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1دورية أكاديمية
المؤلفون: Lore De Kock, Fabienne Ver Donck, Chantal Thys, Anouck Wijgaerts, Koji Eto, Chris Van Geet, Kathleen Freson
المصدر: Haematologica, Vol 106, Iss 12 (2021)
مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Kathleen Freson, Anouck Wijgaerts, Chris Van Geet
المصدر: Platelets, Vol 28, Iss 7, Pp 731-734 (2017)
مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Anouck Wijgaerts, Christine Wittevrongel, Chantal Thys, Timothy Devos, Kathelijne Peerlinck, Marloes R. Tijssen, Chris Van Geet, Kathleen Freson
المصدر: Haematologica, Vol 102, Iss 4 (2017)
مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
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المؤلفون: Chris Van Geet, Fabienne Ver Donck, Anouck Wijgaerts, Koji Eto, Chantal Thys, Kathleen Freson, Lore De Kock
المصدر: Haematologica
مصطلحات موضوعية: Proteome, Gene Expression Profiling, Hematology, Computational biology, Biology, Transcriptome, src-Family Kinases, Proteome profiling, Humans, Phosphorylation, Letters to the Editor, Megakaryocytes, Proto-oncogene tyrosine-protein kinase Src
وصف الملف: Electronic
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc8e47ef85058321337830a31c304408
https://doi.org/10.3324/haematol.2021.279248 -
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المؤلفون: Christine Wittevrongel, Gunnar Buyse, Berten Ceulemans, Anouck Wijgaerts, Chris Van Geet, Hild Van Esch, Sophie Louwette, Michela Di Michele, Chantal Thys, Kathleen Freson, Kate Downes
المصدر: Human molecular genetics
مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Proteome, Nucleosome assembly, Biology, Sudden death, Frameshift mutation, 03 medical and health sciences, 0302 clinical medicine, Atrophy, Internal medicine, Exome Sequencing, Genetics, medicine, Animals, Humans, Frameshift Mutation, Molecular Biology, Zebrafish, Genetics (clinical), Exome sequencing, Neurogenesis, Infant, Newborn, Infant, Nuclear Proteins, General Medicine, Fibroblasts, medicine.disease, Hypotonia, Pedigree, Chemistry, Phenotype, 030104 developmental biology, Endocrinology, 030220 oncology & carcinogenesis, Female, Human medicine, medicine.symptom, Polyneuropathy, Sudden Infant Death
وصف الملف: Print
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc41f1986c5fcef0a0361ebd6bb9db94
https://doi.org/10.1093/hmg/ddaa233 -
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المؤلفون: Kathleen Freson, Anouck Wijgaerts
المصدر: Hématologie. 20:319-328
مصطلحات موضوعية: Physics, Hematology, Molecular biology, Megakaryopoiesis
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::5b91b77708f1f3aab181ab26aef48f56
https://doi.org/10.1684/hma.2014.0970 -
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المؤلفون: Anouck Wijgaerts, C. Van Geet, Kathleen Freson
المصدر: International Journal of Laboratory Hematology. 36:313-325
مصطلحات موضوعية: Blood Platelets, Platelet disorder, Systems biology, Megakaryocyte differentiation, Biochemistry (medical), Clinical Biochemistry, Hematology, General Medicine, Biology, medicine.disease, Gray platelet syndrome, medicine.anatomical_structure, Megakaryocyte, Immunology, Transcriptional regulation, medicine, Humans, Platelet, Blood Platelet Disorders, Bone marrow
