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Items: 1 to 50 of 57

1.

Automated measurement of fetal head circumference using 2D ultrasound images.

van den Heuvel TLA, de Bruijn D, de Korte CL, Ginneken BV.

PLoS One. 2018 Aug 23;13(8):e0200412. doi: 10.1371/journal.pone.0200412. eCollection 2018.

2.

Comparison Study of Low-Cost Ultrasound Devices for Estimation of Gestational Age in Resource-Limited Countries.

van den Heuvel TLA, de Bruijn D, Moens-van de Moesdijk D, Beverdam A, van Ginneken B, de Korte CL.

Ultrasound Med Biol. 2018 Nov;44(11):2250-2260. doi: 10.1016/j.ultrasmedbio.2018.05.023. Epub 2018 Aug 6.

PMID:
30093339
3.

Fluorinated steroids do not improve outcome of isolated atrioventricular block.

Van den Berg NW, Slieker MG, van Beynum IM, Bilardo CM, de Bruijn D, Clur SA, Cornette JM, Frohn-Mulder IM, Haak MC, van Loo-Maurus KE, Manten GT, Rackowitz AB, Rammeloo LA, Reimer A, Rijlaarsdam ME, Freund MW.

Int J Cardiol. 2016 Dec 15;225:167-171. doi: 10.1016/j.ijcard.2016.09.119. Epub 2016 Sep 30.

PMID:
27728859
4.

Next generation sequencing in synovial sarcoma reveals novel gene mutations.

Vlenterie M, Hillebrandt-Roeffen MH, Flucke UE, Groenen PJ, Tops BB, Kamping EJ, Pfundt R, de Bruijn DR, Geurts van Kessel AH, van Krieken HJ, van der Graaf WT, Versleijen-Jonkers YM.

Oncotarget. 2015 Oct 27;6(33):34680-90. doi: 10.18632/oncotarget.5786.

5.

Small biparietal diameter and head circumference are part of the phenotype instead of independent prognostic markers in fetuses with spinal dysraphism.

Cuppen I, de Bruijn D, Geerdink N, Rotteveel JJ, Willemsen MA, van Vugt JM, Pasman JW, Roeleveld N.

Fetal Diagn Ther. 2015;37(2):135-40. doi: 10.1159/000366157. Epub 2014 Nov 12.

PMID:
25402003
6.

Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice.

Balemans MC, Ansar M, Oudakker AR, van Caam AP, Bakker B, Vitters EL, van der Kraan PM, de Bruijn DR, Janssen SM, Kuipers AJ, Huibers MM, Maliepaard EM, Walboomers XF, Benevento M, Nadif Kasri N, Kleefstra T, Zhou H, Van der Zee CE, van Bokhoven H.

Dev Biol. 2014 Feb 15;386(2):395-407. doi: 10.1016/j.ydbio.2013.12.016. Epub 2013 Dec 19.

7.

RevSex duplication-induced and sex-related differences in the SOX9 regulatory region chromatin landscape in human fibroblasts.

Lybæk H, de Bruijn D, den Engelsman-van Dijk AH, Vanichkina D, Nepal C, Brendehaug A, Houge G.

Epigenetics. 2014 Mar;9(3):416-27. doi: 10.4161/epi.27474. Epub 2013 Dec 18.

8.

The mitotic arrest deficient protein MAD2B interacts with the clathrin light chain A during mitosis.

Medendorp K, Vreede L, van Groningen JJ, Hetterschijt L, Brugmans L, Jansen PA, van den Hurk WH, de Bruijn DR, van Kessel AG.

PLoS One. 2010 Nov 30;5(11):e15128. doi: 10.1371/journal.pone.0015128.

9.

Germline epigenetic silencing of the tumor suppressor gene PTPRJ in early-onset familial colorectal cancer.

Venkatachalam R, Ligtenberg MJ, Hoogerbrugge N, Schackert HK, Görgens H, Hahn MM, Kamping EJ, Vreede L, Hoenselaar E, van der Looij E, Goossens M, Churchman M, Carvajal-Carmona L, Tomlinson IP, de Bruijn DR, Van Kessel AG, Kuiper RP.

Gastroenterology. 2010 Dec;139(6):2221-4. doi: 10.1053/j.gastro.2010.08.063. Epub 2010 Oct 29. No abstract available.

PMID:
21036128
10.

The epigenetics of (hereditary) colorectal cancer.

Venkatachalam R, Ligtenberg MJ, Hoogerbrugge N, de Bruijn DR, Kuiper RP, Geurts van Kessel A.

Cancer Genet Cytogenet. 2010 Nov;203(1):1-6. doi: 10.1016/j.cancergencyto.2010.08.013. Review.

