Single dose amoxicillin treatment of acute otitis media von Puczynski, Mark S., Stankiewicz, James A., O'Keefe, J. aul

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Prevalence and prognostic significance of allelic imbalance by single-nucleotide polymorphism analysis in low-risk myelodysplastic syndromes von Mohamedali, Azim, Gäken, Joop, Twine, Natalie A., Ingram, Wendy, Westwood, Nigel, Lea, Nicholas C., Hayden, Janet, Donaldson, Nora, Aul, Carlo, Gattermann, Norbert, Giagounidis, Aristotle, Germing, Ulrich, List, Alan F., Mufti, Ghulam J.

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Frequency of del(12p) is commonly underestimated in myelodysplastic syndromes: Results from a German diagnostic study in comparison with an international control group von Braulke, Friederike, Müller-Thomas, Catharina, Götze, Katharina, Platzbecker, Uwe, Germing, Ulrich, Hofmann, Wolf-Karsten, Giagounidis, Aristoteles A. N., Lübbert, Michael, Greenberg, Peter L., Bennett, John M., Solé, Francesc, Slovak, Marilyn L., Ohyashiki, Kazuma, Le Beau, Michelle M., Tüchler, Heinz, Pfeilstöcker, Michael, Hildebrandt, Barbara, Aul, Carlo, Stauder, Reinhard, Valent, Peter, Fonatsch, Christa, Bacher, Ulrike, Trümper, Lorenz, Haase, Detlef, Schanz, Julie

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Clonality of the stem cell compartment during evolution of myelodysplastic syndromes and other bone marrow failure syndromes von Tiu, R, Gondek, L, O'Keefe, C, Maciejewski, J P

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Chromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AML von Gondek, Lukasz P., Tiu, Ramon, O'Keefe, Christine L., Sekeres, Mikkael A., Theil, Karl S., Maciejewski, Jaroslaw P.

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Application of array‐based whole genome scanning technologies as a cytogenetic tool in haematological malignancies von Maciejewski, Jaroslaw P., Tiu, Ramon V., O’Keefe, Christine

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Characterization of chromosome arm 20q abnormalities in myeloid malignancies using genome-wide single nucleotide polymorphism array analysis von Huh, Jungwon, Tiu, Ramon V., Gondek, Lukasz P., O'Keefe, Christine L., Jasek, Monika, Makishima, Hideki, Jankowska, Ania M., Jiang, Ying, Verma, Amit, Theil, Karl S., McDevitt, Michael A., Maciejewski, Jaroslaw P.

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E3 ligase–defective Cbl mutants lead to a generalized mastocytosis and myeloproliferative disease von Bandi, Srinivasa Rao, Brandts, Christian, Rensinghoff, Marion, Grundler, Rebekka, Tickenbrock, Lara, Köhler, Gabriele, Duyster, Justus, Berdel, Wolfgang E., Müller-Tidow, Carsten, Serve, Hubert, on behalf of the Study Alliance Leukemias, Sargin, Bülent

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Alteration of Epidermal Growth Factor-Dependent Phosphorylation during Rat Liver Regeneration von Rubin, Richard A., O'Keefe, Edward J., Earp, H. Shelton

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High Throughput Screening for Cyanovirin-N Mimetics Binding to HIV-1 gp4l von Beutler, John A., McMahon, James B., Johnson, Tanya R., O'Keefe, Barry R., Buzzell, Randy A., Robbins, Danielle, Gardella, Roberta, Wilson, Jennifer, Boyd, Michael R.

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Born−Haber−Fajans Cycle Generalized:  Linear Energy Relation between Molecules, Crystals, and Metals von Glasser, Leslie, von Szentpály, László

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The expression of mature myeloid cell differentiation markers in acute leukemia von White, Deborah L., Ashman, Leonie K., Dart, Geoffrey W., Zola, Heddy, Toogood, Ian R.G., Kimber, Richard J.

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Age-related mutations and chronic myelomonocytic leukemia von Mason, C C, Khorashad, J S, Tantravahi, S K, Kelley, T W, Zabriskie, M S, Yan, D, Pomicter, A D, Reynolds, K R, Eiring, A M, Kronenberg, Z, Sherman, R L, Tyner, J W, Dalley, B K, Dao, K-H, Yandell, M, Druker, B J, Gotlib, J, O'Hare, T, Deininger, M W

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Corrigendum to “The prevalence and long-term health effects of long Covid among hospitalised and non-hospitalised populations: a systematic review and meta-analysis” von O'Mahoney, Lauren L., Routen, Ash, Gillies, Clare, Ekezie, Winifred, Welford, Anneka, Zhang, Alexa, Karamchandani, Urvi, Simms-Williams, Nikita, Cassambai, Shabana, Ardavani, Ashkon, Wilkinson, Thomas J., Hawthorne, Grace, Curtis, Ffion, Kingsnorth, Andrew P., Almaqhawi, Abdullah, Ward, Thomas, Ayoubkhani, Daniel, Banerjee, Amitava, Calvert, Melanie, Shafran, Roz, Stephenson, Terence, Sterne, Jonathan, Ward, Helen, Evans, Rachael A., Zaccardi, Francesco, Wright, Shaney, Khunti, Kamlesh

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Haploinsufficiency of RPS14 in 5q− syndrome is associated with deregulation of ribosomal‐ and translation‐related genes von Pellagatti, Andrea, Hellström‐Lindberg, Eva, Giagounidis, Aristoteles, Perry, Janet, Malcovati, Luca, Della Porta, Matteo G., Jädersten, Martin, Killick, Sally, Fidler, Carrie, Cazzola, Mario, Wainscoat, James S., Boultwood, Jacqueline

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Simultaneous brain cell type and lineage determined by scRNA-seq reveals stereotyped cortical development von Anderson, Donovan J., Pauler, Florian M., McKenna, Aaron, Shendure, Jay, Hippenmeyer, Simon, Horwitz, Marshall S.

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Identification of a risk dependent microRNA expression signature in myelodysplastic syndromes von Sokol, Lubomir, Caceres, Gisela, Volinia, Stefano, Alder, Hans, Nuovo, Gerard J., Liu, Chang‐Gong, McGraw, Kathy, Clark, Justine A., Sigua, Celia A., Chen, Dung‐Tsa, Moscinski, Lynn, Croce, Carlo M., List, Alan F.

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Van‐den Berghe’s 5q‐ syndrome in 2008 von Mohamedali, Azim, Mufti, Ghulam J.

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Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes von Slovak, Marilyn L, Smith, David D, Bedell, Victoria, Hsu, Ya-Hsuan, O'Donnell, Margaret, Forman, Stephen J, Gaal, Karl, McDaniel, Lisa, Schultz, Roger, Ballif, Blake C, Shaffer, Lisa G

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Splicing factor 3b subunit 1 (Sf3b1) haploinsufficient mice display features of low risk Myelodysplastic syndromes with ring sideroblasts von Visconte, Valeria, Tabarroki, Ali, Zhang, Li, Parker, Yvonne, Hasrouni, Edy, Mahfouz, Reda, Isono, Kyoichi, Koseki, Haruhiko, Sekeres, Mikkael A, Saunthararajah, Yogen, Barnard, John, Lindner, Daniel, Rogers, Heesun J, Tiu, Ramon V

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