نتائج البحث - "Kozyra, Emilia"

العلاقة: Versió postprint del document publicat a: https://doi.org/10.1111/bjh.18330Test; British Journal of Haematology, 2022, vol. 199, num. 4, p. 482-495; https://doi.org/10.1111/bjh.18330Test; info:eu-repo/grantAgreement/EC/H2020/739593/EU//HCEMM; http://hdl.handle.net/2445/191099Test; 726966

الإتاحة: https://doi.org/10.1111/bjh.18330Test
http://hdl.handle.net/2445/191099Test

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5

دورية أكاديمية

GATA2 deficiency and MDS/ AML: Experimental strategies for disease modelling and future therapeutic prospects

المؤلفون: Kotmayer, Lili, Romero‐Moya, Damia, Marin‐Bejar, Oskar, Kozyra, Emilia, Català, Albert, Bigas, Anna, Wlodarski, Marcin W., Bödör, Csaba, Giorgetti, Alessandra

المساهمون: Bundesministerium für Bildung und Forschung, Generalitat de Catalunya, Ministerio de Economía y Competitividad, Nemzeti Kutatási és Technológiai Hivatal, Vera and Joseph Dresner Foundation, American Lebanese Syrian Associated Charities

المصدر: British Journal of Haematology ; volume 199, issue 4, page 482-495 ; ISSN 0007-1048 1365-2141

الإتاحة: https://doi.org/10.1111/bjh.18330Test

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6

دورية أكاديمية

Hematopoietic stem cell transplantation in children and adolescents with GATA2-related myelodysplastic syndrome

المصدر: http://lobid.org/resources/99370676016606441Test#!, 56(11):2732-2741.

مصطلحات موضوعية: Adolescent [MeSH], GATA2 Transcription Factor/genetics [MeSH], Humans [MeSH], Myelodysplastic Syndromes/therapy [MeSH], Paediatrics, Myelodysplastic Syndromes/genetics [MeSH], Stem-cell therapies, Article, Germ-Line Mutation [MeSH], Graft vs Host Disease/etiology [MeSH], Chromosome Deletion [MeSH], Hematopoietic Stem Cell Transplantation/methods [MeSH], Child [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6442902Test; https://doi.org/10.1038/s41409-021-01374-yTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563415Test/

الإتاحة: https://doi.org/10.1038/s41409-021-01374-yTest
https://repository.publisso.de/resource/frl:6442902Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8563415Test/

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7

دورية أكاديمية

Association of unbalanced translocation der(1;7) with germline GATA2 mutations

المؤلفون: Kozyra, Emilia J., Göhring, Gudrun, Hickstein, Dennis D., Calvo, Katherine R., DiNardo, Courtney D., Dworzak, Michael, de Haas, Valerie, Starý, Jan, Hasle, Henrik, Shimamura, Akiko, Fleming, Mark D., Inaba, Hiroto, Lewis, Sara, Hsu, Amy P., Holland, Steven M., Arnold, Danielle E., Mecucci, Cristina, Keel, Siobán B., Bertuch, Alison A., Tawana, Kiran, Barzilai, Shlomit, Hirabayashi, Shinsuke, Onozawa, Masahiro, Lei, Shaohua, Alaiz, Helena, Andrikovics, Hajnalka, Betts, David, Beverloo, Berna H., Buechner, Jochen, Čermák, Martin, Cervera, José, Haus, Olga, Jahnukainen, Kirsi, Manola, Kalliopi N., Nebral, Karin, Pasquali, Francesco, Tchinda, Joelle, Turkiewicz, Dominik, Van Roy, Nadine, Zemanova, Zuzana, Pastor, Victor B., Strahm, Brigitte, Noellke, Peter, Niemeyer, Charlotte M., Schlegelberger, Brigitte, Yoshimi, Ayami, Wlodarski, Marcin W.

المصدر: Kozyra , E J , Göhring , G , Hickstein , D D , Calvo , K R , DiNardo , C D , Dworzak , M , de Haas , V , Starý , J , Hasle , H , Shimamura , A , Fleming , M D , Inaba , H , Lewis , S , Hsu , A P , Holland , S M , Arnold , D E , Mecucci , C , Keel , S B , Bertuch , A A , Tawana , K , Barzilai , S , Hirabayashi , S , ....

العلاقة: https://pure.eur.nl/en/publications/21e7e57d-1ce9-4ba8-8d83-c1ed18832a93Test

الإتاحة: https://doi.org/10.1182/blood.2021012781Test
https://pure.eur.nl/en/publications/21e7e57d-1ce9-4ba8-8d83-c1ed18832a93Test
http://www.scopus.com/inward/record.url?scp=85120756166&partnerID=8YFLogxKTest