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المؤلفون: Claire Lentaigne, Deborah Whitehorn, Tamam Bakchoul, Tadbir K. Bariana, John Bradley, Anne M. Kelly, Anouck Wijgaerts, Jonathan Stephens, Rémi Favier, Chantal Thys, Marc De Maeyer, Augusto Rendon, Sri V V Deevi, Kathelijne Peerlinck, F. Lucy Raymond, Michele P. Lambert, Kathleen Freson, Michael Laffan, D. J. Perry, Sylvia Richardson, Myrto Kostadima, Andrew D Mumford, Kathleen Stirrups, Christopher J. Penkett, Ernest Turro, Sol Schulman, Ilenia Simeoni, Wendy N. Erber, Willem H. Ouwehand, Keith Gomez, Mary Mathias, Paquita Nurden, Sofia Papadia, Chris Van Geet, Steve Austin, Sarah K Westbury, Daniel Greene, Sofie Ashford, Dominik Selleslag, Christine Wittevrongel, Peter William Collins, Carolyn M. Millar, Antony P. Attwood
المساهمون: Med Microbiol, Infect Dis & Infect Prev, MUMC+: DA CDL Algemeen (9), RS: CARIM - R1.04 - Clinical thrombosis and haemostasis, Biochemie, RS: CARIM - R1.03 - Cell biochemistry of thrombosis and haemostasis, Medical Research Council (MRC)
المصدر: Science Translational Medicine, 8(328):328ra30. American Association for the Advancement of Science
Turro, E, Greene, D, Wijgaerts, A, Thys, C, Lentaigne, C, Bariana, T K, Westbury, S K, Kelly, A M, Selleslag, D, Stephens, J C, Papadia, S, Simeoni, I, Penkett, C J, Ashford, S, Attwood, A, Austin, S, Bakchoul, T, Collins, P, Deevi, S V V, Favier, R, Kostadima, M, Lambert, M P, Mathias, M, Millar, C M, Peerlinck, K, Perry, D J, Schulman, S, Whitehorn, D, Wittevrongel, C, De Maeyer, M, Rendon, A, Gomez, K, Erber, W N, Mumford, A D, Nurden, P, Stirrups, K, Bradley, J R, Lucy Raymond, F, Laffan, M A, Van Geet, C, Richardson, S & Freson, K & Ouwehand, W H 2016, ' A dominant gain-of-function mutation in universal tyrosine kinase SRC causes thrombocytopenia, myelofibrosis, bleeding, and bone pathologies ', Science Translational Medicine, vol. 8, no. 328, 328ra30 . https://doi.org/10.1126/scitranslmed.aad7666مصطلحات موضوعية: 0301 basic medicine, Male, Myeloid, Research & Experimental Medicine, chemistry.chemical_compound, 0302 clinical medicine, Megakaryocyte, Chlorocebus aethiops, Src family kinase, Animals, Blood Platelets, Bone and Bones, COS Cells, Cercopithecus aethiops, Female, Hematopoiesis, Hemorrhage, Humans, Mutation, Pedigree, Phenotype, Primary Myelofibrosis, Thrombocytopenia, Transfection, Zebrafish, src-Family Kinases, Medicine (all), PLATELET, 11 Medical and Health Sciences, OSTEOCLASTS, General Medicine, CONFORMATION, medicine.anatomical_structure, Medicine, Research & Experimental, 030220 oncology & carcinogenesis, Stem cell, Tyrosine kinase, Life Sciences & Biomedicine, Proto-oncogene tyrosine-protein kinase Src, GRAY PLATELET SYNDROME, UNRAVEL, IMATINIB, Article, Gray platelet syndrome, 03 medical and health sciences, MEGAKARYOCYTES, OSTEOPETROSIS, medicine, Science & Technology, COMPLEX, business.industry, ZEBRAFISH, BRIDGE-BPD Consortium, Tyrosine phosphorylation, Cell Biology, 06 Biological Sciences, medicine.disease, PODOSOMES, MICE, 030104 developmental biology, chemistry, DEFECT, Immunology, CELLS, Cancer research, RNA, HUMAN PHENOTYPE ONTOLOGY, business, MATRIX
وصف الملف: Print-Electronic; application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3abf3e713632f2d4f4b79dd740d7ce90
https://cris.maastrichtuniversity.nl/en/publications/798e4ad0-d6bf-4108-acbd-b347381a5789