المؤلفون: Haferlach, T, Nagata, Y, Grossmann, V, Okuno, Y, Bacher, U, Nagae, G, Schnittger, S, Sanada, M, Kon, A, Alpermann, T, Yoshida, K, Roller, A, Nadarajah, N, Shiraishi, Y, Shiozawa, Y, Chiba, K, Tanaka, H, Koeffler, HP, Klein, H-U, Dugas, M, Aburatani, H, Kohlmann, A, Miyano, S, Haferlach, C, Kern, W, Ogawa, S

المصدر: Leukemia. 28(2)

مصطلحات موضوعية: Genetic Testing, Clinical Research, Rare Diseases, Human Genome, Genetics, Biotechnology, Cancer, Hematology, Adult, Aged, Aged, 80 and over, Female, Gene Frequency, Genetic Association Studies, Genetic Markers, High-Throughput Nucleotide Sequencing, Humans, Male, Middle Aged, Mutation, Mutation Rate, Myelodysplastic Syndromes, Polymorphism, Single Nucleotide, Prognosis, Proportional Hazards Models, Young Adult, next-generation sequencing, molecular markers, myelodysplastic syndromes, prognostic score, Clinical Sciences, Oncology and Carcinogenesis, Immunology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/07p8r0c1Test

المؤلفون: Jovanovic, J.V., Ivey, A., Vannucchi, A.M., Lippert, E., Leibundgut, E. Oppliger, Cassinat, B., Pallisgaard, N., Maroc, N., Hermouet, S., Nickless, G., Guglielmelli, P., Reijden, B.A. van der, Jansen, J.H., Alpermann, T., Schnittger, S., Bench, A., Tobal, K., Wilkins, B., Cuthill, K., McLornan, D., Yeoman, K., Akiki, S., Bryon, J., Jeffries, S., Jones, A., Percy, M.J., Schwemmers, S., Gruender, A., Kelley, T.W., Reading, S., Pancrazzi, A., McMullin, M.F., Pahl, H.L., Cross, N.C., Harrison, C.N., Prchal, J.T., Chomienne, C., Kiladjian, J.J., Barbui, T., Grimwade, D.

المصدر: Jovanovic, J V; Ivey, A; Vannucchi, A M; Lippert, E; Oppliger Leibundgut, Elisabeth; Cassinat, B; Pallisgaard, N; Maroc, N; Hermouet, S; Nickless, G; Guglielmelli, P; van der Reijden, B A; Jansen, J H; Alpermann, T; Schnittger, S; Bench, A; Tobal, K; Wilkins, B; Cuthill, K; McLornan, D; ... (2013). Establishing optimal quantitative-polymerase chain reaction assays for routine diagnosis and tracking of minimal residual disease in JAK2-V617F-associated myeloproliferative neoplasms: a joint European LeukemiaNet/MPN&MPNr-EuroNet (COST action BM0902) study. Leukemia, 27(10), pp. 2032-2039. Nature Publishing Group 10.1038/leu.2013.219 <http://dx.doi.org/10.1038/leu.2013.219Test>
Leukemia
Leukemia, 27, 2032-9
Leukemia, 27, 10, pp. 2032-9

مصطلحات موضوعية: Adult, Male, Neoplasm, Residual, 610 Medicine & health, Real-Time Polymerase Chain Reaction, Young Adult, hemic and lymphatic diseases, Humans, Transplantation, Homologous, RNA, Messenger, Aged, JAK2-V617F, Immune Regulation Translational research [NCMLS 2], Myeloproliferative Disorders, Reverse Transcriptase Polymerase Chain Reaction, Remission Induction, Janus Kinase 2, Middle Aged, Prognosis, Europe, MRD, qPCR standardization, Cytogenetic Analysis, Mutation, Female, Original Article, Neoplasm Recurrence, Local, Follow-Up Studies, Stem Cell Transplantation

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8db0b9a0e0a05667e1f59be8f8b90e3dTest
https://doi.org/10.1038/leu.2013.219Test

