Unraveling the crucial roles of Meis1 in leukemogenesis and normal hematopoiesis

Classification, subtype discovery, and prediction of outcome in pediatric acute lymphoblastic leukemia by gene expression profiling

Yeoh, A. E. J., Ross, M. E., Shurtleff, S. A., Williams, W. K., Patel, D. H., Mahfouz, R. A., Behm, F. G., Raimondi, S. C., Relling, M. V., Patel, A. R., et al. (2002) · Cancer Cell · doi:10.1016/s1535-6108(02)00032-6 · Cited by 1,914 · see citing works

MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia

Armstrong, S. A., Staunton, J. E., Silverman, L. B., Pieters, R., den Boer, M. L., Minden, M. D., Sallan, S. E., Lander, E. S., Golub, T. R., & Korsmeyer, S. J. (2001) · Nature Genetics · doi:10.1038/ng765 · Cited by 1,721 · see citing works

Bmi-1 determines the proliferative capacity of normal and leukaemic stem cells.

Lessard, J., & Sauvageau, G. (2003) · Nature · doi:10.1038/nature01572 · Cited by 1,452 · see citing works

Acute myeloid leukemia originates from a hierarchy of leukemic stem cell classes that differ in self-renewal capacity

Hope, K. J., Jin, L., & Dick, J. E. (2004) · Nature Immunology · doi:10.1038/ni1080 · Cited by 968 · see citing works

Altered Hox expression and segmental identity in Mll-mutant mice

Yu, B., Hess, J. L., Horning, S. E., Brown, G. A. J., & Korsmeyer, S. J. (1995) · Nature · doi:10.1038/378505a0 · Cited by 872 · see citing works

Hoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b

Kroon, E., Krosl, J., Thorsteinsdottir, U., Baban, S., Buchberg, A. M., & Sauvageau, G. (1998) · The EMBO Journal · doi:10.1093/emboj/17.13.3714 · Cited by 640 · see citing works

Identification and characterization of leukemia stem cells in murine MLL-AF9 acute myeloid leukemia

Somervaille, T. C. P., & Cleary, M. L. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.08.020 · Cited by 582 · see citing works

Enhanced self-renewal of hematopoietic stem cells mediated by the polycomb gene product Bmi-1

Iwama, A., Oguro, H., Negishi, M., Kato, Y., Morita, Y., Tsukui, H., Ema, H., Kamijo, T., Katoh-Fukui, Y., Koseki, H., et al. (2004) · Immunity · doi:10.1016/j.immuni.2004.11.004 · Cited by 515 · see citing works

AML1/ETO-expressing nonleukemic stem cells in acute myelogenous leukemia with 8;21 chromosomal translocation

Miyamoto, T., Weissman, I. L., & Akashi, K. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.13.7521 · Cited by 465 · see citing works

Hematopoietic stem cells express multiple myeloid markers: implications for the origin and targeted therapy of acute myeloid leukemia

Taussig, D. C. (2005) · Blood · doi:10.1182/blood-2005-03-1072 · Cited by 370 · see citing works

Gene expression signatures in MLL-rearranged T-lineage and B-precursor acute leukemias: dominance of HOX dysregulation

Ferrando, A. A., Armstrong, S. A., Neuberg, D. S., Sallan, S. E., Silverman, L. B., Korsmeyer, S. J., & Look, A. T. (2003) · Blood · doi:10.1182/blood-2002-10-3221 · Cited by 350 · see citing works

Hoxa9 and Meis1 Are Key Targets for MLL-ENL-Mediated Cellular Immortalization

Zeisig, B. B., Milne, T., García-Cuéllar, M.-P., Schreiner, S., Martin, M.-E., Fuchs, U., Borkhardt, A., Chanda, S. K., Walker, J. R., Soden, R., et al. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.24.2.617-628.2004 · Cited by 330 · see citing works

Meis1, a PBX1-Related Homeobox Gene Involved in Myeloid Leukemia in BXH-2 Mice

Moskow, J. J., Bullrich, F., Huebner, K., Daar, I. O., & Buchberg, A. M. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.10.5434 · Cited by 329 · see citing works

Hematopoietic, angiogenic and eye defects in Meis1 mutant animals

Hisa, T., Spence, S. E., Rachel, R. A., Fujita, M., Nakamura, T., Ward, J. M., Devor-Henneman, D. E., Saiki, Y., Kutsuna, H., Tessarollo, L., et al. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600038 · Cited by 306 · see citing works

MLL, a mammalian trithorax- group gene, functions as a transcriptional maintenance factor in morphogenesis

Yu, B., Hanson, R. D., Hess, J. L., Horning, S. E., & Korsmeyer, S. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.18.10632 · Cited by 302 · see citing works

Meis1 is an essential and rate-limiting regulator of MLL leukemia stem cell potential.Preprint

Wong, P., Iwasaki, M., Somervaille, T., So, C., & Cleary, M. (2007) · Genes & Development · doi:10.1101/gad.1602107 · Cited by 297 · see citing works

Differential expression of Hox, Meis1, and Pbx1 genes in primitive cells throughout murine hematopoietic ontogeny

Pineault, N., Helgason, C. D., Lawrence, H. J., & Humphries, R. K. (2002) · Experimental Hematology · doi:10.1016/s0301-472x(01)00757-3 · Cited by 278 · see citing works

AbdB-Like Hox Proteins Stabilize DNA Binding by the Meis1 Homeodomain Proteins

Shen, W.-F., Montgomery, J. C., Rozenfeld, S. B., Moskow, J. J., Lawrence, H. J., Buchberg, A. M., & Largman, C. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.11.6448 · Cited by 278 · see citing works

HOXA9 Forms Triple Complexes with PBX2 and MEIS1 in Myeloid Cells

Shen, W.-F., Rozenfeld, S., Kwong, A., Kömüves, L. G., Lawrence, H. J., & Largman, C. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.4.3051 · Cited by 249 · see citing works

Most Acute Myeloid Leukemia Progenitor Cells With Long-Term Proliferative Ability In Vitro and In Vivo Have the Phenotype CD34+/CD71−/HLA-DR−

