Citations for
1ATF4, RUNX2, SP7
Regulation and Role of Transcription Factors in Osteogenesis.
Chan WCW, Tan Z, To MKT, Chan D.
Int J Mol Sci. May 21;22(11):5445. doi: 10.3390/ijms22115445. 2021
2CBFB, IHH, RUNX2, SP7
Molecular Mechanism of Runx2-Dependent Bone Development.
Komori T.
Mol Cells. Feb 29;43(2):168-175. doi: 10.14348/molcells.2019.0244 2020
3LEF1, RUNX2, WNT3, WWTR1
Interaction of LEF1 with TAZ is necessary for the osteoblastogenic activity of Wnt3a.
Kida J, Hata K, Nakamura E, Yagi H, Takahata Y, Murakami T, Maeda Y, Nishimura R.
Sci Rep 8(1):10375. doi: 10.1038/s41598-018-28711-4. 2018
4NFIC, RUNX2, SP7
The Nfic-osterix pathway regulates ameloblast differentiation and enamel formation
Lee DS, Roh SY, Park JC.
Cell Tissue Res. Dec;374(3):531-540. doi: 10.1007/s00441-018-2901-3. Epub 2018 Aug 9 2018
5CAMK2N1, RUNX2
RUNX3 and CAMK2N1 hypermethylation as prognostic marker for epithelial ovarian cancer.
Häfner N, Steinbach D, Jansen L, Diebolder H, Dürst M, Runnebaum IB.
Int J Cancer 138(1):217-28. doi: 10.1002/ijc.29690. 2016
6IPO8, RUNX2
RUNX2 controls human IPO8 basal transcription in Saos-2 cells
Xiong J, Hu Z, Wang T, Xu X, Liu J, Wu P, Che X, Li W.
Mol Med Rep. Aug;14(2):1418-24. doi: 10.3892/mmr.2016.5356. Epub 2016 Jun 1 2016
7RUNX2, SOX6
Functional analyses reveal the essential role of SOX6 and RUNX2 in the communication of chondrocyte and osteoblast.
Zhang Y, Yang TL, Li X, Guo Y.
Osteoporos Int 26(2):553-61. doi: 10.1007/s00198-014-2882-3. Epub 2014 Sep 12. 2015
8KDM6B, RUNX2
JMJD3 promotes chondrocyte proliferation and hypertrophy during endochondral bone formation in mice.
Zhang F, Xu L, Xu L, Xu Q, Li D, Yang Y, Karsenty G, Chen CD.
J Mol Cell Biol 7(1):23-34. doi: 10.1093/jmcb/mjv003. Epub 2015 Jan 13. 2015
9CTNNB1, HDAC7, RUNX2
Histone deacetylase 7 (Hdac7) suppresses chondrocyte proliferation and β-catenin activity during endochondral ossification.
Bradley EW, Carpio LR, Olson EN, Westendorf JJ.
J Biol Chem 290(1):118-26. doi: 10.1074/jbc.M114.596247. Epub 2014 Nov 11. 2015
10RUNX2, WNT1
Crucial roles of canonical Runx2-dependent pathway on Wnt1-induced osteoblastic differentiation of human periodontal ligament fibroblasts.
Kook SH, Heo JS, Lee JC.
Mol Cell Biochem 402(1-2):213-23. doi: 10.1007/s11010-015-2329-y. 2015
11RUNX2, SP7
Sp7 and Runx2 molecular complex synergistically regulate expression of target genes.
Rashid H, Ma C, Chen H, Wang H, Hassan MQ, Sinha K, de Crombrugghe B, Javed A.
Connect Tissue Res 55 Suppl 1:83-7. doi: 10.3109/03008207.2014.923872. 2014
12RUNX2, SMURF1
A feedback loop between RUNX2 and the E3 ligase SMURF1 in regulation of differentiation of human dental pulp stem cells.
Yang F, Xu N, Li D, Guan L, He Y, Zhang Y, Lu Q, Zhang X.
J Endod 40(10):1579-86. doi: 10.1016/j.joen.2014.04.010. Epub 2014 Jun 11. 2014
13RUNX2, SMURF1
A feedback loop between RUNX2 and the E3 ligase SMURF1 in regulation of differentiation of human dental pulp stem cells.
Yang F, Xu N, Li D, Guan L, He Y, Zhang Y, Lu Q, Zhang X.
J Endod 40(10):1579-86. doi: 10.1016/j.joen.2014.04.010. Epub 2014 Jun 11. 2014
14NAA10, RUNX2
NAA10 controls osteoblast differentiation and bone formation as a feedback regulator of Runx2.
Yoon H, Kim HL, Chun YS, Shin DH, Lee KH, Shin CS, Lee DY, Kim HH, Lee ZH, Ryoo HM, Lee MN, Oh GT, Park JW.
Nat Commun 5:5176. doi: 10.1038/ncomms6176. 2014
15MAP2K5, MAPK7, RUNX2
The MEK5/ERK5 pathway mediates fluid shear stress promoted osteoblast differentiation.
Zhao LG, Chen SL, Teng YJ, An LP, Wang J, Ma JL, Xia YY.
Connect Tissue Res 55(2):96-102. doi: 10.3109/03008207.2013.853755. Epub 2014 Jan 10. 2014
16DUP6PM, RUNX2
Pure de novo partial trisomy 6p in a girl with craniosynostosis.
Varvagiannis K, Stefanidou A, Gyftodimou Y, Lord H, Williams L, Sarri C, Pandelia E, Bazopoulou-Kyrkanidou E, Noakes C, Lester T, Wilkie AO, Petersen MB.
Am J Med Genet A m J Med Genet A. 2013 Jan 10. doi: 10.1002/ajmg.a.35727. [Epub ahead of print] 2013
17KAT2B, RUNX2
PCAF acetylates Runx2 and promotes osteoblast differentiation.
Wang CY, Yang SF, Wang Z, Tan JM, Xing SM, Chen DC, Xu SM, Yuan W.
J Bone Miner Metab Bone Miner Metab. 2013 Mar 7. [Epub ahead of print] 2013
18DLX5, GATA4, RUNX2
GATA4 negatively regulates osteoblast differentiation by downregulation of Runx2.
