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Transcriptional Regulation

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

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Pages 2444-2454 | Received 17 Dec 1997, Accepted 09 Feb 1998, Published online: 28 Mar 2023

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Huimin Jiang, Fan Zhang, Takeshi Kurosu & B. Matija Peterlin. (2005) Runx1 Binds Positive Transcription Elongation Factor b and Represses Transcriptional Elongation by RNA Polymerase II: Possible Mechanism of CD4 Silencing. Molecular and Cellular Biology 25:24, pages 10675-10683.
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Kenji Hata, Riko Nishimura, Mio Ueda, Fumiyo Ikeda, Takuma Matsubara, Fumitaka Ichida, Kunihiro Hisada, Takashi Nokubi, Akira Yamaguchi & Toshiyuki Yoneda. (2005) A CCAAT/Enhancer Binding Protein β Isoform, Liver-Enriched Inhibitory Protein, Regulates Commitment of Osteoblasts and Adipocytes. Molecular and Cellular Biology 25:5, pages 1971-1979.
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Naomi Yoshida, Takehiro Ogata, Kenji Tanabe, Songhua Li, Megumi Nakazato, Kazuyoshi Kohu, Toshiro Takafuta, Sandor Shapiro, Yasutaka Ohta, Masanobu Satake & Toshio Watanabe. (2005) Filamin A-Bound PEBP2β/CBFβ Is Retained in the Cytoplasm and Prevented from Functioning as a Partner of the Runx1 Transcription Factor. Molecular and Cellular Biology 25:3, pages 1003-1012.
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Kristie L. Durst, Bart Lutterbach, Tanawan Kummalue, Alan D. Friedman & Scott W. Hiebert. (2003) The inv(16) Fusion Protein Associates with Corepressors via a Smooth Muscle Myosin Heavy-Chain Domain. Molecular and Cellular Biology 23:2, pages 607-619.
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Ting-Lei Gu, Tamara L. Goetz, Barbara J. Graves & Nancy A. Speck. (2000) Auto-Inhibition and Partner Proteins, Core-Binding Factor β (CBFβ) and Ets-1, Modulate DNA Binding by CBFα2 (AML1). Molecular and Cellular Biology 20:1, pages 91-103.
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Tamara L. Goetz, Ting-Lei Gu, Nancy A. Speck & Barbara J. Graves. (2000) Auto-Inhibition of Ets-1 Is Counteracted by DNA Binding Cooperativity with Core-Binding Factor α2. Molecular and Cellular Biology 20:1, pages 81-90.
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Tsukasa Okuda, Kiyoshi Takeda, Yasuko Fujita, Motohiro Nishimura, Shigeki Yagyu, Makie Yoshida, Shizuo Akira, James R. Downing & Tatsuo Abe. (2000) 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. Molecular and Cellular Biology 20:1, pages 319-328.
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Amjad Javed, Soraya Gutierrez, Martin Montecino, André J. van Wijnen, Janet L. Stein, Gary S. Stein & Jane B. Lian. (1999) Multiple Cbfa/AML Sites in the Rat Osteocalcin Promoter Are Required for Basal and Vitamin D-Responsive Transcription and Contribute to Chromatin Organization. Molecular and Cellular Biology 19:11, pages 7491-7500.
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Kannan Thirunavukkarasu, Muktar Mahajan, Keith W. McLarren, Stefano Stifani & Gerard Karsenty. (1998) Two Domains Unique to Osteoblast-Specific Transcription Factor Osf2/Cbfa1 Contribute to Its Transactivation Function and Its Inability To Heterodimerize with Cbfβ. Molecular and Cellular Biology 18:7, pages 4197-4208.
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Lin-Feng Chen, Kosei Ito, Yota Murakami & Yoshiaki Ito. (1998) The Capacity of Polyomavirus Enhancer Binding Protein 2αB (AML1/Cbfa2) To Stimulate Polyomavirus DNA Replication Is Related to Its Affinity for the Nuclear Matrix. Molecular and Cellular Biology 18:7, pages 4165-4176.
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Crossref
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Crossref
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Hui Huang, Andrew J. Woo, Zachary Waldon, Yocheved Schindler, Tyler B. Moran, Helen H. Zhu, Gen-Sheng Feng, Hanno Steen & Alan B. Cantor. (2012) A Src family kinase–Shp2 axis controls RUNX1 activity in megakaryocyte and T-lymphocyte differentiation. Genes & Development 26:14, pages 1587-1601.
