المؤلفون: Filipe R. Pinto, António Lamas, Daniel G. Oliveira, Márcia E. Oliveira, Raquel Faria

المصدر: Acta Médica Portuguesa (2023)

مصطلحات موضوعية: Inflammation/genetics, Myelodysplastic Syndromes/genetics, Ubiquitin-Activating Enzymes/genetics, VEXAS syndrome, Medicine, Medicine (General), R5-920

وصف الملف: electronic resource

العلاقة: https://www.actamedicaportuguesa.com/revista/index.php/amp/article/view/19687Test; https://doaj.org/toc/0870-399XTest; https://doaj.org/toc/1646-0758Test

الوصول الحر: https://doaj.org/article/1f33e427401d43a5908a454c928cf115Test

المؤلفون: Hilberink, J.R., van Zeventer, I.A., Chitu, D.A., Pabst, T., Klein, S.K., Stussi, G., Griskevicius, L., Valk, PJM, Cloos, J., van de Loosdrecht, A.A., Breems, D., van Lammeren-Venema, D., Boersma, R., Jongen-Lavrencic, M., Fehr, M., Hoogendoorn, M., Manz, M.G., Söhne, M., van Marwijk Kooy, R., Deeren, D., van der Poel, MWM, Legdeur, M.C., Tick, L., Chalandon, Y., Ammatuna, E., Blum, S., Löwenberg, B., Ossenkoppele, G.J., Huls, G.

المساهمون: Dutch-Belgian Hemato-Oncology Cooperative Group (HOVON), Swiss Group for Clinical Cancer Research (SAKK), Chitu, D.A., Klein, S.K., Griskevicius, L., Valk, PJM, Cloos, J., van de Loosdrecht, A.A., Breems, D., van Lammeren-Venema, D., Boersma, R., Jongen-Lavrencic, M., Söhne, M., van Marwijk Kooy, R., Deeren, D., van der Poel, MWM, Legdeur, M.C., Tick, L., Ammatuna, E., Löwenberg, B., Ossenkoppele, G.J., Huls, G., Pabst, T., Stussi, G., Fehr, M., Manz, M.G., Chalandon, Y., Blum, S.

المصدر: Blood cancer journal, vol. 13, no. 1, pp. 93

مصطلحات موضوعية: Humans, Male, Female, Aged, Decitabine/therapeutic use, Myelodysplastic Syndromes/genetics, Leukemia, Myeloid, Acute/genetics, Mutation, Treatment Outcome

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/37336890; info:eu-repo/semantics/altIdentifier/eissn/2044-5385; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_4F3DD7E2D5288; https://serval.unil.ch/notice/serval:BIB_4F3DD7E2D528Test; urn:issn:2044-5385; https://serval.unil.ch/resource/serval:BIB_4F3DD7E2D528.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_4F3DD7E2D5288Test

الإتاحة: https://doi.org/10.1038/s41408-023-00850-6Test
https://serval.unil.ch/notice/serval:BIB_4F3DD7E2D528Test
https://serval.unil.ch/resource/serval:BIB_4F3DD7E2D528.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_4F3DD7E2D5288Test

المؤلفون: Ma, Haili, Bizet, Martin, Soares Da Costa, Christelle, Murisier, Frédéric, de Bony, Eric James, Wang, Meng-Ke, Yoshimi, Akihide, Lin, Kuan-Ting, Riching, Kristin M., Wang, Xing, Beckman, John I., Arya, Shailee, Droin, Nathalie, Calonne, Emilie, Hassabi, Bouchra, Zhang, Qing-Yang, Li, Ang, Putmans, Pascale, Malbec, Lionel, Hubert, Céline, Lan, Jie, Mies, Frédérique, Bula Ibula Yanga, Yanga, Solary, Eric, Daniels, Danette, Gupta, Yogesh K., Deplus, Rachel, Abdel-Wahab, Omar, Yang, Yun-Gui, Fuks, François

المصدر: Molecular cell, 83 (23

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Humans, Leukemia -- genetics, Myelodysplastic Syndromes -- genetics, Neoplasms -- genetics, RNA, Messenger -- genetics, RNA-Binding Proteins -- genetics, Serine-Arginine Splicing Factors -- genetics, RNA Methylation -- genetics, NSUN2, RNA methylation, RNA modification, RNA splicing, SRSF2, SRSF2(P95H), cancer, epitranscriptomics, leukemia, m(5)C

