KNAW

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Organisation

Medical Genetics Centre South-West Netherlands - MGC

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Completed research

(the most recent research is at the top)
Collaboration Hemoglobin Regulation and Erythropoiesis: A journey from laboratory to disorders
Collaboration Lipid and fatty acid metabolism: integrated analysis of genetic variation, biomarkers and environmental factors to identify new classifiers of incident MI risk and to maximize biological understanding.
Collaboration Real-Time Visualization of DNA-protein transactions during DNA Recombination: Analysis of Mechanistic Dynamics on Single DNA Molecules
Collaboration Quantitative heritable variation in gene expression as a cause for breast cancer susceptibility
Collaboration Genome analysis and molecular cytogenetics
Commissioner Causes of congenital malformation syndroms
Secretariat Stat signalling in Sezary syndrome
Secretariat The genetic aspects of Complex Regional Pain Syndrome (CRPS) and dystonia-related episodic neurological disorders
Secretariat Development of an in vitro assay for the detection of substances capable of slowing down the ageing process
Secretariat Epigenetics and chromosomal abnormalities in human oocytes
Secretariat Imprint erasure during germ cell development
Secretariat Analysis and mechanisms of the cellular (trancription) response following DNA damage
Secretariat Identification of individuals sensitive for DNA damage inducing agents by means of DNA expression chips
Secretariat Plasticity and dynamics of sensorimotor systems
Secretariat The biological clock
Secretariat Cardiovascular diseases
Secretariat Neurological and neuromuscular diseases
Secretariat Mechanism of apoptin induced apoptosis
Secretariat Applied virology
Secretariat Gene and protein replacement therapy in lysosomal storage diseases
Secretariat New methods for gene transfer
Secretariat Neural development
Secretariat Regulation of p53
Secretariat Transcription and transformation regulation in E1A
Secretariat Chromatin and gene regulation
Secretariat Regulation of gene expression
Secretariat Hemodynamics in fetal cardiac abnormalities
Secretariat Gene expression during embryonic development
Secretariat Gene regulation in neuronal development
Secretariat Gene regulation in haemopoiesis
Secretariat Molecular and cell biological aspects of normal and abnormal embryonic development
Secretariat Regulation of gene expression during early embryonic development
Secretariat Environmental and genetic factors in the clinical expression of familial dysbetalipoproteinemia
Secretariat Influence of ultraviolet light on gene expression involved in differentiation and proliferation in the skin
Secretariat Lipoprotein metabolism and atherosclerosis studies with transgenic mice
Secretariat Genetics of cardiovascular diseases
Secretariat Cell biological and molecular backgrounds of cardiovascular diseases
Secretariat Biostatistics of high-throughput gene expression and haplotype analysis
Secretariat Genetics of multifactorial diseases
Secretariat Chromosomal aberrations in malignancies and congenital syndromes
Secretariat Early diagnostics and screening methods
Secretariat Hereditary renal diseases
Secretariat X-linked disease genes
Secretariat Mechanism of insulin action and candidate genes in diabetes mellitus
Secretariat Relation between clinical, biochemical and genetic heterogeneity in lysosomal storage diseases
Secretariat Hereditary defects in transport processes in the lysosomal membrane
Secretariat Molecular basis of complex diseases
Secretariat Molecular basis of neurogenetic diseases
Secretariat Molecular biological and clinical psychiatric study of the Gilles de la Tourette syndrome
Secretariat Identification and characterisation of genes involved in tuberous sclerosis
Secretariat Molecular and cell biological aspects of hand development
Secretariat Development and application of methods related to carrier studies and prenatal diagnostics
Secretariat Molecular background of X-linked mental retardation
Secretariat Spatial organisation and regulation of genetic information
Secretariat Development and application of molecular cytogenetics
Secretariat Tumour suppressor genes and cancer
Secretariat Chromosome analysis and automation in molecular cytogenetics
Secretariat Chromosomal aberrations in malignancies
Secretariat Molecular cell and chromosome analysis
Secretariat Molecular and genetic tumour pathology of solid tumours
Secretariat Hereditary breast tumours
Secretariat Identification and characterisation of genes involved in tuberous sclerosis
Secretariat Hereditary melanomas, dysplastic nevus syndrome
Secretariat Hereditary intestinal tumours
Secretariat Hereditary melanomas
Secretariat Tumour suppressor genes
Secretariat Genetic instability in model organisms
Secretariat Translesion synthesis
Secretariat Impact of DNA repair processes on the cellular response after induction of DNA damage
Secretariat Chromosome stability
Secretariat Replication of damaged DNA
Secretariat Photoreactivation
Secretariat Base excision repair
Secretariat Repair of double strand breaks and cross-links in DNA

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