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Volumn 31, Issue 2, 2011, Pages 159-166

Aberrant lymphatic development in euploid fetuses with increased nuchal translucency including Noonan syndrome

Author keywords

Lymphatic development; Noonan syndrome; Nuchal edema; Nuchal translucency

Indexed keywords

BIOLOGICAL MARKER; LYMPHOCYTE SURFACE MARKER; NEUROPILIN 1; PLATELET DERIVED GROWTH FACTOR B; PODOPLANIN; PROTEIN LYVE 1; PROTEIN PROX 1; SMOOTH MUSCLE ACTIN; SONIC HEDGEHOG PROTEIN; TRANSCRIPTION FACTOR CDX1; TRANSCRIPTION FACTOR FOXC2; UNCLASSIFIED DRUG; VASCULOTROPIN A; VON WILLEBRAND FACTOR;

EID: 79251498665     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2666     Document Type: Article
Times cited : (21)

References (29)
  • 1
    • 0034729087 scopus 로고    scopus 로고
    • Noonan syndrome: a cryptic condition in early gestation
    • Achiron R, Heggesh J, Grisaru D, et al. 2000. Noonan syndrome: a cryptic condition in early gestation. Am J Med Genet 92(3): 159-165.
    • (2000) Am J Med Genet , vol.92 , Issue.3 , pp. 159-165
    • Achiron, R.1    Heggesh, J.2    Grisaru, D.3
  • 2
    • 63849250390 scopus 로고    scopus 로고
    • Noonan syndrome cardiac defects are caused by PTPN11 acting in endocardium to enhance endocardial-mesenchymal transformation
    • Araki T, Chan G, Newbigging S, Morikawa L, Bronson RT, Neel BG. 2009. Noonan syndrome cardiac defects are caused by PTPN11 acting in endocardium to enhance endocardial-mesenchymal transformation. Proc Natl Acad Sci USA 106(12): 4736-4741.
    • (2009) Proc Natl Acad Sci USA , vol.106 , Issue.12 , pp. 4736-4741
    • Araki, T.1    Chan, G.2    Newbigging, S.3    Morikawa, L.4    Bronson, R.T.5    Neel, B.G.6
  • 3
    • 33646075955 scopus 로고    scopus 로고
    • Nuchal edema and venous-lymphatic phenotype disturbance in human fetuses and mouse embryos with aneuploidy
    • Bekker MN, van den Akker NSM, Bartelings MM, et al. 2006. Nuchal edema and venous-lymphatic phenotype disturbance in human fetuses and mouse embryos with aneuploidy. J Soc Gynecol Investig 13: 209-216.
    • (2006) J Soc Gynecol Investig , vol.13 , pp. 209-216
    • Bekker, M.N.1    van den Akker, N.S.M.2    Bartelings, M.M.3
  • 5
    • 74949127403 scopus 로고    scopus 로고
    • Nuchal translucency and lymphatic system maldevelopment
    • Bellini C, Rutigliani M, Boccardo FM, et al. 2009. Nuchal translucency and lymphatic system maldevelopment. J Perinat Med 37(6): 673-676.
    • (2009) J Perinat Med , vol.37 , Issue.6 , pp. 673-676
    • Bellini, C.1    Rutigliani, M.2    Boccardo, F.M.3
  • 8
    • 69749098035 scopus 로고    scopus 로고
    • Abnormal Shh and FOXC2 expression correlates with aberrant lymphatic development in human fetuses with increased nuchal translucency
    • de Mooij YM, Van Den Akker NM, Bekker MN, et al. 2009. Abnormal Shh and FOXC2 expression correlates with aberrant lymphatic development in human fetuses with increased nuchal translucency. Prenat Diagn 29(9): 840-846.
    • (2009) Prenat Diagn , vol.29 , Issue.9 , pp. 840-846
    • de Mooij, Y.M.1    Van Den Akker, N.M.2    Bekker, M.N.3
  • 9
    • 0028825887 scopus 로고
    • Overexpression of vascular endothelial growth factor in the avian embryo induces hypervascularization and increased vascular permeability without alterations of embryonic pattern formation
