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Items: 1 to 50 of 52

1.

Immersion oil for high-resolution live-cell imaging at 37 degrees C: optical and physical characteristics.

Oomen LC, Sacher R, Brocks HH, Zwier JM, Brakenhoff GJ, Jalink K.

J Microsc. 2008 Nov;232(2):353-61. doi: 10.1111/j.1365-2818.2008.02106.x.

2.

Quantitative image correction and calibration for confocal fluorescence microscopy using thin reference layers and SIPchart-based calibration procedures.

Zwier JM, Oomen L, Brocks L, Jalink K, Brakenhoff GJ.

J Microsc. 2008 Jul;231(Pt 1):59-69. doi: 10.1111/j.1365-2818.2008.02017.x.

3.

Probing microscopic chemical environments with high-intensity chirped pulses.

Buist AH, Mller M, Ghauharali RI, Brakenhoff GJ, Squier JA, Bardeen CJ, Yakovlev VV, Wilson KR.

Opt Lett. 1999 Feb 15;24(4):244-6.

PMID:
18071468
4.

Imaging colloidal particle induced topological defects in a nematic liquid crystal using third harmonic generation microscopy.

Pillai RS, Oh-E M, Yokoyama H, Brakenhoff GJ, Müller M.

Opt Express. 2006 Dec 25;14(26):12976-83.

PMID:
19532191
6.

Characterization of sectioning fluorescence microscopy with thin uniform fluorescent layers: Sectioned Imaging Property or SIPcharts.

Brakenhoff GJ, Wurpel GW, Jalink K, Oomen L, Brocks L, Zwier JM.

J Microsc. 2005 Sep;219(Pt 3):122-32.

7.

Image calibration in fluorescence microscopy.

Zwier JM, Van Rooij GJ, Hofstraat JW, Brakenhoff GJ.

J Microsc. 2004 Oct;216(Pt 1):15-24.

8.

Four-dimensional imaging of chromatin dynamics during the assembly of the interphase nucleus.

Manders EM, Visser AE, Koppen A, de Leeuw WC, van Liere R, Brakenhoff GJ, van Driel R.

Chromosome Res. 2003;11(5):537-47.

PMID:
12971728
9.

Optical far-field microscopy of single molecules with 3.4 nm lateral resolution.

Bloess A, Durand Y, Matsushita M, van Dermeer H, Brakenhoff GJ, Schmidt J.

J Microsc. 2002 Jan;205(Pt 1):76-85.

10.

Fluorescence photobleaching-based image standardization for fluorescence microscopy

Ghauharali RI, Brakenhoff GJ.

J Microsc. 2000 May;198 (Pt 2):88-100.

11.

CARS microscopy with folded BoxCARS phasematching

Muller M, Squier J, De Lange CA, Brakenhoff GJ.

J Microsc. 2000 Feb;197 (Pt 2):150-8.

12.

Image cytometric method for quantifying the relative amount of DNA in bacterial nucleoids using Escherichia coli.

Vischer NO, Huls PG, Ghauharali RI, Brakenhoff GJ, Nanninga N, Woldringh CL.

J Microsc. 1999 Oct;196(Pt 1):61-8.

13.

Third harmonic generation microscopy.

Squier J, Muller M, Brakenhoff G, Wilson KR.

Opt Express. 1998 Oct 26;3(9):315-24.

PMID:
19384376
14.

3D microscopy of transparent objects using third-harmonic generation.

Müller M, Squier J, Wilson KR, Brakenhoff GJ.

J Microsc. 1998 Sep;191(3):266-274.

15.

Dispersion pre-compensation of 15 femtosecond optical pulses for high-numerical-aperture objectives.

Müller M, Squier J, Wolleschensky R, Simon U, Brakenhoff GJ.

J Microsc. 1998 Aug;191(2):141-150.

16.

Optical saturation measurements of fluorophores in solution with pulsed femtosecond excitation and two-dimensional CCD camera detection.

Ghauharali RI, Müller M, Buist AH, Sosnowski TS, Norris TB, Squier J, Brakenhoff GJ.

Appl Opt. 1997 Jun 20;36(18):4320-8.

PMID:
18253462
17.

Apodization and the point-spread autocorrelation function.

Müller M, Brakenhoff GJ.

Appl Opt. 1997 May 1;36(13):2755-62.

PMID:
18253266
18.

