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1دورية أكاديمية
المؤلفون: Thomas Blom, Rutger Meinsma, Franca di Summa, Emile van den Akker, André B. P. van Kuilenburg, Marten Hansen, Godelieve A. M. Tytgat
المصدر: EJNMMI Research, Vol 11, Iss 1, Pp 1-10 (2021)
مصطلحات موضوعية: Megakaryocytes, Thrombocytopenia, Platelets, Meta-iodobenzylguanidine, MIBG, Neuroblastoma, Medical physics. Medical radiology. Nuclear medicine, R895-920
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2191-219X
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2دورية أكاديمية
المؤلفون: Thomas Blom, Rutger Meinsma, Marja Rutgers, Corine Buitenhuis, Marieke Dekken-Van den Burg, André B. P. van Kuilenburg, Godelieve A. M. Tytgat
المصدر: EJNMMI Research, Vol 10, Iss 1, Pp 1-12 (2020)
مصطلحات موضوعية: Meta-iodobenzylguanidine (MIBG), Hematological toxicity, Thrombocytopenia, Platelets, Selective serotonin reuptake inhibitor (SSRI), Medical physics. Medical radiology. Nuclear medicine, R895-920
وصف الملف: electronic resource
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3دورية أكاديميةThe Cytidine Analog Fluorocyclopentenylcytosine (RX-3117) Is Activated by Uridine-Cytidine Kinase 2.
المؤلفون: Dzjemma Sarkisjan, Joris R Julsing, Kees Smid, Daniël de Klerk, André B P van Kuilenburg, Rutger Meinsma, Young B Lee, Deog J Kim, Godefridus J Peters
المصدر: PLoS ONE, Vol 11, Iss 9, p e0162901 (2016)
وصف الملف: electronic resource
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المؤلفون: Doreen Dobritzsch, Judith Meijer, Rutger Meinsma, Dirk Maurer, Ardeshir A. Monavari, Anders Gummesson, Annika Reims, Jorge A. Cayuela, Natalia Kuklina, Jean-François Benoist, Laurence Perrin, Birgit Assmann, Georg F. Hoffmann, Jörgen Bierau, Angela M. Kaindl, André B.P. van Kuilenburg
المساهمون: Laboratory Genetic Metabolic Diseases, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Clinical Genetics, MUMC+: DA KG Lab Centraal Lab (9), RS: FHML non-thematic output
المصدر: Molecular genetics and metabolism, 136(3), 177-185. Academic Press Inc.
Molecular Genetics and Metabolism, 136(3), 177-185. Academic Press
Molecular Genetics and Metabolism, 136(3), 177-185. Academic Press Inc.مصطلحات موضوعية: Purine-Pyrimidine Metabolism, Inborn Errors, Endocrinology, Diabetes and Metabolism, beta-Ureidopropionase, Minigene approach, Biochemistry, AMINOISOBUTYRIC ACID, Amidohydrolases, MECHANISMS, Neurological abnormalities, Endocrinology, SDG 3 - Good Health and Well-being, GENETIC-ANALYSIS, Genetics, RNA Precursors, Animals, Humans, Abnormalities, Multiple, CRYSTAL-STRUCTURE, WHITE FAT, HOMOCARNOSINE, Molecular Biology, Medicinsk genetik, Functional and structural protein analysis, Mammals, Brain Diseases, Movement Disorders, PURIFICATION, Crystal structure, UPB1, DIHYDROPYRIMIDINE DEHYDROGENASE, ALANINE SYNTHASE, Mutation, beta-Alanine, CARNOSINE, Medical Genetics, ß-Ureidopropionase
وصف الملف: application/pdf
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المؤلفون: Iedan R. N. Verly, Yvette A. H. Matser, René Leen, Rutger Meinsma, Marta Fiocco, Jan Koster, Richard Volckmann, Dilara Savci-Heijink, Giuliana Cangemi, Sebastiano Barco, Linda J. Valentijn, Godelieve A. M. Tytgat, André B. P. van Kuilenburg
المساهمون: CCA -Cancer Center Amsterdam, Laboratory Genetic Metabolic Diseases, AII - Cancer immunology, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Oncogenomics, CCA - Cancer Treatment and Quality of Life, Paediatric Oncology, CCA - Imaging and biomarkers
المصدر: JCO Precision Oncology, 6. LIPPINCOTT WILLIAMS & WILKINS
JCO Precision Oncology, 6:e2000447. American Society of Clinical Oncologyمصطلحات موضوعية: N-Myc Proto-Oncogene Protein, Neuroblastoma, Cancer Research, Oncology, Dopamine, Biomarkers, Tumor, Humans, Prospective Studies, Retrospective Studies
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09e0374dba51e3faacf8e291c8764558
https://doi.org/10.1200/po.20.00447 -
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المؤلفون: Marten Hansen, André B.P. van Kuilenburg, Thomas Blom, Emile van den Akker, Rutger Meinsma, Franca di Summa, Godelieve A.M. Tytgat
المساهمون: Landsteiner Laboratory, Paediatric Oncology, Laboratory Genetic Metabolic Diseases, CCA - Cancer biology and immunology, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, CCA - Cancer Treatment and Quality of Life
المصدر: EJNMMI research, 11(1):81. Springer Berlin
EJNMMI Research, Vol 11, Iss 1, Pp 1-10 (2021)
EJNMMI Researchمصطلحات موضوعية: Platelets, R895-920, Pharmacology, Citalopram, Medical physics. Medical radiology. Nuclear medicine, Neuroblastoma, Megakaryocyte, medicine, Radiology, Nuclear Medicine and imaging, Platelet, MIBG, Serotonin transporter, Original Research, biology, business.industry, SERT, medicine.disease, Thrombocytopenia, Haematopoiesis, medicine.anatomical_structure, Norepinephrine transporter, Meta-iodobenzylguanidine, biology.protein, Serotonin, business, Megakaryocytes, medicine.drug
