Search Results - "Hinrichs, John W J"
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Prognostic Value of CTNNB1 Gene Mutation in Primary Sporadic Aggressive Fibromatosis
Published in Annals of surgical oncology (01-05-2015)“…Background Aggressive fibromatosis (AF) comprises tumors with a varying biological behavior. Genetic tumor characteristics may be predictive of recurrence;…”
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One-fits-all pretreatment protocol facilitating Fluorescence In Situ Hybridization on formalin-fixed paraffin-embedded, fresh frozen and cytological slides
Published in Molecular cytogenetics (17-06-2019)“…The Fluorescence In Situ Hybridization (FISH) technique is a very useful tool for diagnostic and prognostic purposes in molecular pathology. However, clinical…”
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Added value of HER-2 amplification testing by multiplex ligation-dependent probe amplification in invasive breast cancer
Published in PloS one (04-12-2013)“…HER-2 is a prognostic and predictive marker, but as yet no technique is perfectly able to identify patients likely to benefit from HER-2 targeted therapies. We…”
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Semi-quantitative CYP2D6 gene doses in relation to metabolic ratios of psychotropics
Published in European journal of clinical pharmacology (01-10-2008)“…Purpose Genetic polymorphisms in cytochrome P450 (CYP) enzyme CYP2D6 have a substantial effect on the success of pharmacotherapy. Different models, including a…”
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Implementation of Novel Molecular Biomarkers for Non-small Cell Lung Cancer in the Netherlands: How to Deal With Increasing Complexity
Published in Frontiers in oncology (22-01-2020)“…The diagnostic landscape of non-small cell lung cancer (NSCLC) is changing rapidly with the availability of novel treatments. Despite high-level healthcare in…”
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EGFR and KRAS mutations in lung carcinomas in the Dutch population: increased EGFR mutation frequency in malignant pleural effusion of lung adenocarcinoma
Published in Cellular oncology (Dordrecht) (01-06-2012)“…Background Frequencies of EGFR and KRAS mutations in non-small cell lung cancer (NSCLC) have predominantly been determined in East Asian and North American…”
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Sociodemographic Characteristics and Screening Outcomes of Women Preferring Self-Sampling in the Dutch Cervical Cancer Screening Programme: A Population-Based Study
Published in Cancer epidemiology, biomarkers & prevention (06-02-2023)“…In the Netherlands, lower high-risk human papillomavirus (hrHPV) positivity but higher cervical intraepithelial neoplasia (CIN) 2+ detection were found in…”
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Targeted Next Generation Sequencing as a Reliable Diagnostic Assay for the Detection of Somatic Mutations in Tumours Using Minimal DNA Amounts from Formalin Fixed Paraffin Embedded Material
Published in PloS one (26-02-2016)“…Targeted Next Generation Sequencing (NGS) offers a way to implement testing of multiple genetic aberrations in diagnostic pathology practice, which is…”
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Therapeutic Drug Monitoring of Antidepressants and Cytochrome P450 Genotyping in General Practice
Published in Journal of clinical pharmacology (01-11-2006)“…In the psychiatric setting, therapeutic drug monitoring and genotyping for cytochrome P450 (CYP) polymorphisms help to ensure and maintain therapeutic drug…”
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Clinical performance of high-risk HPV testing on self-samples versus clinician samples in routine primary HPV screening in the Netherlands: An observational study
Published in The Lancet regional health. Europe (01-12-2021)“…High-risk human papillomavirus (hrHPV) testing on self-collected samples has potential as a primary screening tool in cervical screening, but real-world…”
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Comparison of Next-Generation Sequencing and Mutation-Specific Platforms in Clinical Practice
Published in American journal of clinical pathology (01-04-2015)“…Objectives: To compare next-generation sequencing (NGS) platforms with mutation-specific analysis platforms in a clinical setting, in terms of sensitivity,…”
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Simultaneous Detection of Clinically Relevant Mutations and Amplifications for Routine Cancer Pathology
Published in The Journal of molecular diagnostics : JMD (2015)“…In routine cancer molecular pathology, various independent experiments are required to determine mutation and amplification status of clinically relevant…”
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ATP-binding Cassette Transporters Are Enriched in Non-caveolar Detergent-insoluble Glycosphingolipid-enriched Membrane Domains (DIGs) in Human Multidrug-resistant Cancer Cells
Published in The Journal of biological chemistry (13-02-2004)“…In this study we show that P-glycoprotein in multidrug-resistant 2780AD human ovarian carcinoma cells and multidrug resistance-associated protein 1 in…”
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MRP1 and glucosylceramide are coordinately over expressed and enriched in rafts during multidrug resistance acquisition in colon cancer cells
Published in International journal of cancer (01-07-2004)“…Previously we have described a novel multidrug‐resistant cell line, HT29col, which displayed over expression of the multidrug‐resistance protein 1 (MRP1) and…”
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Drug resistance-associated changes in sphingolipids and ABC transporters occur in different regions of membrane domains
Published in Journal of lipid research (01-11-2005)“…We have recently shown that two ATP binding cassette (ABC) transporters are enriched in Lubrol-resistant noncaveolar membrane domains in multidrug-resistant…”
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Introduction of primary screening using high-risk HPV DNA detection in the Dutch cervical cancer screening programme: a population-based cohort study
Published in BMC medicine (11-12-2019)“…In January 2017, the Dutch cervical cancer screening programme transitioned from cytomorphological to primary high-risk HPV (hrHPV) DNA screening, including…”
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The influence of cytochrome P450 pharmacogenetics on disposition of common antidepressant and antipsychotic medications
Published in Clinical biochemist reviews (01-02-2006)“…Since the identification of all the major drug-metabolising cytochrome P450 (CYP) enzymes and their major gene variants, pharmacogenetics has had a major…”
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Targeted Next Generation Sequencing as a Reliable Diagnostic Assay for the Detection of Somatic Mutations in Tumours Using Minimal DNA Amounts from Formalin Fixed Paraffin Embedded Material: e0149405
Published in PloS one (01-02-2016)“…Background Targeted Next Generation Sequencing (NGS) offers a way to implement testing of multiple genetic aberrations in diagnostic pathology practice, which…”
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