The mechanism of red cell (dis)aggregation investigated by means of direct cell manipulation using multiple optical trapping.

Bronkhorst PJ, Grimbergen J, Brakenhoff GJ, Heethaar RM, Sixma JJ.

Br J Haematol. 1997 Feb;96(2):256-8.

PMID:
9029009
19.

Improved axial resolution by point-spread autocorrelation function imaging.

Brakenhoff GJ, Müller M.

Opt Lett. 1996 Nov 1;21(21):1721-3.

PMID:
19881779
20.

Analysis of efficiency of two-photon versus single-photon absorption of fluorescence generation in biological objects.

Brakenhoff GJ, Müller M, Ghauharali RI.

J Microsc. 1996 Aug;183(Pt 2):140-4.

PMID:
8805826
21.

Real-time two-photon confocal microscopy using a femtosecond, amplified Ti:sapphire system.

Brakenhoff GJ, Squier J, Norris T, Bliton AC, Wade MH, Athey B.

J Microsc. 1996 Mar;181(Pt 3):253-9.

22.

Characterization of high-numerical-aperture lenses by spatial autocorrelation of the focal field.

Muller M, Brakenhoff GJ.

Opt Lett. 1995 Nov 1;20(21):2159. No abstract available.

PMID:
19862283
23.

A new method to study shape recovery of red blood cells using multiple optical trapping.

Bronkhorst PJ, Streekstra GJ, Grimbergen J, Nijhof EJ, Sixma JJ, Brakenhoff GJ.

Biophys J. 1995 Nov;69(5):1666-73.

24.

Measurement of femtosecond pulses in the focal point of a high-numerical-aperture lens by two-photon absorption.

Muller M, Squier J, Brakenhoff GJ.

Opt Lett. 1995 May 1;20(9):1038. No abstract available.

PMID:
19859416
25.

Isolation of single yeast cells by optical trapping.

Grimbergen JA, Visscher K, Gomes de Mesquita DS, Brakenhoff GJ.

Yeast. 1993 Jul;9(7):723-32.

PMID:
8368006
27.

Dynamics of three-dimensional replication patterns during the S-phase, analysed by double labelling of DNA and confocal microscopy.

Manders EM, Stap J, Brakenhoff GJ, van Driel R, Aten JA.

J Cell Sci. 1992 Nov;103 ( Pt 3):857-62.

28.

Confocal microscopy in microgravity research.

Goede AP, Brakenhoff GJ, Woldringh CL, Aalders JW, Imhof JP, van Kralingen P, Mels WA, Schreinemakers P, Zegers A.

Adv Space Res. 1992;12(1):109-12.

PMID:
11536944
29.
30.

Three-dimensional distribution of DNase I-sensitive chromatin regions in interphase nuclei of embryonal carcinoma cells.

de Graaf A, van Hemert F, Linnemans WA, Brakenhoff GJ, de Jong L, van Renswoude J, van Driel R.

Eur J Cell Biol. 1990 Jun;52(1):135-41.

PMID:
2387304
31.

Confocal microscopy as a tool for the study of the intranuclear topography of chromosomes.

van Dekken H, van Rotterdam A, Jonker R, van der Voort HT, Brakenhoff GJ, Bauman JG.

J Microsc. 1990 May;158(Pt 2):207-14.

PMID:
2370652
33.

Spatial topography of a pericentromeric region (1q12) in hemopoietic cells studied by in situ hybridization and confocal microscopy.

van Dekken H, van Rotterdam A, Jonker RR, van der Voort HT, Brakenhoff GJ, Bauman JG.

Cytometry. 1990;11(5):570-8.

34.

Ki-67 detects a nuclear matrix-associated proliferation-related antigen. II. Localization in mitotic cells and association with chromosomes.

Verheijen R, Kuijpers HJ, van Driel R, Beck JL, van Dierendonck JH, Brakenhoff GJ, Ramaekers FC.

J Cell Sci. 1989 Apr;92 ( Pt 4):531-40.

35.

Three-dimensional chromosome arrangement of Crepis capillaris in mitotic prophase and anaphase as studied by confocal scanning laser microscopy.

Oud JL, Mans A, Brakenhoff GJ, van Der Voort HT, van Spronsen EA, Nanninga N.

J Cell Sci. 1989 Mar;92 ( Pt 3):329-39.

36.