PMID:
20951312
11.

Severe Progressive Autism Associated with Two de novo Changes: A 2.6-Mb 2q31.1 Deletion and a Balanced t(14;21)(q21.1;p11.2) Translocation with Long-Range Epigenetic Silencing of LRFN5 Expression.

de Bruijn DR, van Dijk AH, Pfundt R, Hoischen A, Merkx GF, Gradek GA, Lybæk H, Stray-Pedersen A, Brunner HG, Houge G.

Mol Syndromol. 2010 Feb;1(1):46-57. doi: 10.1159/000280290. Epub 2010 Feb 12.

12.

The mitotic arrest deficient protein MAD2B interacts with the small GTPase RAN throughout the cell cycle.

Medendorp K, van Groningen JJ, Vreede L, Hetterschijt L, van den Hurk WH, de Bruijn DR, Brugmans L, van Kessel AG.

PLoS One. 2009 Sep 15;4(9):e7020. doi: 10.1371/journal.pone.0007020.

13.

Differential presentation of tumor antigen-derived epitopes by MHC-class I and antigen-positive tumor cells.

Held G, Neumann F, Sturm C, Kaestner L, Dauth N, de Bruijn DR, Renner C, Lipp P, Pfreundschuh M.

Int J Cancer. 2008 Oct 15;123(8):1841-7. doi: 10.1002/ijc.23728.

14.

Histone deacetylase inhibitors reverse SS18-SSX-mediated polycomb silencing of the tumor suppressor early growth response 1 in synovial sarcoma.

Lubieniecka JM, de Bruijn DR, Su L, van Dijk AH, Subramanian S, van de Rijn M, Poulin N, van Kessel AG, Nielsen TO.

Cancer Res. 2008 Jun 1;68(11):4303-10. doi: 10.1158/0008-5472.CAN-08-0092.

15.

Major sacrococcygeal teratoma in an extreme premature infant: a multidisciplinary approach.

den Otter SC, de Mol AC, Eggink AJ, van Heijst AF, de Bruijn D, Wijnen RM.

Fetal Diagn Ther. 2008;23(1):41-5. Epub 2007 Oct 9.

PMID:
17934297
16.

Ebstein's anomaly with severe hypoplastic and stenotic pulmonary venous connections: an unusual cause of congenital chylothorax.

de Bruijn D, van Oort A, Kapusta L.

Ultrasound Obstet Gynecol. 2007 Nov;30(6):910-2. No abstract available.

17.

The C terminus of the synovial sarcoma-associated SSX proteins interacts with the LIM homeobox protein LHX4.

de Bruijn DR, van Dijk AH, Willemse MP, van Kessel AG.

Oncogene. 2008 Jan 24;27(5):653-62. Epub 2007 Jul 30.

PMID:
17667940
18.

The effect of computer reminders on GPs' prescribing behaviour: a cluster-randomised trial.

Martens JD, van der Weijden T, Severens JL, de Clercq PA, de Bruijn DP, Kester AD, Winkens RA.

Int J Med Inform. 2007 Dec;76 Suppl 3:S403-16. Epub 2007 Jun 14.

PMID:
17569575
19.

Fetal anomaly scan potentially will replace routine AFAFP assays for the detection of neural tube defects.

Kooper AJ, de Bruijn D, van Ravenwaaij-Arts CM, Faas BH, Creemers JW, Thomas CM, Smits AP.

Prenat Diagn. 2007 Jan;27(1):29-33.

PMID:
17154227
20.

The (epi)genetics of human synovial sarcoma.

de Bruijn DR, Nap JP, van Kessel AG.

Genes Chromosomes Cancer. 2007 Feb;46(2):107-17. Review.

PMID:
17117414
21.

The synovial-sarcoma-associated SS18-SSX2 fusion protein induces epigenetic gene (de)regulation.

de Bruijn DR, Allander SV, van Dijk AH, Willemse MP, Thijssen J, van Groningen JJ, Meltzer PS, van Kessel AG.

Cancer Res. 2006 Oct 1;66(19):9474-82.

22.

Targeted disruption of the synovial sarcoma-associated SS18 gene causes early embryonic lethality and affects PPARBP expression.

de Bruijn DR, Peters WJ, Chuva de Sousa Lopes SM, van Dijk AH, Willemse MP, Pfundt R, de Boer P, Geurts van Kessel A.

Hum Mol Genet. 2006 Oct 1;15(19):2936-44. Epub 2006 Aug 22.

PMID:
16926188
23.

Common origin of the human synovial sarcoma associated SS18 and SS18L1 gene loci.

de Bruijn DR, Geurts van Kessel A.

Cytogenet Genome Res. 2006;112(3-4):222-6.

