RUNX1/AML1: A Central Player in Hematopoiesis

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis.

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Definitive Hematopoiesis Is Autonomously Initiated by the AGM Region

Medvinsky, A., & Dzierzak, E. A. (1996) · Cell · doi:10.1016/s0092-8674(00)80165-8 · Cited by 1,548 · see citing works

Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis.

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Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

Song, W.-J., Sullivan, M. G., Legare, R. D., Hutchings, S., Tan, X., Kufrin, D., Ratajczak, J., Resende, I. C., Haworth, C., Hock, R., et al. (1999) · Nature Genetics · doi:10.1038/13793 · Cited by 1,100 · see citing works

t(8;21) breakpoints on chromosome 21 in acute myeloid leukemia are clustered within a limited region of a single gene, AML1.

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Fusion Between Transcription Factor CBFβ/PEBP2β and a Myosin Heavy Chain in Acute Myeloid Leukemia

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Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.

Golub, T. R., Barker, G. F., Bohlander, S. K., Hiebert, S. W., Ward, D. C., Bray-Ward, P., Morgan, E., Raimondi, S. C., Rowley, J. D., & Gilliland, D. G. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.11.4917 · Cited by 704 · see citing works

Transcription factor NF-E2 is required for platelet formation independent of the actions of thrombopoeitin/MGDF in megakaryocyte development

Shivdasani, R. A., Rosenblatt, M., Zucker‐Franklin, D., Jackson, C. W., Hunt, P., Saris, C. J. M., & Orkin, S. H. (1995) · Cell · doi:10.1016/0092-8674(95)90531-6 · Cited by 687 · see citing works

<i>Cbfa2</i> is required for the formation of intra-aortic hematopoietic clusters

North, T., Gu, T.-L., Stacy, T., Wang, Q., Howard, L., Binder, M., Marín-Padilla, M., & Speck, N. A. (1999) · Development · doi:10.1242/dev.126.11.2563 · Cited by 662 · see citing works

The CBFβ Subunit Is Essential for CBFα2 (AML1) Function In Vivo

Wang, Q., Stacy, T., Miller, J. D., Lewis, A. F., Gu, T.-L., Huang, X., Bushweller, J. H., Bories, J.-C., Alt, F. W., Ryan, G., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)81389-6 · Cited by 621 · see citing works

Definitive hematopoietic stem cells first develop within the major arterial regions of the mouse embryo

Bruijn, M. F. T. R. D., Speck, N. A., Peeters, M. C. E., & Dzierzak, E. (2000) · The EMBO Journal · doi:10.1093/emboj/19.11.2465 · Cited by 617 · see citing works

PEBP2/PEA2 represents a family of transcription factors homologous to the products of the Drosophila runt gene and the human AML1 gene.

Ogawa, E., Maruyama, M., Kagoshima, H., Inuzuka, M., Lu, J., Satake, M., Shigesada, K., & Ito, Y. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.14.6859 · Cited by 608 · see citing works

Intraaortic hemopoietic cells are derived from endothelial cells during ontogeny

Jaffredo, T., Gautier, R., Eichmann, A., & Dieterlen‐Lièvre, F. (1998) · Development · doi:10.1242/dev.125.22.4575 · Cited by 580 · see citing works

The transcriptional control of hematopoiesis [see comments]

Shivdasani, R., & Orkin, S. (1996) · Blood · doi:10.1182/blood.v87.10.4025.bloodjournal87104025 · Cited by 560 · see citing works

The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion

Romana, S., Mauchauffe, M., Le Coniat, M., Chumakov, I., Le Paslier, D., Berger, R., & Bernard, O. (1995) · Blood · doi:10.1182/blood.v85.12.3662.bloodjournal85123662 · Cited by 530 · see citing works

A Role for Hematopoietic Stem Cells in Promoting Angiogenesis

Takakura, N., Watanabe, T., Suenobu, S., Yamada, Y., Noda, T., Ito, Y., Satake, M., & Suda, T. (2000) · Cell · doi:10.1016/s0092-8674(00)00025-8 · Cited by 501 · see citing works

Specification of Drosophila Hematopoietic Lineage by Conserved Transcription Factors

