메뉴 건너뛰기




Volumn 297, Issue 5, 2014, Pages 826-833

Craniofacial shape variation in Twist1+/- mutant mice

Author keywords

Craniosynostosis; Geometric morphometrics; Mouse; Saethre Chotzen; Twist1

Indexed keywords

TRANSCRIPTION FACTOR TWIST; TRANSCRIPTION FACTOR TWIST 1; UNCLASSIFIED DRUG; NUCLEAR PROTEIN; TWIST1 PROTEIN, MOUSE;

EID: 84899489358     PISSN: 19328486     EISSN: 19328494     Source Type: Journal    
DOI: 10.1002/ar.22899     Document Type: Article
Times cited : (28)

References (46)
  • 1
    • 0024402829 scopus 로고
    • Intentional cranial vault deformation and induced changes of the cranial base and face
    • Anton SC. 1989. Intentional cranial vault deformation and induced changes of the cranial base and face. Am J Phys Anthropol 79:253-267.
    • (1989) Am J Phys Anthropol , vol.79 , pp. 253-267
    • Anton, S.C.1
  • 2
    • 67549099054 scopus 로고    scopus 로고
    • Requirement for Twist1 in frontonasal and skull vault development in the mouse embryo
    • Bildsoe H, Loebel DA, Jones VJ, Chen YT, Behringer RR, Tam PP. 2009. Requirement for Twist1 in frontonasal and skull vault development in the mouse embryo. Dev Biol 331:176-188.
    • (2009) Dev Biol , vol.331 , pp. 176-188
    • Bildsoe, H.1    Loebel, D.A.2    Jones, V.J.3    Chen, Y.T.4    Behringer, R.R.5    Tam, P.P.6
  • 4
    • 42949105086 scopus 로고    scopus 로고
    • A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003
    • Boulet SL, Rasmussen S, Honein MA. 2008. A population-based study of craniosynostosis in metropolitan Atlanta, 1989-2003. Am J Med Genet Part A 146A:984-991.
    • (2008) Am J Med Genet Part A , vol.146 A , pp. 984-991
    • Boulet, S.L.1    Rasmussen, S.2    Honein, M.A.3
  • 5
    • 0031832127 scopus 로고    scopus 로고
    • The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome
    • Bourgeois P, Bolcato-Bellemin AL, Danse JM, Bloch-Zupan A, Yoshiba K, Stoetzel C, Perrin-Schmitt F. 1998. The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome. Hum Mol Genet 7:945-957.
    • (1998) Hum Mol Genet , vol.7 , pp. 945-957
    • Bourgeois, P.1    Bolcato-Bellemin, A.L.2    Danse, J.M.3    Bloch-Zupan, A.4    Yoshiba, K.5    Stoetzel, C.6    Perrin-Schmitt, F.7
  • 6
    • 0032910450 scopus 로고    scopus 로고
    • Three-dimensional analysis of craniofacial form in a familial rabbit model of nonsyndromic coronal suture synostosis using Euclidean distance matrix analysis
    • Burrows AM, Richtsmeier JT, Mooney MP, Smith TD, Losken HW, Siegel MI. 1999. Three-dimensional analysis of craniofacial form in a familial rabbit model of nonsyndromic coronal suture synostosis using Euclidean distance matrix analysis. Cleft Palate Craniofac J 36:196-206.
    • (1999) Cleft Palate Craniofac J , vol.36 , pp. 196-206
    • Burrows, A.M.1    Richtsmeier, J.T.2    Mooney, M.P.3    Smith, T.D.4    Losken, H.W.5    Siegel, M.I.6
  • 7
    • 0036788297 scopus 로고    scopus 로고
    • Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome
    • Carver E, Oram K, Gridley T. 2002. Craniosynostosis in Twist heterozygous mice: a model for Saethre-Chotzen syndrome. Anat Rec 268:90-92.
    • (2002) Anat Rec , vol.268 , pp. 90-92
    • Carver, E.1    Oram, K.2    Gridley, T.3
  • 8
    • 0028933142 scopus 로고
    • Twist is required in head mesenchyme for cranial neural tube morphogenesis
    • Chen ZF, Behringer RR. 1995. Twist is required in head mesenchyme for cranial neural tube morphogenesis. Genes Dev 9:686-699.
