Charles H C M Buys
Overview
Explore the profile of Charles H C M Buys including associated specialties, affiliations and a list of published articles.
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Articles
24
Citations
643
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Recent Articles
1.
Bakker M, Kerstjens-Frederikse W, Buys C, de Walle H, de Jong-van den Berg L
Birth Defects Res A Clin Mol Teratol
. 2009 Nov;
88(2):94-100.
PMID: 19937603
Background: There is a need for case-control studies of the effect of paroxetine on the occurrence of specific heart defects. Methods: We performed a case-control study with data from a...
2.
Mastenbroek S, Twisk M, van Echten-Arends J, Sikkema-Raddatz B, Korevaar J, Verhoeve H, et al.
N Engl J Med
. 2007 Jul;
357(1):9-17.
PMID: 17611204
Background: Pregnancy rates in women of advanced maternal age undergoing in vitro fertilization (IVF) are disappointingly low. It has been suggested that the use of preimplantation genetic screening of cleavage-stage...
3.
van Tintelen J, Tio R, Kerstjens-Frederikse W, van Berlo J, Boven L, Suurmeijer A, et al.
J Am Coll Cardiol
. 2007 Jun;
49(25):2430-9.
PMID: 17599607
Objectives: The goal of this study was to identify the underlying gene defect in a family with inherited myocardial fibrosis. Background: A large family with an autosomal dominantly inherited form...
4.
Plaza-Menacho I, van der Sluis T, Hollema H, Gimm O, Buys C, Magee A, et al.
J Biol Chem
. 2007 Jan;
282(9):6415-24.
PMID: 17209045
The precise role of STAT3 Ser(727) phosphorylation in RET-mediated cell transformation and oncogenesis is not well understood. In this study, we have shown that familial medullary thyroid carcinoma (FMTC) mutants...
5.
Dijkhuizen T, van Essen T, Van der Vlies P, Verheij J, Sikkema-Raddatz B, van der Veen A, et al.
Am J Med Genet A
. 2006 Oct;
140(22):2482-7.
PMID: 17036314
Imbalances of 3p telomeric sequences cause 3p- and trisomy 3p syndrome, respectively, showing distinct, but also shared clinical features. No causative genes have been identified in trisomy 3p patients, but...
6.
Ter Elst A, Hiemstra B, Van der Vlies P, Kamminga W, van der Veen A, Davelaar I, et al.
Genes Chromosomes Cancer
. 2006 Sep;
45(12):1077-93.
PMID: 16958100
The early and frequent occurrence of deletions at 3p21.3 in lung cancer has led to the consideration of this chromosomal region as a lung cancer (LUCA) critical region with tumor...
7.
Sikkema-Raddatz B, Suijkerbuijk R, van der Vlag J, Stoepker M, Buys C, Meerman G
Prenat Diagn
. 2006 Jul;
26(9):855-60.
PMID: 16821249
Objective: For prenatal cytogenetic diagnosis, cell cultures should be maximally successful. When introducing a change in conditions, e.g. a new batch of medium, the growth potential of a culture is...
8.
Sikkema-Raddatz B, Suijkerbuijk R, Bouman K, de Jong B, Buys C, Meerman G
Prenat Diagn
. 2006 Jul;
26(9):791-800.
PMID: 16821245
Objectives: To investigate the effect of factors involved in cell culturing and slide preparation of amniotic fluid (AF) and chorionic villus biopsies (CVB) for prenatal cytogenetic diagnosis. Methods: The effect...
9.
Angeloni D, Ter Elst A, Wei M, van der Veen A, Braga E, Klimov E, et al.
Genes Chromosomes Cancer
. 2006 Apr;
45(7):676-91.
PMID: 16607615
Homozygous deletions or loss of heterozygosity (LOH) at human chromosome band 3p12 are consistent features of lung and other malignancies, suggesting the presence of a tumor suppressor gene(s) (TSG) at...
10.
Niessen R, Sijmons R, Ou J, Olthof S, Osinga J, Ligtenberg M, et al.
Hum Genet
. 2006 Jan;
119(1-2):206-11.
PMID: 16408224
Biallelic germline mutations of MUTYH-a gene encoding a base excision repair protein-are associated with an increased susceptibility of colorectal cancer. Whether monoallelic MUTYH mutations also increase cancer risk is not...