Crossref
A Bufalino, LMR Paranaíba, AF Gouvêa, LA Gueiros, H Martelli-Júnior, JJ Junior, MA Lopes, E Graner, OP de Almeida, PA Vargas & RD Coletta. (2012) Cleidocranial dysplasia: oral features and genetic analysis of 11 patients. Oral Diseases 18:2, pages 184-190.
Crossref
Zhenbo HuXiaorong GuKristine BaraoidanVinzon IbanezArun SharmaShriHari KadkolReinhold MunkerSteven Ackerman, Giuseppina NuciforaYogen Saunthararajah. (2011) RUNX1 regulates corepressor interactions of PU.1. Blood 117:24, pages 6498-6508.
Crossref
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Crossref
Chenying Zhang, Shuguo Zheng, Yixiang Wang, Yuming Zhao, Junxia Zhu & Lihong Ge. (2010) Mutational analysis of RUNX2 gene in Chinese patients with cleidocranial dysplasia. Mutagenesis 25:6, pages 589-594.
Crossref
Pegine B. Walrad, Saiyu Hang, Genevieve S. Joseph, Julia Salas & J. Peter Gergen. (2010) Distinct Contributions of Conserved Modules to Runt Transcription Factor Activity. Molecular Biology of the Cell 21:13, pages 2315-2326.
Crossref
Joost H.A. Martens & Henk G. Stunnenberg. (2010) The molecular signature of oncofusion proteins in acute myeloid leukemia. FEBS Letters 584:12, pages 2662-2669.
Crossref
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Crossref
H-M Ryoo, H-Y Kang, S-K Lee, K-E Lee & J-W Kim. (2010) RUNX2 mutations in cleidocranial dysplasia patients. Oral Diseases 16:1, pages 55-60.
Crossref
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Crossref
Ryuji Uchino. (2009) Domain analyses of the Runx1 transcription factor responsible for modulating T-cell receptor-β/CD4 and interleukin-4/interferon-γ expression in CD4 + peripheral T lymphocytes . Immunology 128:1, pages 16-24.
Crossref
M-C Kuo, D-C Liang, C-F Huang, Y-S Shih, J-H Wu, T-L Lin & L-Y Shih. (2009) RUNX1 mutations are frequent in chronic myelomonocytic leukemia and mutations at the C-terminal region might predict acute myeloid leukemia transformation. Leukemia 23:8, pages 1426-1431.
Crossref
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He-Yu Zhang, Long Jin, Gail A. Stilling, Katharina H. Ruebel, Kendra Coonse, Yoshinori Tanizaki, Avraham Raz & Ricardo V. Lloyd. (2008) RUNX1 and RUNX2 upregulate Galectin-3 expression in human pituitary tumors. Endocrine 35:1, pages 101-111.
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Ivana M. Djuretic, Fernando Cruz-Guilloty & Anjana Rao. 2009. 1 23 .
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Yoshiaki Ito. 2008. 33 76 .
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Crossref
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Crossref
E Reed-Inderbitzin, I Moreno-Miralles, S K Vanden-Eynden, J Xie, B Lutterbach, K L Durst-Goodwin, K S Luce, B J Irvin, M L Cleary, S J Brandt & S W Hiebert. (2006) RUNX1 associates with histone deacetylases and SUV39H1 to repress transcription. Oncogene 25:42, pages 5777-5786.
Crossref
Hebin Liu, Leif Carlsson & Thomas Grundström. (2006) Identification of an N-terminal Transactivation Domain of Runx1 That Separates Molecular Function from Global Differentiation Function. Journal of Biological Chemistry 281:35, pages 25659-25669.
Crossref
Jennifer J. Westendorf. (2006) Transcriptional co-repressors of Runx2. Journal of Cellular Biochemistry 98:1, pages 54-64.
Crossref
Robert B. Lorsbach & James R. Downing. 2010. Childhood Leukemias. Childhood Leukemias 298 338 .
B.M. Schaubach, H.Y. Wen & R.E. Kellems. (2006) Regulation of Murine Ada Gene Expression in the Placenta by Transcription Factor RUNX1. Placenta 27:2-3, pages 269-277.
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Suk-Chul Bae & Yong Hee Lee. (2006) Phosphorylation, acetylation and ubiquitination: The molecular basis of RUNX regulation. Gene 366:1, pages 58-66.