    • (1995) Genes Dev , vol.9 , pp. 686-699
    • Chen, Z.F.1    Behringer, R.R.2
  • 9
    • 0026718133 scopus 로고
    • Effects of fronto-occipital artificial cranial vault modification on the cranial base and face
    • Cheverud JM, Kohn LA, Konigsberg LW, Leigh SR. 1992. Effects of fronto-occipital artificial cranial vault modification on the cranial base and face. Am J Phys Anthropol 88:323-345.
    • (1992) Am J Phys Anthropol , vol.88 , pp. 323-345
    • Cheverud, J.M.1    Kohn, L.A.2    Konigsberg, L.W.3    Leigh, S.R.4
  • 11
    • 0035002962 scopus 로고    scopus 로고
    • The effect of neurocranial surgery on basicranial morphology in isolated sagittal craniosynostosis
    • DeLeon VB, Zumpano MP, Richtsmeier JT. 2001. The effect of neurocranial surgery on basicranial morphology in isolated sagittal craniosynostosis. Cleft Palate Craniofac J 38:134-146.
    • (2001) Cleft Palate Craniofac J , vol.38 , pp. 134-146
    • DeLeon, V.B.1    Zumpano, M.P.2    Richtsmeier, J.T.3
  • 14
    • 38849132555 scopus 로고    scopus 로고
    • Down-regulation of ubiquitin ligase Cbl induced by Twist haploinsufficiency in Saethre-Chotzen syndrome results in increased PI3K/Akt signaling and osteoblast proliferation
    • Guenou H, Kaabeche K, Dufour C, Miraoui H, Marie P. 2006. Down-regulation of ubiquitin ligase Cbl induced by Twist haploinsufficiency in Saethre-Chotzen syndrome results in increased PI3K/Akt signaling and osteoblast proliferation. Am J Pathol 169:1303-1311.
    • (2006) Am J Pathol , vol.169 , pp. 1303-1311
    • Guenou, H.1    Kaabeche, K.2    Dufour, C.3    Miraoui, H.4    Marie, P.5
  • 15
    • 20444448111 scopus 로고    scopus 로고
    • 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. 2005. A role for fibroblast growth factor receptor-2 in the altered osteoblast phenotype induced by Twist haploinsufficiency in the Saethre-Chotzen syndrome. Hum Mol Genet 14:1429-1439.
    • (2005) Hum Mol Genet , vol.14 , pp. 1429-1439
    • Guenou, H.1    Kaabeche, K.2    Mee, S.L.3    Marie, P.J.4
  • 16
    • 80052737779 scopus 로고    scopus 로고
    • Persistent expression of Twist1 in chondrocytes causes growth plate abnormalities and dwarfism in mice
    • Guzzo R, Andreeva V, Spicer D, Drissi M. 2011. Persistent expression of Twist1 in chondrocytes causes growth plate abnormalities and dwarfism in mice. Int J Dev Biol 55:641-647.
    • (2011) Int J Dev Biol , vol.55 , pp. 641-647
    • Guzzo, R.1    Andreeva, V.2    Spicer, D.3    Drissi, M.4
  • 18
    • 84866018266 scopus 로고    scopus 로고
    • Interrelationship of cranial suture fusion, basicranial development, and resynostosis following suturectomy in Twist1+/- mice, a murine model of Saethre-Chotzen syndrome
    • Hermann C, Lee C, Gadepalli S, Lawrence K, Richards M, Olivares-Navarrete R, Williams J, Schwartz Z, Boyan B. 2012. Interrelationship of cranial suture fusion, basicranial development, and resynostosis following suturectomy in Twist1+/- mice, a murine model of Saethre-Chotzen syndrome. Calcif Tissue Int 91:255-266.
    • (2012) Calcif Tissue Int , vol.91 , pp. 255-266
    • Hermann, C.1    Lee, C.2    Gadepalli, S.3    Lawrence, K.4    Richards, M.5    Olivares-Navarrete, R.6    Williams, J.7    Schwartz, Z.8    Boyan, B.9
  • 21
    • 84864027660 scopus 로고    scopus 로고
    • S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome
    • S252W is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome. Dev Biol 368:283-293.
    • (2012) Dev Biol , vol.368 , pp. 283-293
    • Holmes, G.1    Basilico, C.2
  • 22
    • 84881670219 scopus 로고    scopus 로고
    • Second family with the Boston-type craniosynostosis syndrome: novel mutation and expansion of the clinical spectrum
    • Janssen A, Hosen MJ, Jeannin P, Coucke PJ, De Paepe A, Vanakker OM. 2013. Second family with the Boston-type craniosynostosis syndrome: novel mutation and expansion of the clinical spectrum. Am J Med Genet Part A 161A:2352-2357.
    • (2013) Am J Med Genet Part A , vol.161 A , pp. 2352-2357
    • Janssen, A.1    Hosen, M.J.2    Jeannin, P.3    Coucke, P.J.4    De Paepe, A.5    Vanakker, O.M.6
  • 23
    • 0033870788 scopus 로고    scopus 로고
    • A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis?
    • Johnson D, Wall SA, Mann S, Wilkie AO. 2000. A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis? Eur J Hum Genet 8:571-577.
    • (2000) Eur J Hum Genet , vol.8 , pp. 571-577
    • Johnson, D.1    Wall, S.A.2    Mann, S.3    Wilkie, A.O.4
  • 25
    • 78650839801 scopus 로고    scopus 로고
    • MorphoJ: an integrated software package for geometric morphometrics
    • Klingenberg CP. 2011. MorphoJ: an integrated software package for geometric morphometrics. Mol Ecol Resour 11:353-357.
    • (2011) Mol Ecol Resour , vol.11 , pp. 353-357
    • Klingenberg, C.P.1
  • 26
    • 45849105613 scopus 로고    scopus 로고
    • Roles of FGFR2 and TWIST in human craniosynostosis: insights from genetic mutations in cranial osteoblasts
    • Marie PJ, Kaabeche K, Guenou H. 2008. Roles of FGFR2 and TWIST in human craniosynostosis: insights from genetic mutations in cranial osteoblasts. Front Oral Biol 12:144-159.
    • (2008) Front Oral Biol , vol.12 , pp. 144-159
    • Marie, P.J.1    Kaabeche, K.2    Guenou, H.3
  • 27
    • 0022908897 scopus 로고
    • Cranial base changes following surgical treatment of craniosynostosis
    • Marsh JL, Vannier MW. 1986. Cranial base changes following surgical treatment of craniosynostosis. Cleft Palate J 23(Suppl 1):9-18.
    • (1986) Cleft Palate J , vol.23 , Issue.SUPPL 1 , pp. 9-18
    • Marsh, J.L.1    Vannier, M.W.2
  • 31
    • 77956988604 scopus 로고    scopus 로고
    • Pivotal role of Twist in skeletal biology and pathology
    • Miraoui H, Marie P. 2010. Pivotal role of Twist in skeletal biology and pathology. Gene 468:1-7.
    • (2010) Gene , vol.468 , pp. 1-7
    • Miraoui, H.1    Marie, P.2
  • 32
    • 0031816780 scopus 로고    scopus 로고
    • A rabbit model of human familial, nonsyndromic unicoronal suture synostosis. I. Synostotic onset, pathology, and sutural growth patterns
    • Mooney MP, Siegel MI, Burrows AM, Smith TD, Losken HW, Dechant J, Cooper G, Kapucu MR. 1998. A rabbit model of human familial, nonsyndromic unicoronal suture synostosis. I. Synostotic onset, pathology, and sutural growth patterns. Childs Nerv Syst 14:236-246.
    • (1998) Childs Nerv Syst , vol.14 , pp. 236-246
    • Mooney, M.P.1    Siegel, M.I.2    Burrows, A.M.3    Smith, T.D.4    Losken, H.W.5    Dechant, J.6    Cooper, G.7    Kapucu, M.R.8
  • 33
  • 35
    • 79960064424 scopus 로고    scopus 로고
    • Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes
    • Purushothaman R, Cox TC, Maga AM, Cunningham ML. 2011. Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes. Birth Defects Res A Clin Mol Teratol 91:603-609.