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8

دورية أكاديمية

Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes

المؤلفون: Sahoo, Sushree S., Pastor, Victor B., Goodings, Charnise, Voss, Rebecca K., Kozyra, Emilia J., Szvetnik, Amina, Noellke, Peter, Dworzak, Michael, Starý, Jan, Locatelli, Franco, Masetti, Riccardo, Schmugge, Markus, Moerloose, Barbara De, Catala, Albert, Kállay, Krisztián, Turkiewicz, Dominik, Hasle, Henrik, Buechner, Jochen, Jahnukainen, Kirsi, Ussowicz, Marek, Polychronopoulou, Sophia, Smith, Owen P., Fabri, Oksana, Barzilai, Shlomit, Haas, Valérie De, Baumann, Irith, Schwarz-Furlan, Stephan, Niewisch, Marena, Sauer, M.G. (Martin), Burkhardt, B. (Birgit), Lang, P. (Peter), Bader, P. (Peter), Beier, R. (Rita), Müller, I. (Ingo), Albert, M.H. (Michael), Meisel, R. (Roland), Schulz, A. (Ansgar), Cario, G. (Gunnar), Panda, P.K. (Pritam), Wehrle, J. (Julius), Hirabayashi, S. (Shinsuke), Derecka, M. (Marta), Durruthy-Durruthy, R. (Robert), Göhring, G. (Gudrun), Yoshimi-Noellke, A. (Ayami), Ku, M. (Manching), Lebrecht, D. (Dirk), Erlacher, M. (Miriam), Flotho, C. (Christian), Strahm, B. (Brigitte), Niemeyer, Charlotte M., Wlodarski, M.W. (Marcin)

المصدر: Sahoo , S S , Pastor , V B , the European Working Group of MDS in Children (EWOG-MDS) , Goodings , C , Voss , R K , Kozyra , E J , Szvetnik , A , Noellke , P , Dworzak , M , Starý , J , Locatelli , F , Masetti , R , Schmugge , M , Moerloose , B D , Catala , A , Kállay , K , Turkiewicz , D , Hasle , H , Buechner , J , Jahnukainen , K , Ussowicz , M , Polychronopoulou , S , ....

مصطلحات موضوعية: /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being, name=SDG 3 - Good Health and Well-being

العلاقة: https://pure.eur.nl/en/publications/b2bc766f-746f-4208-a1ce-e2eb46d830d3Test

الإتاحة: https://doi.org/10.1038/s41591-021-01511-6Test
https://pure.eur.nl/en/publications/b2bc766f-746f-4208-a1ce-e2eb46d830d3Test
http://www.scopus.com/inward/record.url?scp=85116777637&partnerID=8YFLogxKTest
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330547Test/

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9

دورية أكاديمية

Publisher Correction: Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes

المؤلفون: Sahoo, Sushree S., Pastor, Victor B., Goodings, Charnise, Voss, Rebecca K., Kozyra, Emilia J., Szvetnik, Amina, Noellke, Peter, Dworzak, Michael, Starý, Jan, Locatelli, Franco, Masetti, Riccardo, Schmugge, Markus, De Moerloose, Barbara, Catala, Albert, Kállay, Krisztián, Turkiewicz, Dominik, Hasle, Henrik, Buechner, Jochen, Jahnukainen, Kirsi, Ussowicz, Marek, Polychronopoulou, Sophia, Smith, Owen P., Fabri, Oksana, Barzilai, Shlomit, de Haas, Valerie, Baumann, Irith, Schwarz-Furlan, Stephan, Moerloose, Barbara De, Kallay, Krisztián, Smith, Owen, Haas, Valérie De, Gohring, Gudrun, Niemeyer, Charlotte, Nebral, Karin, Simonitsch-Kluppp, Ingrid, Paepe, Pascale De, Van Roy, Nadine, Campr, Vit, Zemanova, Zuzana, Clasen-Linde, Erik, Plesner, Tine, Schlegelberger, Brigitte, Rudelius, Martina, Manola, Kalliopi, Stefanaki, Kalliopi, Csomor, Judit, Andrikovics, Hajnalka, Betts, David, O’Sullivan, Maureen

المصدر: Nature Medicine ; volume 27, issue 12, page 2248-2248 ; ISSN 1078-8956 1546-170X

مصطلحات موضوعية: General Biochemistry, Genetics and Molecular Biology, General Medicine

الإتاحة: https://doi.org/10.1038/s41591-021-01632-yTest
https://www.nature.com/articles/s41591-021-01632-y.pdfTest
https://www.nature.com/articles/s41591-021-01632-yTest

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10

دورية أكاديمية

Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency

المؤلفون: Kozyra, Emilia J, Pastor, Victor B, Schmugge, Markus

المصدر: Kozyra, Emilia J; Pastor, Victor B; et al; Schmugge, Markus (2020). Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency. Leukemia, 34(10):2673-2687.

مصطلحات موضوعية: Medical Clinic, 610 Medicine & health, Anesthesiology and Pain Medicine, Cancer Research, Hematology

وصف الملف: application/pdf

العلاقة: https://www.zora.uzh.ch/id/eprint/199944/1/s41375-020-0899-5%281%29.pdfTest; info:pmid/32555368; urn:issn:0887-6924

الإتاحة: https://doi.org/10.5167/uzh-19994410.1038/s41375-020-0899-5Test
https://www.zora.uzh.ch/id/eprint/199944Test/
https://www.zora.uzh.ch/id/eprint/199944/1/s41375-020-0899-5%281%29.pdfTest

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