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1دورية أكاديمية
المؤلفون: Ritter, Malte, Klimiankou, Maksim, Klimenkova, Olga, Schambach, AxelAff2, Aff3, Hoffmann, Dirk, Schmidt, Amy, Kanz, Lothar, Link, Daniel C., Welte, Karl, Skokowa, JuliaAff1
المصدر: Annals of Hematology. 99(10):2329-2338
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2دورية أكاديمية
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3دورية أكاديمية
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المؤلفون: Julia Skokowa, Axel Schambach, Amy P. Schmidt, Maksim Klimiankou, Malte U Ritter, Dirk Hoffmann, Karl Welte, Daniel C. Link, Lothar Kanz, Olga Klimenkova
المصدر: Annals of Hematology
مصطلحات موضوعية: Male, Neutropenia, Myeloid, Mice, Transgenic, G-CSFR mutations, Biology, medicine.disease_cause, Colony-Forming Units Assay, Mice, chemistry.chemical_compound, hemic and lymphatic diseases, Receptors, Colony-Stimulating Factor, medicine, Animals, Congenital Bone Marrow Failure Syndromes, Preleukemia, Myeloid Cells, RNA, Messenger, Congenital Neutropenia, Severe congenital neutropenia, Inflammation, Myelopoiesis, Mutation, RUNX1 mutations, Gene Expression Profiling, Bone marrow failure, Wild type, Myeloid leukemia, Hematology, General Medicine, Hematopoietic Stem Cells, medicine.disease, Immunity, Innate, Recombinant Proteins, Specific Pathogen-Free Organisms, Mice, Inbred C57BL, medicine.anatomical_structure, Pre-leukemia bone marrow failure syndrome, RUNX1, chemistry, Core Binding Factor Alpha 2 Subunit, Cancer research, Original Article, Bone marrow, Cell Division
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المؤلفون: Yokota, Asumi, Huo, Li, Lan, Fengli, Wu, Jianqiang, Huang, Gang
المصدر: Molecules and Cells
مصطلحات موضوعية: RUNX1 mutations, hemic and lymphatic diseases, pathogenesis, Hematologic Neoplasms, embryonic structures, Core Binding Factor Alpha 2 Subunit, Mutation, Humans, clinical incidence and prognosis, Minireview, targeted therapy
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::3e1fbc533c588fc4727ac94a41cbad36
http://europepmc.org/articles/PMC7057846 -
6دورية أكاديمية
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المؤلفون: Aline Renneville, Judith C. W. Marsh, Carolyn Owen, Andrew Green, Rogier Mous, Jude Fitzgibbon, Andrew R. Hallahan, David Taussig, Jun Wang, Josep F. Nomdedeu, Ahad F. Al Seraihi, Mark Layton, Nikolas Pontikos, Doris Steinemann, Kim Reay, Vincent Plagnol, Rachel Protheroe, Tim Ripperger, Susanna Akiki, Joanne Mason, Upal Hossain, Henrik Hjorth-Hansen, Anne Uyttebroeck, Amanda J. Walne, Nigel H. Russell, Jenna Alnajar, Nele Hug, Claude Preudhomme, Jamie Cavenagh, Findlay Bewicke-Copley, Csaba Bödör, Kiran Tawana, Adrian Bloor, Cynthia L. Toze, Alicia Ellison, Paula Page, Gabriela Sciuccati, Inderjeet Dokal, Tom Vulliamy, John K. Wu, Jiri Pavlu, Peter Vandenberghe, Hemanth Tummala, Elspeth Payne, Michael L. Barnett, David T. Bowen, Brigitte Schlegelberger, Priyanka Mehta, Ana Rio-Machin, Alison Male, Shirleny Cardoso, Hannah Armes, Anand Saggar, Sarah Lawson, Nuria Pujol-Moix, Javier F. Cáceres, Pierre Fenaux, Sally Killick
المصدر: Nature Communications
r-IIB SANT PAU: Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut dInvestigació Biomèdica Sant Pau (IIB Sant Pau)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
Rio-machin, A, Vulliamy, T, Hug, N, Walne, A, Tawana, K, Cardoso, S, Ellison, A, Pontikos, N, Wang, J, Tummala, H, Al Seraihi, A F, Alnajar, J, Bewicke-Copley, F, Armes, H, Barnett, M, Bloor, A, Bodor, C, Bowen, D, Fenaux, P, Green, A, Hallahan, A, Hjorth-Hansen, H, Hossain, U, Killick, S, Lawson, S, Layton, M, Male, A M, Marsh, J, Mehta, P, Mous, R, Nomdedeu, J F, Owen, C, Pavlu, J, Payne, E, Protheroe, R, Predhomme, C, Pujol-Moix, N, Renneville, A, Russell, N, Saggar, A, Sciuccati, G, Taussig, D, Toze, C, Uyttebroeck, A, Vandenberghe, P, Schlegelberger, B, Ripperger, T, Steinemann, D, Wu, J, Mason, J, Page, P, El Akiki, S, Reay, K, Cavenagh, J D, Plagnol, V, Caceres, J F, Fitzgibbon, J & Dokal, I 2020, ' The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants ', Nature Communications . https://doi.org/10.1038/s41467-020-14829-5
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instnameمصطلحات موضوعية: 0301 basic medicine, Myeloid, Adenosine Deaminase, Vesicular Transport Proteins, General Physics and Astronomy, DYSKERATOSIS-CONGENITA, Whole Exome Sequencing, Cohort Studies, 0302 clinical medicine, hemic and lymphatic diseases, CEBPA, Cancer genomics, RUNX1 MUTATIONS, lcsh:Science, Exome sequencing, MYELODYSPLASTIC SYNDROME, Genetics, Multidisciplinary, Receptors, Interleukin-17, Myeloid leukemia, SAMD9L MUTATIONS CAUSE, Pedigree, Multidisciplinary Sciences, Leukemia, Leukemia, Myeloid, Acute, medicine.anatomical_structure, 030220 oncology & carcinogenesis, Science & Technology - Other Topics, RNA Helicases, Platelet disorder, Science, LINE, ACUTE MYELOID-LEUKEMIA, Platelet Membrane Glycoproteins, Biology, General Biochemistry, Genetics and Molecular Biology, Article, Acute myeloid leukaemia, 03 medical and health sciences, Germline mutation, PLATELET DISORDER, Exome Sequencing, medicine, Humans, MECHANISTIC INSIGHTS, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, Science & Technology, Perforin, Myelodysplastic syndromes, General Chemistry, Axonemal Dyneins, medicine.disease, Nonsense Mediated mRNA Decay, SELF-RENEWAL, 030104 developmental biology, Myelodysplastic Syndromes, lcsh:Q
وصف الملف: Electronic; application/pdf
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المصدر: Chinese Journal of Hematology
مصطلحات موضوعية: Adult, Male, RUNX1 mutations, Myeloid neoplasms, Hematopoietic Stem Cell Transplantation, 预后, Middle Aged, Prognosis, 髓系肿瘤, 异基因造血干细胞移植, 论著, Leukemia, Myeloid, Acute, RUNX1突变, Allogeneic hematopoietic stem cell transplantation, Core Binding Factor Alpha 2 Subunit, Mutation, Humans, Transplantation, Homologous, Female, Aged, Retrospective Studies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::29946a5ba1cb168c6b89d5ae94a66e5b
http://europepmc.org/articles/PMC7348223 -
9دورية أكاديمية
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10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.