Lebestky, T., Chang, T., Hartenstein, V., & Banerjee, U. K. (2000) · Science · doi:10.1126/science.288.5463.146 · Cited by 494 · see citing works

Transcriptional repression by AML1 and LEF-1 is mediated by the TLE/Groucho corepressors

Levanon, D., Goldstein, R. E., Bernstein, Y., Tang, H., Goldenberg, D., Stifani, S., Paroush, Z., & Groner, Y. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.20.11590 · Cited by 467 · see citing works

Cloning and Characterization of Subunits of the T-Cell Receptor and Murine Leukemia Virus Enhancer Core-Binding Factor

Wang, S., Wang, Q., Crute, B. E., Melnikova, I. N., Keller, S. R., & Speck, N. A. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.6.3324-3339.1993 · Cited by 435 · see citing works

Biallelic and Heterozygous Point Mutations in the Runt Domain of theAML1/PEBP2B Gene Associated With Myeloblastic Leukemias

Osato, M., Asou, N., Abdalla, E., Hoshino, K., Yamasaki, H., Okubo, T., Suzushima, H., Takatsuki, K., Kanno, T., Shigesada, K., et al. (1999) · Blood · doi:10.1182/blood.v93.6.1817.406k36_1817_1824 · Cited by 395 · see citing works

Absence of fetal liver hematopoiesis in mice deficient in transcriptional coactivator core binding factor beta.

Sasaki, K., Yagi, H., Bronson, R. T., Tominaga, K., Matsunashi, T., Deguchi, K., Tani, Y., Kishimoto, T., & Komori, T. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.22.12359 · Cited by 366 · see citing works

In Vitro Generation of Lymphohematopoietic Cells from Endothelial Cells Purified from Murine Embryos

Nishikawa, S.-I., Nishikawa, S., Kawamoto, H., Yoshida, H., Kizumoto, M., Kataoka, H., & Katsura, Y. (1998) · Immunity · doi:10.1016/s1074-7613(00)80581-6 · Cited by 352 · see citing works

The runt domain identifies a new family of heterometric transcriptional regulators

Kagoshima, H., Shigesada, K., Satake, M., Ito, Y., Miyoshi, H., Ohki, M., Pepling, M., & Gergen, P. (1993) · Trends in Genetics · doi:10.1016/0168-9525(93)90026-e · Cited by 326 · see citing works

Generation of the AML1‐EVI‐1 fusion gene in the t(3;21)(q26;q22) causes blastic crisis in chronic myelocytic leukemia.

Mitani, K., Ogawa, S., Tanaka, T., Miyoshi, H., Kurokawa, M., Mano, H., Yazaki, Y., Ohki, M., & Hirai, H. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06288.x · Cited by 323 · see citing works

The Drosophila segmentation gene runt encodes a novel nuclear regulatory protein that is also expressed in the developing nervous system.Preprint

Kania, M. A., Bonner, A., Duffy, J. B., & Gergen, J. P. (1990) · Genes & Development · doi:10.1101/gad.4.10.1701 · Cited by 288 · see citing works

Dimerization with PEBP2β protects RUNX1/AML1 from ubiquitin–proteasome‐mediated degradation

Huang, G., Shigesada, K., Ito, K., Wee, H., Yokomizo, T., & Ito, Y. (2001) · The EMBO Journal · doi:10.1093/emboj/20.4.723 · Cited by 283 · see citing works

Consistent intergenic splicing and production of multiple transcripts between AML1 at 21q22 and unrelated genes at 3q26 in (3;21)(q26;q22) translocations.

