[1] Higuchi M, Yoshida S, Ueharu H, et al. PRRX1 and PRRX2 distinctively participate in pituitary organogenesis and a cell-supply system[J]. Medline Plus, 2014, 357(1): 323-325.
[2] Cserjesi P, Lilly B, Bryson L, et al. MHox: A mesodermally restricted homeodomain protein that binds an essential site in the muscle creatine kinase enhancer[J]. Development, 1992, 115(4): 1087-1101.
[3] Kern M J, Witte D P, Valerius M T, et al. A novel murine homeobox gene isolated by a tissue specific PCR cloning strategy[J]. Nucleic Acids Res, 1992, 20(19): 5189-5195.
[4] Krumlauf R, Holland P W, Mcvey J H, et al. Developmental and spatial patterns of expression of the mouse homeobox gene[J]. Development, 1987, 99(4): 603-617.
[5] Higuchi M, Kato T, Chen M, et al. Temporospatial gene expression of Prx1 and Prx2 is involved in morphogenesis of cranial placode-derived tissues through epithelio-mesenchymal interaction during rat embryogenesis[J]. Cell Tissue Res, 2013, 353(1): 27-40.
[6] Leussink B, Brouwer A, Khattabi M, et al. Expression patterns of the paired-related homeobox genes MHox/Prrx1 and S8/Prx2 suggest roles in development of the heart and the forebrain[J]. Mech Dev, 1995, 52(1): 51-64.
[7] Kern M J, Argao E A, Birkenmeier E H, et al. Genomic organization and chromosome localization of the murine homeobox gene Pmx[J]. Genomics, 1994, 19(2): 334-340.
[8] Opstelten D J,Vogels R,Robert B,et al. The mouse homeobox gene S8 is expressed during embryogenesis predominantly in mesenchyme[J]. Mech Dev, 1991, 34(1): 29-41.
[9] Kongsuwan K, Webb E, Housiaux P, et al. Expression of multiple homeobox genes within diverse mammalian haemopoietic lineages[J]. Embo J, 1988, 7(7): 2131-2138.
[10] van Schaick H S, Smidt M P, Rovescalli A C, et al. Homeobox gene Prx3 expression in rodent brain and extraneural tissues[J]. Proc Natl Acad Sci USA, 1997, 94(24): 12993-12998.
[11] 张玉娟, 催 巍. 人SHOX2基因的生物学作用及与疾病关系的研究[J]. 中国卫生检验杂志, 2013, 23(9): 2112-2114.
[12] Norris R A, Scott K K, Moore C S, et al. Human PRRX1 and PRRX2 genes: Cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome[J]. Mamm Genome, 2000, 11(11): 1000-1005.
[13] Schneider K U, Dietrich D, Fleischhacker M, et al. Correlation of SHOX2 gene amplification and DNA methylation in lung cancer tumors[J]. BMC Cancer, 2011, 11(10):102-104.
[14] Martin J F, Bradley A, Olson E N. The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages[J]. Genes Dev, 1995, 9(10): 1237-1249.
[15] Nakamura T, Yamazaki Y, Hatano Y, et al. NUP98 is fused to PMX1 homeobox gene in human acute myelogenous leukemia with chromosome translocation[J]. Blood, 1999, 94(2):741-745.
[16] Fritz D, Stefanovic B. RNA-binding protein RBMS3 is expressed in activated hepatic stellate cells and liver fibrosis and increases expression of transcription factor Prrx1[J]. J Mol Biol, 2007, 371(3):585-595.
[17] Bergwerff M, Tenberger A C, Deruit M C, et al. Patterns of paired-related homeobox genes PRX1 and PRX2 suggest involvement in matrix modulation in the developing chick vascular system[J]. Dev Dyn, 1998, 213(1): 59-70.
[18] Du B, Cawthorn W P, Su A, et al. The transcription factor paired-related homeobox 1 (Prrx1) inhibits adipogenesis by activating transforming growth factor-β (TGFβ) signaling[J]. J Biol Chem, 2013, 288(5): 3036-3047.
[19] Mitchell J M,Hicklin D M, Doughty P M,et al. The Prx1 homeobox gene is critical for molar tooth morphogenesis[J].Dent Res,2006,85(10):888-893.
[20] White P, Thomas D W, Fong S. Deletion of the homeobox gene PRX-2 affects fetal but not adult fibroblast wound healing responses[J]. H Feta Fibr, 2003, 120(1): 135-144.
[21] Yoshida T, Hoofnagle M H, Owens G K. Myocardin and Prx1 contribute to angiotensinⅡ-induced expression of smooth muscle alpha-actin[J]. Circ Res, 2004, 94(8): 1075-1082.