Song I, Kim K, Kim JH, Lee YK, Jung HJ, Byun HO, Yoon G, Kim N.
BMB Rep MB Rep. 2013 Dec 22. pii: 2539. [Epub ahead of print] 2013
19BGLAP, IBSP, KDM6B, RUNX2, SP7
Histone demethylase Jmjd3 regulates osteoblast differentiation via transcription factors Runx2 and osterix.
Yang D, Okamura H, Nakashima Y, Haneji T.
J Biol Chem 288(47):33530-41. doi: 10.1074/jbc.M113.497040. Epub 2013 Oct 8. 2013
20RUNX2, TSSC1
Runx2 induces bone osteolysis by transcriptional suppression of TSSC1.
Wang DC, Wang HF, Yuan ZN.
Biochem Biophys Res Commun 438(4):635-9. doi: 10.1016/j.bbrc.2013.07.131. Epub 2013 Aug 8. 2013
21CBL, RUNX2, STAT5A
Promotion of osteoblast differentiation in mesenchymal cells through Cbl-mediated control of STAT5 activity.
Dieudonne FX, Sévère N, Biosse-Duplan M, Weng JJ, Su Y, Marie PJ.
Stem Cells 31(7):1340-9. doi: 10.1002/stem.1380. 2013
22AXIN2, HDAC3, RUNX2
Runx2 protein represses Axin2 expression in osteoblasts and is required for craniosynostosis in Axin2-deficient mice.
McGee-Lawrence ME, Li X, Bledsoe KL, Wu H, Hawse JR, Subramaniam M, Razidlo DF, Stensgard BA, Stein GS, van Wijnen AJ, Lian JB, Hsu W, Westendorf JJ.
J Biol Chem 288(8):5291-302. doi: 10.1074/jbc.M112.414995. Epub 2013 Jan 7. 2013
23ALCAM, RUNX2
Hierarchical organization of osteoblasts reveals the significant role of CD166 in hematopoietic stem cell maintenance and function.
Chitteti BR, Cheng YH, Kacena MA, Srour EF.
Bone 54(1):58-67. doi: 10.1016/j.bone.2013.01.038. Epub 2013 Jan 28. 2013
24DCLK1, RUNX2
The microtubule-associated protein DCAMKL1 regulates osteoblast function via repression of Runx2.
Zou W, Greenblatt MB, Brady N, Lotinun S, Zhai B, de Rivera H, Singh A, Sun J, Gygi SP, Baron R, Glimcher LH, Jones DC.
J Exp Med 210(9):1793-806. doi: 10.1084/jem.20111790. Epub 2013 Aug 5. 2013
25RUNX2, RUNX3
Functional role of Runx3 in the regulation of aggrecan expression during cartilage development.
Wigner NA, Soung do Y, Einhorn TA, Drissi H, Gerstenfeld LC.
J Cell Physiol 228(11):2232-42. doi: 10.1002/jcp.24396. 2013
26RUNX2, S100A16
S100A16 inhibits osteogenesis but stimulates adipogenesis.
Li D, Zhang R, Zhu W, Xue Y, Zhang Y, Huang Q, Liu M, Liu Y.
Mol Biol Rep 40(5):3465-73. doi: 10.1007/s11033-012-2413-2. Epub 2013 Mar 25. 2013
27ATF6, RUNX2, XBP1
XBP1S associates with RUNX2 and regulates chondrocyte hypertrophy.
Liu Y, Zhou J, Zhao W, Li X, Jiang R, Liu C, Guo FJ.
J Biol Chem 287(41):34500-13. doi: 10.1074/jbc.M112.385922. Epub 2012 Aug 3. Retraction in: J Biol Chem. 2015 Apr 24;290(17):10643. 2012
28CEBPB, EPAS1, MMP13, RUNX2
C/EBPB and RUNX2 cooperate to degrade cartilage with MMP-13 as the target and HIF-2á as the inducer in chondrocytes.
Hirata M, Kugimiya F, Fukai A, Saito T, Yano F, Ikeda T, Mabuchi A, Sapkota BR, Akune T, Nishida N, Yoshimura N, Nakagawa T, Tokunaga K, Nakamura K, Chung UI, Kawaguchi H.
Hum Mol Genet 21(5):1111-23. doi: 10.1093/hmg/ddr540. Epub 2011 Nov 17. 2012
29MMP13, RUNX2, SP7
Osterix regulates calcification and degradation of chondrogenic matrices through matrix metalloproteinase 13 (MMP13) expression in association with transcription factor Runx2 during endochondral ossification.
Nishimura R, Wakabayashi M, Hata K, Matsubara T, Honma S, Wakisaka S, Kiyonari H, Shioi G, Yamaguchi A, Tsumaki N, Akiyama H, Yoneda T.
J Biol Chem 287(40):33179-90. Epub 2012 Aug 6. 2012
30RUNX2, SRF
Serum response factor regulates bone formation via IGF-1 and Runx2 signals.
Chen J, Yuan K, Mao X, Miano JM, Wu H, Chen Y.
J Bone Miner Res 27(8):1659-68. doi: 10.1002/jbmr.1607. 2012
31EHMT2, RUNX2
Recruitment of coregulator G9a by Runx2 for selective enhancement or suppression of transcription.
Purcell DJ, Khalid O, Ou CY, Little GH, Frenkel B, Baniwal SK, Stallcup MR.
J Cell Biochem 113(7):2406-14. doi: 10.1002/jcb.24114. 2012
32HIF1A, RUNX2, VEGFA
Runx2 protein stabilizes hypoxia-inducible factor-1α through competition with von Hippel-Lindau protein (pVHL) and stimulates angiogenesis in growth plate hypertrophic chondrocytes.
Lee SH, Che X, Jeong JH, Choi JY, Lee YJ, Lee YH, Bae SC, Lee YM.
J Biol Chem 287(18):14760-71. doi: 10.1074/jbc.M112.340232. Epub 2012 Feb 20. 2012
33RUNX2
Biomechanical stimulation of osteoblast gene expression requires phosphorylation of the RUNX2 transcription factor.
