메뉴 건너뛰기




Volumn 24, Issue 4, 2000, Pages 391-395

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BONE DEFECT; BONE GROWTH; CARTILAGE CELL; CELL DIFFERENTIATION; CELL PROLIFERATION; CHONDROGENESIS; CONTROLLED STUDY; EMBRYO; ENCHONDRAL OSSIFICATION; GENE LOSS; MORPHOGENESIS; MOUSE; MUTANT; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SKULL DEVELOPMENT;

EID: 0034029571     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/74231     Document Type: Article
Times cited : (641)

References (29)
  • 1
    • 0027431005 scopus 로고
    • A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
    • Jabs, E.W. et al. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 75, 443-450 (1993).
    • (1993) Cell , vol.75 , pp. 443-450
    • Jabs, E.W.1
  • 2
    • 0029800845 scopus 로고    scopus 로고
    • The molecular basis of Boston-type craniosynostosis: The Pro148 → his mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences
    • Ma, L., Golden, S., Wu, L. & Maxson, R. The molecular basis of Boston-type craniosynostosis: the Pro148 → His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences. Hum. Mol. Genet. 5, 1915-1920 (1996).
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1915-1920
    • Ma, L.1    Golden, S.2    Wu, L.3    Maxson, R.4
  • 3
    • 0034074417 scopus 로고    scopus 로고
    • Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification
    • Wilkie, A.O.M. et al. Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification. Nature Genet. 24, 387-390 (2000).
    • (2000) Nature Genet. , vol.24 , pp. 387-390
    • Wilkie, A.O.M.1
  • 4
    • 0033555425 scopus 로고    scopus 로고
    • Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: A possible mechanism for MSX2-mediated craniosynostosis in humans
    • Liu, Y.H. et al. Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans. Dev. Biol. 205, 260-274 (1999).
    • (1999) Dev. Biol. , vol.205 , pp. 260-274
    • Liu, Y.H.1
  • 5
    • 0033562384 scopus 로고    scopus 로고
    • Ectopic Msx2 overexpression inhibits and Msx2 antisense stimulates calvarial osteoblast differentiation
    • Dodig, M. et al. Ectopic Msx2 overexpression inhibits and Msx2 antisense stimulates calvarial osteoblast differentiation. Dev. Biol. 209, 298-307 (1999).
    • (1999) Dev. Biol. , vol.209 , pp. 298-307
    • Dodig, M.1
  • 6
    • 0032541970 scopus 로고    scopus 로고
    • Reciprocal regulation of osteocalcin transcription by the homeodomain proteins Msx2 and Dlx5
    • Newberry, E.P., Latifi, T. & Towler, D.A. Reciprocal regulation of osteocalcin transcription by the homeodomain proteins Msx2 and Dlx5. Biochemistry 37, 16360-16368 (1998).
    • (1998) Biochemistry , vol.37 , pp. 16360-16368
    • Newberry, E.P.1    Latifi, T.2    Towler, D.A.3
  • 7
    • 0029750190 scopus 로고    scopus 로고
    • Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein
    • Vortkamp, A. et al. Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein. Science 273, 613-622 (1996).
    • (1996) Science , vol.273 , pp. 613-622
    • Vortkamp, A.1
  • 8
    • 0028057743 scopus 로고
    • Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene
    • Karaplis, A.C. et al. Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene. Genes Dev. 8, 277-289 (1994).
    • (1994) Genes Dev. , vol.8 , pp. 277-289
    • Karaplis, A.C.1
  • 9
    • 9344241375 scopus 로고    scopus 로고
    • PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth
    • Lanske, B. et al. PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth. Science 273, 663-666 (1996).
    • (1996) Science , vol.273 , pp. 663-666
    • Lanske, B.1
  • 10
    • 0029887927 scopus 로고    scopus 로고
    • Haploinsufficiency of parathyroid hormone-related peptide (PTHrP) results in abnormal postnatal bone development
    • Amizuka, N. et al. Haploinsufficiency of parathyroid hormone-related peptide (PTHrP) results in abnormal postnatal bone development. Dev. Biol. 175, 166-176 (1996).
    • (1996) Dev. Biol. , vol.175 , pp. 166-176
    • Amizuka, N.1
  • 11
    • 0000767102 scopus 로고
    • Seizures associated with the Catlin mark
    • Kite, W.C. Jr Seizures associated with the Catlin mark. Neurology 11, 345-348 (1961).
    • (1961) Neurology , vol.11 , pp. 345-348
    • Kite W.C., Jr.1
  • 12
    • 0031764610 scopus 로고    scopus 로고
    • Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice
    • Pennachio, L.A. et al. Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice. Nature Genet. 20, 251-258 (1998).
    • (1998) Nature Genet. , vol.20 , pp. 251-258
    • Pennachio, L.A.1
  • 13
    • 0031928291 scopus 로고    scopus 로고
    • The cells and molecules that make a cerebellum
    • Goldwitz, D. & Hamre, K. The cells and molecules that make a cerebellum, Trends Neurosci. 21, 375-382 (1998).
    • (1998) Trends Neurosci. , vol.21 , pp. 375-382
    • Goldwitz, D.1    Hamre, K.2
  • 15
    • 0028292605 scopus 로고
    • Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development
    • Satokata, I. & Maas, R. Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development. Nature Genet. 6, 348-356 (1994).