وصف الملف: 2 full-text file(s): application/pdf | application/pdf

العلاقة: uri/info:doi/10.1016/j.molcel.2023.11.003; uri/info:pii/S1097-2765(23)00919-X; uri/info:pmid/38065062; uri/info:scp/85178093467; https://dipot.ulb.ac.be/dspace/bitstream/2013/368902/6/Ma2023.pdfTest; https://dipot.ulb.ac.be/dspace/bitstream/2013/368902/1/elsevier_352546.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/368902Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/368902Test
https://dipot.ulb.ac.be/dspace/bitstream/2013/368902/6/Ma2023.pdfTest
https://dipot.ulb.ac.be/dspace/bitstream/2013/368902/1/elsevier_352546.pdfTest

المؤلفون: Hecht, Anna, Meyer, Julia A., Jann, Johann-Christoph, Sockel, Katja, Giagounidis, Aristoteles, Götze, Katharina S., Letsch, Anne, Haase, Detlef, Schlenk, Richard F., Haferlach, Torsten, Schafhausen, Philippe, Bug, Gesine, Lübbert, Michael, Thol, Felicitas, Büsche, Guntram, Schuler, Esther, Nowak, Verena, Obländer, Julia, Fey, Stephanie, Müller, Nadine, Metzgeroth, Georgia, Hofmann, Wolf-Karsten, Germing, Ulrich, Nolte, Florian, Reinwald, Mark, Nowak, Daniel

المصدر: http://lobid.org/resources/99370678538206441Test#!, 100(6):1463-1471.

مصطلحات موضوعية: Myelodysplastic syndromes, Deletion 5q, Female [MeSH], Aged, 80 and over [MeSH], Chromosomes, Human, Pair 5/genetics [MeSH], Aged [MeSH], DNA Methylation/drug effects [MeSH], Adult [MeSH], Humans [MeSH], Lenalidomide, Treatment Outcome [MeSH], Antineoplastic Agents/pharmacology [MeSH], Middle Aged [MeSH], Myelodysplastic Syndromes/genetics [MeSH], Original Article, Male [MeSH], Myelodysplastic Syndromes/drug therapy [MeSH], Antineoplastic Agents/therapeutic use [MeSH], Chromosome Deletion [MeSH], DNA methylation, Lenalidomide/pharmacology [MeSH], Lenalidomide/therapeutic use [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6447833Test; https://doi.org/10.1007/s00277-021-04492-1Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116243Test/

الإتاحة: https://doi.org/10.1007/s00277-021-04492-1Test
https://repository.publisso.de/resource/frl:6447833Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116243Test/

المؤلفون: Owattanapanich, Weerapat, Herzig, Julia, Jahn, Nikolaus, Panina, Ekaterina, Ruchutrakool, Theera, Kungwankiattichai, Smith, Issaragrisil, Surapol, Döhner, Hartmut, Döhner, Konstanze

المصدر: http://lobid.org/resources/99370678538206441Test#!, 100(8):1983-1993.

مصطلحات موضوعية: Female [MeSH], Mutation [MeSH], Adult [MeSH], Humans [MeSH], Prospective Studies [MeSH], Myelodysplastic Syndromes/therapy [MeSH], Middle Aged [MeSH], Myelodysplastic Syndromes/genetics [MeSH], Thailand, Thailand/epidemiology [MeSH], DNA (Cytosine-5-)-Methyltransferases/genetics [MeSH], Original Article, Acute myeloid leukemia, Genetic, Male [MeSH], Leukemia, Myeloid, Acute/epidemiology [MeSH], Acute/genetics [MeSH], Myelodysplastic Syndromes/epidemiology [MeSH], fms-Like Tyrosine Kinase 3/genetics [MeSH], Next-generation sequencing, Acute/therapy [MeSH], Molecular, High-Throughput Nucleotide Sequencing [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6447821Test; https://doi.org/10.1007/s00277-021-04513-zTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285357Test/

الإتاحة: https://doi.org/10.1007/s00277-021-04513-zTest
https://repository.publisso.de/resource/frl:6447821Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285357Test/

المؤلفون: Bortnick, Rachel, Wlodarski, Marcin, de Haas, Valerie, De Moerloose, Barbara, Dworzak, Michael, Hasle, Henrik, masetti, riccardo, Starý, Jan, Turkiewicz, Dominik, Ussowicz, Marek, Kozyra, Emilia, Albert, Michael, Bader, Peter, Bordon, Victoria, Cario, Gunnar, Beier, Rita, Schulte, Johannes Hubertus, Bresters, Dorine, Müller, Ingo, Pichler, Herbert, Sedlacek, Petr, Sauer, Martin G., Zecca, Marco, Göhring, Gudrun, Yoshimi, Ayami, Noellke, Peter, Erlacher, Miriam, Locatelli, Franco, Niemeyer, Charlotte, Strahm, Brigitte

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/

المؤلفون: Stomper, Julia, Meier, Ruth, Ma, Tobias, Pfeifer, Dietmar, Ihorst, Gabriele, Blagitko-Dorfs, Nadja, Greve, Gabriele, Zimmer, Dennis, Platzbecker, Uwe, Hagemeijer, Anne, Schmitt-Graeff, Ingrid, Lübbert, Michael

المصدر: http://lobid.org/resources/99370675582406441Test#!, 13(1):77.