Li Y, Ge C, Long JP, Begun DL, Rodriguez JA, Goldstein SA, Franceschi RT.
J Bone Miner Res 27(6):1263-74. doi: 10.1002/jbmr.1574. 2012
34RUNX2
Targeting Runx2 expression in hypertrophic chondrocytes impairs endochondral ossification during early skeletal development.
Ding M, Lu Y, Abbassi S, Li F, Li X, Song Y, Geoffroy V, Im HJ, Zheng Q.
J Cell Physiol 227(10):3446-56. doi: 10.1002/jcp.24045. 2012
35RUNX2
Genomic promoter occupancy of runt-related transcription factor RUNX2 in Osteosarcoma cells identifies genes involved in cell adhesion and motility.
van der Deen M, Akech J, Lapointe D, Gupta S, Young DW, Montecino MA, Galindo M, Lian JB, Stein JL, Stein GS, van Wijnen AJ.
J Biol Chem 287(7):4503-17. doi: 10.1074/jbc.M111.287771. Epub 2011 Dec 9. 2012
36HTR2A, HTR2B, HTR2C, PTHLH, RUNX2
Mammary gland serotonin regulates parathyroid hormone-related protein and other bone-related signals.
Hernandez LL, Gregerson KA, Horseman ND.
Am J Physiol Endocrinol Metab 302(8):E1009-15. doi: 10.1152/ajpendo.00666.2011. Epub 2012 Feb 7. 2012
37ATF6, BGLAP, BMP2, RUNX2
BMP2 protein regulates osteocalcin expression via Runx2-mediated Atf6 gene transcription.
Jang WG, Kim EJ, Kim DK, Ryoo HM, Lee KB, Kim SH, Choi HS, Koh JT.
J Biol Chem 287(2):905-15. doi: 10.1074/jbc.M111.253187. Epub 2011 Nov 18. 2012
38NELL1, RUNX2, SOX9
Calvarial cleidocraniodysplasia-like defects with ENU-induced Nell-1 deficiency.
Zhang X, Ting K, Pathmanathan D, Ko T, Chen W, Chen F, Lee H, James AW, Siu RK, Shen J, Culiat CT, Soo C.
J Craniofac Surg 23(1):61-6. doi: 10.1097/SCS.0b013e318240c8c4. 2012
39PIP, RUNX2
Runx2 controls a feed-forward loop between androgen and prolactin-induced protein (PIP) in stimulating T47D cell proliferation.
Baniwal SK, Little GH, Chimge NO, Frenkel B.
J Cell Physiol 227(5):2276-82. doi: 10.1002/jcp.22966. 2012
40FOXO1, RUNX2
FOXO1 inhibits Runx2 transcriptional activity and prostate cancer cell migration and invasion.
Zhang H, Pan Y, Zheng L, Choe C, Lindgren B, Jensen ED, Westendorf JJ, Cheng L, Huang H.
Cancer Res 71(9):3257-67. Epub 2011 Apr 19. 2011
41RUNX2
The role of runt-related transcription factor 2 (Runx2) in the late stage of odontoblast differentiation and dentin formation.
Li S, Kong H, Yao N, Yu Q, Wang P, Lin Y, Wang J, Kuang R, Zhao X, Xu J, Zhu Q, Ni L.
Biochem Biophys Res Commun 410(3):698-704. Epub 2011 Jun 15. 2011
42BMP2, RUNX2
Bone morphogenetic protein-2 activates NADPH oxidase to increase endoplasmic reticulum stress and human coronary artery smooth muscle cell calcification.
Liberman M, Johnson RC, Handy DE, Loscalzo J, Leopold JA.
Biochem Biophys Res Commun 413(3):436-41. Epub 2011 Aug 30. 2011
43PANX3, RUNX2
Pannexin 3 is a novel target for Runx2, expressed by osteoblasts and mature growth plate chondrocytes.
Bond SR, Lau A, Penuela S, Sampaio AV, Underhill TM, Laird DW, Naus CC.
J Bone Miner Res 26(12):2911-22. doi: 10.1002/jbmr.509. 2011
44COL10A1, RUNX2
Runx2 contributes to murine Col10a1 gene regulation through direct interaction with its cis-enhancer.
Li F, Lu Y, Ding M, Napierala D, Abbassi S, Chen Y, Duan X, Wang S, Lee B, Zheng Q.
J Bone Miner Res 26(12):2899-910. doi: 10.1002/jbmr.504. 2011
45RUNX2
Early onset of Runx2 expression caused craniosynostosis, ectopic bone formation, and limb defects.
Maeno T, Moriishi T, Yoshida CA, Komori H, Kanatani N, Izumi S, Takaoka K, Komori T.
Bone 49(4):673-82. doi: 10.1016/j.bone.2011.07.023. Epub 2011 Jul 23. 2011
46HMGB2, LEF1, RUNX2
Expression patterns and function of chromatin protein HMGB2 during mesenchymal stem cell differentiation.
Taniguchi N, Caramés B, Hsu E, Cherqui S, Kawakami Y, Lotz M.
J Biol Chem 286(48):41489-98. doi: 10.1074/jbc.M111.236984. Epub 2011 Sep 2. 2011
47NKX3-2, RUNX2
Nkx3.2-induced suppression of Runx2 is a crucial mediator of hypoxia-dependent maintenance of chondrocyte phenotypes.
Kawato Y, Hirao M, Ebina K, Tamai N, Shi K, Hashimoto J, Yoshikawa H, Myoui A.
Biochem Biophys Res Commun 416(1-2):205-10. doi: 10.1016/j.bbrc.2011.11.026. Epub 2011 Nov 10. 2011
48NKX2-1, RUNX2
Thyroid-specific gene expression in chondrocytes.
Endo T, Kobayashi T.
Biochem Biophys Res Commun 416(3-4):227-31. doi: 10.1016/j.bbrc.2011.08.122. Epub 2011 Sep 16. 2011
49FGF2, RUNX2
Fibroblast growth factor-2 induces osteogenic differentiation through a Runx2 activation in vascular smooth muscle cells.