    • Flamme I, von RM, Drexler HC, Syed-Ali S, Risau W. 1995. Overexpression of vascular endothelial growth factor in the avian embryo induces hypervascularization and increased vascular permeability without alterations of embryonic pattern formation. Dev Biol 171(2): 399-414.
    • (1995) Dev Biol , vol.171 , Issue.2 , pp. 399-414
    • Flamme, I.1    von, R.M.2    Drexler, H.C.3    Syed-Ali, S.4    Risau, W.5
  • 12
  • 13
    • 24944534593 scopus 로고    scopus 로고
    • VEGF-A and FGF-2 synergistically promote neoangiogenesis through enhancement of endogenous PDGF-B-PDGFRbeta signaling
    • Kano MR, Morishita Y, Iwata C, et al. 2005. VEGF-A and FGF-2 synergistically promote neoangiogenesis through enhancement of endogenous PDGF-B-PDGFRbeta signaling. J Cell Sci 118(Pt 16): 3759-3768.
    • (2005) J Cell Sci , vol.118 , Issue.PT 16 , pp. 3759-3768
    • Kano, M.R.1    Morishita, Y.2    Iwata, C.3
  • 14
    • 57349108541 scopus 로고    scopus 로고
    • PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome
    • Ko JM, Kim JM, Kim GH, Yoo HW. 2008. PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome. J Hum Genet 53(11-12): 999-1006.
    • (2008) J Hum Genet , vol.53 , Issue.11-12 , pp. 999-1006
    • Ko, J.M.1    Kim, J.M.2    Kim, G.H.3    Yoo, H.W.4
  • 15
    • 0032560844 scopus 로고    scopus 로고
    • VEGF/VPF overexpression in skin of transgenic mice induces angiogenesis, vascular hyperpermeability and accelerated tumor development
    • Larcher F, Murillas R, Bolontrade M, Conti CJ, Jorcano JL. 1998. VEGF/VPF overexpression in skin of transgenic mice induces angiogenesis, vascular hyperpermeability and accelerated tumor development. Oncogene 17(3): 303-311.
    • (1998) Oncogene , vol.17 , Issue.3 , pp. 303-311
    • Larcher, F.1    Murillas, R.2    Bolontrade, M.3    Conti, C.J.4    Jorcano, J.L.5
  • 16
    • 0036070186 scopus 로고    scopus 로고
    • sonic hedgehog and vascular endothelial growth factor act upstream of the Notch pathway during arterial endothelial differentiation
    • Lawson ND, Vogel AM, Weinstein BM. 2002. sonic hedgehog and vascular endothelial growth factor act upstream of the Notch pathway during arterial endothelial differentiation. Dev Cell 3(1): 127-136.
    • (2002) Dev Cell , vol.3 , Issue.1 , pp. 127-136
    • Lawson, N.D.1    Vogel, A.M.2    Weinstein, B.M.3
  • 17
    • 0033607817 scopus 로고    scopus 로고
    • Vascular endothelial growth factor (VEGF) and VEGF-C show overlapping binding sites in embryonic endothelia and distinct sites in differentiated adult endothelia
    • Lymboussaki A, Olofsson B, Eriksson U, Alitalo K. 1999. Vascular endothelial growth factor (VEGF) and VEGF-C show overlapping binding sites in embryonic endothelia and distinct sites in differentiated adult endothelia. Circ Res 85(11): 992-999.
    • (1999) Circ Res , vol.85 , Issue.11 , pp. 992-999
    • Lymboussaki, A.1    Olofsson, B.2    Eriksson, U.3    Alitalo, K.4
  • 19
    • 18544386859 scopus 로고    scopus 로고
    • Lymphatic endothelial reprogramming of vascular endothelial cells by the Prox-1 homeobox transcription factor
    • Petrova TV, Makinen T, Makela TP, et al. 2002. Lymphatic endothelial reprogramming of vascular endothelial cells by the Prox-1 homeobox transcription factor. EMBO J 21(17): 4593-4599.
