메뉴 건너뛰기




Volumn 63, Issue 5, 2005, Pages 253-257

Immunohistochemical expression of p63 in human prenatal tooth primordia

Author keywords

Development; Histochemical; Human; Malformation; p63 gene; Tooth

Indexed keywords

HEMATOXYLIN; PROTEIN P63;

EID: 27144492019     PISSN: 00016357     EISSN: None     Source Type: Journal    
DOI: 10.1080/00016350510019919     Document Type: Article
Times cited : (10)

References (19)
  • 1
    • 0033594491 scopus 로고    scopus 로고
    • P63 is a P53 homologue required for limb and epidermal morphogenesis
    • Mills AA, Zheng B, Wang XJ, Vogel H, Roop DR, Bradley A. P63 is a P53 homologue required for limb and epidermal morphogenesis. Nature 1999;398(6729):708-13.
    • (1999) Nature , vol.398 , Issue.6729 , pp. 708-713
    • Mills, A.A.1    Zheng, B.2    Wang, X.J.3    Vogel, H.4    Roop, D.R.5    Bradley, A.6
  • 2
    • 0033594485 scopus 로고    scopus 로고
    • P63 is essential for regenerative proliferation in limb, craniofacial and epithelial development
    • Yang A, Schweitzer R, Sun D, Kaghad M, Walker N, Bronson RT, et al. P63 is essential for regenerative proliferation in limb, craniofacial and epithelial development. Nature 1999; 398(6729):714-18.
    • (1999) Nature , vol.398 , Issue.6729 , pp. 714-718
    • Yang, A.1    Schweitzer, R.2    Sun, D.3    Kaghad, M.4    Walker, N.5    Bronson, R.T.6
  • 3
    • 0028958081 scopus 로고
    • Ectoderm-mesenchyme and mesenchyme-mesenchyme interactions regulate Msx-1 expression and cellular differentiation in the murine limb bud
    • Wang Y, Sassoon D. Ectoderm-mesenchyme and mesenchyme-mesenchyme interactions regulate Msx-1 expression and cellular differentiation in the murine limb bud. Dev Biol 1995;168:374-82.
    • (1995) Dev Biol , vol.168 , pp. 374-382
    • Wang, Y.1    Sassoon, D.2
  • 4
    • 0037108134 scopus 로고    scopus 로고
    • P63 gene mutations and human developmental syndromes
    • Brunner HG, Hamel BC, Bokhoven Hv H. P63 gene mutations and human developmental syndromes. Am J Med Genet 2002; 112:284-90.
    • (2002) Am J Med Genet , vol.112 , pp. 284-290
    • Brunner, H.G.1    Hamel, B.C.2    Bokhoven, Hv.H.3
  • 6
    • 0035992715 scopus 로고    scopus 로고
    • Prenatal diagnosis of acro-dermatoungual-lacrimal-tooth syndrome, a dominantly inherited ectrodactyly
    • O'Brien KE, Shorrock J, Bianchi DW. Prenatal diagnosis of acro-dermatoungual-lacrimal-tooth syndrome, a dominantly inherited ectrodactyly. J Ultrasound Med 2002;21:921-5.
    • (2002) J Ultrasound Med , vol.21 , pp. 921-925
    • O'Brien, K.E.1    Shorrock, J.2    Bianchi, D.W.3
  • 8
  • 9
    • 0029974761 scopus 로고    scopus 로고
    • The EEC syndrome: A literature study
    • Roelfsema NM, Cobben JM. The EEC syndrome: a literature study. Clin Dysmorphol 1996;5:115-27.
    • (1996) Clin Dysmorphol , vol.5 , pp. 115-127
    • Roelfsema, N.M.1    Cobben, J.M.2
  • 10
    • 0029088987 scopus 로고
    • Twenty-four cases of the EEC syndrome: Clinical presentation and management
    • Buss PW, Hughes HE, Clarke A. Twenty-four cases of the EEC syndrome: clinical presentation and management. J Med Genet 1995;32:716-23.
    • (1995) J Med Genet , vol.32 , pp. 716-723
    • Buss, P.W.1    Hughes, H.E.2    Clarke, A.3
  • 11
    • 0017118874 scopus 로고
    • The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: An autosomal dominant condition
    • Hay RJ, Wells RS. The syndrome of ankyloblepharon, ectodermal defects and cleft lip and palate: an autosomal dominant condition. Br J Dermatol 1976;94:277-89.
    • (1976) Br J Dermatol , vol.94 , pp. 277-289
    • Hay, R.J.1    Wells, R.S.2
  • 13
    • 0033071807 scopus 로고    scopus 로고
    • Limb mammary syndrome: A new genetic disorder with mammary hypoplasia, ectrodactyly, and other hand/foot anomalies maps to human chromosome 3q27
    • van Bokhoven H, Jung M, Smits AP, van Beersum S, Ruschendorf F, van Steensel M, et al. Limb mammary syndrome: a new genetic disorder with mammary hypoplasia, ectrodactyly, and other hand/foot anomalies maps to human chromosome 3q27. Am J Hum Genet 1999;64:538-46.
    • (1999) Am J Hum Genet , vol.64 , pp. 538-546
    • Van Bokhoven, H.1    Jung, M.2    Smits, A.P.3    Van Beersum, S.4    Ruschendorf, F.5    Van Steensel, M.6
  • 16
    • 0034255855 scopus 로고    scopus 로고
    • Characterization of the expression pattern of P63 alpha and delta Np63 alpha in benign and malignant oral epithelial lesions
    • Nylander K, Coates PJ, Hall PA. Characterization of the expression pattern of P63 alpha and delta Np63 alpha in benign and malignant oral epithelial lesions. Int J Cancer 2000;87:368-72.
    • (2000) Int J Cancer , vol.87 , pp. 368-372
    • Nylander, K.1    Coates, P.J.2    Hall, P.A.3
  • 17
    • 0031883625 scopus 로고    scopus 로고
    • The life history of an embryonic signaling center: BMP-4 induces P21 and is associated with apoptosis in the mouse tooth enamel knot
    • Jernvall J, Aberg T, Kettunen P, Keranen S, Thesleff, I. The life history of an embryonic signaling center: BMP-4 induces P21 and is associated with apoptosis in the mouse tooth enamel knot. Development 1998;125:161-9.
    • (1998) Development , vol.125 , pp. 161-169
    • Jernvall, J.1    Aberg, T.2    Kettunen, P.3    Keranen, S.4    Thesleff, I.5
  • 18
  • 19
    • 0036538566 scopus 로고    scopus 로고
    • Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in P63
    • Duijf PH, Vanmolkot KR, Propping P, Friedl W, Krieger E, McKeon F, et al. Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in P63. Hum Mol Genet 2002;11:799-804.
    • (2002) Hum Mol Genet , vol.11 , pp. 799-804
    • Duijf, P.H.1    Vanmolkot, K.R.2    Propping, P.3    Friedl, W.4    Krieger, E.5    McKeon, F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.