Nakahara T, Sato H, Shimizu T, Tanaka T, Matsui H, Kawai-Kowase K, Sato M, Iso T, Arai M, Kurabayashi M.
Biochem Biophys Res Commun 394(2):243-8. Epub 2009 Nov 10. 2010
50RUNX2, TLE1, UBTF
Transcriptional corepressor TLE1 functions with Runx2 in epigenetic repression of ribosomal RNA genes.
Ali SA, Zaidi SK, Dobson JR, Shakoori AR, Lian JB, Stein JL, van Wijnen AJ, Stein GS.
Proc Natl Acad Sci U S A 107(9):4165-9. Epub 2010 Feb 16. 2010
51RUNX2
Runx2 association with progression of prostate cancer in patients: mechanisms mediating bone osteolysis and osteoblastic metastatic lesions.
Akech J, Wixted JJ, Bedard K, van der Deen M, Hussain S, Guise TA, van Wijnen AJ, Stein JL, Languino LR, Altieri DC, Pratap J, Keller E, Stein GS, Lian JB.
Oncogene 29(6):811-21. Epub 2009 Nov 16. 2010
52RUNX2
FGF2-activated ERK mitogen-activated protein kinase enhances Runx2 acetylation and stabilization.
Park OJ, Kim HJ, Woo KM, Baek JH, Ryoo HM.
J Biol Chem 285(6):3568-74. Epub 2009 Dec 10. 2010
53RUNX2
Runx2 regulates survivin expression in prostate cancer cells.
Lim M, Zhong C, Yang S, Bell AM, Cohen MB, Roy-Burman P.
Lab Invest 90(2):222-33. Epub 2009 Nov 30. 2010
54RUNX2
Regulation of bone development and extracellular matrix protein genes by RUNX2.
Komori T.
Cell Tissue Res 339(1):189-95. Epub 2009 Aug 1. Review. 2010
55CCD, RUNX2
Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2.
El-Gharbawy AH, Peeden JN Jr, Lachman RS, Graham JM Jr, Moore SR, Rimoin DL.
Am J Med Genet A 152A(1):169-74.PMID: 20014132 2010
56RUNX2
Copy number variation analysis in single-suture craniosynostosis: Multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis.
Mefford HC, Shafer N, Antonacci F, Tsai JM, Park SS, Hing AV, Rieder MJ, Smyth MD, Speltz ML, Eichler EE, Cunningham ML.
Am J Med Genet A 152A(9):2203-10.PMID: 20683987 2010
57HES1, HES2, ID4, RUNX2
Id4, a new candidate gene for senile osteoporosis, acts as a molecular switch promoting osteoblast differentiation.
Tokuzawa Y, Yagi K, Yamashita Y, Nakachi Y, Nikaido I, Bono H, Ninomiya Y, Kanesaki-Yatsuka Y, Akita M, Motegi H, Wakana S, Noda T, Sablitzky F, Arai S, Kurokawa R, Fukuda T, Katagiri T, Schönbach C, Suda T, Mizuno Y, Okazaki Y.
PLoS Genet 6(7):e1001019.PMID: 20628571 2010
58ARID4A, RUNX2
Retinoblastoma binding protein-1 (RBP1) is a Runx2 coactivator and promotes osteoblastic differentiation.
Monroe DG, Hawse JR, Subramaniam M, Spelsberg TC.
BMC Musculoskelet Disord 11:104.PMID: 20509905 2010
59MMP20, ODAM, RUNX2
The odontogenic ameloblast-associated protein (ODAM) cooperates with RUNX2 and modulates enamel mineralization via regulation of MMP-20.
Lee HK, Lee DS, Ryoo HM, Park JT, Park SJ, Bae HS, Cho MI, Park JC.
J Cell Biochem 111(3):755-67. 2010
60FOXO1, RUNX2
Foxo1, a novel regulator of osteoblast differentiation and skeletogenesis.
Teixeira CC, Liu Y, Thant LM, Pang J, Palmer G, Alikhani M.
J Biol Chem 285(40):31055-65. Epub 2010 Jul 22. 2010
61RUNX2, ZNF521
Zfp521 controls bone mass by HDAC3-dependent attenuation of Runx2 activity.
Hesse E, Saito H, Kiviranta R, Correa D, Yamana K, Neff L, Toben D, Duda G, Atfi A, Geoffroy V, Horne WC, Baron R.
J Cell Biol 191(7):1271-83. Epub 2010 Dec 20. 2010
62HDAC7, RUNX2
Bone morphogenic protein 2 activates protein kinase D to regulate histone deacetylase 7 localization and repression of Runx2.
Jensen ED, Gopalakrishnan R, Westendorf JJ.
J Biol Chem 284(4):2225-34. Epub 2008 Nov 21. 2009
63RUNX2, SNAI1
Snail1 controls bone mass by regulating Runx2 and VDR expression during osteoblast differentiation.
de Frutos CA, Dacquin R, Vega S, Jurdic P, Machuca-Gayet I, Nieto MA.
EMBO J 28(6):686-96. Epub 2009 Feb 5. 2009
64CCD, RUNX2
A Runx2 threshold for the cleidocranial dysplasia phenotype.
Lou Y, Javed A, Hussain S, Colby J, Frederick D, Pratap J, Xie R, Gaur T, van Wijnen AJ, Jones SN, Stein GS, Lian JB, Stein JL.
Hum Mol Genet 18(3):556-68. Epub 2008 Nov 20. 2009
65MMP13, PTH, RUNX2
Identification and characterization of Runx2 phosphorylation sites involved in matrix metalloproteinase-13 promoter activation.
Selvamurugan N, Shimizu E, Lee M, Liu T, Li H, Partridge NC.
FEBS Lett 583(7):1141-6. Epub 2009 Mar 3. 2009
66HDAC4, RUNX2, VEGFA
HDAC4 represses vascular endothelial growth factor expression in chondrosarcoma by modulating RUNX2 activity.
Sun X, Wei L, Chen Q, Terek RM.