Nucifora, G., Begy, C. R., Kobayashi, H., Roulston, D., Claxton, D. F., Pedersen-Bjergaard, J., Parganas, E., Ihle, J. N., & Rowley, J. D. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.9.4004 · Cited by 256 · see citing works

Haploinsufficiency of AML1 Affects the Temporal and Spatial Generation of Hematopoietic Stem Cells in the Mouse Embryo

Cai, Z., Bruijn, M. F. T. R. D., Ma, X., Dortland, B. R., Luteijn, T., Downing, J. R., & Dzierzak, E. A. (2000) · Immunity · doi:10.1016/s1074-7613(00)00042-x · Cited by 253 · see citing works

Mouse embryonic hematopoiesis

Dzierzak, E. A. (1995) · Trends in Genetics · doi:10.1016/s0168-9525(00)89107-6 · Cited by 246 · see citing works

A Mechanism of Repression by Acute Myeloid Leukemia-1, the Target of Multiple Chromosomal Translocations in Acute Leukemia

Lutterbach, B. A., Westendorf, J. J., Linggi, B. E., Isaac, S., Seto, E., & Hiebert, S. W. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.1.651 · Cited by 245 · see citing works

The Partner Gene of AML1 in t(16;21) Myeloid Malignancies Is a Novel Member of the MTG8(ETO) Family

Gamou, T., Kitamura, E., Hosoda, F., Shimizu, K., Shinohara, K., Hayashi, Y., Nagase, T., Yokoyama, Y., & Ohki, M. (1998) · Blood · doi:10.1182/blood.v91.11.4028 · Cited by 238 · see citing works

Potential intraembryonic hemogenic sites at pre-liver stages in the mouse

García-Porrero, J. A., Godin, I., & Dieterlen-Li�vre, F. (1995) · Anatomy and Embryology · doi:10.1007/bf00240375 · Cited by 234 · see citing works

CD34 Expression Patterns During Early Mouse Development Are Related to Modes of Blood Vessel Formation and Reveal Additional Sites of Hematopoiesis

Wood, H. B., May, G. E., Healy, L. E., Enver, T., & Morriss‐Kay, G. M. (1997) · Blood · doi:10.1182/blood.v90.6.2300 · Cited by 212 · see citing works

Intrinsic Transcriptional Activation-Inhibition Domains of the Polyomavirus Enhancer Binding Protein 2/Core Binding Factor α Subunit Revealed in the Presence of the β Subunit

Kanno, T., Kanno, Y., Chen, L.-F., Ogawa, E., Kim, W.-Y., & Ito, Y. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.5.2444 · Cited by 192 · see citing works

Patterning of cells in the Drosophila eye by Lozenge, which shares homologous domains with AML1.

Daga, A., Karlovich, C. A., Dumstrei, K., & Banerjee, U. (1996) · Genes &amp; Development · doi:10.1101/gad.10.10.1194 · Cited by 188 · see citing works

Hematopoiesis in the fetal liver is impaired by targeted mutagenesis of a gene encoding a non-DNA binding subunit of the transcription factor, polyomavirus enhancer binding protein 2/core binding factor

Niki, M., Okada, H., Takano, H., Kuno, J., Tani, K., Hibino, H., Asano, S., Ito, Y., Satake, M., & Noda, T. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.11.5697 · Cited by 181 · see citing works

Molecular basis of tissue‐specific gene expression mediated by the Runt domain transcription factor PEBP2/CBF

Ito, Y. (1999) · Genes to Cells · doi:10.1046/j.1365-2443.1999.00298.x · Cited by 179 · see citing works

Requirement of <i>Runx1/AML1/PEBP2αB</i> for the generation of haematopoietic cells from endothelial cells

Yokomizo, T., Ogawa, M., Osato, M., Kanno, T., Yoshida, H., Fujimoto, T., Fraser, S., Nishikawa, S., Okada, H., Satake, M., et al. (2001) · Genes to Cells · doi:10.1046/j.1365-2443.2001.00393.x · Cited by 176 · see citing works

A New Transcription Factor Family Associated with Human Leukemias

Speck, N. A., & Stacy, T. (1995) · Critical Reviews in Eukaryotic Gene Expression · doi:10.1615/critreveukargeneexpr.v5.i3-4.60 · Cited by 163 · see citing works

Expression of the Runt Domain-Encoding PEBP2 α Genes in T cells during Thymic Development

Satake, M., Nomura, S., Yamaguchi‐Iwai, Y., Takahama, Y., Hashimoto, Y., Niki, M., Kitamura, Y., & Ito, Y. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.3.1662 · Cited by 157 · see citing works

Expression of the human acute myeloid leukemia gene AML1 is regulated by two promoter regions.