المؤلفون: Tapper, W., Jones, A.V., Kralovics, R., Harutyunyan, A.S., Zoi, K., Leung, W., Godfrey, A.L., Guglielmelli, P., Callaway, A., Ward, D., Aranaz, P., White, H.E., Waghorn, K., Lin, F., Chase, A.J., Baxter, E., Maclean, C., Nangalia, J., Chen, E., Evans, P., Short, M., Jack, A., Wallis, L., Oscier, D., Duncombe, A.S., Schuh, A., Mead, A.J., Griffiths, M., Ewing, J., Gale, R.E., Schnittger, S., Haferlach, T., Stegelmann, F., Döhner, K., Grallert, H., Strauch, K., Tanaka, T., Bandinelli, S., Giannopoulos, A., Pieri, L., Mannarelli, C., Gisslinger, H., Barosi, G., Cazzola, M., Reiter, A., Harrison, C.N., Campbell, P.J., Green, A.R., Vannucchi, A.M., Cross, N.C.P.

المصدر: Nature Communications
Nat. Commun. 6:6691 (2015)

مصطلحات موضوعية: Adult, Male, Genotype, Genes, myb, Polymorphism, Single Nucleotide, Article, Cohort Studies, Gene Frequency, GTP-Binding Proteins, hemic and lymphatic diseases, Proto-Oncogenes, Humans, Genetic Predisposition to Disease, HSP70 Heat-Shock Proteins, Polycythemia Vera, Telomerase, Alleles, Aged, Myeloproliferative Disorders, Genetic Variation, food and beverages, Janus Kinase 2, Middle Aged, Biochemistry, Genetics and Molecular Biology (all), Chemistry (all), Physics and Astronomy (all), MECOM, TERT, JAK2, HBS1L-MYB, myeloproliferative, Peptide Elongation Factors, MDS1 and EVI1 Complex Locus Protein, DNA-Binding Proteins, Case-Control Studies, Mutation, Female, Calreticulin, Receptors, Thrombopoietin, Thrombocythemia, Essential, Transcription Factors

وصف الملف: text; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::af4de8e77111910f7e836273abe58d9dTest
http://hdl.handle.net/2158/1012272Test