    • (2011) Birth Defects Res A Clin Mol Teratol , vol.91 , pp. 603-609
    • Purushothaman, R.1    Cox, T.C.2    Maga, A.M.3    Cunningham, M.L.4
  • 36
    • 84855478714 scopus 로고    scopus 로고
    • Normal and disease-related biological functions of Twist1 and underlying molecular mechanisms
    • Qin Q, Xu Y, He T, Qin C, Xu J. 2012. Normal and disease-related biological functions of Twist1 and underlying molecular mechanisms. Cell Res 22:90-106.
    • (2012) Cell Res , vol.22 , pp. 90-106
    • Qin, Q.1    Xu, Y.2    He, T.3    Qin, C.4    Xu, J.5
  • 37
    • 0028263955 scopus 로고
    • Saethre-Chotzen syndrome
    • Reardon W, Winter RM. 1994. Saethre-Chotzen syndrome. J Med Genet 31:393-396.
    • (1994) J Med Genet , vol.31 , pp. 393-396
    • Reardon, W.1    Winter, R.M.2
  • 42
    • 0037084824 scopus 로고    scopus 로고
    • Twist haploinsufficiency in Saethre-Chotzen syndrome induces calvarial osteoblast apoptosis due to increased TNFalpha expression and caspase-2 activation
    • Yousfi M, Lasmoles F, El Ghouzzi V, Marie PJ. 2002a. Twist haploinsufficiency in Saethre-Chotzen syndrome induces calvarial osteoblast apoptosis due to increased TNFalpha expression and caspase-2 activation. Hum Mol Genet 11:359-369.
    • (2002) Hum Mol Genet , vol.11 , pp. 359-369
    • Yousfi, M.1    Lasmoles, F.2    El Ghouzzi, V.3    Marie, P.J.4
  • 43
    • 0035016726 scopus 로고    scopus 로고
    • Increased bone formation and decreased osteocalcin expression induced by reduced TWIST dosage in Saethre-Chotzen syndrome
    • Yousfi M, Lasmoles F, Lomri A, Delannoy P, Marie PJ. 2001. Increased bone formation and decreased osteocalcin expression induced by reduced TWIST dosage in Saethre-Chotzen syndrome. J Clin Invest 107:1153-1161.
    • (2001) J Clin Invest , vol.107 , pp. 1153-1161
    • Yousfi, M.1    Lasmoles, F.2    Lomri, A.3    Delannoy, P.4    Marie, P.J.5
  • 44
    • 0036387218 scopus 로고    scopus 로고
    • TWIST inactivation reduces CBFA1/RUNX2 expression and DNA binding to the osteocalcin promoter in osteoblasts
    • Yousfi M, Lasmoles F, Marie PJ. 2002b. TWIST inactivation reduces CBFA1/RUNX2 expression and DNA binding to the osteocalcin promoter in osteoblasts. Biochem Biophys Res Commun 297:641-644.
    • (2002) Biochem Biophys Res Commun , vol.297 , pp. 641-644
    • Yousfi, M.1    Lasmoles, F.2    Marie, P.J.3
  • 45
    • 84883760208 scopus 로고    scopus 로고
    • Analysis of Snail1 function and regulation by Twist1 in palatal fusion
    • Yu W, Zhang Y, Ruest L, Svoboda K. 2013. Analysis of Snail1 function and regulation by Twist1 in palatal fusion. Front Physiol 4:1-10.
    • (2013) Front Physiol , vol.4 , pp. 1-10
    • Yu, W.1    Zhang, Y.2    Ruest, L.3    Svoboda, K.4
  • 46
    • 84859761872 scopus 로고    scopus 로고
    • Specific inactivation of Twist1 in the mandibular arch neural crest cells affects the development of the ramus and reveals interactions with Hand2
    • Zhang Y, Blackwell E, McKnight M, Knutsen G, Vu W, Ruest L. 2012. Specific inactivation of Twist1 in the mandibular arch neural crest cells affects the development of the ramus and reveals interactions with Hand2. Dev Dyn 241:924-940.
    • (2012) Dev Dyn , vol.241 , pp. 924-940
    • Zhang, Y.1    Blackwell, E.2    McKnight, M.3    Knutsen, G.4    Vu, W.5    Ruest, L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.