PMID:
16484776
24.

SSX cancer testis antigens are expressed in most multiple myeloma patients: co-expression of SSX1, 2, 4, and 5 correlates with adverse prognosis and high frequencies of SSX-positive PCs.

Taylor BJ, Reiman T, Pittman JA, Keats JJ, de Bruijn DR, Mant MJ, Belch AR, Pilarski LM.

J Immunother. 2005 Nov-Dec;28(6):564-75.

PMID:
16224274
25.

Prospective study on the expression of cancer testis genes and antibody responses in 100 consecutive patients with primary breast cancer.

Mischo A, Kubuschok B, Ertan K, Preuss KD, Romeike B, Regitz E, Schormann C, de Bruijn D, Wadle A, Neumann F, Schmidt W, Renner C, Pfreundschuh M.

Int J Cancer. 2006 Feb 1;118(3):696-703.

26.

Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome.

Kleefstra T, Smidt M, Banning MJ, Oudakker AR, Van Esch H, de Brouwer AP, Nillesen W, Sistermans EA, Hamel BC, de Bruijn D, Fryns JP, Yntema HG, Brunner HG, de Vries BB, van Bokhoven H.

J Med Genet. 2005 Apr;42(4):299-306.

27.

The cancer-related protein SSX2 interacts with the human homologue of a Ras-like GTPase interactor, RAB3IP, and a novel nuclear protein, SSX2IP.

de Bruijn DR, dos Santos NR, Kater-Baats E, Thijssen J, van den Berk L, Stap J, Balemans M, Schepens M, Merkx G, van Kessel AG.

Genes Chromosomes Cancer. 2002 Jul;34(3):285-98.

PMID:
12007189
28.

Expression of SSX genes in human osteosarcomas.

Naka N, Araki N, Nakanishi H, Itoh K, Mano M, Ishiguro S, de Bruijn DR, Myoui A, Ueda T, Yoshikawa H.

Int J Cancer. 2002 Apr 1;98(4):640-2. No abstract available.

29.

The MLL fusion partner AF10 binds GAS41, a protein that interacts with the human SWI/SNF complex.

Debernardi S, Bassini A, Jones LK, Chaplin T, Linder B, de Bruijn DR, Meese E, Young BD.

Blood. 2002 Jan 1;99(1):275-81.

30.

SYT associates with human SNF/SWI complexes and the C-terminal region of its fusion partner SSX1 targets histones.

Kato H, Tjernberg A, Zhang W, Krutchinsky AN, An W, Takeuchi T, Ohtsuki Y, Sugano S, de Bruijn DR, Chait BT, Roeder RG.

J Biol Chem. 2002 Feb 15;277(7):5498-505. Epub 2001 Dec 4. Erratum in: J Biol Chem 2002 Apr 19;277(16):14350.

31.

Mapping and characterization of the mouse and human SS18 genes, two human SS18-like genes and a mouse Ss18 pseudogene.

de Bruijn DR, Kater-Baats E, Eleveld M, Merkx G, Geurts Van Kessel A.

Cytogenet Cell Genet. 2001;92(3-4):310-9.

PMID:
11435705
32.

The synovial sarcoma associated protein SYT interacts with the acute leukemia associated protein AF10.

de Bruijn DR, dos Santos NR, Thijssen J, Balemans M, Debernardi S, Linder B, Young BD, Geurts van Kessel A.

Oncogene. 2001 May 31;20(25):3281-9.

33.

Molecular mechanisms underlying human synovial sarcoma development.

dos Santos NR, de Bruijn DR, van Kessel AG.

Genes Chromosomes Cancer. 2001 Jan;30(1):1-14. Review.

PMID:
11107170
34.

Construction of a 350-kb sequence-ready 11q13 cosmid contig encompassing the markers D11S4933 and D11S546: mapping of 11 genes and 3 tumor-associated translocation breakpoints.

van Asseldonk M, Schepens M, de Bruijn D, Janssen B, Merkx G, Geurts van Kessel A.

Genomics. 2000 May 15;66(1):35-42.

PMID:
10843802
35.

Heterogeneous expression of the SSX cancer/testis antigens in human melanoma lesions and cell lines.

dos Santos NR, Torensma R, de Vries TJ, Schreurs MW, de Bruijn DR, Kater-Baats E, Ruiter DJ, Adema GJ, van Muijen GN, van Kessel AG.

Cancer Res. 2000 Mar 15;60(6):1654-62.

36.

Delineation of the protein domains responsible for SYT, SSX, and SYT-SSX nuclear localization.

dos Santos NR, de Bruijn DR, Kater-Baats E, Otte AP, van Kessel AG.

