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Volumn 132, Issue 19, 2005, Pages 4397-4406

Shox2-deficient mice exhibit a rare type of incomplete clefting of the secondary palate

Author keywords

Cleft palate; Epithelial mesenchymal interaction; Mouse; Shox2

Indexed keywords

BONE MORPHOGENETIC PROTEIN; FIBROBLAST GROWTH FACTOR 10; FIBROBLAST GROWTH FACTOR RECEPTOR 2; FIBROBLAST GROWTH FACTOR RECEPTOR 2C; HOMEODOMAIN PROTEIN; UNCLASSIFIED DRUG;

EID: 27644592957     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: 10.1242/dev.02013     Document Type: Article
Times cited : (126)

References (55)
  • 1
    • 9644257521 scopus 로고    scopus 로고
    • The cellular and molecular etiology of the cleft secondary palate in Fgf10 mutant mice
    • Alappat, S. R., Zhang, Z., Suzuki, K., Zhang, X., Liu, H., Jiang, R., Yamada, G. and Chen, Y. P. (2005). The cellular and molecular etiology of the cleft secondary palate in Fgf10 mutant mice. Dev. Biol. 277, 102-113.
    • (2005) Dev. Biol. , vol.277 , pp. 102-113
    • Alappat, S.R.1    Zhang, Z.2    Suzuki, K.3    Zhang, X.4    Liu, H.5    Jiang, R.6    Yamada, G.7    Chen, Y.P.8
  • 2
    • 0030788742 scopus 로고    scopus 로고
    • De Lange syndrome: Subjective and objective comparison of the classical and mild phenotypes
    • Allanson, J. E., Hennekam, R. C. and Ireland, M. (1997). De Lange syndrome: subjective and objective comparison of the classical and mild phenotypes. J. Med. Genet. 34, 645-650.
    • (1997) J. Med. Genet. , vol.34 , pp. 645-650
    • Allanson, J.E.1    Hennekam, R.C.2    Ireland, M.3
  • 4
    • 0026584439 scopus 로고
    • An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
    • Baldwin, C. T., Hoth, C. F., Amos, J. A., da-Silva, E. O. and Milunsky, A. (1992). An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature 355, 637-638.
    • (1992) Nature , vol.355 , pp. 637-638
    • Baldwin, C.T.1    Hoth, C.F.2    Amos, J.A.3    da-Silva, E.O.4    Milunsky, A.5
  • 5
    • 0031040450 scopus 로고    scopus 로고
    • Ectopic application of BMP-2 and BMP-4 can change patterning of developing chick facial primordia
    • Barlow, A. J. and Francis-West, P. H. (1997). Ectopic application of BMP-2 and BMP-4 can change patterning of developing chick facial primordia. Development 124, 391-398.
    • (1997) Development , vol.124 , pp. 391-398
    • Barlow, A.J.1    Francis-West, P.H.2
  • 7
    • 0029956078 scopus 로고    scopus 로고
    • Evidence from normal expression and targeted misexpression that Bone Morphogenetic Protein-4 (Bmp-4) plays a role in mouse embryonic lung morphogenesis
    • Bellusci, S., Henderson, R., Winnier, G., Oikawa, T. and Hogan, B. L. M. (1996). Evidence from normal expression and targeted misexpression that Bone Morphogenetic Protein-4 (Bmp-4) plays a role in mouse embryonic lung morphogenesis. Development 122, 1693-1702.
    • (1996) Development , vol.122 , pp. 1693-1702
    • Bellusci, S.1    Henderson, R.2    Winnier, G.3    Oikawa, T.4    Hogan, B.L.M.5
  • 9
    • 0030879040 scopus 로고    scopus 로고
    • Homeobox genes and disease
    • Boncinelli, E. (1997). Homeobox genes and disease. Curr. Opin. Genet. Dev. 7, 331-337.