المؤلفون: Haaß, Wiltrud, Kleiner, Helga, Schweizerische Arbeitsgemeinschaft für Klinische Krebsforschung, Morgner, A., Herbst, R., Matek, W., Lamberti, C., Zöller, T., Koch, B., Marth, T., Henzel, A., Wagner, S., Woska, E., German CML Study Group, Neumann, F., Hoffknecht, M. M., Illmer, T., Wolf, T., Ehninger, G., Kiani, A., Platzbecker, U., Aul, C., Badrakhan, C. D., Giagounidis, A., Wernli, M., Flaßhove, M., Henneke, F., Moritz, T., Simon, M., Müller, L. L., Janz, R., Eckart, M., Häcker, B., Rech, D., Mackensen, A., Bargetzi, M., Krause, S. W., Staib, P., Schlegel, F., Wätzig, K., Rudolph, R., Wattad, M., Baur, F. K., Heit, W., Beelen, D. W., Hüttmann, A., Fischer von Weikersthal, L., Novotny, J., Trenschel, R., Lindemann, A., Linck, D., Jäger, E., Al-Batran, Salah-Eddin, Ottmann, O. G., Serve, H., Reiber, T., Semsek, D., Gro, V., Waller, C., Kühnemund, A., Hoeffkes, H. G., Lambertz, H., Schulz, L., Tajrobehkar, K., Mittermüller, J., Rummel, M. J., Burchardt, A., Pralle, H., Müller, S., Runde, V., Klei, M., Westheider, J., Hoyer, A., Tessen, H. W., Hesse, A., Trümper, L., Binder, C., Schmidt, C. A., Hirt, C., Hahn, M., Sieber, M., Eschenburg, H., Wilhelm, S., Depenbusch, R., Rösel, S., Eimermacher, H., Spohn, C., Moeller, R., Schmitz, N., Nickelsen, M., Schlimok, G., Engel, E., Haatanen, T., Hollburg, W., Platz, D., Köster, H., Bokemeyer, C., Schafhausen, P., Grote-Metke, A., Bechtel, B., Hemeier, M., Reichert, D., Sosada, M., Ganser, A., Schlegelberger, B., Ho, A. D., Rohlfing, S., Dengler, J., Petersen, V., Porowski, P., Hahn, L., Dietzfelbinger, H., Weiß, Christel, Janssen, J., Gröschel, W., Bartholomäus, A., Pfreundschuh, M., Kemmerling, M., Hansen, R., Reeb, M., Link, H., Mahlmann, S., Mezger, J., Schatz, M., Furkert, J., Schmier, M., Gatter, J., Neumann, S., Heymanns, J., Steinmetz, H. T., Schmitz, S., Scheid, C., Planker, M., Frieling, T., Lollert, A., Mandel, T., Neise, M., Schröder, M., Greif, D., Kempf, B., März, W., Kremers, S., Müller, L., Hartmann, F., Heil, G., Goldmann, B., Majunke, P. J., Heinkele, P., Gregor, M., Theobald, M., Fischer, T., Thomas, S., Hensel, M., Plöger, C., Schuster, D., Brust, J., Hieber, U., Paliege, R., Hehlmann, R., Neubauer, A., Burchert, A., Graeven, U., Lange, C., Schmidt, G., Völkl, S., Schmidt, B., Hitz, H., Spiekermann, K., Reichert, P., Hiddemann, W., Haferlach, T., Haferlach, C., Schnittger, S., Stötzer, O., Scheidegger, C., Fischer, C., Berdel, W. E., Koppele, A., Hebart, H., Fuss, H., Snaga, A., Schmidt, P., Hoffmann, R., Reschke, D., Zirpel, I., Sauer, M., Lenk, G., Theilmann, L., Sandritter, B., Neben, K., Schenk, M., Dengler, R., Herr, W., Krause, S., Braun, B., Günther, E., Wacker, A., Pihusch, R., Baldus, M., Matzdorff, A., Staiger, H. J., Pollmeier, G., Grimminger, W., Geer, T., Schanz, S., Jür, C., Gassmann, W., Seitz, K., Kaesberger, J., Mück, R., Heim, D., Illerhaus, G., Denzlinger, C., Fiechtner, H., Springer, G., Hoffmann, D., Jacki, S. H., Kanz, L., Bross-Bach, U., Döhner, H., Stegelmann, F., Haferlach, Claudia, Gratwohl, A., Kalhori, N., Langer, W., Nusch, A., Wei, J., Kamp, T., Schadeck-Gressel, C., Schwerdtfeger, R., Josten, K. M., Klein, O., Fett, W., Tichelli, A., Strotkötter, H., Maintz, C., Groschek, M., Schlag, R., Elsel, W., Schüler, F., Dölken, G., Lindemann, H. W., Wolf, H. H., Schmoll, H. J., Korsten, S., Braumann, D., Hoelzer, P., Kleeberg, U., Hossfeld, D., Lange, E., Schubert, J., Weischer, H., Dürk, H. A., Kirchner, H. H., Bu, E C., Henesser, D., Sievers, B., Freier, W., Kaiser, U., Peest, D., Römer, E., Hermann, T., Fauser, A., Valverde, M. L., Menzel, J., Kemper, J., le Coutre, P., Hochhaus, A., La Rosée, P., Bentz, M., Prümmer, O., Kneba, M., Strack, U., Schoch, R., Severin, K., Stauch, M., Arnold, R., Karbach, U., Vehling-Kaiser, U., Köchling, G., Wei, U., Middeke, H., Neuhaus, T., Martin, H., Fetscher, S., Schmielau, J., Kämpfe, D., Ludwig, W. D., Uppenkamp, M., Wei, B., Thum, P., Wuillemin, W., Hofmann, W. K., Griesshammer, M., Tischler, H. J., Becker, M., Hanfstein, B., Müller, M., Ratei, R., Saußele, S., Lunscken, C., Kolb, H. J., Lutz, L., Hentrich, M., Nerl, C., Wendtner, C., Ladda, E., Gnad, M., Teutsch, C., Suna, H., Schmidt, E., Koschmieder, S., Falge, C., Wandt, H., Wilhelm, M., Köhne, C. H., Schweiger, C., Müller-Naendrup, C., Frühauf, S., Ludwig, F., Ranft, K., Dencausse, Y., Baake, G., Ritter, P. R., Kloke, O., Göttler, B., Schick, H. D., Schlegelberger, Brigitte, Urmersbach, A., Weidenhöfer, S., Weidinger, P., Wacker, D., Wehmeyer, J., Kreuser, E. D., Schlenska-Lange, A., Edinger, R., Andreesen, R., Wehmeier, A., Stahlhut, K., Blau, I., Käfer, G., Cerny, T., Hess, U., Priebe-Richter, C., Stange-Budumlu, O., Demandt, M., Freunek, G., Heidemann, E., Schleicher, J., Mergenthaler, H. G., Ihle, H., Boewer, C., Zeller, C., Laubenstein, H. P., Rendenbach, B., Clemens, M., Waladkhani, A. R., Forstbauer, H., Müller, F., Brettner, S., Raghavachar, A., Sperling, C., Kunzmann, V., Goebeler, M. E., Gmür, J., Schelenz, C., Koschuth, A., Kingreen, D., Heßling, J., Derwahl, K. M., Oldenkott, B., Müller, Martin C., Englisch, H. J., Thiel, E., Burmeister, T., Notter, M., de Wit, M., Rothaug, W., Büschel, G., Beyer, J., Dahmen, E., Hehlmann, Rüdiger, Biaggi, C., Lämmle, B., Friess, D., Baerlocher, G., Oppliger Leibundgut, E., Tobler, A., Just, M., Schäfer, E., Behringer, D., Brandt, M., Hofmann, Wolf-Karsten, Schmiegel, W., Vaupel, H. A., Verbeek, W., Ko, Y. D., Sauerbruch, T., Hahn-Ast, C., Janzen, V., Schmidt-Wolf, Ingo G. H., Trenn, G., Fabarius, Alice, van der Linde, M., Pommerien, W., Fritz, L., Krauter, J., Lordick, F., Fritsch, G., Pflüger, K. H., Diekmann, C., Kullmer, J., Doering, G., Seifarth, Wolfgang, Munzinger, H., Hertenstein, B., Peyn, A., Mayer, J., Zácková, D., Kujickova, J., Stier, S., Wejda, B., Möller-Faßbender, F., Hänel, M.