Ghozi, M. C., Bernstein, Y., Negreanu, V., Levanon, D., & Groner, Y. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.5.1935 · Cited by 152 · see citing works

TLE, the Human Homolog of Groucho, Interacts with AML1 and Acts as a Repressor of AML1-Induced Transactivation

Imai, Y., Kurokawa, M., Tanaka, K., Friedman, A. D., Ogawa, S., Mitani, K., Yazaki, Y., & Hirai, H. (1998) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1998.9705 · Cited by 121 · see citing works

Expression and Function of a Stem Cell Promoter for the Murine CBFα2 Gene: Distinct Roles and Regulation in Natural Killer and T Cell Development

Telfer, J. C., & Rothenberg, E. V. (2001) · Developmental Biology · doi:10.1006/dbio.2000.9991 · Cited by 88 · see citing works

The AML1 Transcription Factor Functions to Develop and Maintain Hematogenic Precursor Cells in the Embryonic Aorta–Gonad–Mesonephros Region

Mukouyama, Y.-S., Chiba, N., Hara, T., Okada, H., Ito, Y., Kanamaru, R., Miyajima, A., Satake, M., & Watanabe, T. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9617 · Cited by 81 · see citing works

Expression of runt in the mouse embryo

Simeone, A., Daga, A., & Calabi, F. (1995) · Developmental Dynamics · doi:10.1002/aja.1002030107 · Cited by 73 · see citing works

Biological Characteristics of the Leukemia-Associated Transcriptional Factor AML1 Disclosed by Hematopoietic Rescue of AML1 -Deficient Embryonic Stem Cells by Using a Knock-in Strategy

Okuda, T., Takeda, K., Fujita, Y., Nishimura, M., Yagyu, S., Yoshida, M., Akira, S., Downing, J. R., & Abe, T. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.1.319-328.2000 · Cited by 66 · see citing works

Identification of an Alternatively Spliced Form of the Mouse AML1/RUNX1 Gene Transcript AML1c and Its Expression in Early Hematopoietic Development

Fujita, Y., Nishimura, M., Taniwaki, M., Abe, T., & Okuda, T. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.4513 · Cited by 57 · see citing works

In vivo interactions of the Drosophila Hairy and Runt transcriptional repressors with target promoters.

Jiménez, G., Pinchin, S. M., & Ish‐Horowicz, D. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb01100.x · Cited by 45 · see citing works

Cell signaling and transcriptional regulation of osteoblast lineage commitment, differentiation, bone formation, and homeostasis

Zhu, S., Chen, W., Masson, A., & Li, Y. (2024) · Cell Discovery · doi:10.1038/s41421-024-00689-6 · Cited by 513 · see citing works

Hypoxia-induced microRNA-424 expression in human endothelial cells regulates HIF-α isoforms and promotes angiogenesis

Ghosh, G., Subramanian, I. V., Adhikari, N., Zhang, X., Joshi, H. P., Basi, D. L., Chandrashekhar, Y., Hall, J. L., Roy, S., Zeng, Y., et al. (2010) · Journal of Clinical Investigation · doi:10.1172/jci42980 · Cited by 417 · see citing works

Hematopoietic stem cell fate is established by the Notch-Runx pathway

Burns, C. E., Traver, D., Mayhall, E., Shepard, J. L., & Zon, L. I. (2005) · Genes &amp; Development · doi:10.1101/gad.1337005 · Cited by 401 · see citing works

Hematopoietic stem cells proliferate until after birth and show a reversible phase-specific engraftment defect

Bowie, M. B., McKnight, K. D., Kent, D. G., McCaffrey, L., Hoodless, P. A., & Eaves, C. J. (2006) · Journal of Clinical Investigation · doi:10.1172/jci28310 · Cited by 380 · see citing works

Current knowledge on psoriasis and autoimmune diseases

McCormick, T. S., Ayala‐Fontanez, N., & Soler, D. C. (2016) · Psoriasis Targets and Therapy · doi:10.2147/ptt.s64950 · Cited by 270 · see citing works