J Biol Chem 284(33):21881-90. Epub 2009 Jun 9.PMID: 19509297 2009
67FGF8, RUNX2
FGF8 regulates myogenesis and induces Runx2 expression and osteoblast differentiation in cultured cells.
Omoteyama K, Takagi M.
J Cell Biochem 106(4):546-52.PMID: 19170063 2009
68DSPP, RUNX2, SP7
Runx2, osx, and dspp in tooth development.
Chen S, Gluhak-Heinrich J, Wang YH, Wu YM, Chuang HH, Chen L, Yuan GH, Dong J, Gay I, MacDougall M.
J Dent Res 88(10):904-9. 2009
69CCD, RUNX2
De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia.
Purandare SM, Mendoza-Londono R, Yatsenko SA, Napierala D, Scott DA, Sibai T, Casas K, Wilson P, Lee J, Muneer R, Leonard JC, Ramji FG, Lachman R, Li S, Stankiewicz P, Lee B, Mulvihill JJ.
Am J Med Genet A 146(4):453-8. 2008
70RUNX2, SP7
Upregulation of Runx2 and Osterix during in vitro chondrogenesis of human adipose-derived stromal cells.
Rich JT, Rosov‡ I, Nolta JA, Myckatyn TM, Sandell LJ, McAlinden A.
Biochem Biophys Res Commun 372(1):230-5. Epub 2008 May 13. 2008
71RUNX2, TRPS1
Uncoupling of chondrocyte differentiation and perichondrial mineralization underlies the skeletal dysplasia in tricho-rhino-phalangeal syndrome.
Napierala D, Sam K, Morello R, Zheng Q, Munivez E, Shivdasani RA, Lee B.
Hum Mol Genet 17(14):2244-54. Epub 2008 Apr 17. 2008
72AIRE, ATR, BCOR, CCD, COL1A1, COL1A2, CRDAI, CYP27B1, DLX", FTC1, GALNT3, HPC3, NHS, OFCD, OI1A, OI1B, PCNT, PDDR, PGA1, RUNX2, SCKL, SCKL1, SCKL2, SCKL3, SHH, SIOD, SMARCAL1, TDOS, VDDR2, VDR, WHS
The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvement.
Bailleul-Forestier I, Berdal A, Vinckier F, de Ravel T, Fryns JP, Verloes A.
Eur J Med Genet 51(5):383-408. Epub 2008 May 23. Review. 2008
73GPER1, RGS2, RUNX2
Runx2 regulates G protein-coupled signaling pathways to control growth of osteoblast progenitors.
Teplyuk NM, Galindo M, Teplyuk VI, Pratap J, Young DW, Lapointe D, Javed A, Stein JL, Lian JB, Stein GS, van Wijnen AJ.
J Biol Chem 283(41):27585-97. Epub 2008 Jul 14. 2008
74RUNX2, SP7
BMP2 regulates Osterix through Msx2 and Runx2 during osteoblast differentiation.
Matsubara T, Kida K, Yamaguchi A, Hata K, Ichida F, Meguro H, Aburatani H, Nishimura R, Yoneda T.
J Biol Chem 283(43):29119-25. Epub 2008 Aug 14. 2008
75NELL1, RUNX2
Involvement of MAPK signaling molecules and Runx2 in the NELL1-induced osteoblastic differentiation.
Bokui N, Otani T, Igarashi K, Kaku J, Oda M, Nagaoka T, Seno M, Tatematsu K, Okajima T, Matsuzaki T, Ting K, Tanizawa K, Kuroda S.
FEBS Lett 582(2):365-71. Epub 2007 Dec 17.PMID: 18082140 2008
76RUNX2
Runx2 represses myocardin-mediated differentiation and facilitates osteogenic conversion of vascular smooth muscle cells.
Tanaka T, Sato H, Doi H, Yoshida CA, Shimizu T, Matsui H, Yamazaki M, Akiyama H, Kawai-Kowase K, Iso T, Komori T, Arai M, Kurabayashi M.
Mol Cell Biol 28(3):1147-60. Epub 2007 Nov 26.PMID: 18039851 2008
77RUNX1, RUNX2, RUNX3, STAT5B
Physical and functional interactions between STAT5 and Runx transcription factors.
Ogawa S, Satake M, Ikuta K.
J Biochem 143(5):695-709. Epub 2008 Feb 22.PMID: 18296717 2008
78RUNX1, RUNX2, CCD, FPDAML
Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.
Matheny CJ, Speck ME, Cushing PR, Zhou Y, Corpora T, Regan M, Newman M, Roudaia L, Speck CL, Gu TL, Griffey SM, Bushweller JH, Speck NA.
EMBO J 26(4):1163-75. Epub 2007 Feb 8. 2007
79NELL1, RUNX2
Craniosynostosis-associated gene nell-1 is regulated by runx2.
Truong T, Zhang X, Pathmanathan D, Soo C, Ting K.
J Bone Miner Res 22(1):7-18. 2007
80NFATC2, RUNX2
Regulation of NFATc2 gene expression by the transcription factor Runx2.
Thirunavukkarasu K, Pei Y, Moore TL, Wei T, Wang H, Chandrasekhar S.
Mol Biol Rep 34(1):1-10. Epub 2006 Nov 11. 2007
81RUNX2
Mitotic control of RUNX2 phosphorylation by both CDK1/cyclin B kinase and PP1/PP2A phosphatase in osteoblastic cells.
Rajgopal A, Young DW, Mujeeb KA, Stein JL, Lian JB, van Wijnen AJ, Stein GS.
J Cell Biochem 100(6):1509-17. 2007
82CCD, RUNX2
A novel mutation of gene CBFA1/RUNX2 in cleidocranial dysplasia.
Lo Muzio L, Tetè S, Mastrangelo F, Cazzolla AP, Lacaita MG, Margaglione M, Campisi G.
Ann Clin Lab Sci 37(2):115-20. 2007
83RUNX1, RUNX2, RUNX3
Runx3/AML2/Cbfa3 regulates early and late chondrocyte differentiation.
Soung do Y, Dong Y, Wang Y, Zuscik MJ, Schwarz EM, O'Keefe RJ, Drissi H.