المصدر: PLOS ONE 10(6), e0129648 (2015). doi:10.1371/journal.pone.0129648
PLoS ONE

مصطلحات موضوعية: Adult, Aged, 80 and over, Chromosome Aberrations, Adolescent, Fusion Proteins, bcr-abl, Antineoplastic Agents, Chromosome Breakage, Middle Aged, Clonal Evolution, Young Adult, hemic and lymphatic diseases, Cell Line, Tumor, Leukemia, Myelogenous, Chronic, BCR-ABL Positive, Proteolysis, Imatinib Mesylate, Humans, Blast Crisis, Separase, Research Article, Aged

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f18d0c27f6478a3f7c9bf13d9356962Test

المؤلفون: Strehl, S, Meyer, C, Kowarz, E, Hofmann, J, Renneville, A, Zuna, J, Trka, J, Ben Abdelali, R, Macintyre, E, De Braekeleer, E, De Braekeleer, M, Delabesse, E, de Oliveira, MP, Cavé, H, Clappier, E, van Dongen, JJM, Balgobind, BV, van den HeuvelEibrink, MM, Beverloo, HB, PanzerGrümayer, R, TeiglerSchlegel, A, Harbott, J, Kjeldsen, E, Schnittger, S, Koehl, U, Gruhn, B, Heidenreich, O, Chan, LC, Yip, SF, Krzywinski, M, Eckert, C, Möricke, A, Schrappe, M, Alonso, CN, Schäfer, BW, Krauter, J, Lee, DA, zur Stadt, U, Te Kronnie, G, Sutton, R, Izraeli, S, Trakhtenbrot, L, Lo Nigro, L, Tsaur, G, Fechina, L, Szczepanski, T, Ilencikova, D, Molkentin, M, Burmeister, T, Dingermann, T, Klingebiel, T, Marschalek, R