Blair, A., Hogge, D. E., & Sutherland, H. J. (1998) · Blood · doi:10.1182/blood.v92.11.4325 · Cited by 237 · see citing works

NUP98–HOXA9 expression in hemopoietic stem cells induces chronic and acute myeloid leukemias in mice

KROON, E. J., Þorsteinsdóttir, U., Mayotte, N., Nakamura, T., & Sauvageau, G. (2001) · The EMBO Journal · doi:10.1093/emboj/20.3.350 · Cited by 225 · see citing works

Expression of HOX genes, HOX cofactors, and MLL in phenotypically and functionally defined subpopulations of leukemic and normal human hematopoietic cells

Kawagoe, H., Humphries, R. K., Blair, A., Sutherland, H., & Hogge, D. E. (1999) · Leukemia · doi:10.1038/sj.leu.2401410 · Cited by 222 · see citing works

Interaction of MLL Amino Terminal Sequences with Menin Is Required for Transformation

Caslini, C., Yang, Z., El-Osta, M., Milne, T. A., Slany, R. K., & Hess, J. L. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-2369 · Cited by 217 · see citing works

Leukemogenic MLL Fusion Proteins Bind across a Broad Region of the Hox a9 Locus, Promoting Transcription and Multiple Histone Modifications

Milne, T. A., Martin, M. E., Brock, H. W., Slany, R. K., & Hess, J. L. (2005) · Cancer Research · doi:10.1158/0008-5472.can-05-1041 · Cited by 181 · see citing works

Upregulation of Meis1 and HoxA9 in acute lymphocytic leukemias with the t(4 : 11) abnormality

Rozovskaia, T., Feinstein, E., Mor, O., Foà, R., Blechman, J. A., Nakamura, T., Croce, C. M., Cimino, G. G., & Canaani, E. (2001) · Oncogene · doi:10.1038/sj.onc.1204174 · Cited by 181 · see citing works

c-Myb is an essential downstream target for homeobox-mediated transformation of hematopoietic cells

Hess, J. L., Bittner, C. B., Zeisig, D. T., Bach, C., Fuchs, U., Borkhardt, A., Frampton, J., & Slany, R. K. (2006) · Blood · doi:10.1182/blood-2005-12-5014 · Cited by 165 · see citing works

Induction of acute myeloid leukemia in mice by the human leukemia-specific fusion gene NUP98-HOXD13 in concert with Meis1

Pineault, N., Buske, C., Feuring‐Buske, M., Abramovich, C., Rosten, P., Hogge, D. E., Aplan, P. D., & Humphries, R. K. (2003) · Blood · doi:10.1182/blood-2002-08-2484 · Cited by 148 · see citing works

Molecular characterization of acute leukemias by use of microarray technology

Kohlmann, A., Schoch, C., Schnittger, S., Dugas, M., Hiddemann, W., Kern, W., & Haferlach, T. (2003) · Genes Chromosomes and Cancer · doi:10.1002/gcc.10225 · Cited by 145 · see citing works

HOXB6 overexpression in murine bone marrow immortalizes a myelomonocytic precursor in vitro and causes hematopoietic stem cell expansion and acute myeloid leukemia in vivo

Fischbach, N. A., Rozenfeld, S. B., Shen, W.-F., Fong, S., Chrobak, D., Ginzinger, D. G., Kogan, S. C., Radhakrishnan, A., Beau, M. M. L., Largman, C., et al. (2004) · Blood · doi:10.1182/blood-2004-04-1583 · Cited by 137 · see citing works

The versatile mixed lineage leukaemia gene MLL and its many associations in leukaemogenesis

Daser, A., & Rabbitts, T. H. (2005) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2005.01.007 · Cited by 129 · see citing works

Meis1 programs transcription of FLT3 and cancer stem cell character, using a mechanism that requires interaction with Pbx and a novel function of the Meis1 C-terminus

Wang, G. G., Pasillas, M. P., & Kamps, M. P. (2005) · Blood · doi:10.1182/blood-2004-12-4664 · Cited by 127 · see citing works

Nup98-HoxA9 immortalizes myeloid progenitors, enforces expression of Hoxa9, Hoxa7 and Meis1, and alters cytokine-specific responses in a manner similar to that induced by retroviral co-expression of Hoxa9 and Meis1

Calvo, K. R., Sykes, D. B., Pasillas, M. P., & Kamps, M. P. (2002) · Oncogene · doi:10.1038/sj.onc.1205516 · Cited by 120 · see citing works

Distinct functions of homeodomain-containing and homeodomain-less isoforms encoded by homothoraxPreprint

Noro, B., Culí, J., McKay, D. J., Zhang, W., & Mann, R. S. (2006) · Genes & Development · doi:10.1101/gad.1412606 · Cited by 112 · see citing works

Gene expression patterns associated with recurrent chromosomal translocations in acute lymphoblastic leukemia

Fine, B. M., Stanulla, M., Schrappe, M., Ho, M., Viehmann, S. F., Harbott, J., & Boxer, L. M. (2003) · Blood · doi:10.1182/blood-2003-05-1518 · Cited by 108 · see citing works

Persistent Transactivation by Meis1 Replaces Hox Function in Myeloid Leukemogenesis Models: Evidence for Co-Occupancy of Meis1-Pbx and Hox-Pbx Complexes on Promoters of Leukemia-Associated Genes

Wang, G. G., Pasillas, M. P., & Kamps, M. P. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.26.10.3902-3916.2006 · Cited by 97 · see citing works

Differential and Common Leukemogenic Potentials of Multiple NUP98-Hox Fusion Proteins Alone or with Meis1

Pineault, N., Abramovich, C., Ohta, H., & Humphries, R. K. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.5.1907-1917.2004 · Cited by 91 · see citing works

The MLL gene and translocations involving chromosomal band 11q23 in acute leukemia.

