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Items: 29

1.

High detection rate of clinically relevant genomic abnormalities in plasma cells enriched from patients with multiple myeloma.

Stevens-Kroef M, Weghuis DO, Croockewit S, Derksen L, Hooijer J, Elidrissi-Zaynoun N, Siepman A, Simons A, Kessel AG.

Genes Chromosomes Cancer. 2012 Nov;51(11):997-1006. doi: 10.1002/gcc.21982. Epub 2012 Jul 25.

PMID:
22833442
2.

Microarray-based genomic profiling as a diagnostic tool in acute lymphoblastic leukemia.

Simons A, Stevens-Kroef M, El Idrissi-Zaynoun N, van Gessel S, Weghuis DO, van den Berg E, Waanders E, Hoogerbrugge P, Kuiper R, van Kessel AG.

Genes Chromosomes Cancer. 2011 Dec;50(12):969-81. doi: 10.1002/gcc.20919. Epub 2011 Aug 31.

PMID:
21882283
3.

Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification.

Stevens-Kroef M, Simons A, Gorissen H, Feuth T, Weghuis DO, Buijs A, Raymakers R, Geurts van Kessel A.

Cancer Genet Cytogenet. 2009 Dec;195(2):97-104. doi: 10.1016/j.cancergencyto.2009.06.020.

PMID:
19963108
4.

Detection of cryptic subtelomeric imbalances in fetuses with ultrasound abnormalities.

Faas BH, Nillesen W, Vermeer S, Weghuis DO, de Leeuw N, Smits AP, van Ravenswaaij-Arts CM.

Eur J Med Genet. 2008 Nov-Dec;51(6):511-9. doi: 10.1016/j.ejmg.2008.07.002. Epub 2008 Jul 19.

PMID:
18691679
5.

t(7;12)(q36;p13) and t(7;12)(q32;p13)--translocations involving ETV6 in children 18 months of age or younger with myeloid disorders.

Slater RM, von Drunen E, Kroes WG, Weghuis DO, van den Berg E, Smit EM, van der Does-van den Berg A, van Wering E, Hählen K, Carroll AJ, Raimondi SC, Beverloo HB.

Leukemia. 2001 Jun;15(6):915-20. Review.

6.

Fluorescence in situ hybridization analysis shows the frequent occurrence of 14q32.3 rearrangements with involvement of immunoglobulin switch regions in myeloma cell lines.

Kuipers J, Vaandrager JW, Weghuis DO, Pearson PL, Scheres J, Lokhorst HM, Clevers H, Bast BJ.

Cancer Genet Cytogenet. 1999 Mar;109(2):99-107.

PMID:
10087940
7.

Genomic organization and chromosomal localization of three members of the UDP-N-acetylgalactosamine: polypeptide N-acetylgalactosaminyltransferase family.

Bennett EP, Weghuis DO, Merkx G, van Kessel AG, Eiberg H, Clausen H.

Glycobiology. 1998 Jun;8(6):547-55.

PMID:
9592121
8.

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
9.

Identification of a human heart FABP pseudogene located on chromosome 13.

Prinsen CF, Weghuis DO, Kessel AG, Veerkamp JH.

Gene. 1997 Jul 9;193(2):245-51.

PMID:
9256083
10.

Structure and chromosomal localization of the human anti-müllerian hormone type II receptor gene.

Visser JA, McLuskey A, van Beers T, Weghuis DO, van Kessel AG, Grootegoed JA, Themmen AP.

Biochem Biophys Res Commun. 1995 Oct 24;215(3):1029-36.

PMID:
7488027
11.

Comparative genomic hybridization analysis of human sarcomas: I. Occurrence of genomic imbalances and identification of a novel major amplicon at 1q21-q22 in soft tissue sarcomas.

Forus A, Weghuis DO, Smeets D, Fodstad O, Myklebost O, van Kessel AG.

Genes Chromosomes Cancer. 1995 Sep;14(1):8-14.

PMID:
8527390
12.

Comparative genomic hybridization analysis of human sarcomas: II. Identification of novel amplicons at 6p and 17p in osteosarcomas.

Forus A, Weghuis DO, Smeets D, Fodstad O, Myklebost O, Geurts van Kessel A.

Genes Chromosomes Cancer. 1995 Sep;14(1):15-21.

PMID:
8527379
13.

Detection of numerical alterations for chromosomes 7 and 12 in benign thyroid lesions by in situ hybridization. Histological implications.

Criado B, Barros A, Suijkerbuijk RF, Weghuis DO, Seruca R, Fonseca E, Castedo S.

Am J Pathol. 1995 Jul;147(1):136-44.

14.

Fine mapping of the human bone morphogenetic protein-4 gene (BMP4) to chromosome 14q22-q23 by in situ hybridization.

van den Wijngaard A, Weghuis DO, Boersma CJ, van Zoelen EJ, Geurts van Kessel A, Olijve W.