مصطلحات موضوعية: Adult, Child, Chromosome Breakage, Chromosomes, Human, Pair 11 - genetics - ultrastructure, Computational Biology, Polymerase Chain Reaction, Recombination, Genetic, Translocation, Biopsy, DNA, Neoplasm - blood - genetics, Gene Duplication, Humans, Leukemia - genetics, Myeloid-Lymphoid Leukemia Protein - genetics, Neoplasm Proteins - genetics, Oncogene Proteins, Fusion - genetics, Bone Marrow - chemistry - pathology, Acute Disease

العلاقة: Leukemia; http://www.scopus.com/mlt/select.url?eid=2-s2.0-68749120703&selection=ref&srcTest=s&origin=recordpage; Leukemia, 2009, v. 23 n. 8, p. 1490-1499; 4141695; 1499; 181199; WOS:000268862000017; http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0887-6924&volume=23&issue=8&spage=1490&epage=1499&date=2009&atitle=New+insights+to+the+MLL+recombinome+of+acute+leukemiasTest; eid_2-s2.0-68749120703; 1490; http://hdl.handle.net/10722/126723Test; 23

الإتاحة: https://doi.org/10.1038/leu.2009.33Test
http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0887-6924&volume=23&issue=8&spage=1490&epage=1499&date=2009&atitle=New+insights+to+the+MLL+recombinome+of+acute+leukemiasTest
http://hdl.handle.net/10722/126723Test

المؤلفون: Ulrike Bacher, Tamara Alpermann, T Haferlach, Claudia Haferlach, Wolfgang Kern, Manja Meggendorfer, Carlo Gambacorti-Passerini, Susanne Schnittger

المساهمون: Meggendorfer, M, Bacher, U, Alpermann, T, Haferlach, C, Kern, W, GAMBACORTI PASSERINI, C, Haferlach, T, Schnittger, S

مصطلحات موضوعية: Adult, Male, Cancer Research, Mutation rate, medicine.medical_specialty, Myeloid, Isochromosome, SETBP1, Biology, medicine.disease_cause, Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative, Young Adult, Mutation Rate, Bone Marrow, Internal medicine, medicine, Humans, Proto-Oncogene Proteins c-cbl, Aged, Chromosome 7 (human), Aged, 80 and over, Mutation, Hematology, Nuclear Proteins, Middle Aged, medicine.disease, Myelodysplastic-Myeloproliferative Diseases, Isochromosomes, Repressor Proteins, Leukemia, medicine.anatomical_structure, Oncology, Myelodysplastic Syndromes, Cancer research, Atypical chronic myeloid leukemia, Female, Chromosome Deletion, Carrier Proteins, Chromosomes, Human, Pair 7

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1ee441f6d0c6b465466020c2a39822eTest
http://hdl.handle.net/10281/44120Test

المؤلفون: Pellegrino Musto, Antony B. Holmes, Victoria A. Wells, Livio Trentin, Stefano Pileri, Robin Foà, Gianpietro Semenzato, Claudia Haferlach, Roberta Pacini, Brunangelo Falini, Oliver Elliott, Maria Paola Martelli, Susanne Schnittger, Laura Pasqualucci, Arcangelo Liso, Vladimir Trifonov, Valentina Pettirossi, Raul Rabadan, Gianluca Schiavoni, Wolfgang Kern, Alessandro Pulsoni, Enrico Tiacci, Luca Arcaini, Achille Ambrosetti, Giovanni Pizzolo, Monia Capponi, Torsten Haferlach, Roberta Mannucci, Caterina Patti, Laurent Farinelli, Francesco Forconi, Giorgio Inghirami, Alessandra Pucciarini, Francesco Di Raimondo, Paolo Sportoletti, Barbara Bigerna