[22] Jone F S, Meech R, Edelman D B, et al.Prx1 controls vascular smooth muscle cell proliferation and tenascin-C expression and is upregulated with Prx2 in pulmonary vascular disease[J]. Circ Res,2001, 89(11): 131-138.
[23] Ten B D, Brouwer A, Korving J, et al. Prx1 and Prx2 in skeletogenesis: Roles in the craniofacial region, inner ear and limbs[J]. Development, 1998, 125(19): 3831-3842.
[24] White P, Thomas D W, Fong S, et al. Deletion of the homeobox gene PRX-2 affects fetal but not adult fibroblast wound healing responses[J]. J Invest Dermatol, 2003, 120(1): 135-144.
[25] Kong S, Opstelten D J, Vogels R et al. The mouse homeobox gene, S8, is expressed during embryogenesis predominantly in mesenchyme[J]. Mech Dev, 1999, 32(1):29-41.
[26] Balic A, Adams D, Mina M, et al. Prx1 and Prx2 cooperatively regulate the morphogenesis of the medial region of the mandibular process[J]. H Nation Institutes, 2009, 238(10): 2599-2613.
[27] Lu M F, Cheng H T, Kern M J, et al. prx-1 functions cooperatively with another paired-related homeobox gene, Prx-2, to maintain cell fates within the craniofacial mesenchyme[J]. Development, 1999, 126(3): 495-504.
[28] 聂 磊, 韩 梅. 同源异型盒基因对血管平滑肌细胞的调控作用[J]. 细胞生物学杂志, 2004,26(13):352-356.
[29] Higuchi M, Kato T, Yoshida S, et al. PRRX1 and PRRX2 positive mesenchymal stem/progenitor cells are involved in vasculogenesis during ratembryonic pituitary development[J].Cell Tissue Res, 2015, 361(2):557-565.
[30] Karpe F, Pinnick K E. Biology of upper-body and lower-body adipose tissue-link to whole-body phenotypes[J].Nat Rev Endocrinol, 2015, 11(2):90-100.
[31] Stelnicki E J, Arbeit J, Cass D L, et al. Modulation of the human homeobox genes PRX-2 and HOXB13 in scarless fetal wounds[J]. J Invest Dermatol, 1998, 11(1): 57-63.
[32] Susa T, Ishikawa A, Kato T, et al. Molecular cloning of paired related homeobox (Prx2) as a novel pituitary transcription factor[J]. Development, 2009, 55(5): 502-511.
[33] ten Berge D, Brouwer A, Korving J, et al. Prx1 and Prx2 are upstream regulators of sonic hedgehog and control cell proliferation during mandibular arch morphogenesis[J]. Development, 2001, 128(15): 2929-2938.
[34] Smith T M, Lozanoff S, Iyyanar P P, et al. Molecular signaling along the anterior-posterior axis of early palate development[J].Front Physiol,2013, 3(10):488-491.
[35] Censani M, Anyane K, Wapner R, et al. Rare inheritance of Leri-Weill syndrome due to crossover of short stature homeobox gene (SHOX) deletions between X and Y chromosomes: A case report[J]. Int J Pediatr Endocrinol, 2013, 2013(1): 1-13.
[36] Gross R, Giese K, Pagel J. HMG domain proteins: Architectural elements in the assembly of nucleoprotein structures[J]. Trends Genet, 1994, 10(3): 94-100.
[37] Yu L, Liu H, Yan M, et al. Shox2 is required for chondrocyte proliferation and maturation in proximal limb skeleton[J]. Dev Biol, 2007, 306(2): 549-559.
[38] Vickerman L, Neufeld S, Cobb J. Shox2 function couples neural, muscular and skeletal development in the proximal forelimb[J]. Dev Biol, 2011, 350(2): 323-336.
[39] Song H F, Chai J K, Chen M L, et al. The significance and the expression of homeobox genes during human burn wound healing[J]. Chinese Journal of Burns, 2003,19(2):112-115.
[40] Lee K Y, Yamamoto Y, Boucher J, et al. Shox2 is a molecular determinant of depot-specific adipocyte function[J]. PNAS, 2013, 110(28): 11409-11414.
[41] Laurikkala J, Mikkola M, Mustonen T, et al. TNF signaling via the ligand-receptor pair ectodysplasin and edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis[J]. Dev Biol, 2001, 229(2):443-455.
[42] Li X, Liang W, Weng X, et al. Overexpression of Shox2 leads to congenital dysplasia of the temporomandibular joint in mice[J]. Int J Mol Sci, 2014, 15(8): 13135-13150. |