Braekeleer, M. D., Morel, F., Bris, M. L., Herry, A., & Douet‐Guilbert, N. (2005) · PubMed · Cited by 90 · see citing works

Frequent co‐expression of HoxA9 and Meis1 genes in infant acute lymphoblastic leukaemia with MLL rearrangement

Imamura, T., Morimoto, A., Takanashi, M., Hibi, S., Sugimoto, T., Ishii, E., & Imashuku, S. (2002) · British Journal of Haematology · doi:10.1046/j.1365-2141.2002.03803.x · Cited by 82 · see citing works

Two distinct gene expression signatures in pediatric acute lymphoblastic leukemia with MLL rearrangements.

Tsutsumi, S., Taketani, T., Nishimura, K., Ge, X., Taki, T., Sugita, K., Ishii, E., Hanada, R., Ohki, M., Aburatani, H., et al. (2003) · PubMed · Cited by 81 · see citing works

The Flt3 receptor tyrosine kinase collaborates with NUP98-HOX fusions in acute myeloid leukemia

Palmqvist, L., Argiropoulos, B., Pineault, N., Abramovich, C., Sly, L. M., Krystal, G., Wan, A. N. C., & Humphries, R. K. (2006) · Blood · doi:10.1182/blood-2005-12-007005 · Cited by 63 · see citing works

Expression ofHOXGenes in Acute Leukemia Cell Lines with and withoutMLLTranslocations

Quentmeier, H., Dirks, W. G., MacLeod, R. A. F., Reinhardt, J., Zaborski, M., & Drexler, H. G. (2003) · Leukemia & lymphoma/Leukemia and lymphoma · doi:10.1080/10428190310001609942 · Cited by 59 · see citing works

Molecular Pathogenesis of MLL-Associated Leukemias

Eguchi, M., Eguchi‐Ishimae, M., & Greaves, M. F. (2005) · International Journal of Hematology · doi:10.1532/ijh97.05042 · Cited by 50 · see citing works

Molecular dissection of Meis1 reveals 2 domains required for leukemia induction and a key role for Hoxa gene activation

Mamo, A. (2006) · Blood · doi:10.1182/blood-2005-06-2244 · Cited by 47 · see citing works

Transplantable cell lines generated with NUP98–Hox fusion genes undergo leukemic progression by Meis1 independent of its binding to DNA

Pineault, N., Abramovich, C., & Humphries, R. K. (2005) · Leukemia · doi:10.1038/sj.leu.2403696 · Cited by 38 · see citing works

The hunt for cancer-initiating cells: a history stemming from leukemia

Buzzeo, M. P., Scott, E. W., & Cogle, C. R. (2007) · Leukemia · doi:10.1038/sj.leu.2404768 · Cited by 36 · see citing works

Flt3 is dispensable to the Hoxa9/Meis1 leukemogenic cooperation

Morgado, E., Albouhair, S., & Lavau, C. (2007) · Blood · doi:10.1182/blood-2006-01-039586 · Cited by 28 · see citing works

True

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The Distinct Metabolic Profile of Hematopoietic Stem Cells Reflects Their Location in a Hypoxic Niche

Simsek, T., Kocabas, F., Zheng, J., DeBerardinis, R. J., Mahmoud, A. I., Olson, E. N., Schneider, J. W., Zhang, C. C., & Sadek, H. A. (2010) · Cell Stem Cell · doi:10.1016/j.stem.2010.07.011 · Cited by 1,101 · see citing works

Proteolysis-Targeting Chimeras as Therapeutics and Tools for Biological Discovery

Burslem, G. M., & Crews, C. M. (2020) · Cell · doi:10.1016/j.cell.2019.11.031 · Cited by 1,079 · see citing works

Densely Interconnected Transcriptional Circuits Control Cell States in Human Hematopoiesis

Novershtern, N., Subramanian, A., Lawton, L. N., Mak, R. H., Haining, W. N., McConkey, M. E., Habib, N., Yosef, N., Chang, C. Y., Shay, T., et al. (2011) · Cell · doi:10.1016/j.cell.2011.01.004 · Cited by 942 · see citing works

Meis1 regulates postnatal cardiomyocyte cell cycle arrest

Mahmoud, A. I., Kocabaş, F., Muralidhar, S. A., Kimura, W., Koura, A. S., Thet, S., Porrello, E. R., & Sadek, H. A. (2013) · Nature · doi:10.1038/nature12054 · Cited by 559 · see citing works

EWS-FLI-1 modulates miRNA145 and SOX2 expression to initiate mesenchymal stem cell reprogramming toward Ewing sarcoma cancer stem cellsPreprint

Riggi, N., Suvà, M.-L., Vito, C. D., Provero, P., Stehle, J., Baumer, K., Cironi, L., Janiszewska, M., Petricevic, T., Suvà, D., et al. (2010) · Genes & Development · doi:10.1101/gad.1899710 · Cited by 279 · see citing works

Meis1 regulates the metabolic phenotype and oxidant defense of hematopoietic stem cells

Kocabaş, F., Zheng, J., Thet, S., Copeland, N. G., Jenkins, N. A., DeBerardinis, R. J., Zhang, C. C., & Sadek, H. A. (2012) · Blood · doi:10.1182/blood-2012-05-432260 · Cited by 235 · see citing works

Hypoxia and Metabolic Properties of Hematopoietic Stem Cells

Zhang, C. C., & Sadek, H. A. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.5019 · Cited by 154 · see citing works

Effective Menin inhibitor-based combinations against AML with MLL rearrangement or NPM1 mutation (NPM1c)

Fiskus, W. C., Boettcher, S., Daver, N. G., Mill, C. P., Sasaki, K., Birdwell, C. E., Davis, J. A., Takahashi, K., Kadia, T. M., Dinardo, C. D., et al. (2022) · Blood Cancer Journal · doi:10.1038/s41408-021-00603-3 · Cited by 134 · see citing works

Essential role of BRG, the ATPase subunit of BAF chromatin remodeling complexes, in leukemia maintenance

Buscarlet, M., Krasteva, V., Ho, L., Simon, C., Hébert, J., Wilhelm, B. T., Crabtree, G. R., Sauvageau, G., Thibault, P., & Lessard, J. A. (2014) · Blood · doi:10.1182/blood-2013-02-483495 · Cited by 124 · see citing works

