstrodt, F. Crepin, E. Veghel-Plandsoen, M. van Duijn, C.M. van Bartels, C.C.M. Meijers, C.
2002-05-01
The transcription factor GATA6 is essential for branching morphogenesis and epithelial cell differentiation during fetal pulmonary development (Article)
Keijzer, R. Tuyl, M. van Meijers, C. Post, M.R. Tibboel, D. Koutsourakis, M. Grosveld, F.G.
2001-01-01
A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome) (Article)
Brooks, A.S. Breuning, M.H. Osinga, J. Smagt, J.J. van der Catsman-Berrevoets, C.E. Buys, C.H.C.M. Meijers, C. Hofstra, R.M.
1999-01-01
Constipation as the presenting symptom in de novo multiple endocrine neoplasia type 2B (Article)
Krijger, R.R. de Brooks, A.S. Harst, E. van der Hofstra, R.M. Bruining, H.A. Molenaar, J.C. Meijers, C.
1998-01-01
The murine homologue of HIRA, a DiGeorge syndrome candidate gene, is expressed in embryonic structures affected in human CATCH22 patients (Article)
Wilming, L.G. Snoeren, C.A. Rijswijk, A.L. van Meijers, C. Grosveld, F.G.
1997-01-01
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