[1] Monterisi S, Lo Riso P, Russo K, et al. HOXB7 overexpression in lung cancer is a hallmark of acquired stemlike phenotype[J]. Oncogene, 2018, 37(26): 3575-3588. DOI: 10.1038/s41388-018-0229-9.
[2] Hu H, Chen Y, Cheng S, et al. Dysregulated expression of homebox gene HOXA13 is correlated with the poor prognosis in bladder cancer[J]. Wien Klin Wochenschr, 2017, 129(11-12): 391397. DOI: 10.1007/s0050801611084.
[3] Skvarova Kramarzova K, Fiser K, Mejstrikova E, et al. Homeobox gene expression in acute myeloid leukemia is linked to typical underlying molecular aberrations[J]. J Hematol Oncol, 2014, 7: 94. DOI: 10.1186/s1304501400940.
[4] Futreal PA, Cochran C, Rosenthal J, et al. Isolation of a diverged homeobox gene, MOX1, from the BRCA1 region on 17q21 by solution hybrid capture[J]. Hum Mol Genet, 1994, 3(8): 1359-1364.
[5] Sawamiphak S, Stainier DY. Developmental biology: it takes muscle to make blood cells[J]. Nature, 2014, 512(7514): 257-258. DOI: 10.1038/nature13740.
[6] Karaca E, Yuregir OO, Bozdogan ST, et al. Rare variants in the notch signaling pathway describe a novel type of autosomal recessive KlippelFeil syndrome[J]. Am J Med Genet A, 2015, 167A(11): 2795-2799. DOI: 10.1002/ajmg.a.37263.
[7] Wu B, Zhang L, Zhu YH, et al. Mesoderm/mesenchyme homeobox gene 1 promotes vascular smooth muscle cell phenotypic modulation and vascular remodeling[J]. Int J Cardiol, 2018, 251: 82-89. DOI: 10.1016/j.ijcard.2017.10.098.
[8] Nguyen PD, Gurevich DB, Sonntag C, et al. Muscle stem cells undergo extensive clonal drift during tissue growth via Meox1mediated induction of G2 cellcycle arrest[J]. Cell Stem Cell, 2017, 21(1): 107-119, e6. DOI: 10.1016/j.stem.2017.06.003.
[9] Lefebvre M, DieuxCoeslier A, Baujat G, et al. Diagnostic strategy in segmentation defect of the vertebrae: a retrospective study of 73 patients[J]. J Med Genet, 2018, 55(6): 422-429. DOI: 10.1136/jmedgenet-2017-104939.
[10] Dauer MVP, Currie PD, Berger J. Skeletal malformations of Meox1deficient zebrafish resemble human KlippelFeil syndrome[J]. J Anat, 2018, 233(6): 687-695. DOI: 10.1111/joa.12890.
[11] Thiaville MM, Stoeck A, Chen L, et al. Identification of PBX1 target genes in cancer cells by global mapping of PBX1 binding sites[J]. PLoS One, 2012, 7(5): e36054. DOI: 10.1371/journal.pone.0036054.
[12] Chen X, Jung JG, ShajahanHaq AN, et al. ChIPBIT: bayesian inference of target genes using a novel joint probabilistic model of ChIPseq profiles[J]. Nucleic Acids Res, 2016, 44(7): e65. DOI: 10.1093/nar/gkv1491.
[13] Wei X, Yu L, Li Y. PBX1 promotes the cell proliferation via JAK2/STAT3 signaling in clear cell renal carcinoma[J]. Biochem Biophys Res Commun, 2018, 500(3): 650-657. DOI: 10.1016/j.bbrc.2018.04.127.
[14] Sun L, Burnett J, Gasparyan M, et al. Novel cancer stem cell targets during epithelial to mesenchymal transition in PTENdeficient trastuzumabresistant breast cancer[J]. Oncotarget, 2016, 7(32): 5140851422. DOI: 10.18632/oncotarget.9839.
[15] Peng C, Lou HL, Liu F, et al. Enhanced identification of potential pleiotropic genetic variants for bone mineral density and breast cancer[J]. Calcif Tissue Int, 2017, 101(5): 489-500. DOI: 10.1007/s00223-017-0308-x.
[16] Sun L, Yuan H, Burnett J, et al. MEOX1 promotes tumor progression and predicts poor prognosis in human nonsmallcell lung cancer[J]. Int J Med Sci, 2019, 16(1): 68-74. DOI: 10.7150/ijms.27595.
[17] Zhu ZY, Wang XL, Li DP. Silencing of MEOX1 gene inhibits proliferation and promotes apoptosis of LNCaP cells in prostate cancer[J]. Cancer Biother Radiopharm, 2019, 34(2): 91-102. DOI: 10.1089/cbr.2018.2545.
[18] Linn SC, West RB, Pollack JR, et al. Gene expression patterns and gene copy number changes in dermatofibrosarcoma protuberans[J]. Am J Pathol, 2003, 163(6): 2383-2395. DOI: 10.1016/S00029440(10)635936.
[19] Rodrigo I, Bovolenta P, Mankoo BS, et al. Meox homeodomain proteins are required for Bapx1 expression in the sclerotome and activate its transcription by direct binding to its promoter[J]. Mol Cell Biol, 2004, 24(7): 2757-2766.
[20] Lu D, Wang J, Li J, et al. Meox1 accelerates myocardial hypertrophic decompensation through Gata4[J]. Cardiovasc Res, 2018, 114(2): 300-311. DOI: 10.1093/cvr/cvx222.
[21] Savage J, Voronova A, Mehta V, et al. Canonical Wnt signaling regulates Foxc1/2 expression in P19 cells[J]. Differentiation, 2010, 79(1): 31-40. DOI: 10.1016/j.diff.2009.08.008.
[22] Stamataki D, Kastrinaki M, Mankoo BS, et al. Homeodomain proteins Mox1 and Mox2 associate with Pax1 and Pax3 transcription factors[J]. FEBS Lett, 2001, 499(3): 274-278.
[23] Wissmüller S, Kosian T, Wolf M, et al. The highmobilitygroup domain of Sox proteins interacts with DNAbinding domains of many transcription factors[J]. Nucleic Acids Res, 2006, 34(6): 1735-1744. DOI: 10.1093/nar/gkl105. |