Iron, dopamine, genetics, and hormones in the pathophysiology of restless legs syndrome

Khan, F. H., Ahlberg, C. D., Chow, C. A., Shah, D. R., & Koo, B. B. (2017) · Journal of Neurology · doi:10.1007/s00415-017-8431-1 · Cited by 114 · see citing works

Vitamin C-induced epigenomic remodelling in IDH1 mutant acute myeloid leukaemia

Mingay, M., Chaturvedi, A., Bilenky, M., Cao, Q., Jackson, L., Hui, T., Moksa, M., Heravi-Moussavi, A., Humphries, R. K., Heuser, M., et al. (2018) · Leukemia · doi:10.1038/leu.2017.171 · Cited by 94 · see citing works

Activity of menin inhibitor ziftomenib (KO-539) as monotherapy or in combinations against AML cells with MLL1 rearrangement or mutant NPM1

Fiskus, W. C., Daver, N. G., Boettcher, S., Mill, C. P., Sasaki, K., Birdwell, C. E., Davis, J. A., Das, K., Takahashi, K., Kadia, T. M., et al. (2022) · Leukemia · doi:10.1038/s41375-022-01707-w · Cited by 84 · see citing works

Hypoxic metabolism in human hematopoietic stem cells

Kocabaş, F., Xie, L., Xie, J., Yu, Z., DeBerardinis, R. J., Kimura, W., Thet, S., Elshamy, A. F., Abouellail, H. A., Muralidhar, S. A., et al. (2015) · Cell & Bioscience · doi:10.1186/s13578-015-0020-3 · Cited by 79 · see citing works

Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US population

Yang, Q., Li, L., Chen, Q., Foldvary‐Schaefer, N., Ondo, W. G., & Wang, Q. K. (2011) · Sleep Medicine · doi:10.1016/j.sleep.2011.06.006 · Cited by 78 · see citing works

MEIS transcription factors in development and disease

Schulte, D., & Geerts, D. (2019) · Development · doi:10.1242/dev.174706 · Cited by 77 · see citing works

Mechanisms of iron metabolism in Caenorhabditis elegans

Anderson, C. P., & Leibold, E. A. (2014) · Frontiers in Pharmacology · doi:10.3389/fphar.2014.00113 · Cited by 74 · see citing works

PPM1K Regulates Hematopoiesis and Leukemogenesis through CDC20-Mediated Ubiquitination of MEIS1 and p21.

Liu, X.-Y., Zhang, F., Zhang, Y., Li, X., Chen, C.-Q., Zhou, M., Yu, Z., Liu, Y.-X., Zhao, Y.-Z., Hao, X., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.140 · Cited by 66 · see citing works

Identification of Pbx1 , a Potential Oncogene, as a Notch3 Target Gene in Ovarian Cancer

Park, J. T., Shih, I., & Wang, T. (2008) · Cancer Research · doi:10.1158/0008-5472.can-08-0517 · Cited by 74 · see citing works

A crucial role for the ubiquitously expressed transcription factor Sp1 at early stages of hematopoietic specification

Gilmour, J., Assi, S. A., Jägle, U., Kulu, D., van de Werken, H. J. G., Clarke, D., Westhead, D. R., Philipsen, S., & Bonifer, C. (2014) · Development · doi:10.1242/dev.106054 · Cited by 71 · see citing works

Dpp dependent Hematopoietic stem cells give rise to Hh dependent blood progenitors in larval lymph gland of Drosophila

Dey, N. S., Ramesh, P., Chugh, M., Mandal, S., & Mandal, L. (2016) · eLife · doi:10.7554/elife.18295 · Cited by 66 · see citing works

GPR84 sustains aberrant β-catenin signaling in leukemic stem cells for maintenance of MLL leukemogenesis.

Dietrich, P. A., Yang, C., Leung, H., Lynch, J., Gonzales, E., Liu, B., Haber, M., Norris, M., Wang, J.-L., & Wang, J. (2014) · Blood · doi:10.1182/blood-2013-10-532523 · Cited by 58 · see citing works

Targeting of epigenetic co-dependencies enhances anti-AML efficacy of Menin inhibitor in AML with MLL1-r or mutant NPM1

Fiskus, W. C., Mill, C. P., Birdwell, C. E., Davis, J. A., Das, K., Boettcher, S., Kadia, T. M., Dinardo, C. D., Takahashi, K., Loghavi, S., et al. (2023) · Blood Cancer Journal · doi:10.1038/s41408-023-00826-6 · Cited by 56 · see citing works

LncRNA SNORD3A specifically sensitizes breast cancer cells to 5-FU by sponging miR-185-5p to enhance UMPS expression

Luo, L., Zhang, J., Tang, H., Zhai, D., Huang, D., Li, L., Wang, X., Liu, T., Zhang, Q., Zhang, Z., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-2557-2 · Cited by 55 · see citing works

Acute Myeloid Leukemia and the Wnt Pathway

Eaves, C. J., & Humphries, R. K. (2010) · New England Journal of Medicine · doi:10.1056/nejmcibr1003522 · Cited by 52 · see citing works

HOXB13 interaction with MEIS1 modifies proliferation and gene expression in prostate cancer

Johng, D., Torga, G., Ewing, C. M., Jin, K., Norris, J. D., McDonnell, D. P., & Isaacs, W. B. (2018) · The Prostate · doi:10.1002/pros.23747 · Cited by 49 · see citing works

MEIS2 Is an Oncogenic Partner in AML1-ETO-Positive AML

Naidu, V. M., Klappacher, J., Oswald, F., Mulaw, M. A., Mandoli, A., Thiel, V. N., Bamezai, S., Feder, K., Martens, J. H. A., Rawat, V. P. S., et al. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.05.094 · Cited by 47 · see citing works

MEIS-mediated suppression of human prostate cancer growth and metastasis through HOXB13-dependent regulation of proteoglycans

VanOpstall, C., Perike, S., Brechka, H., Gillard, M., Lamperis, S. M., Zhu, B., Brown, R. M., Bhanvadia, R. R., & Griend, D. J. V. (2020) · eLife · doi:10.7554/elife.53600 · Cited by 47 · see citing works

Beyond Hox: the role of ParaHox genes in normal and malignant hematopoiesis

Rawat, V. P. S., Humphries, R. K., & Buske, C. (2012) · Blood · doi:10.1182/blood-2012-02-385898 · Cited by 46 · see citing works

The role of meis1 in primitive and definitive hematopoiesis during zebrafish development

Cvejic, A., Serbanovic‐Canic, J., Stemple, D. L., & Ouwehand, W. H. (2010) · Haematologica · doi:10.3324/haematol.2010.027698 · Cited by 44 · see citing works

Trithorax, Hox, and TALE-class homeodomain proteins ensure cell survival through repression of the BH3-only gene egl-1.