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المؤلفون: Rutger Meinsma, Marja Rutgers, Marieke Dekken-Van den Burg, Thomas Blom, Godelieve A.M. Tytgat, Corine K.M. Buitenhuis, André B.P. van Kuilenburg
المساهمون: Laboratory Genetic Metabolic Diseases, CCA - Cancer biology and immunology, Amsterdam Gastroenterology Endocrinology Metabolism
المصدر: EJNMMI research, 10(1):78. Springer Berlin
EJNMMI Research
EJNMMI Research, Vol 10, Iss 1, Pp 1-12 (2020)مصطلحات موضوعية: lcsh:Medical physics. Medical radiology. Nuclear medicine, Platelets, Sertraline, biology, Selective serotonin reuptake inhibitor (SSRI), business.industry, lcsh:R895-920, Hematological toxicity, Fluvoxamine, Pharmacology, Citalopram, medicine.disease, Thrombocytopenia, Meta-iodobenzylguanidine (MIBG), Norepinephrine transporter, Desipramine, Neuroblastoma, medicine, biology.protein, Radiology, Nuclear Medicine and imaging, Serotonin, business, Serotonin transporter, medicine.drug, Original Research
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbcfbc144a08664293c72da9296916c5
https://pure.amc.nl/en/publications/selective-serotonin-reuptake-inhibitors-ssris-prevent-metaiodobenzylguanidine-mibg-uptake-in-platelets-without-affecting-neuroblastoma-tumor-uptake(e99bfeab-6f89-423c-aefe-d0cb19711392).html -
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المؤلفون: Maja Tarailo-Graovac, André B.P. van Kuilenburg, Colin Jd Ross, Doreen Dobritzsch, Judith Meijer, Rutger Meinsma, Clara D.M. van Karnebeek, Wyeth W. Wasserman, Britt I. Drögemöller, Lida Zoetekouw, Dirk Maurer, Jerry Vockley
المساهمون: Laboratory Genetic Metabolic Diseases, AGEM - Inborn errors of metabolism, Amsterdam Neuroscience - Cellular & Molecular Mechanisms, Paediatric Metabolic Diseases
المصدر: Human mutation, 39(7), 947-953. Wiley-Liss Inc.
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Heterozygote, Adolescent, Dihydropyrimidine Dehydrogenase Deficiency, Genotype, Mutation, Missense, Biology, Compound heterozygosity, Loss of heterozygosity, 03 medical and health sciences, symbols.namesake, Dihydropyrimidine dehydrogenase deficiency, Genetics, medicine, Humans, Missense mutation, Exome, Dihydrouracil Dehydrogenase (NADP), Genetics (clinical), Sequence Deletion, Sanger sequencing, Whole genome sequencing, Whole Genome Sequencing, Chromosome Mapping, Infant, Exons, medicine.disease, Introns, Phenotype, 030104 developmental biology, Child, Preschool, Paraparesis, Spastic, symbols, Female, DPYD
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المؤلفون: Rutger Meinsma, Tetsuya Ito, Yoriko Watanabe, Lida Zoetekouw, Jeroen Roelofsen, Yoko Nakajima, Judith Meijer, Doreen Dobritzsch, Chunhua Zhang, André B.P. van Kuilenburg, Kyoko Tashiro, Xu Wang
المساهمون: AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, CCA -Cancer Center Amsterdam, Laboratory Genetic Metabolic Diseases
المصدر: Molecular genetics and metabolism, 122(4), 216-222. Academic Press Inc.
مصطلحات موضوعية: Male, Models, Molecular, 0301 basic medicine, endocrine system, Endocrinology, Diabetes and Metabolism, Mutant, Mutation, Missense, Biochemistry, Amidohydrolases, 03 medical and health sciences, Endocrinology, Atrophy, Asian People, Gene Frequency, Japan, Catalytic Domain, Genetics, medicine, Humans, Point Mutation, Missense mutation, Child, Uracil, Molecular Biology, Gene, chemistry.chemical_classification, biology, Point mutation, Brain, Genetic Variation, Infant, Active site, medicine.disease, 030104 developmental biology, Enzyme, chemistry, Child, Preschool, Dihydropyrimidinase, biology.protein, Female, Crystallization, Metabolism, Inborn Errors
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المؤلفون: A. B. P. Van Kuilenburg, Rutger Meinsma
المساهمون: Laboratory Genetic Metabolic Diseases
المصدر: Nucleosides, nucleotides & nucleic acids, 35(10-12), 613-618. Marcel Dekker Inc.
مصطلحات موضوعية: 0301 basic medicine, Gene Expression, Cytidine, Biochemistry, Substrate Specificity, law.invention, Neuroblastoma, 03 medical and health sciences, chemistry.chemical_compound, Pyrimidine analogue, Adenosine Triphosphate, 0302 clinical medicine, law, Escherichia coli, Genetics, medicine, Humans, Uridine, Kinase, General Medicine, medicine.disease, Ribonucleoside, Molecular biology, Kinetics, 030104 developmental biology, chemistry, Cell culture, 030220 oncology & carcinogenesis, Recombinant DNA, Molecular Medicine, Uridine Kinase, Nucleoside-Phosphate Kinase