The Bone-specific Expression of Runx2 Oscillates during the Cell Cycle to Support a G1-related Antiproliferative Function in Osteoblasts

Galindo, M. A., Pratap, J., Young, D. W., Hovhannisyan, H., Im, H., Choi, J., Lian, J. B., Stein, J. L., Stein, G. S., & van Wijnen, A. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m413665200 · Cited by 240 · see citing works

Association of a putative regulatory polymorphism in the <i>PD‐1</i> gene with susceptibility to type 1 diabetes

Nielsen, C., Hansen, D., Husby, S., Jacobsen, B. B., & Lillevang, S. T. (2003) · Tissue Antigens · doi:10.1046/j.1399-0039.2003.00136.x · Cited by 232 · see citing works

Myocardial Infarction Activates CCR2+ Hematopoietic Stem and Progenitor Cells

Dutta, P., Sager, H. B., Stengel, K. R., Naxerova, K., Courties, G., Sáez, B., Silberstein, L., Heidt, T., Sebas, M., Sun, Y., et al. (2015) · Cell stem cell · doi:10.1016/j.stem.2015.04.008 · Cited by 219 · see citing works

Adaptive and Innate Immunity in Psoriasis and Other Inflammatory Disorders

Schön, M. P. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01764 · Cited by 197 · see citing works

Runx2 mediates FGF signaling from epithelium to mesenchyme during tooth morphogenesis

Åberg, T., Wang, X., Kim, J. H., Yamashiro, T., Bei, M., Rice, R., Ryoo, H., & Thesleff, I. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.02.012 · Cited by 182 · see citing works

Genome‐Wide DNA Methylation Patterns in Naive CD4+ T Cells From Patients With Primary Sjögren's Syndrome

Altorok, N., Coit, P., Hughes, T. K., Koelsch, K. A., Stone, D. U., Rasmussen, A., Radfar, L., Scofield, R. H., Sivils, K. L. M., Farris, A. D., et al. (2013) · Arthritis & Rheumatology · doi:10.1002/art.38264 · Cited by 171 · see citing works

An important role for RUNX3 in human L1 transcription and retrotransposition

Yang, N. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg663 · Cited by 167 · see citing works

Etv2/ER71 induces vascular mesoderm from Flk1+PDGFRα+ primitive mesoderm

Kataoka, H., Hayashi, M., Nakagawa, R., Tanaka, Y., Izumi, N., Nishikawa, S., Jakt, L. M., Tarui, H., & Nishikawa, S. (2011) · Blood · doi:10.1182/blood-2011-05-352658 · Cited by 166 · see citing works

Genome-wide prediction of cis-regulatory regions using supervised deep learning methods

Li, Y., Shi, W., & Wasserman, W. W. (2018) · BMC Bioinformatics · doi:10.1186/s12859-018-2187-1 · Cited by 123 · see citing works

Isolation and characterization of runxa and runxb, zebrafish members of the runt family of transcriptional regulators

Burns, C. E., DeBlasio, T., Zhou, Y., Zhang, J., Zon, L. I., & Nimer, S. D. (2002) · Experimental Hematology · doi:10.1016/s0301-472x(02)00955-4 · Cited by 120 · see citing works

Altered Runx1 Subnuclear Targeting Enhances Myeloid Cell Proliferation and Blocks Differentiation by Activating a miR-24/MKP-7/MAPK Network

Zaidi, S. K., Dowdy, C. R., van Wijnen, A. J., Lian, J. B., Raza, A., Stein, J. L., Croce, C. M., & Stein, G. S. (2009) · Cancer Research · doi:10.1158/0008-5472.can-09-1567 · Cited by 115 · see citing works

Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways

Tang, C.-Y., Wu, M., Zhao, D., Edwards, D. N., McVicar, A., Luo, Y., Zhu, G., Wang, Y., Zhou, H., Chen, W., et al. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009233 · Cited by 111 · see citing works

When the good go bad: Mutant NPM1 in acute myeloid leukemia

Kunchala, P., Kuravi, S., Jensen, R. A., McGuirk, J. P., & Balusu, R. (2017) · Blood Reviews · doi:10.1016/j.blre.2017.11.001 · Cited by 99 · 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