    • (1997) Curr. Opin. Genet. Dev. , vol.7 , pp. 331-337
    • Boncinelli, E.1
  • 11
    • 0000473573 scopus 로고    scopus 로고
    • Signaling loops in the reciprocal epithelial-mesenchymal interactions of mammalian tooth development
    • (ed. C.-M, Chuong), Austin, TX: RG Landes
    • Chen, Y. P. and Maas, R. (1998). Signaling loops in the reciprocal epithelial-mesenchymal interactions of mammalian tooth development. In Molecular basis of epithelial appendage morphogenesis (ed. C.-M, Chuong), pp. 265-282. Austin, TX: RG Landes.
    • (1998) Molecular Basis of Epithelial Appendage Morphogenesis , pp. 265-282
    • Chen, Y.P.1    Maas, R.2
  • 12
    • 0029802695 scopus 로고    scopus 로고
    • Msxl controls inductive signaling during mammalian tooth morphogenesis
    • Chen, Y. P., Bei, M., Woo, I., Satokata, I. and Maas, R. (1996). Msxl controls inductive signaling during mammalian tooth morphogenesis. Development 122, 3035-3044.
    • (1996) Development , vol.122 , pp. 3035-3044
    • Chen, Y.P.1    Bei, M.2    Woo, I.3    Satokata, I.4    Maas, R.5
  • 14
  • 16
    • 0033961133 scopus 로고    scopus 로고
    • An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signaling during mouse organogenesis
    • De Moerlooze, L., Spencer-Dene, B., Revest, J., Hajihosseni, M., Rosewell, I. and Dickson, C. (2000). An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signaling during mouse organogenesis. Development 127, 483-492.
    • (2000) Development , vol.127 , pp. 483-492
    • De Moerlooze, L.1    Spencer-Dene, B.2    Revest, J.3    Hajihosseni, M.4    Rosewell, I.5    Dickson, C.6
  • 18
    • 0015089693 scopus 로고
    • Congeital defects in the hard palate
    • Fara, M. (1971). Congeital defects in the hard palate. Plast. Reconstr. Surg. 48, 44-47.
    • (1971) Plast. Reconstr. Surg. , vol.48 , pp. 44-47
    • Fara, M.1
  • 20
    • 0021695259 scopus 로고
    • Epithelial-mesenchymal interactions during vertebrate palatogenesis
    • Ferguson, M. W. J. and Honig, L. S. (1984). Epithelial-mesenchymal interactions during vertebrate palatogenesis. Curr. Top. Dev. Biol. 19, 138-164.
    • (1984) Curr. Top. Dev. Biol. , vol.19 , pp. 138-164
    • Ferguson, M.W.J.1    Honig, L.S.2
  • 21
    • 0029114035 scopus 로고
    • The occurrence of the blepharophimosis, ptosis, epicanthus inversus syndrome and Langer type of mesomelic dwarfism in the same patient. Evidence of the location of Langer type of mesomelic dwarfism at 3q22.3-q23?
    • Fryns, J. P. (1995). The occurrence of the blepharophimosis, ptosis, epicanthus inversus syndrome and Langer type of mesomelic dwarfism in the same patient. Evidence of the location of Langer type of mesomelic dwarfism at 3q22.3-q23? Clin. Genet. 48, 111-112.
    • (1995) Clin. Genet. , vol.48 , pp. 111-112
    • Fryns, J.P.1
  • 23
    • 0026949405 scopus 로고
    • Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene
    • Glaser, T., Walton, D. S. and Maas, R. L. (1992). Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene. Nat. Genet. 2, 232-239.
    • (1992) Nat. Genet. , vol.2 , pp. 232-239
    • Glaser, T.1    Walton, D.S.2    Maas, R.L.3
  • 24
    • 0017104216 scopus 로고
    • Developmental aspects of secondary palate development
    • Greene, R. M. and Pratt, R. M. (1976). Developmental aspects of secondary palate development. J. Embryol. Exp. Morph. 36, 225-245.