مصطلحات موضوعية: Aged, 80 and over [MeSH], Aged [MeSH], DNA Copy Number Variations/genetics [MeSH], EZH2, Histones/genetics [MeSH], Protein expression, H3K27 trimethylation, Mutations, Myelodysplastic Syndromes/genetics [MeSH], Cohort Studies [MeSH], Gene Expression/genetics [MeSH], Acute myeloid leukemia, Survival, Male [MeSH], Promoter methylation, Leukemia, Myeloid, Acute/genetics [MeSH], Mutation/genetics [MeSH], Female [MeSH], Adult [MeSH], Humans [MeSH], Enhancer of Zeste Homolog 2 Protein/genetics [MeSH], Middle Aged [MeSH], Cancer epigenetics and diagnostics, Research, Prognosis [MeSH], Young Adult [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6463995Test; https://doi.org/10.1186/s13148-021-01052-2Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8043064Test/

الإتاحة: https://doi.org/10.1186/s13148-021-01052-2Test
https://repository.publisso.de/resource/frl:6463995Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8043064Test/

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 , ....

مصطلحات موضوعية: DEFICIENCY, FAMILIAL MYELODYSPLASTIC SYNDROME, HIGH-FREQUENCY, Translocation, Genetic, Humans, Middle Aged, Male, GATA2 Transcription Factor/deficiency, Young Adult, Myelodysplastic Syndromes/genetics, Adolescent, Germ-Line Mutation, Adult, Female, Child

وصف الملف: application/pdf

الإتاحة: https://doi.org/10.1182/blood.2021012781Test
https://pure.au.dk/portal/da/publications/association-of-unbalanced-translocation-der17-with-germline-gata2-mutationsTest(b4d967c4-ad06-46a8-bb21-cca80c2b181e).html
https://pure.au.dk/ws/files/274410748/Primary_cytotoxic_T_cell_lymphomas_harbor_recurrent_targetable_alterations_in_the_JAK_STAT_pathway.pdfTest
http://www.scopus.com/inward/record.url?scp=85120756166&partnerID=8YFLogxKTest

المصدر: Blood Cancer Journal. 13(1)

مصطلحات موضوعية: Male, Myeloid, Leukemia, Treatment Outcome, Decitabine/therapeutic use, Mutation, Humans, Female, Acute/genetics, Myelodysplastic Syndromes/genetics, Aged

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od________83::07451efcefdc941e05f11fcbeeb5153cTest
https://doi.org/10.1038/s41408-023-00850-6Test

المؤلفون: Eileen Wedge, Ulvi Ahmadov, Thomas B. Hansen, Zongliang Gao, Morten Tulstrup, Christophe Côme, Sridhar Nonavinkere Srivatsan, Tanzir Ahmed, Jakob S. Jespersen, Balthasar C. Schlotmann, Claudia Schöllkopf, Klas Raaschou-Jensen, Niels Ødum, Jørgen Kjems, Rasmus O. Bak, Matthew J. Walter, Kirsten Grønbæk, Lasse S. Kristensen

المصدر: Wedge, E, Ahmadov, U, Hansen, T B, Gao, Z, Tulstrup, M, Côme, C, Nonavinkere Srivatsan, S, Ahmed, T, Jespersen, J S, Schlotmann, B C, Schöllkopf, C, Raaschou-Jensen, K, Ødum, N, Kjems, J, Bak, R O, Walter, M J, Grønbæk, K & Kristensen, L S 2023, ' Impact of U2AF1 mutations on circular RNA expression in myelodysplastic neoplasms ', Leukemia, vol. 37, no. 5, pp. 1113-1125 . https://doi.org/10.1038/s41375-023-01866-4Test

مصطلحات موضوعية: Cancer Research, Mice, Splicing Factor U2AF/genetics, Oncology, Doxycycline, Neoplasms, RNA Splicing, RNA, Circular/genetics, Mutation, Animals, Hematology, RNA Splicing Factors/genetics, Myelodysplastic Syndromes/genetics

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d552d18cfb6225451b91d289182d9379Test
https://pure.au.dk/portal/da/publications/impact-of-u2af1-mutations-on-circular-rna-expression-inTest-myelodysplastic-neoplasms(3de8bf0a-a973-4385-b2c9-1ac1bb734ed6).html