Publications

Studies in health technology and informatics

The development of a new information model for a pediatric cancer registry on late treatment sequelae in The Netherlands.

24-02-2001

Molecular and biochemical parasitology

Tandemly repeated DNA is a target for the partial replacement of thymine by beta-D-glucosyl-hydroxymethyluracil in Trypanosoma brucei.

01-07-2000

The EMBO journal

The modified base J is the target for a novel DNA-binding protein in kinetoplastid protozoans.

15-11-1999

Nature cell biology

Rac regulates phosphorylation of the myosin-II heavy chain, actinomyosin disassembly and cell spreading.

01-08-1999

Molecular and cellular biology

Biosynthesis and function of the modified DNA base beta-D-glucosyl-hydroxymethyluracil in Trypanosoma brucei.

01-10-1998

Molecular and biochemical parasitology

The modified DNA base beta-D-glucosyl-hydroxymethyluracil is not found in the tsetse fly stages of Trypanosoma brucei.

01-07-1998

Molecular and biochemical parasitology

Changes in expression site control and DNA modification in Trypanosoma brucei during differentiation of the bloodstream form to the procyclic form.

15-05-1998

Analytical biochemistry

The modified DNA base beta-D-glucosylhydroxymethyluracil confers resistance to micrococcal nuclease and is incompletely recovered by 32P-postlabeling.

01-05-1998

Proceedings of the National Academy of Sciences of the United States of America

beta-D-glucosyl-hydroxymethyluracil is a conserved DNA modification in kinetoplastid protozoans and is abundant in their telomeres.

03-03-1998

Molecular and biochemical parasitology

Control of VSG gene expression sites in Trypanosoma brucei.

01-03-1998

Molecular and biochemical parasitology

beta-D-glucosyl-hydroxymethyluracil, a novel base in African trypanosomes and other Kinetoplastida.

01-12-1997

Genes & development

Localization of the modified base J in telomeric VSG gene expression sites of Trypanosoma brucei.

01-12-1997

The Journal of biological chemistry

Targeting of Tiam1 to the plasma membrane requires the cooperative function of the N-terminal pleckstrin homology domain and an adjacent protein interaction domain.

07-11-1997

The Journal of cell biology

The guanine nucleotide exchange factor Tiam1 affects neuronal morphology; opposing roles for the small GTPases Rac and Rho.

03-11-1997

Behring Institute Mitteilungen

Mechanisms of antigenic variation in African trypanosomes.

01-03-1997

Nucleic acids research

The telomeric GGGTTA repeats of Trypanosoma brucei contain the hypermodified base J in both strands.

01-07-1996

Current topics in microbiology and immunology

Role of Tiam 1 in Rac-mediated signal transduction pathways.

01-01-1996

Archives of medical research

Antigenic variation in trypanosomes.

01-01-1996

Oncogene

Oncogenic activity of Tiam1 and Rac1 in NIH3T3 cells.

07-12-1995

Cell

Antigenic variation in malaria.

14-07-1995

Cell

beta-D-glucosyl-hydroxymethyluracil: a novel modified base present in the DNA of the parasitic protozoan T. brucei.

17-12-1993

Cold Spring Harbor symposia on quantitative biology

Control of antigenic variation in African trypanosomes.

01-01-1993

Oncogene

Mutation of the human neu protein facilitates down-modulation by monoclonal antibodies.

01-04-1990

Oncogene

Differentiation-dependent expression of provirus-activated int-1 oncogene in clonal cell lines derived from a mouse mammary tumor.

01-04-1990

The development of a new information model for a pediatric cancer registry on late treatment sequelae in The Netherlands.

Tandemly repeated DNA is a target for the partial replacement of thymine by beta-D-glucosyl-hydroxymethyluracil in Trypanosoma brucei.

The modified base J is the target for a novel DNA-binding protein in kinetoplastid protozoans.

Rac regulates phosphorylation of the myosin-II heavy chain, actinomyosin disassembly and cell spreading.

Biosynthesis and function of the modified DNA base beta-D-glucosyl-hydroxymethyluracil in Trypanosoma brucei.

The modified DNA base beta-D-glucosyl-hydroxymethyluracil is not found in the tsetse fly stages of Trypanosoma brucei.

Changes in expression site control and DNA modification in Trypanosoma brucei during differentiation of the bloodstream form to the procyclic form.

The modified DNA base beta-D-glucosylhydroxymethyluracil confers resistance to micrococcal nuclease and is incompletely recovered by 32P-postlabeling.

beta-D-glucosyl-hydroxymethyluracil is a conserved DNA modification in kinetoplastid protozoans and is abundant in their telomeres.

Control of VSG gene expression sites in Trypanosoma brucei.

beta-D-glucosyl-hydroxymethyluracil, a novel base in African trypanosomes and other Kinetoplastida.

Localization of the modified base J in telomeric VSG gene expression sites of Trypanosoma brucei.

Targeting of Tiam1 to the plasma membrane requires the cooperative function of the N-terminal pleckstrin homology domain and an adjacent protein interaction domain.

The guanine nucleotide exchange factor Tiam1 affects neuronal morphology; opposing roles for the small GTPases Rac and Rho.

Mechanisms of antigenic variation in African trypanosomes.

The telomeric GGGTTA repeats of Trypanosoma brucei contain the hypermodified base J in both strands.

Role of Tiam 1 in Rac-mediated signal transduction pathways.

Antigenic variation in trypanosomes.

Oncogenic activity of Tiam1 and Rac1 in NIH3T3 cells.

Antigenic variation in malaria.

beta-D-glucosyl-hydroxymethyluracil: a novel modified base present in the DNA of the parasitic protozoan T. brucei.

Control of antigenic variation in African trypanosomes.

Mutation of the human neu protein facilitates down-modulation by monoclonal antibodies.

Differentiation-dependent expression of provirus-activated int-1 oncogene in clonal cell lines derived from a mouse mammary tumor.

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