    • (1976) J. Embryol. Exp. Morph. , vol.36 , pp. 225-245
    • Greene, R.M.1    Pratt, R.M.2
  • 25
    • 0037382630 scopus 로고    scopus 로고
    • Expression of mouse Tbx22 support its role in palatogenesis and glossogenesis
    • Herr, A., Meunier, D., Müller, I., Rump, A., Fundele, R., Ropers, H. H. and Nuber, U. A. (2003). Expression of mouse Tbx22 support its role in palatogenesis and glossogenesis. Dev. Dyn. 226, 579-586.
    • (2003) Dev. Dyn. , vol.226 , pp. 579-586
    • Herr, A.1    Meunier, D.2    Müller, I.3    Rump, A.4    Fundele, R.5    Ropers, H.H.6    Nuber, U.A.7
  • 26
    • 0025898874 scopus 로고
    • A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome
    • Ireland, M., English, C., Cross, I., Houlsby, W. T. and Burn, J. (1991). A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome. J. Med. Genet. 28, 639-640.
    • (1991) J. Med. Genet. , vol.28 , pp. 639-640
    • Ireland, M.1    English, C.2    Cross, I.3    Houlsby, W.T.4    Burn, J.5
  • 27
    • 0242719725 scopus 로고    scopus 로고
    • Conditional inactivation of Tgfbr2 in cranial neural crest causes cleft palate and calvaria defects
    • Ito, Y., Yeo, J. Y., Chytil, A., Han, J., Bringas, P., Jr, Nakajima, A., Shuler, C., Moses, H. L. and Chai, Y. (2003). Conditional inactivation of Tgfbr2 in cranial neural crest causes cleft palate and calvaria defects. Development 130, 5269-5280.
    • (2003) Development , vol.130 , pp. 5269-5280
    • Ito, Y.1    Yeo, J.Y.2    Chytil, A.3    Han, J.4    Bringas Jr., P.5    Nakajima, A.6    Shuler, C.7    Moses, H.L.8    Chai, Y.9
  • 28
    • 0029006411 scopus 로고
    • Prenatal craniofacial development: New insights on normal and abnormal mechanisms
    • Johnston, M. C. and Bronsky, P. T. (1995). Prenatal craniofacial development: new insights on normal and abnormal mechanisms. Crit. Rev. Oral. Biol. Med. 6, 368-422.
    • (1995) Crit. Rev. Oral Biol. Med. , vol.6 , pp. 368-422
    • Johnston, M.C.1    Bronsky, P.T.2
  • 31
    • 4043104765 scopus 로고    scopus 로고
    • Odd-skipped related 2 (Osr2) encodes a key intrinsic regulator of secondary palate growth and morphogenesis
    • Lan, Y., Ovitt, C. E., Cho, E.-S., Maltby, K. M., Wang, Q. and Jiang, R. (2004). Odd-skipped related 2 (Osr2) encodes a key intrinsic regulator of secondary palate growth and morphogenesis. Development 131, 3207-3216.
    • (2004) Development , vol.131 , pp. 3207-3216
    • Lan, Y.1    Ovitt, C.E.2    Cho, E.-S.3    Maltby, K.M.4    Wang, Q.5    Jiang, R.6
  • 33
    • 0019458853 scopus 로고
    • Cleft of the hard palate with soft palate integrity
    • Mitts, T. F., Garrett, W. S. and Hurwitz, D. J. (1981). Cleft of the hard palate with soft palate integrity. Cleft Palate J. 18, 204-206.
    • (1981) Cleft Palate J. , vol.18 , pp. 204-206
    • Mitts, T.F.1    Garrett, W.S.2    Hurwitz, D.J.3
  • 34
    • 0032169255 scopus 로고    scopus 로고
    • Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities
    • Peters, H., Neubuser, A., Kratochwil, K. and Balling, R. (1998). Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities. Genes Dev. 12, 2735-2747.
    • (1998) Genes Dev. , vol.12 , pp. 2735-2747
    • Peters, H.1    Neubuser, A.2    Kratochwil, K.3    Balling, R.4
  • 35
    • 0030940217 scopus 로고    scopus 로고
    • Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
    • Rao, E., Weiss, B., Fukami, M., Rump, A., Niesler, B., Mertz, A., Muroya, K., Binder, G., Kirsch, S., Winkelmann, M. et al. (1997). Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nat. Genet. 16, 54-63.
