Menezes A, Jones R, Shrestha A, Nicholson R, Leckenby A, Azevedo A
Leukemia. 2022; 36(7):1769-1780.
PMID: 35490198
PMC: 9252899.
DOI: 10.1038/s41375-022-01577-2.
Gong L, Odilov B, Han F, Liu F, Sun Y, Zhang N
Genes Genomics. 2022; 44(6):683-690.
PMID: 35235174
PMC: 9120113.
DOI: 10.1007/s13258-022-01229-w.
Inchingolo A, Patano A, Coloccia G, Ceci S, Inchingolo A, Marinelli G
Medicina (Kaunas). 2021; 57(12).
PMID: 34946295
PMC: 8709258.
DOI: 10.3390/medicina57121350.
Tintut Y, Honda H, Demer L
Biomolecules. 2021; 11(10).
PMID: 34680115
PMC: 8533507.
DOI: 10.3390/biom11101482.
Saharudin S, Sanusi S, Ponnuraj K
Clin Oral Investig. 2021; 26(2):1261-1268.
PMID: 34453594
DOI: 10.1007/s00784-021-04098-x.
Secondary cytogenetic abnormalities in core-binding factor AML harboring inv(16) vs t(8;21).
Han S, Mrozek K, Voutsinas J, Wu Q, Morgan E, Vestergaard H
Blood Adv. 2021; 5(10):2481-2489.
PMID: 34003250
PMC: 8152510.
DOI: 10.1182/bloodadvances.2020003605.
Integrated analysis of ceRNA network and tumor-infiltrating immune cells in esophageal cancer.
Chen Y, Zhou H, Wang Z, Huang Z, Wang J, Zheng M
Biosci Rep. 2021; 41(5).
PMID: 33960364
PMC: 8164107.
DOI: 10.1042/BSR20203804.
Extracellular Vesicle-Mediated Bone Remodeling and Bone Metastasis: Implications in Prostate Cancer.
Patil K, Soekmadji C
Subcell Biochem. 2021; 97:297-361.
PMID: 33779922
DOI: 10.1007/978-3-030-67171-6_12.
Transcriptional Programming in Arteriosclerotic Disease: A Multifaceted Function of the Runx2 (Runt-Related Transcription Factor 2).
Chen Y, Zhao X, Wu H
Arterioscler Thromb Vasc Biol. 2020; 41(1):20-34.
PMID: 33115268
PMC: 7770073.
DOI: 10.1161/ATVBAHA.120.313791.
Runx3 prevents spontaneous colitis by directing the differentiation of anti-inflammatory mononuclear phagocytes.
Hantisteanu S, Dicken Y, Negreanu V, Goldenberg D, Brenner O, Leshkowitz D
PLoS One. 2020; 15(5):e0233044.
PMID: 32453801
PMC: 7250423.
DOI: 10.1371/journal.pone.0233044.
RUNX3 Inhibits the Invasion and Metastasis of Human Colon Cancer HT-29 Cells by Upregulating MMP-2/9.
Xue J, Wu X, Qu M, Guo F, Han L, Sun G
Evid Based Complement Alternat Med. 2020; 2020:5978131.
PMID: 32184893
PMC: 7063181.
DOI: 10.1155/2020/5978131.
Inhibition of Vif-Mediated Degradation of APOBEC3G through Competitive Binding of Core-Binding Factor Beta.
Miyagi E, Welbourn S, Sukegawa S, Fabryova H, Kao S, Strebel K
J Virol. 2020; 94(7).
PMID: 31941780
PMC: 7081906.
DOI: 10.1128/JVI.01708-19.
Identification of variants associated with cleidocranial dysplasia.
Gao X, Li K, Fan Y, Sun Y, Luo X, Wang L
Hereditas. 2019; 156:31.
PMID: 31548836
PMC: 6747736.
DOI: 10.1186/s41065-019-0107-7.
RUNX family: Oncogenes or tumor suppressors (Review).
Otalora-Otalora B, Henriquez B, Lopez-Kleine L, Rojas A
Oncol Rep. 2019; 42(1):3-19.
PMID: 31059069
PMC: 6549079.
DOI: 10.3892/or.2019.7149.
RUNX proteins desensitize multiple myeloma to lenalidomide via protecting IKZFs from degradation.
Zhou N, Gutierrez-Uzquiza A, Zheng X, Chang R, Vogl D, Garfall A
Leukemia. 2019; 33(8):2006-2021.
PMID: 30760870
PMC: 6687534.
DOI: 10.1038/s41375-019-0403-2.
Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: A case report and literature review.
Ma D, Wang X, Guo J, Zhang J, Cai T
Medicine (Baltimore). 2018; 97(32):e11328.
PMID: 30095610
PMC: 6133463.
DOI: 10.1097/MD.0000000000011328.
Runx1-Stat3 signaling regulates the epithelial stem cells in continuously growing incisors.
Sarper S, Inubushi T, Kurosaka H, Minagi H, Kuremoto K, Sakai T
Sci Rep. 2018; 8(1):10906.
PMID: 30026553
PMC: 6053438.
DOI: 10.1038/s41598-018-29317-6.
Chemoresistance‑related long non‑coding RNA expression profiles in human breast cancer cells.
Huang L, Zeng L, Chu J, Xu P, Lv M, Xu J
Mol Med Rep. 2018; 18(1):243-253.
PMID: 29749447
PMC: 6059676.
DOI: 10.3892/mmr.2018.8942.
The Transcription Factor Runx3 Establishes Chromatin Accessibility of cis-Regulatory Landscapes that Drive Memory Cytotoxic T Lymphocyte Formation.
Wang D, Diao H, Getzler A, Rogal W, Frederick M, Milner J
Immunity. 2018; 48(4):659-674.e6.
PMID: 29669249
PMC: 6750808.
DOI: 10.1016/j.immuni.2018.03.028.
A novel Alu-mediated microdeletion in the RUNX2 gene in a Chinese patient with cleidocranial dysplasia.
Qian Y, Zhang Y, Wei B, Zhang M, Yang J, Leng C
J Genet. 2018; 97(1):137-143.
PMID: 29666333