J Bone Miner Res 22(8):1260-70. 2007
84FLNB, RUNX2
Filamin B represses chondrocyte hypertrophy in a Runx2/Smad3-dependent manner.
Zheng L, Baek HJ, Karsenty G, Justice MJ.
J Cell Biol 178(1):121-8. 2007
85RUNX2, TRAM2
Identification of novel Runx2 targets in osteoblasts: cell type-specific BMP-dependent regulation of Tram2.
Pregizer S, Barski A, Gersbach CA, García AJ, Frenkel B.
J Cell Biochem 102(6):1458-71.PMID: 17486635 2007
86RUNX2
Runx2 deficiency and defective subnuclear targeting bypass senescence to promote immortalization and tumorigenic potential.
Zaidi SK, Pande S, Pratap J, Gaur T, Grigoriu S, Ali SA, Stein JL, Lian JB, van Wijnen AJ, Stein GS.
Proc Natl Acad Sci U S A 104(50):19861-6. Epub 2007 Dec 5. 2007
87FGF18, RUNX2
Runx2 inhibits chondrocyte proliferation and hypertrophy through its expression in the perichondrium.
Hinoi E, Bialek P, Chen YT, Rached MT, Groner Y, Behringer RR, Ornitz DM, Karsenty G.
Genes Dev 20(21):2937-42. Epub 2006 Oct 18. 2006
88CMPD1, RUNX2, SOX9
Dominance of SOX9 function over RUNX2 during skeletogenesis.
Zhou G, Zheng Q, Engin F, Munivez E, Chen Y, Sebald E, Krakow D, Lee B.
Proc Natl Acad Sci U S A 103(50):19004-9. Epub 2006 Dec 1. 2006
89RUNX2
Cbfa-1 (Runx-2) and osteocalcin expression by human osteoblasts in heparin osteoporosis in vitro.
Handschin AE, Egermann M, Trentz O, Wanner GA, Kock HJ, Zund G, Trentz OA.
Clin Appl Thromb Hemost 12(4):465-72. 2006
90TGFB1, TGFBR1, RUNX2
Repetitive exposure to TGF-beta suppresses TGF-beta type I receptor expression by differentiated osteoblasts.
Kim KK, Ji C, Chang W, Wells RG, Gundberg CM, McCarthy TL, Centrella M.
Gene 379:175-84. Epub 2006 May 19. 2006
91RUNX2
Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype.
Kim HJ, Nam SH, Kim HJ, Park HS, Ryoo HM, Kim SY, Cho TJ, Kim SG, Bae SC, Kim IS, Stein JL, van Wijnen AJ, Stein GS, Lian JB, Choi JY.
J Cell Physiol 207(1):114-22. 2006
92BMP4, RUNX2
Different roles of Runx2 during early neural crest-derived bone and tooth development.
James MJ, JŠrvinen E, Wang XP, Thesleff I.
J Bone Miner Res 21(7):1034-44. 2006
93RUNX2, SMAD6, SMURF1
Smad6 interacts with Runx2 and mediates Smad ubiquitin regulatory factor 1-induced Runx2 degradation.
Shen R, Chen M, Wang YJ, Kaneki H, Xing L, O'keefe RJ, Chen D.
J Biol Chem 281(6):3569-76. Epub 2005 Nov 18. 2006
94RUNX2
Impaired intranuclear trafficking of Runx2 (AML3/CBFA1) transcription factors in breast cancer cells inhibits osteolysis in vivo.
Javed A, Barnes GL, Pratap J, Antkowiak T, Gerstenfeld LC, van Wijnen AJ, Stein JL, Lian JB, Stein GS.
Proc Natl Acad Sci U S A 102(5):1454-9. Epub 2005 Jan 21. 2005
95TWIST1, FGFR2, ACS3, RUNX2
A role for fibroblast growth factor receptor-2 in the altered osteoblast phenotype induced by Twist haploinsufficiency in the Saethre-Chotzen syndrome.
Guenou H, Kaabeche K, Mee SL, Marie PJ.
Hum Mol Genet 14(11):1429-39. Epub 2005 Apr 13. 2005
96CCD, RUNX2
Dysregulation of chondrogenesis in human cleidocranial dysplasia.
Zheng Q, Sebald E, Zhou G, Chen Y, Wilcox W, Lee B, Krakow D.
Am J Hum Genet 77(2):305-12. Epub 2005 Jun 10. 2005
97CCD, HPE3, SHH, RUNX2
Holoprosencephaly and cleidocranial dysplasia in a patient due to two position-effect mutations: case report and review of the literature.
Fernandez BA, Siegel-Bartelt J, Herbrick JA, Teshima I, Scherer SW.
Clin Genet 68(4):349-59. 2005
98IBSP, RUNX2
Cooperative interactions between RUNX2 and homeodomain protein-binding sites are critical for the osteoblast-specific expression of the bone sialoprotein gene.
Roca H, Phimphilai M, Gopalakrishnan R, Xiao G, Franceschi RT.
J Biol Chem 280(35):30845-55. Epub 2005 Jul 5. 2005
99CCD, RUNX2
Functional analysis of a novel RUNX2 missense mutation found in a family with cleidocranial dysplasia.
Puppin C, Pellizzari L, Fabbro D, Fogolari F, Tell G, Tessa A, Santorelli FM, Damante G.
J Hum Genet 50(12):679-83. Epub 2005 Oct 22. 2005
100CBFB, MYH11, RUNX2
Identification of genes that synergize with Cbfb-MYH11 in the pathogenesis of acute myeloid leukemia.
Castilla LH, Perrat P, Martinez NJ, Landrette SF, Keys R, Oikemus S, Flanegan J, Heilman S, Garrett L, Dutra A, Anderson S, Pihan GA, Wolff L, Liu PP.
Proc Natl Acad Sci U S A 101(14):4924-9. Epub 2004 Mar 24. 2004
101HDAC4, RUNX2
HDAC4: a corepressor controlling bone development.
Hug BA.
Cell 119(4):448-9. 2004
102HDAC4, RUNX2
Histone deacetylase 4 controls chondrocyte hypertrophy during skeletogenesis.