    • (1997) Nat. Genet. , vol.16 , pp. 54-63
    • Rao, E.1    Weiss, B.2    Fukami, M.3    Rump, A.4    Niesler, B.5    Mertz, A.6    Muroya, K.7    Binder, G.8    Kirsch, S.9    Winkelmann, M.10
  • 37
    • 0029744104 scopus 로고    scopus 로고
    • Cloning and characterization of four murine homeobox genes
    • Rovescalli, A. C., Asoh, S. and Nirenberg, M. (1996), Cloning and characterization of four murine homeobox genes. Proc. Natl. Acad. Sci. USA 93, 10691-10696.
    • (1996) Proc. Natl. Acad. Sci. USA , vol.93 , pp. 10691-10696
    • Rovescalli, A.C.1    Asoh, S.2    Nirenberg, M.3
  • 38
    • 0020682278 scopus 로고
    • Experimental induction of an incomplete hard-palate cleft in the rat
    • Schupbach, P. M. (1983). Experimental induction of an incomplete hard-palate cleft in the rat. Oral Surg. Oral Med. Oral Pathol. 55, 2-9.
    • (1983) Oral Surg. Oral Med. Oral Pathol. , vol.55 , pp. 2-9
    • Schupbach, P.M.1
  • 40
    • 0031935317 scopus 로고    scopus 로고
    • A new human homeobox gene OGI2X is a member of the most conserved homeobox gene family and is expressed during heart development in mouse
    • Semina, E. V., Reiter, R. S. and Murray, J. C. (1998). A new human homeobox gene OGI2X is a member of the most conserved homeobox gene family and is expressed during heart development in mouse. Hum. Mol. Genet. 7, 415-422.
    • (1998) Hum. Mol. Genet. , vol.7 , pp. 415-422
    • Semina, E.V.1    Reiter, R.S.2    Murray, J.C.3
  • 43
    • 0021662054 scopus 로고
    • Morphogenesis of a complex organ: Vertebrate palate development
    • Slavkin, H. C. (1984). Morphogenesis of a complex organ: vertebrate palate development. Curr. Top. Dev. Biol. 19, 1-16.
    • (1984) Curr. Top. Dev. Biol. , vol.19 , pp. 1-16
    • Slavkin, H.C.1
  • 46
    • 0028943567 scopus 로고
    • Regulation of organogenesis: Common molecular mechanisms regulating the development of teeth and other organs
    • Thesleff, I., Vaahtokari, I. and Partanen, A.-M. (1995). Regulation of organogenesis: Common molecular mechanisms regulating the development of teeth and other organs. Int. J. Dev. Biol. 39, 35-50.
    • (1995) Int. J. Dev. Biol. , vol.39 , pp. 35-50
    • Thesleff, I.1    Vaahtokari, I.2    Partanen, A.-M.3
  • 48
    • 2642565901 scopus 로고    scopus 로고
    • NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion protein and fly Nipped-B, is mutated in Cornelia de Lange syndrome
    • Tonkin, E. T., Wang, T. J., Lisgo, S., Bamshad, M. J. and Strachan, T. (2004). NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion protein and fly Nipped-B, is mutated in Cornelia de Lange syndrome. Nat. Genet. 36, 636-641.
    • (2004) Nat. Genet. , vol.36 , pp. 636-641
    • Tonkin, E.T.1    Wang, T.J.2    Lisgo, S.3    Bamshad, M.J.4    Strachan, T.5
  • 49
    • 0034028899 scopus 로고    scopus 로고
    • MSX1 mutation is associated with orofacial clefting and tooth agenesis in human
    • Van den Boogaard, M.-J. H., Dorland, M., Beemer, F. A. and van Amstel, H. K. P. (2000). MSX1 mutation is associated with orofacial clefting and tooth agenesis in human. Nat. Genet. 24, 342-343.