المساهمون: Tiacci E, Trifonov V, Schiavoni G, Holmes A, Kern W, Martelli MP, Pucciarini A, Bigerna B, Pacini R, Wells VA, Sportoletti P, Pettirossi V, Mannucci R, Elliott O, Liso A, Ambrosetti A, Pulsoni A, Forconi F, Trentin L, Semenzato G, Inghirami G, Capponi M, Di Raimondo F, Patti C, Arcaini L, Musto P, Pileri S, Haferlach C, Schnittger S, Pizzolo G, Foà R, Farinelli L, Haferlach T, Pasqualucci L, Rabadan R, Falini B.

مصطلحات موضوعية: Male, Lymphoma, Hairy Cell, genetics/metabolism/pathology, Hypereosinophilic Syndrome, Medicine, Missense mutation, genetics, Extracellular Signal-Regulated MAP Kinases, Exome, Hairy Cell Leukemia Variant, Sanger sequencing, Leukemia, Hairy Cell, Leukemia, Massive parallel sequencing, protein kinase, General Medicine, Middle Aged, MAP Kinase Kinase Kinases, Leukemia, Myeloid, symbols, Female, Sequence Analysis, Mastocytosis, Adult, Proto-Oncogene Proteins B-raf, Lymphoma, B-Cell, Genomics, Article, symbols.namesake, Humans, Adult, Aged, Extracellular Signal-Regulated MAP Kinases, metabolism, Female, Humans, Leukemia, genetics/metabolism/pathology, Lymphoma, B-Cell, genetics/pathology, MAP Kinase Kinase Kinases, metabolism, Male, Middle Aged, Mutation, Proto-Oncogene Proteins B-raf, genetics, Sequence Analysis, DNA, Hairy cell leukemia, Aged, business.industry, genetics/pathology, Sequence Analysis, DNA, medicine.disease, hairy cell leukemia", braf", BRAF MUTATIONS, Myelodysplastic Syndromes, Mutation, Cancer research, business, metabolism

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b00bbe5b187269dfc3ce984d47060fa0Test
http://hdl.handle.net/11585/122981Test

المؤلفون: Tamara Weiss, Aline Renneville, Giuseppe Saglio, Joop H. Jansen, Hans Beier Ommen, Adrian van der Heijden, Vincent H.J. van der Velden, Bert A. van der Reijden, Fabienne Hermitte, Daniel Cilloni, Jelena V. Jovanovic, Sarah B. Daly, David Grimwade, Enrico Gottardi, Barbara Izzo, Robert Kerrin Hills, Josep F. Nomdedeu, Susanne Schnittger, Claude Preudhomme, Milena Fava

المساهمون: Hematology, Immunology, Cilloni, D1, Renneville, A, Hermitte, F, Hills, Rk, Daly, S, Jovanovic, Jv, Gottardi, E, Fava, M, Schnittger, S, Weiss, T, Izzo, Barbara, Nomdedeu, J, van der Heijden, A, van der Reijden, Ba, Jansen, Jh, van der Velden, Vh, Ommen, H, Preudhomme, C, Saglio, G, Grimwade, D.

المصدر: Journal of Clinical Oncology, 27, 5195-201
Journal of Clinical Oncology, 27(31), 5195-5201. American Society of Clinical Oncology
Journal of Clinical Oncology, 27, 31, pp. 5195-201
JOURNAL OF CLINICAL ONCOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Journal of clinical oncology 27 (2009): 5195–5201. doi:10.1200/JCO.2009.22.4865
info:cnr-pdr/source/autori:Cilloni D. ; Renneville A. ; Hermitte F. ; Hills R.K. ; Daly S. ; Jovanovic J.V. ; Gottardi E. ; Fava M ; Schnittger S. ; Weiss T. ; Izzo B. ; Nomdedeu, J. ; van der Heijden A. ; van der Reijden B. A. ; Jansen J. H. ; van der Velden V. H. ; Ommen H. ; Preudhomme C. ; Saglio G. ; Grimwade D./titolo:Real-Time Quantitative Polymerase Chain Reaction Detection of Minimal Residual Disease by Standardized WT1 Assay to Enhance Risk Stratification in Acute Myeloid Leukemia: A European LeukemiaNet Study/doi:10.1200%2FJCO.2009.22.4865/rivista:Journal of clinical oncology/anno:2009/pagina_da:5195/pagina_a:5201/intervallo_pagine:5195–5201/volume:27