Potts, M. B., Wang, D., & Cameron, S. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.02.022 · Cited by 50 · see citing works

Development of Small Molecule MEIS Inhibitors that modulate HSC activity

Turan, R. D., Albayrak, E., Uslu, M., Si̇yah, P., Alyazici, L. Y., Kalkan, B. M., Aslan, G. S., Yücel, D., Aksöz, M., Tüysüz, E. C., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-64888-3 · Cited by 41 · see citing works

Upregulation of CD11b and CD86 through LSD1 inhibition promotes myeloid differentiation and suppresses cell proliferation in human monocytic leukemia cells

Fang, J., Ying, H., Mao, T., Fang, Y., Lu, Y., Wang, H., Zang, I., Wang, Z., Lin, Y., Zhao, M., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.18564 · Cited by 39 · see citing works

MEIS1, PREP1, and PBX4 Are Differentially Expressed in Acute Lymphoblastic Leukemia: Association of MEIS1 Expression with Higher Proliferation and Chemotherapy Resistance

Rosales-Aviña, J. A., Torres-Flores, J., Aguilar‐Lemarroy, A., Gurrola‐Díaz, C. M., Hernández‐Flores, G., Ortiz‐Lazareno, P. C., Lerma-Díaz, J. M., Célis, R. D., Gonzalez-Ramella, O. R., Barrera‐Chairez, E., et al. (2011) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/1756-9966-30-112 · Cited by 37 · see citing works

Transcriptome Profiling Reveals Disruption of Innate Immunity in Chronic Heavy Ethanol Consuming Female Rhesus Macaques

Sureshchandra, S., Rais, M., Stull, C., Grant, K. A., & Messaoudi, I. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159295 · Cited by 35 · see citing works

Higher expression levels of the HOXA9 gene, closely associated with MLL-PTD and EZH2 mutations, predict inferior outcome in acute myeloid leukemia

Gao, L., Sun, J., Liu, F., Zhang, H., & Ma, Y.-G. (2016) · OncoTargets and Therapy · doi:10.2147/ott.s95279 · Cited by 35 · see citing works

RE-IIBP Methylates H3K79 and Induces MEIS1-mediated Apoptosis via H2BK120 Ubiquitination by RNF20

Park, J. W., Kim, K., Kim, J., Chae, Y., Jeong, O.-S., & Seo, S. (2015) · Scientific Reports · doi:10.1038/srep12485 · Cited by 34 · see citing works

Three-amino-acid-loop-extension homeodomain factor Meis3 regulates cell survival via PDK1

Liu, J., Wang, Y., Birnbaum, M. J., & Stoffers, D. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1007001107 · Cited by 34 · see citing works

HOXA9 and MEIS1 gene overexpression in the diagnosis of childhood acute leukemias: Significant correlation with relapse and overall survival

Adamaki, M., Lambrou, G. Ι., Athanasiadou, A., Vlahopoulos, S., Papavassiliou, A. G., & Moschovi, M. A. (2015) · Leukemia Research · doi:10.1016/j.leukres.2015.04.012 · Cited by 33 · see citing works

Correlation Between Meis1 and Msi1 in Esophageal Squamous Cell Carcinoma

Moghbeli, M., Rad, A., Farshchian, M., Taghehchian, N., Gholamin, M., & Abbaszadegan, M. R. (2016) · Journal of Gastrointestinal Cancer · doi:10.1007/s12029-016-9824-6 · Cited by 29 · see citing works

Genome-wide assessment of recurrent genomic imbalances in canine leukemia identifies evolutionarily conserved regions for subtype differentiation

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Identification of E74-like factor 1 (ELF1) as a transcriptional regulator of the Hox cofactor MEIS1

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Cell lineage and cell death: Caenorhabditis elegans and cancer research

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Zebrafish hoxd4a Acts Upstream of meis1.1 to Direct Vasculogenesis, Angiogenesis and Hematopoiesis

Amali, A. A., Sie, L., Winkler, C., & Featherstone, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058857 · Cited by 28 · see citing works

Meis1 regulates proliferation of non-small-cell lung cancer cells.

Li, W., Huang, K., Guo, H., & Cui, G. (2014) · PubMed Central · doi:10.3978/j.issn.2072-1439.2014.06.03 · Cited by 28 · see citing works

The Molecular Genetics of Restless Legs Syndrome

Rye, D. B. (2015) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2015.05.015 · Cited by 27 · see citing works

The Corepressor Rcor1 Is Essential for Normal Myeloerythroid Lineage Differentiation

Yao, H., Goldman, D. C., Fan, G., Mandel, G., & Fleming, W. (2015) · Stem Cells · doi:10.1002/stem.2086 · Cited by 26 · see citing works

The molecular basis of restless legs syndrome

Freeman, A. A. H., & Rye, D. B. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.07.001 · Cited by 25 · see citing works

Integrated analysis of DNA methylation and microRNA regulation of the lung adenocarcinoma transcriptome

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Aberrant EVI1 splicing contributes to EVI1-rearranged leukemia

Tanaka, A., Nakano, T. A., Nomura, M., Yamazaki, H., Bewersdorf, J. P., Mulet‐Lazaro, R., Hogg, S. J., Liu, B., Penson, A., Yokoyama, A., et al. (2022) · Blood · doi:10.1182/blood.2021015325 · Cited by 25 · see citing works