    • (2000) Nat. Genet. , vol.24 , pp. 342-343
    • Van den Boogaard, M.-J.H.1    Dorland, M.2    Beemer, F.A.3    van Amstel, H.K.P.4
  • 50
    • 0030017452 scopus 로고    scopus 로고
    • A human MSX1 homeodomain missense mutation causes selective tooth agenesis
    • Vastardis, H., Karimbux, N., Guthua, S. W., Seidman, J. G. and Seidman, C. E. (1996). A human MSX1 homeodomain missense mutation causes selective tooth agenesis. Nat. Genet. 13, 417-421.
    • (1996) Nat. Genet. , vol.13 , pp. 417-421
    • Vastardis, H.1    Karimbux, N.2    Guthua, S.W.3    Seidman, J.G.4    Seidman, C.E.5
  • 51
    • 0032953373 scopus 로고    scopus 로고
    • Msx1 is required for the induction of Patched by Sonic hedgehog in the mammalian tooth germ
    • Zhang, Y., Zhao, X., Hu, Y., St Amand, T., Zhang, M., Ramamurthy, R., Qiu, M. and Chen, Y. P. (1999). Msx1 is required for the induction of Patched by Sonic hedgehog in the mammalian tooth germ. Dev. Dyn. 215, 45-53.
    • (1999) Dev. Dyn. , vol.215 , pp. 45-53
    • Zhang, Y.1    Zhao, X.2    Hu, Y.3    St Amand, T.4    Zhang, M.5    Ramamurthy, R.6    Qiu, M.7    Chen, Y.P.8
  • 52
    • 0034010334 scopus 로고    scopus 로고
    • A new function of BMP4: Dual role for BMP4 in regulation of Sonic hedgehog expression in the mouse tooth germ
    • Zhang, Y., Zhang, Z., Zhao, X., Yu, X., Hu, Y., Geronimo, B., Fromm, S. H. and Chen, Y. P. (2000). A new function of BMP4: dual role for BMP4 in regulation of Sonic hedgehog expression in the mouse tooth germ. Development 127, 1431-1443.
    • (2000) Development , vol.127 , pp. 1431-1443
    • Zhang, Y.1    Zhang, Z.2    Zhao, X.3    Yu, X.4    Hu, Y.5    Geronimo, B.6    Fromm, S.H.7    Chen, Y.P.8
  • 53
    • 0036714198 scopus 로고    scopus 로고
    • Rescue of cleft palate in Msx1-deficient mice by transgenic Bmp4 reveals a network of BMP and Shh signaling in the regulation of mammalian palatogenesis
    • Zhang, Z., Song, Y., Zhao, X., Zhang, X., Fermin, C. and Chen, Y. P. (2002). Rescue of cleft palate in Msx1-deficient mice by transgenic Bmp4 reveals a network of BMP and Shh signaling in the regulation of mammalian palatogenesis. Development 129, 4135-4146.
    • (2002) Development , vol.129 , pp. 4135-4146
    • Zhang, Z.1    Song, Y.2    Zhao, X.3    Zhang, X.4    Fermin, C.5    Chen, Y.P.6
  • 54
    • 0033745316 scopus 로고    scopus 로고
    • Transgenically ectopic expression of Bmp4 to Msx1 mutant dental mesenchyme restores downstream gene expression but represses Shh and Bmp2 in the enamel knot of wild type tooth germ
    • Zhao, X., Zhang, Z., Song, Y., Zhang, X., Zhang, Y., Hu, Y., Fromm, S. H. and Chen, Y. P. (2000). Transgenically ectopic expression of Bmp4 to Msx1 mutant dental mesenchyme restores downstream gene expression but represses Shh and Bmp2 in the enamel knot of wild type tooth germ. Mech. Dev. 99, 29-38.
    • (2000) Mech. Dev. , vol.99 , pp. 29-38
    • Zhao, X.1    Zhang, Z.2    Song, Y.3    Zhang, X.4    Zhang, Y.5    Hu, Y.6    Fromm, S.H.7    Chen, Y.P.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.