Exp Cell Res. 2000 Apr 10;256(1):192-202.

PMID:
10739666
37.

Double chambered right ventricle: delineation by multiplane transoesophageal echocardiography.

Sreeram N, de Bruijn D, Hitchcock JF.

Int J Cardiol. 1998 Oct 30;66(3):309-11.

PMID:
9874084
38.

Masked t(X;18)(p11;q11) in a biphasic synovial sarcoma revealed by FISH and RT-PCR.

Geurts van Kessel A, de Bruijn D, Hermsen L, Janssen I, dos Santos NR, Willems R, Makkus L, Schreuder H, Veth R.

Genes Chromosomes Cancer. 1998 Oct;23(2):198-201.

PMID:
9739025
39.

Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit.

van den Heuvel L, Ruitenbeek W, Smeets R, Gelman-Kohan Z, Elpeleg O, Loeffen J, Trijbels F, Mariman E, de Bruijn D, Smeitink J.

Am J Hum Genet. 1998 Feb;62(2):262-8.

40.

Towards the isolation of a human malignant extragonadal germ cell tumour-associated breakpoint in chromosome 11q13.

Sinke RJ, van Asseldonk M, de Bruijn D, Strijk JA, Merkx G, Olde Weghuis D, de Jong B, Oosterhuis JW, Geurts van Kessel A.

APMIS. 1998 Jan;106(1):73-8; discussion 78-9.

PMID:
9524564
41.

Human growth-differentiation factor 3 (hGDF3): developmental regulation in human teratocarcinoma cell lines and expression in primary testicular germ cell tumours.

Caricasole AA, van Schaik RH, Zeinstra LM, Wierikx CD, van Gurp RJ, van den Pol M, Looijenga LH, Oosterhuis JW, Pera MF, Ward A, de Bruijn D, Kramer P, de Jong FH, van den Eijnden-van Raaij AJ.

Oncogene. 1998 Jan 8;16(1):95-103.

42.

The human TRIDENT/HFH-11/FKHL16 gene: structure, localization, and promoter characterization.

Korver W, Roose J, Heinen K, Weghuis DO, de Bruijn D, van Kessel AG, Clevers H.

Genomics. 1997 Dec 15;46(3):435-42.

PMID:
9441747
43.

Nuclear localization of SYT, SSX and the synovial sarcoma-associated SYT-SSX fusion proteins.

dos Santos NR, de Bruijn DR, Balemans M, Janssen B, Gärtner F, Lopes JM, de Leeuw B, Geurts van Kessel A.

Hum Mol Genet. 1997 Sep;6(9):1549-58.

PMID:
9285793
44.

Molecular cytogenetics of bone and soft tissue tumors.

Geurts van Kessel A, dos Santos NR, Simons A, de Bruijn D, Forus A, Fodstad O, Myklebost O, Balemans M, Baats E, Olde Weghuis D, Suijkerbuijk RF, van den Berg E, Molenaar WM, de Leeuw B.

Cancer Genet Cytogenet. 1997 May;95(1):67-73. Review. No abstract available.

PMID:
9140455
45.

Identification and characterization of interactions between the vertebrate polycomb-group protein BMI1 and human homologs of polyhomeotic.

Gunster MJ, Satijn DP, Hamer KM, den Blaauwen JL, de Bruijn D, Alkema MJ, van Lohuizen M, van Driel R, Otte AP.

Mol Cell Biol. 1997 Apr;17(4):2326-35.

46.
47.

Isolation and characterization of the mouse homolog of SYT, a gene implicated in the development of human synovial sarcomas.

de Bruijn DR, Baats E, Zechner U, de Leeuw B, Balemans M, Olde Weghuis D, Hirning-Folz U, Geurts van Kessel AG.

Oncogene. 1996 Aug 1;13(3):643-8.

PMID:
8760306
48.

Air travel and adults with cyanotic congenital heart disease.

Harinck E, Hutter PA, Hoorntje TM, Simons M, Benatar AA, Fischer JC, de Bruijn D, Meijboom EJ.

Circulation. 1996 Jan 15;93(2):272-6.

PMID:
8548899
49.

Normal development, growth and reproduction in cellular retinoic acid binding protein-I (CRABPI) null mutant mice.

de Bruijn DR, Oerlemans F, Hendriks W, Baats E, Ploemacher R, Wieringa B, Geurts van Kessel A.

Differentiation. 1994 Dec;58(2):141-8.

PMID:
7890139
50.

Crystallographic modelling.

Driessen RA, Loopstra BO, de Bruijn DP, Kuipers HP, Schenk H.

J Comput Aided Mol Des. 1988 Oct;2(3):225-33.

PMID:
3236050

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