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K. Bollerot, S. Romero, D. Dunon & T. Jaffredo. (2005) Core binding factor in the early avian embryo: cloning of Cbfβ and combinatorial expression patterns with Runx1. Gene Expression Patterns 6:1, pages 29-39.
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Hideyo HiraiIgor M SamokhvalovTetsuhiro FujimotoSatomi NishikawaJiro ImanishiShin-Ichi Nishikawa. (2005) Involvement of Runx1 in the down-regulation of fetal liver kinase-1 expression during transition of endothelial cells to hematopoietic cells. Blood 106:6, pages 1948-1955.
Crossref
Tania M. Schroeder, Eric D. Jensen & Jennifer J. Westendorf. (2005) Runx2: A master organizer of gene transcription in developing and maturing osteoblasts. Birth Defects Research Part C: Embryo Today: Reviews 75:3, pages 213-225.
Crossref
Kristina Jackson Behan, Jason Fair, Shalini Singh, Michael Bogwitz, Trent Perry, Vladimir Grubor, Fiona Cunningham, Charles D. Nichols, Tara L. Cheung, Philip Batterham & John Archie Pollock. (2005) Alternative splicing removes an Ets interaction domain from Lozenge during Drosophila eye development. Development Genes and Evolution 215:8, pages 423-435.
Crossref
Joseph R. Biggs, Youhong Zhang, Luke F. Peterson, Marileila Garcia, Dong-Er Zhang & Andrew S. Kraft. (2005) Phosphorylation of AML1/RUNX1 Regulates Its Degradation and Nuclear Matrix Association. Molecular Cancer Research 3:7, pages 391-401.
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Yoko Fukushima-NakaseYoshinori NaoeIchiro TaniuchiHajime HosoiTohru SugimotoTsukasa Okuda. (2005) Shared and distinct roles mediated through C-terminal subdomains of acute myeloid leukemia/Runt-related transcription factor molecules in murine development. Blood 105:11, pages 4298-4307.
Crossref
Jill Wildonger & Richard S. Mann. (2005) The t(8;21) translocation converts AML1 into a constitutive transcriptional repressor. Development 132:10, pages 2263-2272.
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Lan Anh Nguyen, Pier Paolo Pandolfi, Yukiko Aikawa, Yusuke Tagata, Misao Ohki & Issay Kitabayashi. (2005) Physical and functional link of the leukemia-associated factors AML1 and PML. Blood 105:1, pages 292-300.
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Youhong Zhang, Joseph R. Biggs & Andrew S. Kraft. (2004) Phorbol Ester Treatment of K562 Cells Regulates the Transcriptional Activity of AML1c through Phosphorylation. Journal of Biological Chemistry 279:51, pages 53116-53125.
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Hisako Gunji, Kazuo Waga, Fumihiko Nakamura, Kazuhiro Maki, Ko Sasaki, Yuichi Nakamura & Kinuko Mitani. (2004) TEL/AML1 shows dominant-negative effects over TEL as well as AML1. Biochemical and Biophysical Research Communications 322:2, pages 623-630.
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Yoshiaki Ito. (2004) Oncogenic potential of the RUNX gene family: ‘Overview’. Oncogene 23:24, pages 4198-4208.
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Luke F Peterson & Dong-Er Zhang. (2004) The 8;21 translocation in leukemogenesis. Oncogene 23:24, pages 4255-4262.
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Motohiro NishimuraYoko Fukushima-NakaseYasuko FujitaMitsushige NakaoShogo TodaNobuo KitamuraTatsuo AbeTsukasa Okuda. (2004) VWRPY motif–dependent and –independent roles of AML1/Runx1 transcription factor in murine hematopoietic development. Blood 103:2, pages 562-570.
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Lina Zhang, Stephen M Lukasik, Nancy A Speck & John H Bushweller. (2003) Structural and functional characterization of Runx1, CBFβ, and CBFβ-SMMHC. Blood Cells, Molecules, and Diseases 30:2, pages 147-156.
Crossref
Taketoshi Yoshida, Hirokazu Kanegane, Motomi Osato, Masatoshi Yanagida, Toshio Miyawaki, Yoshiaki Ito & Katsuya Shigesada. (2003) Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype–phenotype correlations. Blood Cells, Molecules, and Diseases 30:2, pages 184-193.
Crossref
Norio Asou. (2003) The role of a Runt domain transcription factor AML1/RUNX1 in leukemogenesis and its clinical implications. Critical Reviews in Oncology/Hematology 45:2, pages 129-150.