Homeobox gene Meis1 modulates cardiovascular regeneration

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Condensate-Promoting ENL Mutation Drives Tumorigenesis In Vivo Through Dynamic Regulation of Histone Modifications and Gene Expression

Liu, Y.-M., Li, Q.-L., Song, L., Gong, C., Tang, S., Budinich, K. A., Vanderbeck, A., Mathias, K. M., Wertheim, G. B., Nguyen, S. C., et al. (2024) · Cancer Discovery · doi:10.1158/2159-8290.cd-23-0876 · Cited by 15 · see citing works

Transcriptional Activation by MEIS1A in Response to Protein Kinase A Signaling Requires the Transducers of Regulated CREB Family of CREB Co-activators

Goh, S.-L., Looi, Y., Shen, H., Fang, J. Q., Bodner, C., Houle, M., Ng, A. C., Screaton, R. A., & Featherstone, M. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.005090 · Cited by 22 · see citing works

The cancer paradigms of mammalian regeneration: can mammals regenerate as amphibians?

Sarig, R., & Tzahor, E. (2016) · Carcinogenesis · doi:10.1093/carcin/bgw103 · Cited by 22 · see citing works

The homeodomain transcription factor MEIS1 triggers chemokine expression and is involved in CD8+ T‐lymphocyte infiltration in early stage ovarian cancer

Karapetsas, A., Tokamani, M., Evangelou, C., & Sandaltzopoulos, R. (2018) · Molecular Carcinogenesis · doi:10.1002/mc.22840 · Cited by 21 · see citing works

Two new targeted alleles for the comprehensive analysis of M eis1 functions in the mouse

González‐Lázaro, M., Roselló‐Díez, A., Delgado, I., Carramolino, L., Sanguino, M. A., Giovinazzo, G., & Torres, M. (2014) · genesis · doi:10.1002/dvg.22833 · Cited by 21 · see citing works

Meis1 is specifically upregulated in kidney myofibroblasts during aging and injury but is not required for kidney homeostasis or fibrotic response

Chang-Panesso, M., Kadyrov, F. F., Machado, F. G., Kumar, A. R., & Humphreys, B. D. (2018) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00030.2018 · Cited by 21 · see citing works

Promoter methylation and expression levels of selected hematopoietic genes in pediatric B-cell acute lymphoblastic leukemia

Musialik‐Świetlińska, E., Bujko, M., Kober, P., Wypych, A., Gawle‐Krawczyk, K., Matysiak, M. J., & SIEDLECKI, J. A. (2015) · Blood Research · doi:10.5045/br.2015.50.1.26 · Cited by 20 · see citing works

Meis1 establishes the pre-hemogenic endothelial state prior to Runx1 expression

Coulombe, P., Cole, G., Fentiman, A., Parker, J., Yung, E., Bilenky, M., Degefie, L. T., Lac, P., Ling, M. Y. M., Tam, D., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-40283-0 · Cited by 20 · see citing works

Promoter DNA methylation and expression levels of HOXA4, HOXA5 and MEIS1 in acute myeloid leukemia

Musialik‐Świetlińska, E., Bujko, M., Kober, P., Grygorowicz, M. A., Libura, M. A., Przestrzelska, M., Juszczyński, P., Borg, K., Florek, I., Jakóbczyk, M., et al. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.3196 · Cited by 19 · see citing works

Role of MAML1 and MEIS1 in Esophageal Squamous Cell Carcinoma Depth of Invasion

Abbaszadegan, M. R., & Moghbeli, M. (2017) · Pathology & Oncology Research · doi:10.1007/s12253-017-0243-1 · Cited by 19 · see citing works

De Novo Generation of Human Hematopoietic Stem Cells from Pluripotent Stem Cells for Cellular Therapy

Ding, J., Li, Y., & Larochelle, A. (2023) · Cells · doi:10.3390/cells12020321 · Cited by 17 · see citing works

Discrete regulatory modules instruct hematopoietic lineage commitment and differentiation

Georgolopoulos, G., Psatha, N., Iwata, M., Nishida, A., Som, T., Yiangou, M., Stamatoyannopoulos, J. A., & Vierstra, J. D. (2021) · Nature Communications · doi:10.1038/s41467-021-27159-x · Cited by 16 · see citing works

Transcriptional Regulation of Stem Cell and Cancer Stem Cell Metabolism

Alptekin, A., Ye, B., & Ding, H. (2017) · Current Stem Cell Reports · doi:10.1007/s40778-017-0071-y · Cited by 16 · see citing works

Elucidating the importance and regulation of key enhancers for human MEIS1 expression

Xiang, P., Yang, X., Escano, L., Dhillon, I., Schneider, E. M., Clemans-Gibbon, J., Wei, W., Wong, J., Wang, S. X., Tam, D., et al. (2022) · Leukemia · doi:10.1038/s41375-022-01602-4 · Cited by 15 · see citing works

Comparative analysis of the Mexico City Prospective Study and the UK Biobank identifies ancestry-specific effects on clonal hematopoiesis

Wen, S., Kuri-Morales, P. A., Hu, F., Nag, A., Tachmazidou, I., Deevi, S. V. V., Taiy, H., Smith, K. R., Loesch, D. P., Burren, O. S., et al. (2025) · Nature Genetics · doi:10.1038/s41588-025-02085-6 · Cited by 18 · see citing works

The TALE homeodomain transcription factor MEIS1 activates the pro‐metastatic melanoma cell adhesion molecule Mcam to promote migration of pancreatic cancer cells

von Burstin, J., Bachhuber, F., Paul, M. C., Schmid, R. M., & Rustgi, A. K. (2016) · Molecular Carcinogenesis · doi:10.1002/mc.22547 · Cited by 15 · see citing works

Meis1 Regulates Postnatal Cardiomyocyte Cell Cycle Arrest

Muralidhar, S. A., & Sadek, H. A. (2016) · Springer eBooks · doi:10.1007/978-4-431-54628-3_11 · Cited by 15 · see citing works

Molecular Profiling of Conjunctival Epithelial Side-Population Stem Cells: Atypical Cell Surface Markers and Sources of a Slow-Cycling Phenotype