    • (1994) Nature Genet. , vol.6 , pp. 348-356
    • Satokata, I.1    Maas, R.2
  • 16
    • 0031764335 scopus 로고    scopus 로고
    • FGFs and BMP4 induce both Msx1-independent and Msx1-dependent signaling pathways in early tooth development
    • Bei, M. & Maas, R. FGFs and BMP4 induce both Msx1-independent and Msx1-dependent signaling pathways in early tooth development. Development 125, 4325-4333 (1998).
    • (1998) Development , vol.125 , pp. 4325-4333
    • Bei, M.1    Maas, R.2
  • 17
    • 0026762590 scopus 로고
    • Expression patterns of the homeobox gene, Hox-8, in the mouse embryo suggest a role in specifying tooth initiation and shape
    • MacKenzie, A., Ferguson, M.W. & Sharpe, P.T. Expression patterns of the homeobox gene, Hox-8, in the mouse embryo suggest a role in specifying tooth initiation and shape. Development 115, 403-420 (1992).
    • (1992) Development , vol.115 , pp. 403-420
    • MacKenzie, A.1    Ferguson, M.W.2    Sharpe, P.T.3
  • 18
    • 0027931643 scopus 로고
    • FGF5 as a regulator of the hair growth cycle: Evidence from targeted and spontaneous mutations
    • Hébert, J.M., Rosenquist, T., Gotz, J. & Martin, G.R. FGF5 as a regulator of the hair growth cycle: evidence from targeted and spontaneous mutations. Cell 78, 1017-1025 (1994).
    • (1994) Cell , vol.78 , pp. 1017-1025
    • Hébert, J.M.1    Rosenquist, T.2    Gotz, J.3    Martin, G.R.4
  • 20
    • 0342722337 scopus 로고    scopus 로고
    • Regulation of Msx-1, Msx-2, Bmp-2, and Bmp-4 during foetal and postnatal mammary gland development
    • Phippard, D.J. et al. Regulation of Msx-1, Msx-2, Bmp-2, and Bmp-4 during foetal and postnatal mammary gland development. Development 122, 2729-2737 (1996).
    • (1996) Development , vol.122 , pp. 2729-2737
    • Phippard, D.J.1
  • 21
    • 0028963780 scopus 로고
    • Digit tip regeneration correlates with regions of Msx1 (Hox 7) expression in fetal and newborn mice
    • Reginelli, A.D., Wang, Y.Q., Sassoon, D. & Muneoka, K. Digit tip regeneration correlates with regions of Msx1 (Hox 7) expression in fetal and newborn mice. Development 121, 1065-1076 (1995).
    • (1995) Development , vol.121 , pp. 1065-1076
    • Reginelli, A.D.1    Wang, Y.Q.2    Sassoon, D.3    Muneoka, K.4
  • 22
    • 0025307712 scopus 로고
    • Hereditary cranium bifidium and symmetric parietal formina are the same entity
    • Little, B.B., Knoll, K.A., Klein, V.R. & Heller, K.B. Hereditary cranium bifidium and symmetric parietal formina are the same entity. Am. J. Med. Genet. 35, 453-458 (1990).
    • (1990) Am. J. Med. Genet. , vol.35 , pp. 453-458
    • Little, B.B.1    Knoll, K.A.2    Klein, V.R.3    Heller, K.B.4
  • 23
    • 0029067515 scopus 로고
    • Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family
    • Preis, S., Engelbrecht, V. & Lenard, H.G. Aplasia cutis congenita and enlarged parietal foramina (Catlin marks) in a family. Acta Paediatr. 84, 701-702 (1995).
    • (1995) Acta Paediatr. , vol.84 , pp. 701-702
    • Preis, S.1    Engelbrecht, V.2    Lenard, H.G.3
  • 25
    • 0032842838 scopus 로고    scopus 로고
    • Eya7-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia
    • Xu, P.-X. et al. Eya7-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia. Nature Genet. 23, 113-117 (1999).
    • (1999) Nature Genet. , vol.23 , pp. 113-117
    • Xu, P.-X.1
  • 26
    • 0024412399 scopus 로고
    • Epithelial cytodifferentiation and extracellular matrix formation in enamel free areas of the occlusal cusp during development of mouse molars: Light and electron microscopic studies
    • Sakakura, Y., Fujiwara, N. & Nawa, T. Epithelial cytodifferentiation and extracellular matrix formation in enamel free areas of the occlusal cusp during development of mouse molars: light and electron microscopic studies. Am. J. Anat. 184, 287-297 (1989).
    • (1989) Am. J. Anat. , vol.184 , pp. 287-297
    • Sakakura, Y.1    Fujiwara, N.2    Nawa, T.3
  • 27
    • 0344054050 scopus 로고    scopus 로고
    • A comprehensive guide for the recognition and classification of distinct stages of hair follicle morphogenesis
    • Paus, R. et al. A comprehensive guide for the recognition and classification of distinct stages of hair follicle morphogenesis. J. Invest. Dermatol. 113, 523-532 (1999).
    • (1999) J. Invest. Dermatol. , vol.113 , pp. 523-532
    • Paus, R.1
  • 28
    • 0030955557 scopus 로고    scopus 로고
    • Basal cell carcinomas in mice overexpressing sonic hedgehog
    • Oro, A.E. et al. Basal cell carcinomas in mice overexpressing Sonic hedgehog. Science 276, 817-821 (1997).
    • (1997) Science , vol.276 , pp. 817-821
    • Oro, A.E.1
  • 29
    • 0027945654 scopus 로고
    • Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1 deficient mice
    • van Genderen, C. et al. Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1 deficient mice. Genes Dev. 8, 2691-2703 (1994).
    • (1994) Genes Dev. , vol.8 , pp. 2691-2703
    • Van Genderen, C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.