Crossref
Hee‐Jun Wee, Gang Huang, Katsuya Shigesada & Yoshiaki Ito. (2002) Serine phosphorylation of RUNX2 with novel potential functions as negative regulatory mechanisms. EMBO reports 3:10, pages 967-974.
Crossref
Taketoshi Yoshida, Hirokazu Kanegane, Motomi Osato, Masatoshi Yanagida, Toshio Miyawaki, Yoshiaki Ito & Katsuya Shigesada. (2002) Functional Analysis of RUNX2 Mutations in Japanese Patients with Cleidocranial Dysplasia Demonstrates Novel Genotype-Phenotype Correlations. The American Journal of Human Genetics 71:4, pages 724-738.
Crossref
Stefan Bäckström, Magnus Wolf-Watz, Christine Grundström, Torleif Härd, Thomas Grundström & Uwe H. Sauer. (2002) The RUNX1 Runt Domain at 1.25Å Resolution: A Structural Switch and Specifically Bound Chloride Ions Modulate DNA Binding. Journal of Molecular Biology 322:2, pages 259-272.
Crossref
Nancy A. Speck & D. Gary Gilliland. (2002) Core-binding factors in haematopoiesis and leukaemia. Nature Reviews Cancer 2:7, pages 502-513.
Crossref
Florence Bernardin & Alan D Friedman. (2002) AML1 stimulates G1 to S progression via its transactivation domain. Oncogene 21:20, pages 3247-3252.
Crossref
Nancy A. Speck. 2002. Wiley Encyclopedia of Molecular Medicine. Wiley Encyclopedia of Molecular Medicine.
John T. Swarthout, Richard C. D'Alonzo, Nagarajan Selvamurugan & Nicola C. Partridge. (2002) Parathyroid hormone-dependent signaling pathways regulating genes in bone cells. Gene 282:1-2, pages 1-17.
Crossref
Richard C. D'Alonzo, Nagarajan Selvamurugan, Stephen M. Krane & Nicola C. Partridge. 2002. Principles of Bone Biology. Principles of Bone Biology 251 264 .
Tsukasa Okuda, Motohiro Nishimura, Mitsushige Nakao & Yasuko Fujitaa. (2001) RUNX1/AML1: A Central Player in Hematopoiesis. International Journal of Hematology 74:3, pages 252-257.
Crossref
Z. S. Xiao, Shi-Guang Liu, T. K. Hinson & L. D. Quarles. (2001) Characterization of the upstream mouseCbfa1/Runx2 promoter. Journal of Cellular Biochemistry 82:4, pages 647-659.
Crossref
Jonathan D Licht. (2001) AML1 and the AML1-ETO fusion protein in the pathogenesis of t(8;21) AML. Oncogene 20:40, pages 5660-5679.
Crossref
S. Kaleem Zaidi, Amjad Javed, Je-Yong Choi, André J. van Wijnen, Janet L. Stein, Jane B. Lian & Gary S. Stein. (2001) A specific targeting signal directs Runx2/Cbfa1 to subnuclear domains and contributes to transactivation of the osteocalcin gene. Journal of Cell Science 114:17, pages 3093-3102.
Crossref
Mondira Kundu & Pu Paul Liu. (2001) Function of the inv(16) fusion gene CBFB-MYH11. Current Opinion in Hematology 8:4, pages 201-205.
Crossref
Husseini K. Manji, Gregory J. Moore & Guang Chen. (2018) Bipolar disorder: leads from the molecular and cellular mechanisms of action of mood stabilisers. British Journal of Psychiatry 178:S41, pages s107-s119.
Crossref
Takashi Nagata & Milton H Werner. (2001) Functional mutagenesis of AML1/RUNX1 and PEBP2β/CBFβ define distinct, non-overlapping sites for DNA recognition and heterodimerization by the runt domain1 1Edited by M. Yaniv. Journal of Molecular Biology 308:2, pages 191-203.
Crossref
Yasuko Fujita, Motohiro Nishimura, Masafumi Taniwaki, Tatsuo Abe & Tsukasa Okuda. (2001) Identification of an Alternatively Spliced Form of the Mouse AML1/RUNX1 Gene Transcript AML1c and Its Expression in Early Hematopoietic Development. Biochemical and Biophysical Research Communications 281:5, pages 1248-1255.