Akinci, M. A., Turner, H. C., Taveras, M., Barash, A., Wang, Z., Reinach, P. S., & Wolosin, J. M. (2009) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.08-2861 · Cited by 14 · see citing works

Mechanisms and Therapeutic Targets of Cardiac Regeneration: Closing the Age Gap

Castellan, R. F. P., & Meloni, M. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00007 · Cited by 14 · see citing works

Tumorigenic and Antiproliferative Properties of the TALE-Transcription Factors MEIS2D and MEIS2A in Neuroblastoma

Groß, A., Schulz, C., Kolb, J., Köster, J., Wehner, S., Czaplinski, S., Khilan, A., Rohrer, H., Harter, P. N., Klingebiel, T. E., et al. (2018) · Cancer Research · doi:10.1158/0008-5472.can-17-1860 · Cited by 13 · see citing works

C-terminal domain of MEIS1 converts PKNOX1 (PREP1) into a HOXA9-collaborating oncoprotein

Bisaillon, R., Wilhelm, B. T., Krošl, J., & Sauvageau, G. (2011) · Blood · doi:10.1182/blood-2011-05-354076 · Cited by 13 · see citing works

Role of Meis1 in mitochondrial gene transcription of pancreatic cancer cells

Tomoeda, M., Yuki, M., Kubo, C., Yoshizawa, H., Kitamura, M., Nagata, S., Nishizawa, Y., & Tomita, Y. (2011) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2011.06.066 · Cited by 13 · see citing works

Interplay between FLI-1 and the LDB1 complex in murine erythroleukemia cells and during megakaryopoiesis

Giraud, G., Kolovos, P., Boltsis, I., van Staalduinen, J., Guyot, B., Weiss‐Gayet, M., van IJcken, W. F. J., Morlé, F., & Grosveld, F. G. (2021) · iScience · doi:10.1016/j.isci.2021.102210 · Cited by 11 · see citing works

Targeting lysine demethylase 6B ameliorates ASXL1 truncation–mediated myeloid malignancies in preclinical models

Ge, G., Zhang, P., Sui, P., Shi, C., Yang, H., Guo, Y., Rubalcava, I. P., Noor, A., Delma, C. R., Agosto-Peña, J., et al. (2023) · Journal of Clinical Investigation · doi:10.1172/jci163964 · Cited by 10 · see citing works

RLS-associated MEIS transcription factors control distinct processes in human neural stem cells

Kittke, V., Zhao, C., Lam, D. D., Harrer, P., Krężel, W., Schormair, B., Oexle, K., & Winkelmann, J. (2024) · Scientific Reports · doi:10.1038/s41598-024-80266-9 · Cited by 9 · see citing works

A knock-in mouse strain facilitates dynamic tracking and enrichment of MEIS1

Xiang, P., Wei, W., Hofs, N., Clemans-Gibbon, J., Maetzig, T., Lai, C. K., Dhillon, I., May, C. G., Rüschmann, J., Schneider, E. M., et al. (2017) · Blood Advances · doi:10.1182/bloodadvances.2017010355 · Cited by 9 · see citing works

Dental Epithelial Stem Cells Express the Developmental Regulator Meis1

Navarro, M. S., Delgado, I., Torres, M., Mustonen, T., Michon, F., & Rice, D. P. C. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00249 · Cited by 9 · see citing works

Delineating MEIS1 cis-regulatory elements active in hematopoietic cells

Xiang, P., Wei, W., Lo, C., Rosten, P. M., Hou, J., Hoodless, P. A., Bilenky, M., Bonifer, C., Cockerill, P. N., Kirkpatrick, A. M., et al. (2013) · Leukemia · doi:10.1038/leu.2013.287 · Cited by 8 · see citing works

Fluorescent genetic barcoding for cellular multiplex analyses

Maetzig, T., Morgan, M. A., & Schambach, A. (2018) · Experimental Hematology · doi:10.1016/j.exphem.2018.08.001 · Cited by 8 · see citing works

The NCOR-HDAC3 co-repressive complex modulates the leukemogenic potential of the transcription factor ERG

Kugler, E., Madiwale, S., Yong, D., Thoms, J. A. I., Birger, Y., Sykes, D. B., Schmoellerl, J., Drakul, A., Priebe, V., Yassin, M., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-41067-2 · Cited by 7 · see citing works

MEIS1-mediated Apoptosis via TNFR1 in Endometriosis

Wang, W., Fu, F., Li, Y., Li, S., Yuan, M., Wang, T., Ren, W., Wei, J., Chen, D., Wang, S., et al. (2025) · Reproductive Sciences · doi:10.1007/s43032-025-01801-1 · Cited by 5 · see citing works

Association of controlled ovarian hyperstimulation treatment with down-regulation of key regulators involved in embryonic implantation in mice

Xiong, M., Zhang, H., Jin, L., Ai, J., Huang, Z., & Zhu, G. (2011) · Journal of Huazhong University of Science and Technology [Medical Sciences] · doi:10.1007/s11596-011-0486-0 · Cited by 5 · see citing works

Npm1 haploinsufficiency in collaboration with MEIS1 is sufficient to induce AML in mice

Muranyi, A., Ammer, T., Kechter, A., Rawat, V. P. S., Sinha, A., González-Menéndez, I., Quintanilla‐Martínez, L., Azoitei, A., Güneş, Ç., Mupo, A., et al. (2022) · Blood Advances · doi:10.1182/bloodadvances.2022007015 · Cited by 5 · see citing works

Overcoming menin inhibitor resistance in AML cells with combinations including BET proteins and a dual BRG1/BRM inhibitor

Fiskus, W. C., Mill, C. P., Issa, G. C., Piel, J. C., Collins, M. P., Hentemann, M., Cuglievan, B., Hou, H., Jain, A., Malovannaya, A., et al. (2026) · Blood · doi:10.1182/blood.2025031486 · Cited by 4 · see citing works

Evaluation of the HOXA9 and MEIS1 genes as a potential biomarker in adult acute myeloid leukemia