Prediction of DNA binding motifs from 3D models of transcription factors; identifying TLX3 regulated genes

Pujato, M. A., Kieken, F., Skiles, A. A., Tapinos, N., & Fiser, A. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku1228 · Cited by 93 · see citing works

Proteome-Wide Analysis of Disease-Associated SNPs That Show Allele-Specific Transcription Factor Binding

Butter, F., Davison, L., Viturawong, T., Scheibe, M., Vermeulen, M., Todd, J. A., & Mann, M. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002982 · Cited by 91 · see citing works

Epigenetic Modifications in Acute Myeloid Leukemia: Prognosis, Treatment, and Heterogeneity

Goldman, S. L., Hassan, C., Khunte, M., Soldatenko, A., Jong, Y., Afshinnekoo, E., & Mason, C. E. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00133 · Cited by 86 · see citing works

RUNX1 contributes to the mesenchymal subtype of glioblastoma in a TGFβ pathway-dependent manner

Zhao, K., Cui, X., Wang, Q., Fang, C., Tan, Y., Wang, Y., Yi, K., Yang, C., You, H., Shang, R., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-2108-x · Cited by 77 · see citing works

Functional anatomy of the hair follicle: The Secondary Hair Germ

Panteleyev, A. A. (2018) · Experimental Dermatology · doi:10.1111/exd.13666 · Cited by 74 · see citing works

Role of RUNX in autoimmune diseases linking rheumatoid arthritis, psoriasis and lupus.

Alarcón-Riquelme, M. E. (2004) · Arthritis Research · doi:10.1186/ar1203 · Cited by 71 · see citing works

Liver ergothioneine accumulation in a guinea pig model of non-alcoholic fatty liver disease. A possible mechanism of defence?

Cheah, I. K.-M., Tang, R. M. Y., Ye, P., Yew, T. S. Z., Lim, K. H. C., & Halliwell, B. B. (2015) · Free Radical Research · doi:10.3109/10715762.2015.1099642 · Cited by 70 · see citing works

Runt-related transcription factor 1 is required for murine osteoblast differentiation and bone formation

Tang, J., Xie, J., Chen, W., Tang, C.-Y., Wu, J., Wang, Y., Zhou, X., Zhou, H., & Li, Y. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.007896 · Cited by 60 · see citing works

mab-2encodes RNT-1, aC. elegansRunx homologue essential for controlling cell proliferation in a stem cell-like developmental lineage

Nimmo, R. A., Antebi, A., & Woollard, A. C. S. (2005) · Development · doi:10.1242/dev.02102 · Cited by 60 · see citing works

RUNX transcription factors: association with pediatric asthma and modulated by maternal smoking

Haley, K. J., Lasky-Su, J., Manoli, S. E., Smith, L. A., Shahsafaei, A., Weiss, S. T., & Tantisira, K. (2011) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00348.2010 · Cited by 58 · see citing works

Braddock–Carey syndrome: A 21q22 contiguous gene syndrome encompassing RUNX1

Braddock, S. R., South, S. T., Schiffman, J. D., Longhurst, M. C., Rowe, L. R., & Carey, J. C. (2016) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.37870 · Cited by 51 · see citing works

AML1/RUNX1 mutations are infrequent, but related to AML‐M0, acquired trisomy 21, and leukemic transformation in pediatric hematologic malignancies

Taketani, T., Taki, T., Takita, J., Tsuchida, M., Hanada, R., Hongo, T., Kaneko, T., Manabe, A., Ida, K., & Hayashi, Y. (2003) · Genes Chromosomes and Cancer · doi:10.1002/gcc.10246 · Cited by 51 · see citing works

A RUNX trio with a taste for autoimmunity

Alarcón-Riquelme, M. E. (2003) · Nature Genetics · doi:10.1038/ng1203-299 · Cited by 51 · see citing works

Number of RUNX1 mutations, wild-type allele loss and additional mutations impact on prognosis in adult RUNX1-mutated AML

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Zfrp8, theDrosophilaortholog ofPDCD2,functions in lymph gland development and controls cell proliferation

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