Crossref
Magnus Wolf-Watz, Stefan Bäckström, Thomas Grundström, Uwe Sauer & Torleif Härd. (2001) Chloride binding by the AML1/Runx1 transcription factor studied by NMR. FEBS Letters 488:1-2, pages 81-84.
Crossref
Jochen Hess, Dominique Porte, Christine Munz & Peter Angel. (2001) AP-1 and Cbfa/Runt Physically Interact and Regulate Parathyroid Hormone-dependent MMP13 Expression in Osteoblasts through a New Osteoblast-specific Element 2/AP-1 Composite Element. Journal of Biological Chemistry 276:23, pages 20029-20038.
Crossref
Keith W. McLarren, Francesca M. Theriault & Stefano Stifani. (2001) Association with the Nuclear Matrix and Interaction with Groucho and RUNX Proteins Regulate the Transcription Repression Activity of the Basic Helix Loop Helix Factor Hes1. Journal of Biological Chemistry 276:2, pages 1578-1584.
Crossref
Jane B. Lian & Gary S. Stein. 2001. Osteoporosis. Osteoporosis 21 71 .
Akihiko Yokoyama, Yasushi Kawaguchi, Issay Kitabayashi, Misao Ohki & Kanji Hirai. (2001) The Conserved Domain CR2 of Epstein–Barr Virus Nuclear Antigen Leader Protein Is Responsible Not Only for Nuclear Matrix Association but Also for Nuclear Localization. Virology 279:2, pages 401-413.
Crossref
Janice C. Telfer & Ellen V. Rothenberg. (2001) Expression and Function of a Stem Cell Promoter for the Murine CBFα2 Gene: Distinct Roles and Regulation in Natural Killer and T Cell Development. Developmental Biology 229:2, pages 363-382.
Crossref
John C Wheeler, Katsuya Shigesada, J Peter Gergen & Yoshiaki Ito. (2000) Mechanisms of transcriptional regulation by Runt domain proteins. Seminars in Cell & Developmental Biology 11:5, pages 369-375.
Crossref
James R Downing, Masakazu Higuchi, Noel Lenny & Allen Eng-Juh Yeoh. (2000) Alterations of the AML1 transcription factor in human leukemia. Seminars in Cell & Developmental Biology 11:5, pages 347-360.
Crossref
John H Bushweller. (2000) CBF—A biophysical perspective. Seminars in Cell & Developmental Biology 11:5, pages 377-382.
Crossref
Yu-Wen Zhang, Natsuo Yasui, Kosei Ito, Gang Huang, Makiko Fujii, Jun-ichi Hanai, Hiroshi Nogami, Takahiro Ochi, Kohei Miyazono & Yoshiaki Ito. (2000) A RUNX2/PEBP2 αA/ CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia . Proceedings of the National Academy of Sciences 97:19, pages 10549-10554.
Crossref
Thomas L. McCarthy, Changhua Ji, Yun Chen, Kenneth K. Kim, Masayoshi Imagawa, Yoshiaki Ito & Michael Centrella. (2000) Runt Domain Factor (Runx)-dependent Effects on CCAAT/ Enhancer-binding Protein δ Expression and Activity in Osteoblasts. Journal of Biological Chemistry 275:28, pages 21746-21753.
Crossref
A. JavedB. GuoS. HiebertJ.Y. ChoiJ. GreenS.C. ZhaoM.A. OsborneS. StifaniJ.L. SteinJ.B. LianA.J. van WijnenG.S. Stein. (2000) Groucho/TLE/R-esp proteins associate with the nuclear matrix and repress RUNX (CBF(alpha)/AML/PEBP2(alpha)) dependent activation of tissue-specific gene transcription. Journal of Cell Science 113:12, pages 2221-2231.
Crossref
AC Ward, DM Loeb, AA Soede-Bobok, IP Touw & AD Friedman. (2000) Regulation of granulopoiesis by transcription factors and cytokine signals. Leukemia 14:6, pages 973-990.
Crossref
Evangelia Pardali, Xiao-Qi Xie, Panagiotis Tsapogas, Susumu Itoh, Konstantinos Arvanitidis, Carl-Henrik Heldin, Peter ten Dijke, Thomas Grundström & Paschalis Sideras. (2000) Smad and AML Proteins Synergistically Confer Transforming Growth Factor β1 Responsiveness to Human Germ-line IgA Genes. Journal of Biological Chemistry 275:5, pages 3552-3560.