Three-dimensional visualization methods for confocal microscopy.

van der Voort HT, Brakenhoff GJ, Baarslag MW.

J Microsc. 1989 Feb;153(Pt 2):123-32.

PMID:
2709405
37.

Three-dimensional imaging in fluorescence by confocal scanning microscopy.

Brakenhoff GJ, van der Voort HT, van Spronsen EA, Nanninga N.

J Microsc. 1989 Feb;153(Pt 2):151-9.

PMID:
2651673
38.

Ki-67 detects a nuclear matrix-associated proliferation-related antigen. I. Intracellular localization during interphase.

Verheijen R, Kuijpers HJ, Schlingemann RO, Boehmer AL, van Driel R, Brakenhoff GJ, Ramaekers FC.

J Cell Sci. 1989 Jan;92 ( Pt 1):123-30.

39.

Three-dimensional confocal fluorescence microscopy.

Brakenhoff GJ, van Spronsen EA, van der Voort HT, Nanninga N.

Methods Cell Biol. 1989;30:379-98. Review. No abstract available.

PMID:
2648116
40.

Visualization and analysis techniques for three dimensional information acquired by confocal microscopy.

Brakenhoff GJ, van der Voort HT, Baarslag MW, Mans B, Oud JL, Zwart R, van Driel R.

Scanning Microsc. 1988 Dec;2(4):1831-8.

PMID:
3238377
41.

3-dimensional imaging of biological structures by high resolution confocal scanning laser microscopy.

Brakenhoff GJ, van der Voort HT, van Spronsen EA, Nanninga N.

Scanning Microsc. 1988 Mar;2(1):33-40.

PMID:
3285458
42.

Three-dimensional imaging by confocal scanning fluorescence microscopy.

Brakenhoff GJ, van der Voort HT, van Spronsen EA, Nanninga N.

Ann N Y Acad Sci. 1986;483:405-15. No abstract available.

PMID:
2436520
43.

Three-dimensional chromatin distribution in neuroblastoma nuclei shown by confocal scanning laser microscopy.

Brakenhoff GJ, van der Voort HT, van Spronsen EA, Linnemans WA, Nanninga N.

Nature. 1985 Oct 24-30;317(6039):748-9.

PMID:
4058582
44.

Confocal scanning light microscopy of the Escherichia coli nucleoid: comparison with phase-contrast and electron microscope images.

Valkenburg JA, Woldringh CL, Brakenhoff GJ, van der Voort HT, Nanninga N.

J Bacteriol. 1985 Feb;161(2):478-83.

45.

Topography of the insertion of LamB protein into the outer membrane of Escherichia coli wild-type and lac-lamB cells.

Vos-Scheperkeuter GH, Pas E, Brakenhoff GJ, Nanninga N, Witholt B.

J Bacteriol. 1984 Aug;159(2):440-7.

46.

Bacterial anatomy in retrospect and prospect.

Nanninga N, Brakenhoff GJ, Meijer M, Woldringh CL.

Antonie Van Leeuwenhoek. 1984;50(5-6):433-60. Review.

PMID:
6442119
47.

Analysis by electron microscopy of the variable segment in the maxi-circle of kinetoplast DNA from Trypanosoma brucei.

Borst P, Weijers PJ, Brakenhoff GJ.

Biochim Biophys Acta. 1982 Dec 31;699(3):272-80. No abstract available.

PMID:
7159594
48.

Kinetoplast DNA in the insect trypanosomes Crithidia luciliae and Crithidia fasciculata. III. Heteroduplex analysis of the C. luciliae minicircles.

Hoeijmakers JH, Weijers PJ, Brakenhoff GJ, Borst P.

Plasmid. 1982 May;7(3):221-9. No abstract available.

PMID:
7100301
49.

The banding pattern of the segment 46A-48C in Drosophila hydeï polytene chromosomes as studied by confocal scanning light microscopy (CSLM).

Grond CJ, Derksen J, Brakenhoff GJ.

Exp Cell Res. 1982 Apr;138(2):458-62. No abstract available.

PMID:
7075699
50.

Visualization of the nucleoid in living bacteria on poly-lysine coated surfaces by the immersion technique.

Binnerts JS, Woldringh CL, Brakenhoff GJ.

J Microsc. 1982 Mar;125(Pt 3):359-63. No abstract available.

PMID:
7045374

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