Abdelrahman, A. M., Tolba, F. M., Kamal, H. M., Abdellateif, M. S., Ahmed, H. A., & Hassan, N. M. (2023) · Egyptian Journal of Medical Human Genetics · doi:10.1186/s43042-023-00391-4 · Cited by 4 · see citing works

Differential transcriptional control of hematopoiesis in congenital and cyclic neutropenia patients harboring ELANE mutations

Zeidler, A., Borbaran-Bravo, N., Dannenmann, B., Ritter, M. U., Nasri, M., Klimiankou, M., Kandabarau, S., Zahabi, A., König, J., Zeidler, C., et al. (2023) · Haematologica · doi:10.3324/haematol.2023.284033 · Cited by 3 · see citing works

MEIS1: From functional versatility to post-transcriptional/translational regulation

Fahim, S. A., Sobky, S. A. E., Abdellatif, A., Fawzy, I. O., & Abdelaziz, A. I. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123683 · Cited by 3 · see citing works

Lead Optimization and Structure–Activity Relationship Studies on Myeloid Ecotropic Viral Integration Site 1 Inhibitor

Turgutalp, B., Uslu, M., Helvacıoğlu, S., Charehsaz, M., Gürdal, E. E., Sippl, W., Kocabaş, F., & Yarım, M. (2021) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.1c00972 · Cited by 3 · see citing works

Triple-negative Thrombocythemia and Subsequent Acute Lymphoblastic Leukemia with Additional Somatic Mutations

Tsuboi, Y., Sakamoto, T., Makishima, K., Suehara, Y., Hattori, K., Kurita, N., Yokoyama, Y., Kato, T., Nishikii, H., Obara, N., et al. (2022) · Internal Medicine · doi:10.2169/internalmedicine.0269-22 · Cited by 2 · see citing works

Gene Expression Profile Regulated by CREB in K562 Cell Line

Xia, H., Gong, Z., Lian, Y., Zhou, J. H. S., & Wang, X. (2016) · Transplantation Proceedings · doi:10.1016/j.transproceed.2016.04.023 · Cited by 2 · see citing works

Comparative analysis of 136,401 Admixed Americans and 419,228 Europeans reveals ancestry-specific genetic determinants of clonal haematopoiesisPreprint

Wen, S., Kuri-Morales, P. A., Hu, F., Nag, A., Tachmazidou, I., Deevi, S. V. V., Taiy, H., Smith, K. R., Loesch, D. P., Burren, O. S., et al. (2024) · medRxiv · doi:10.1101/2024.02.07.24302442 · Cited by 2 · see citing works

Elucidating the risk factors and oncogene drivers of acute myeloid leukemia

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Chromatin dynamics during hematopoiesis reveal discrete regulatory modules instructing differentiationPreprint

Georgolopoulos, G., Psatha, N., Iwata, M., Nishida, A., Som, T., Yiangou, M., Stamatoyannopoulos, J. A., & Vierstra, J. D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.04.02.022566 · Cited by 1 · see citing works

The role of prolyl hydroxylases in the function of leukaemic stem cells and the development of leukaemia

Smith, G. (2015) · Enlighten: Theses (The University of Glasgow)

Characterization of the putative CALM/AF10 collaborator Meis1 in leukemia development

Sen, D. (2013) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.16070

Molecular mechanisms of pathogenesis of myeloproliferative neoplasms: deregulation of genes involved in cell proliferation and apoptosis

Spasovski, V. (2012) · doi:10.2298/bg20121227spasovski

Additional file 1 of Evaluation of the HOXA9 and MEIS1 genes as a potential biomarker in adult acute myeloid leukemia

Abdelrahman, A. M., Tolba, F. M., Kamal, H. M., Abdellateif, M. S., Ahmed, H. A., & Hassan, N. M. (2023) · Figshare · doi:10.6084/m9.figshare.22601588

Sclerotomal hematopoiesis in vertebrate embryos contributes to robustness of the blood system

Jiang, Z., Li, T., Song, Y., Chen, L., Qiu, J., Zhou, F., Wu, X., Wang, J., & Meng, A. (2026) · National Science Review · doi:10.1093/nsr/nwag035

Cooperative reading of DECA-CCAAT composite element by the TALE/NF-Y/Sp2 transcription factors

Bernardini, A., Gnesutta, N., & Mantovani, R. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.151345

The role of MEIS inhibitors in cardiac regeneration and protection

Mammadova, A. (2024) · doi:10.70675/26f419bdzeecdz4816z8ff0z9800989c228b

Progress in the role of MEIS1 in MLL-association leukemia

刘琳, 叶启东, & 汤静燕 (2009) · International journal of pediatrics · doi:10.3760/cma.j.issn.1673-4408.2009.06.006

Linkage of Meis1 leukemogenic activity to multiple downstream effectors including Trib2 and Ccl3

Argiropoulos, B., Palmqvist, L., Yung, E., Kuchenbauer, F. C., Heuser, M., Sly, L. M., Wan, A. N. C., Krystal, G., & Humphries, R. K. (2008) · Experimental Hematology · doi:10.1016/j.exphem.2008.02.011 · Cited by 64 · see citing works

Meis1 programs transcription of FLT3 and cancer stem cell character, using a mechanism that requires interaction with Pbx and a novel function of the Meis1 C-terminus

Wang, G. G., Pasillas, M. P., & Kamps, M. P. (2005) · Blood · doi:10.1182/blood-2004-12-4664 · Cited by 127 · see citing works

Dual actions of Meis1 inhibit erythroid progenitor development and sustain general hematopoietic cell proliferation

Cai, M., Langer, E. M., Gill, J. G., Satpathy, A. T., Albring, J. C., Wumesh, K. C., Murphy, T. L., & MURPHY, K. M. M. (2012) · Blood · doi:10.1182/blood-2012-01-403139 · Cited by 53 · see citing works

Identification of Meis1 Target Genes Involved in the Induction of AML in Collaboration with NUP98-HOXD13.

Palmqvist, L., Argiropoulos, B., & Humphries, R. K. (2006) · Blood · doi:10.1182/blood.v108.11.1404.1404