Crossref
Osamu Narumi, Seiichi Mori, Shuken Boku, Yoshihito Tsuji, Nobuo Hashimoto, Shin-Ichi Nishikawa & Yoshifumi Yokota. (2000) OUT, a Novel Basic Helix-Loop-Helix Transcription Factor with an Id-like Inhibitory Activity. Journal of Biological Chemistry 275:5, pages 3510-3521.
Crossref
Yu-Wen Zhang, Natsuo Yasui, Naoki Kakazu, Tatsuo Abe, Kenzo Takada, Shosuke Imai, Motohiko Sato, Shintaro Nomura, Takahiro Ochi, Shigeharu Okuzumi, Hiroshi Nogami, Toshiro Nagai, Hirohumi Ohashi & Yoshiaki Ito. (2000) PEBP2αA/CBFA1 mutations in Japanese cleidocranial dysplasia patients. Gene 244:1-2, pages 21-28.
Crossref
Bart Lutterbach, Jennifer J. Westendorf, Bryan Linggi, Stuart Isaac, Edward Seto & Scott W. Hiebert. (2000) A Mechanism of Repression by Acute Myeloid Leukemia-1, the Target of Multiple Chromosomal Translocations in Acute Leukemia. Journal of Biological Chemistry 275:1, pages 651-656.
Crossref
Keith W. McLarren, Rita Lo, Diane Grbavec, Kannan Thirunavukkarasu, Gerard Karsenty & Stefano Stifani. (2000) The Mammalian Basic Helix Loop Helix Protein HES-1 Binds to and Modulates the Transactivating Function of the Runt-related Factor Cbfa1. Journal of Biological Chemistry 275:1, pages 530-538.
Crossref
Katherine R Calvo, Paul Knoepfler, Shannon McGrath & Mark P Kamps. (2000) An inhibitory switch derepressed by Pbx, Hox, and Meis/Prep1 partners regulates DNA-binding by Pbx1 and E2a-Pbx1 and is dispensable for myeloid immortalization by E2a-Pbx1. Oncogene 18:56, pages 8033-8043.
Crossref
Sandra McNeil, Congmei Zeng, Kimberly S. Harrington, Scott Hiebert, Jane B. Lian, Janet L. Stein, André J. van Wijnen & Gary S. Stein. (1999) The t(8;21) chromosomal translocation in acute myelogenous leukemia modifies intranuclear targeting of the AML1/CBFα2 transcription factor. Proceedings of the National Academy of Sciences 96:26, pages 14882-14887.
Crossref
Husseini K. Manji, Robert McNamara, Guang Chen & Robert H. Lenox. (1999) Signalling pathways in the brain: Cellular transduction of mood stabilisation in the treatment of manic-depressive illness. Australian and New Zealand Journal of Psychiatry 33:s1, pages S65-S83.
Crossref
Yoshiaki Ito. (1999) Molecular basis of tissue-specific gene expression mediated by the Runt domain transcription factor PEBP2/CBF. Genes to Cells 4:12, pages 685-696.
Crossref
I. Quack, B. Vonderstrass, M. Stock, AS Aylsworth, A. Becker, L. Brueton, PJ Lee, F. Majewski, JB Mulliken, M. Suri, M. Zenker, S. Mundlos & F. Otto. (1999) Mutation Analysis of Core Binding Factor A1 in Patients with Cleidocranial Dysplasia. The American Journal of Human Genetics 65:5, pages 1268-1278.
Crossref
Bart Lutterbach, Yue Hou, Kristie L. Durst & Scott W. Hiebert. (1999) The inv(16) encodes an acute myeloid leukemia 1 transcriptional corepressor. Proceedings of the National Academy of Sciences 96:22, pages 12822-12827.
Crossref
Jun-ichi Hanai, Lin Feng Chen, Tomohiko Kanno, Naoko Ohtani-Fujita, Woo Young Kim, Wei-Hui Guo, Takeshi Imamura, Yasuhiro Ishidou, Minoru Fukuchi, Meng-Jiao Shi, Janet Stavnezer, Masahiro Kawabata, Kohei Miyazono & Yoshiaki Ito. (1999) Interaction and Functional Cooperation of PEBP2/CBF with Smads. Journal of Biological Chemistry 274:44, pages 31577-31582.