Genomics. 1995 Jun 10;27(3):559-60. No abstract available.

PMID:
7558046
15.

Genomic cloning of the human histo-blood group ABO locus.

Bennett EP, Steffensen R, Clausen H, Weghuis DO, Geurts van Kessel A.

Biochem Biophys Res Commun. 1995 Jun 6;211(1):347. No abstract available.

PMID:
7779106
16.

The human E48 antigen, highly homologous to the murine Ly-6 antigen ThB, is a GPI-anchored molecule apparently involved in keratinocyte cell-cell adhesion.

Brakenhoff RH, Gerretsen M, Knippels EM, van Dijk M, van Essen H, Weghuis DO, Sinke RJ, Snow GB, van Dongen GA.

J Cell Biol. 1995 Jun;129(6):1677-89.

17.

The mouse gene Ptprf encoding the leukocyte common antigen-related molecule LAR: cloning, characterization, and chromosomal localization.

Schaapveld RQ, van den Maagdenberg AM, Schepens JT, Weghuis DO, Geurts van Kessel A, Wieringa B, Hendriks WJ.

Genomics. 1995 May 1;27(1):124-30.

PMID:
7665159
18.

Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene.

de Coo R, Buddiger P, Smeets H, Geurts van Kessel A, Morgan-Hughes J, Weghuis DO, Overhauser J, van Oost B.

Genomics. 1995 Apr 10;26(3):461-6.

PMID:
7607668
19.

Interphase cytogenetic analysis of distinct X-chromosomal translocation breakpoints in synovial sarcoma.

Janz M, De Leeuw B, Weghuis DO, Werner M, Nolte M, Geurts Van Kessel A, Nordheim A, Hipskind RA.

J Pathol. 1995 Apr;175(4):391-6.

PMID:
7790992
20.

Genomic cloning of the human histo-blood group ABO locus.

Bennett EP, Steffensen R, Clausen H, Weghuis DO, van Kessel AG.

Biochem Biophys Res Commun. 1995 Jan 5;206(1):318-25. Erratum in: Biochem Biophys Res Commun. 1995 Jun 6;211(1):347.

PMID:
7598760
21.

Definition of a new entity of malignant extragonadal germ cell tumors.

van Echten J, de Jong B, Sinke RJ, Weghuis DO, Sleijfer DT, Oosterhuis JW.

Genes Chromosomes Cancer. 1995 Jan;12(1):8-15.

PMID:
7534118
22.

Genomic organization and chromosomal assignment of the human voltage-gated Na+ channel beta 1 subunit gene (SCN1B).

Makita N, Sloan-Brown K, Weghuis DO, Ropers HH, George AL Jr.

Genomics. 1994 Oct;23(3):628-34.

PMID:
7851891
23.

Molecular cloning of the synovial sarcoma-specific translocation (X;18)(p11.2;q11.2) breakpoint.

de Leeuw B, Balemans M, Weghuis DO, Seruca R, Janz M, Geraghty MT, Gilgenkrantz S, Ropers HH, Geurts van Kessel A.

Hum Mol Genet. 1994 May;3(5):745-9.

PMID:
8081361
24.

Molecular characterization of a recurring complex chromosomal translocation in two human extragonadal germ cell tumors.

Sinke RJ, Weghuis DO, Suijkerbuijk RF, Tanigami A, Nakamura Y, Larsson C, Weber G, de Jong B, Oosterhuis JW, Molenaar WM, et al.

Cancer Genet Cytogenet. 1994 Mar;73(1):11-6.

PMID:
8174069
25.

Assignment of the human gene for the water channel of renal collecting duct Aquaporin 2 (AQP2) to chromosome 12 region q12-->q13.

Deen PM, Weghuis DO, Sinke RJ, Geurts van Kessel A, Wieringa B, van Os CH.

Cytogenet Cell Genet. 1994;66(4):260-2.

PMID:
7512890
26.

The human gene for water channel aquaporin 1 (AQP1) is localized on chromosome 7p15-->p14.

Deen PM, Weghuis DO, Geurs van Kessel A, Wieringa B, van Os CH.

Cytogenet Cell Genet. 1994;65(4):243-6.

PMID:
7504987
27.

Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints.

Sinke RJ, de Leeuw B, Janssen HA, Weghuis DO, Suijkerbuijk RF, Meloni AM, Gilgenkrantz S, Berger W, Ropers HH, Sandberg AA, et al.

Hum Genet. 1993 Oct 1;92(3):305-8.

PMID:
8406438
28.

Cloning, chromosomal localization, and functional expression of the alpha 1 subunit of the L-type voltage-dependent calcium channel from normal human heart.

Schultz D, Mikala G, Yatani A, Engle DB, Iles DE, Segers B, Sinke RJ, Weghuis DO, Klöckner U, Wakamori M, et al.

Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6228-32.

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