Vega RB, Matsuda K, Oh J, Barbosa AC, Yang X, Meadows E, McAnally J, Pomajzl C, Shelton JM, Richardson JA, Karsenty G, Olson EN.
Cell 119(4):555-66. 2004
103RUNX2
Insulin-like growth factor-1 regulates endogenous RUNX2 activity in endothelial cells through a phosphatidylinositol 3-kinase/ERK-dependent and Akt-independent signaling pathway.
Qiao M, Shapiro P, Kumar R, Passaniti A.
J Biol Chem 279(41):42709-18. Epub 2004 Aug 09. 2004
104SMURF1, RUNX2
Smurf1 inhibits osteoblast differentiation and bone formation in vitro and in vivo.
Zhao M, Qiao M, Harris SE, Oyajobi BO, Mundy GR, Chen D.
J Biol Chem 279(13):12854-9. Epub 2003 Dec 29. 2004
105RUNX2, SOST
Cbfa1/RUNX2 directs specific expression of the sclerosteosis gene (SOST).
Sevetson B, Taylor S, Pan Y.
J Biol Chem 279(14):13849-58. Epub 2004 Jan 22. 2004
106ALX1, GATA1, MSX2, RUNX2
Identification of genes responsible for osteoblast differentiation from human mesodermal progenitor cells.
Qi H, Aguiar DJ, Williams SM, La Pean A, Pan W, Verfaillie CM.
Proc Natl Acad Sci U S A 100(6):3305-10. 2003
107RUNX2, SP7
Transcriptional mechanisms in osteoblast differentiation and bone formation.
Nakashima K, de Crombrugghe B.
Trends Genet 19(8):458-66. 2003
108LGALS3, RUNX1, RUNX2, RUNX3
Expression of galectin-3 in skeletal tissues is controlled by Runx2.
Stock M, Schafer H, Stricker S, Gross G, Mundlos S, Otto F.
J Biol Chem 278(19):17360-7. Epub 2003 Feb 25. 2003
109CCD, RUNX2
Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype-phenotype correlations.
Yoshida T, Kanegane H, Osato M, Yanagida M, Miyawaki T, Ito Y, Shigesada K.
Blood Cells Mol Dis 30(2):184-93. 2003
110PPARG, RUNX2
Activation of peroxisome proliferator-activated receptor-gamma inhibits the Runx2-mediated transcription of osteocalcin in osteoblasts.
Jeon MJ, Kim JA, Kwon SH, Kim SW, Park KS, Park SW, Kim SY, Shin CS.
J Biol Chem 278(26):23270-7. Epub 2003 Apr 18. 2003
111RUNX2, BMP7
Transcriptional regulation of the human Runx2/Cbfa1 gene promoter by bone morphogenetic protein-7.
Tou L, Quibria N, Alexander JM.
Mol Cell Endocrinol 205(1-2):121-9. 2003
112CCD, RUNX2
Mutations in the RUNX2 gene in patients with cleidocranial dysplasia.
Otto F, Kanegane H, Mundlos S.
Hum Mutat 19(3):209-16. Review. 2002
113RUNX2, CCD
New mutations in the CBFA1 gene in two Mexican patients with cleidocranial dysplasia.
Machuca-Tzili L, Monroy-Jaramillo N, Gonzalez-Del Angel A, Kofman-Alfaro S.
Clin Genet 61(5):349-53. 2002
114RUNX2
Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations.
Yoshida T, Kanegane H, Osato M, Yanagida M, Miyawaki T, Ito Y, Shigesada K.
Am J Hum Genet 71(4):724-38. 2002
115CBFB, RUNX2
Cbfbeta interacts with Runx2 and has a critical role in bone development.
Kundu M, Javed A, Jeon JP, Horner A, Shum L, Eckhaus M, Muenke M, Lian JB, Yang Y, Nuckolls GH, Stein GS, Liu PP.
Nat Genet 32(4):639-44. 2002
116CBFB, RUNX2
The core-binding factor beta subunit is required for bone formation and hematopoietic maturation.
Miller J, Horner A, Stacy T, Lowrey C, Lian JB, Stein G, Nuckolls GH, Speck NA.
Nat Genet 32(4):645-9. 2002
117RUNX2
Alleles of RUNX2/CBFA1 gene are associated with differences in bone mineral density and risk of fracture.
Vaughan T, Pasco JA, Kotowicz MA, Nicholson GC, Morrison NA.
J Bone Miner Res 17(8):1527-34. 2002
118RUNX2
Runx2, a multifunctional transcription factor in skeletal development.
Komori T.
J Cell Biochem 87(1):1-8. Review. 2002
119DMP1, RUNX2
Dentin matrix protein 1, a target molecule for Cbfa1 in bone, is a unique bone marker gene.
Fen JQ, Zhang J, Dallas SL, Lu Y, Chen S, Tan X, Owen M, Harris SE, MacDougall M.
J Bone Miner Res 17(10):1822-31. 2002
120FGFR2, RUNX2
Fibroblast growth factor 2 induction of the osteocalcin gene requires MAPK activity and phosphorylation of the osteoblast transcription factor, Cbfa1/Runx2.
Xiao G, Jiang D, Gopalakrishnan R, Franceschi RT.
J Biol Chem 277(39):36181-7. Epub 2002 Aug 28. 2002
121RUNX2
Characterization of an osteoblast-specific enhancer element in the CBFA1 gene.
Zambotti A, Makhluf H, Shen J, Ducy P.
J Biol Chem 277(44):41497-506. Epub 2002 Aug 16. 2002
122CCD, RUNX2
Cleidocranial dysplasia with decreased bone density and biochemical findings of hypophosphatasia.
Morava E, Karteszi J, Weisenbach J, Caliebe A, Mundlos S, Mehes K.
Eur J Pediatr 161(11):619-22. Epub 2002 Oct 09. 2002
123SMAD3, RUNX2, TGFB1
TGF-beta-induced repression of CBFA1 by Smad3 decreases cbfa1 and osteocalcin expression and inhibits osteoblast differentiation.
