메뉴 건너뛰기




Volumn 60, Issue 3, 2001, Pages 165-172

Distal limb malformations: Underlying mechanisms and clinical associations

Author keywords

Apical ectodermal ridge; Congenital abnormalities; Dactylaplasia; Ectrodactyly; EEC syndrome; Limb development; Limb malformations; p63; Split hand foot malformation

Indexed keywords

BIOLOGICAL MARKER; DACTYLIN; GROWTH FACTOR; PROTEIN P63; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

EID: 0034775067     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2001.600301.x     Document Type: Short Survey
Times cited : (33)

References (74)
  • 1
    • 26344434725 scopus 로고
    • Genetics and inheritance
    • The Care of Congenital Hand Anomalies St Louis: Quality Medical Publishing
    • (1994)
    • Flatt, A.E.1
  • 8
    • 0030790518 scopus 로고    scopus 로고
    • The mesenchymal factor, Fgf-10, initiates and maintains the outgrowth of the chick limb bud through interaction with Fgf-8 an apical ectodermal factor
    • (1997) Development , vol.124 , pp. 2235-2244
    • Ohuchi, H.1    Nakagawa, T.2    Yamamoto, A.3
  • 9
    • 0028930947 scopus 로고
    • Interaction between the signaling molecules WNT7a and SHH during vertebrate limb development: Dorsal signals regulate anteroposterior patterning
    • (1995) Cell , vol.80 , pp. 939-947
    • Yang, Y.1    Niswander, L.2
  • 11
    • 0027165874 scopus 로고
    • Fgf-4 maintains polarizing activity of posterior limb bud cells in vivo and in vitro
    • (1993) Development , vol.119 , pp. 199-206
    • Vogel, A.1    Tickle, C.2
  • 14
    • 84924843883 scopus 로고
    • The proximo-distal sequence of origin of the parts of the chick wing and the role of ectoderm
    • (1948) J Exp Zool , vol.108 , pp. 363-403
    • Saunders, J.W.1
  • 16
    • 0028951117 scopus 로고
    • Dorsalizing signal wnt7a required for normal polarity of DV and AP axes of mouse limb
    • (1995) Nature , vol.374 , pp. 350-353
    • Parr, B.A.1    McMahon, A.P.2
  • 19
    • 0028959288 scopus 로고
    • The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo
    • (1995) Development , vol.121 , pp. 439-451
    • Crossley, P.H.1    Martin, G.R.2
  • 26
    • 0029146659 scopus 로고
    • Cloning, expression, and chromosomal location of SHH and IHH: Two human homologues of the Drosophila segment polarity gene hedgehog
    • (1995) Genomics , vol.28 , pp. 44-51
    • Marigo, V.1    Roberts, D.J.2    Lee, S.M.3
  • 29
    • 0026454567 scopus 로고
    • Why we have (only) five fingers per hand. Hox genes and the evolution of paired limbs
    • (1992) Development , vol.116 , pp. 289-296
    • Tabin, C.J.1
  • 31
    • 17544386960 scopus 로고    scopus 로고
    • A chick wingless mutation causes abnormality in maintenance of Fgf8 expression in the wing apical ridge, resulting in loss of the dorsoventral boundary
    • (1997) Mech Dev , vol.62 , pp. 3-13
    • Ohuchi, H.1    Shibusawa, M.2    Nakagawa, T.3
  • 34
    • 0034656111 scopus 로고    scopus 로고
    • Targeted misexpression of constitutively active BMP receptor-IB causes bifurcation, duplication, and posterior transformation of digit in mouse limb
    • (2000) Dev Biol , vol.220 , pp. 154-167
    • Zhang, Z.1    Yu, X.2    Zhang, Y.3
  • 35
    • 0019828005 scopus 로고
    • Dactylaplasia in mice: A two-locus model for development anomalies
    • (1981) J Hered , vol.72 , pp. 234-237
    • Chai, C.K.1
  • 45
    • 0032161624 scopus 로고    scopus 로고
    • p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities
    • (1998) Mol Cell , vol.2 , pp. 305-316
    • Yang, A.1    Kaghad, M.2    Wang, Y.3
  • 46
  • 52
    • 0028958081 scopus 로고
    • Ectoderm-mesenchyme and mesenchyme-mesenchyme interactions regulate Msx-1 expression and cellular differentiation in the murine limb bud
    • (1995) Dev Biol , vol.168 , pp. 374-382
    • Wang, Y.1    Sassoon, D.2
  • 60
    • 0028153548 scopus 로고
    • Congenital abnormalities associated with limb deficiency defects: A population study based on cases from the Hungarian Congenital Malformation Registry (1975-1984)
    • (1994) Am J Med Genet , vol.49 , pp. 52-66
    • Evans, J.A.1    Vitez, M.2    Czeizel, A.3
  • 67
    • 0026671579 scopus 로고
    • EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2-q21.3
    • (1992) Clin Genet , vol.42 , pp. 101
    • Qumsiyeh, M.B.1
  • 71
    • 0027964261 scopus 로고
    • Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
    • (1994) Cell , vol.78 , pp. 335-342
    • Shiang, R.1    Thompson, L.M.2    Zhu, Y.Z.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.