مصطلحات موضوعية: Oncology, Adult, Cancer Research, medicine.medical_specialty, Myeloid, Genes, Wilms Tumor, Neoplasm, Residual, Adolescent, DNA Mutational Analysis, Gene Expression, European LeukemiaNet, Young Adult, Immune Regulation [NCMLS 2], Translational research [ONCOL 3], Risk Factors, Internal medicine, hemic and lymphatic diseases, Antineoplastic Combined Chemotherapy Protocols, medicine, Biomarkers, Tumor, Humans, Risk factor, Child, Aged, business.industry, Reverse Transcriptase Polymerase Chain Reaction, Hazard ratio, Myeloid leukemia, Combination chemotherapy, Middle Aged, medicine.disease, Prognosis, Minimal residual disease, Leukemia, Leukemia, Myeloid, Acute, medicine.anatomical_structure, Child, Preschool, Immunology, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e60a1982432de6f2c9dcc785d425dee1Test
http://hdl.handle.net/2066/81742Test

المؤلفون: Frank Griesinger, Jan Trka, Claudia Schoch, Rolf Marschalek, M. G. Ennas, Helena Kempski, Elizabeth Macintyre, Björn Schneider, Emanuele Angelucci, T. Klingebiel, S. Jakob, Rob Pieters, Oskar A. Haas, M L den Boer, U. Zur Stadt, M W J C Jansen, Hugh J.M. Brady, Martin Schrappe, Eric Delabesse, Christian Meyer, Johann Greil, J. J. M. Van Dongen, Theodor Dingermann, A. Attarbaschi, Thomas Burmeister, Sabine Strehl, Beat W. Schäfer, Tomasz Szczepański, Martin Stanulla, C Eckert, Felix Niggli, Susanne Schnittger, Andrea Biondi, Ulrike Koehl, Jan Zuna, Luca Lo Nigro

المساهمون: Immunology, Pediatrics, Meyer, C, Schneider, B, Jakob, S, Strehl, S, Attarbaschi, A, Schnittger, S, Schoch, C, Jansen, M, Dongen, J, Boer, M, Pieters, R, Ennas, M, Angelucci, E, Koehl, U, Greil, J, Griesinger, F, zur Stadt, U, Eckert, C, Szczepanski, T, Niggli, F, Schafer, B, Kempski, H, Brady, H, Zuna, J, Trka, J, Nigro, L, Biondi, A, Delabesse, E, Macintyre, E, Stanulla, M, Schrappe, M, Haas, O, Burmeister, T, Dingermann, T, Klingebiel, T, Marschalek, R

المصدر: Leukemia, 20, 777-784. Nature Publishing Group

مصطلحات موضوعية: Adult, MLL, Cancer Research, Methyltransferase, Oncogene Proteins, Fusion, Methylation, partner gene, Translocation, Genetic, Histones, Fusion gene, chromosomal translocation, hemic and lymphatic diseases, Histone methylation, medicine, Humans, acute leukemia, Child, Gene, Chromosome Aberrations, Genetics, Acute leukemia, Leukemia, biology, Chromosome Mapping, DNA, Histone-Lysine N-Methyltransferase, Hematology, medicine.disease, genomic DNA, Histone, Oncology, Acute Disease, biology.protein, Myeloid-Lymphoid Leukemia Protein

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db1fb51bc90dfa277d96e1d845c4675eTest
https://pure.eur.nl/en/publications/a52eb93c-afb1-4f20-80f7-685f62b399a5Test