Alliston T, Choy L, Ducy P, Karsenty G, Derynck R.
EMBO J 20(9):2254-72. 2001
124RUNX2
Runx2: a novel oncogenic effector revealed by in vivo complementation and retroviral tagging.
Blyth K, Terry A, Mackay N, Vaillant F, Bell M, Cameron ER, Neil JC, Stewart M.
Oncogene 20(3):295-302. 2001
125RUNX2
Analysis of type-I and type-II RUNX2 protein expression in osteoblasts.
Sudhakar S, Katz MS, Elango N.
Biochem Biophys Res Commun 286(1):74-9. 2001
126RUNX2, TGFB1, TNFRSF11B
Stimulation of osteoprotegerin (OPG) gene expression by transforming growth factor-beta (TGF-beta). Mapping of the OPG promoter region that mediates TGF-beta effects.
Thirunavukkarasu K, Miles RR, Halladay DL, Yang X, Galvin RJ, Chandrasekhar S, Martin TJ, Onyia JE.
J Biol Chem 276(39):36241-50. 2001
127CBFB, RUNX2
Structural basis for the heterodimeric interaction between the acute leukaemia-associated transcription factors AML1 and CBFbeta.
Warren AJ, Bravo J, Williams RL, Rabbitts TH.
EMBO J 19(12):3004-15. 2000
128CCD, RUNX2
PEBP2alphaA/CBFA1 mutations in Japanese cleidocranial dysplasia patients.
Zhang YW, Yasui N, Kakazu N, Abe T, Takada K, Imai S, Sato M, Nomura S, Ochi T, Okuzumi S, Nogami H, Nagai T, Ohashi H, Ito Y.
Gene 244(1-2):21-8. 2000
129RUNX2
A RUNX2/PEBP2alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia.
Zhang YW, Yasui N, Ito K, Huang G, Fujii M, Hanai J, Nogami H, Ochi T, Miyazono K, Ito Y.
Proc Natl Acad Sci U S A 97(19):10549-54. 2000
130RUNX2
Cbfa1 is a positive regulatory factor in chondrocyte maturation.
Enomoto H, Enomoto-Iwamoto M, Iwamoto M, Nomura S, Himeno M, Kitamura Y, Kishimoto T, Komori T.
J Biol Chem 275(12):8695-702. 2000
131CCD, RUNX2
A novel missense mutation of the CBFA1 gene in a family with cleidocranial dysplasia (CCD) and variable expressivity.
Golan I, Preising M, Wagener H, Baumert U, Niederdellmann H, Lorenz B, Mussig D.
J Craniofac Genet Dev Biol 20(3):113-20. 2000
132CCD, RUNX2
Cleidocranial dysplasia : clinical and molecular genetics.
Mundlos S.
J Med Genet 36 : 177-182. 1999
133RUNX2, CCD
CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.
Zhou G, et al.
Hum Mol Genet 8(12):2311-2316 1999
134RUNX1, RUNX2, RUNX3
Runt domains take the lead in hematopoiesis and osteogenesis.
Werner MH, Shigesada K, Ito Y.
Nat Med 5(12):1356-7. No abstract available 1999
135RUNX2
Genomic organization, expression of the human CBFA1 gene, and evidence for an alternative splicing event affecting protein function.
Geoffroy V, et al.
Mamm Genome 9 : 54-57. 1998
136RUNX2
Genomic structure and isoform expression of the mouse, rat and human Cbfa1/Osf2 transcription factor.
Xiao ZS, et al.
Gene 214 : 187-197. 1998
137RUNX2, ETS1, SPP1
Transcriptional regulation of osteopontin gene in vivo by PEBP2alphaA/CBFA1 and ETS1 in the skeletal tissues.
Sato M, et al.
Oncogene 17 : 1517-1525. 1998
138RUNX2, CCD
Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development.
Otto F, Thornell AP, Crompton T, Denzel A, Gilmour KC, Rosewell IR, Stamp GW, Beddington RS, Mundlos S, Olsen BR, Selby PB, Owen MJ.
Cell 89(5):765-71. 1997
139RUNX2
Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts.
Komori T, Yagi H, Nomura S, Yamaguchi A, Sasaki K, Deguchi K, Shimizu Y, Bronson RT, Gao YH, Inada M, Sato M, Okamoto R, Kitamura Y, Yoshiki S, Kishimoto T.
Cell 89(5):755-64. 1997
140RUNX2, CCD
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.
Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, Lindhout D, Cole WG, Henn W, Knoll JH, Owen MJ, Mertelsmann R, Zabel BU, Olsen BR.
Cell 89(5):773-9. 1997
141RUNX2, CCD
Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation.
Ducy P, Zhang R, Geoffroy V, Ridall AL, Karsenty G.
Cell 89(5):747-54. 1997
142RUNX2, CCD
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.
Lee B, Thirunavukkarasu K, Zhou L, Pastore L, Baldini A, Hecht J, Geoffroy V, Ducy P, Karsenty G.
Nat Genet 16(3):307-10. 1997
143RUNX2
The cDNA cloning of the transcripts of human PEBP2alphaA/CBFA1 mapped to 6p12.3-p21.1, the locus for cleidocranial dysplasia.
Zhang YW, Bae SC, Takahashi E, Ito Y.
Oncogene 15(3):367-71. 1997
144RUNX2
Runt homology domain proteins in osteoblast differentiation: AML3/CBFA1 is a major component of a bone-specific complex.
Banerjee C, McCabe LR, Choi JY, Hiebert SW, Stein JL, Stein GS, Lian JB.
J Cell Biochem 66(1):1-8. 1997
145CCD,RUNX2
Mapping of the gene for cleidocranial dysplasia in the historical (Arnold) kindred and evidence for locus homogeneity.
Ramesar RS, et al.
J Med Genet 33 : 511-514. 1996
146AML1, AMLT2, AMLT3, RUNX2, RUNX1, RUNX3
AML1, AML2, and AML3, the human members of the runt domain gene-family : cDNA structure, expression, and chromosomal localization.
Levanon D, et al.
Genomics 23 : 425-432. 1994