Crossref
Marcelo J Berardi, Chaohong Sun, Michael Zehr, Frits Abildgaard, Jeff Peng, Nancy A Speck & John H Bushweller. (1999) The Ig fold of the core binding factor α Runt domain is a member of a family of structurally and functionally related Ig-fold DNA-binding domains. Structure 7:10, pages 1247-1256.
Crossref
Haruhiko Akiyama, Tomohiko Kanno, Hiromu Ito, Anne Terry, Jim Neil, Yoshiaki Ito & Takashi Nakamura. (1999) Positive and negative regulation of chondrogenesis by splice variants of PEBP2?A/CBF?1 in clonal mouse EC cells, ATDC5. Journal of Cellular Physiology 181:1, pages 169-178.
Crossref
Ellen V. Rothenberg, Janice C. Telfer & Michele K. Anderson. (1999) Transcriptional regulation of lymphocyte lineage commitment. BioEssays 21:9, pages 726-742.
Crossref
Hideki Ogihara, Tomohiko Kanno, Eiichi Morii, Dae-Ki Kim, Young-Mi Lee, Motohiko Sato, Woo-Young Kim, Shintaro Nomura, Yoshiaki Ito & Yukihiko Kitamura. (1999) Synergy of PEBP2/CBF with mi transcription factor (MITF) for transactivation of mouse mast cell protease 6 gene. Oncogene 18:32, pages 4632-4639.
Crossref
James R. Downing. (1999) THE AML1-ETO CHIMAERIC TRANSCRIPTION FACTOR IN ACUTE MYELOID LEUKAEMIA: BIOLOGY AND CLINICAL SIGNIFICANCE. British Journal of Haematology 106:2, pages 296-308.
Crossref
Eiichi Morii, Hideki Ogihara, Tomohiko Kanno, Dae-Ki Kim, Shintaro Nomura, Yoshiaki Ito & Yukihiko Kitamura. (1999) Identification of the Region of mi Transcription Factor Which Is Responsible for the Synergy with PEBP2/CBF. Biochemical and Biophysical Research Communications 261:1, pages 53-57.
Crossref
Trista North, Ting-Lei Gu, Terryl Stacy, Qing Wang, Louisa Howard, Michael Binder, Miguel Marín-Padilla & Nancy A. Speck. (1999) Cbfa2 is required for the formation of intra-aortic hematopoietic clusters . Development 126:11, pages 2563-2575.
Crossref
Magnus Wolf-Watz, Xiao-Qi Xie, Magnus Holm, Thomas Grundstrom & Torleif Hard. (1999) Solution properties of the free and DNA-bound Runt domain of AML1. European Journal of Biochemistry 261:1, pages 251-260.
Crossref
Motomi OsatoNorio AsouEssam AbdallaKoyu HoshinoHiroshi YamasakiToshiya OkuboHitoshi SuzushimaKiyoshi TakatsukiTomohiko KannoKatsuya ShigesadaYoshiaki Ito. (1999) Biallelic and Heterozygous Point Mutations in the Runt Domain of theAML1/PEBP2B Gene Associated With Myeloblastic Leukemias. Blood 93:6, pages 1817-1824.
Crossref
Hideyuki Harada, Shuzo Tagashira, Masanori Fujiwara, Shinji Ogawa, Takashi Katsumata, Akira Yamaguchi, Toshihisa Komori & Masashi Nakatsuka. (1999) Cbfa1 Isoforms Exert Functional Differences in Osteoblast Differentiation. Journal of Biological Chemistry 274:11, pages 6972-6978.
Crossref
Guang Chen, Wei-Zhang Zeng, Pei-Xiong Yuan, Li-Dong Huang, Yi-Ming Jiang, Zhen-Hua Zhao & Husseini K. Manji. (1999) The Mood-Stabilizing Agents Lithium and Valproate RobustlIncrease the Levels of the Neuroprotective Protein bcl-2 in the CNS. Journal of Neurochemistry 72:2, pages 879-882.
Crossref
Jennifer J. Westendorf & Scott W. Hiebert. (1999) Mammalian runt-domain proteins and their roles in hematopoiesis, osteogenesis, and leukemia. Journal of Cellular Biochemistry 75:S32, pages 51-58.
Crossref
B.J. GRAVES, D.O. COWLEY, T.L. GOETZ, J.M. PETERSEN, M.D. JONSEN & M.E. GILLESPIE. (1998) Autoinhibition as a Transcriptional Regulatory Mechanism. Cold Spring Harbor Symposia on Quantitative Biology 63:0, pages 621-630.
Crossref

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