    • (2002) EMBO J , vol.21 , Issue.17 , pp. 4593-4599
    • Petrova, T.V.1    Makinen, T.2    Makela, T.P.3
  • 20
    • 0034960583 scopus 로고    scopus 로고
    • The morphogen Sonic hedgehog is an indirect angiogenic agent upregulating two families of angiogenic growth factors
    • Pola R, Ling LE, Silver M, et al. 2001. The morphogen Sonic hedgehog is an indirect angiogenic agent upregulating two families of angiogenic growth factors. Nat Med 7(6): 706-711.
    • (2001) Nat Med , vol.7 , Issue.6 , pp. 706-711
    • Pola, R.1    Ling, L.E.2    Silver, M.3
  • 21
    • 0031080033 scopus 로고    scopus 로고
    • First trimester isolated fetal nuchal lucency: significance and outcome
    • Reynders CS, Pauker SP, Benacerraf BR. 1997. First trimester isolated fetal nuchal lucency: significance and outcome. J ltrasound Med 16(2): 101-105.
    • (1997) J ltrasound Med , vol.16 , Issue.2 , pp. 101-105
    • Reynders, C.S.1    Pauker, S.P.2    Benacerraf, B.R.3
  • 22
    • 0032146382 scopus 로고    scopus 로고
    • UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks of gestation. Fetal Medicine Foundation First Trimester Screening Group
    • Snijders RJ, Noble P, Sebire N, Souka A, Nicolaides KH. 1998. UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10-14 weeks of gestation. Fetal Medicine Foundation First Trimester Screening Group. Lancet 352(9125): 343-346.
    • (1998) Lancet , vol.352 , Issue.9125 , pp. 343-346
    • Snijders, R.J.1    Noble, P.2    Sebire, N.3    Souka, A.4    Nicolaides, K.H.5
  • 23
    • 0031926213 scopus 로고    scopus 로고
    • Defects and syndromes in chromosomally normal fetuses with increased nuchal translucency thickness at 10-14 weeks of gestation
    • Souka AP, Snijders RJ, Novakov A, Soares W, Nicolaides KH. 1998. Defects and syndromes in chromosomally normal fetuses with increased nuchal translucency thickness at 10-14 weeks of gestation. Ultrasound Obstet Gynecol 11(6): 391-400.
    • (1998) Ultrasound Obstet Gynecol , vol.11 , Issue.6 , pp. 391-400
    • Souka, A.P.1    Snijders, R.J.2    Novakov, A.3    Soares, W.4    Nicolaides, K.H.5
  • 24
    • 0034920539 scopus 로고    scopus 로고
    • Outcome of pregnancy in chromosomally normal fetuses with increased nuchal translucency in the first trimester
    • Souka AP, Krampl E, Bakalis S, Heath V, Nicolaides KH. 2001. Outcome of pregnancy in chromosomally normal fetuses with increased nuchal translucency in the first trimester. Ultrasound Obstet Gynecol 18(1): 9-17.
    • (2001) Ultrasound Obstet Gynecol , vol.18 , Issue.1 , pp. 9-17
    • Souka, A.P.1    Krampl, E.2    Bakalis, S.3    Heath, V.4    Nicolaides, K.H.5
  • 26
    • 0032999749 scopus 로고    scopus 로고
    • A screening program for trisomy 21 at 10-14 weeks using fetal nuchal translucency, maternal serum free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A
    • Spencer K, Souter V, Tul N, Snijders R, Nicolaides KH. 1999. A screening program for trisomy 21 at 10-14 weeks using fetal nuchal translucency, maternal serum free beta-human chorionic gonadotropin and pregnancy-associated plasma protein-A. Ultrasound Obstet Gynecol 13(4): 231-237.
    • (1999) Ultrasound Obstet Gynecol , vol.13 , Issue.4 , pp. 231-237
    • Spencer, K.1    Souter, V.2    Tul, N.3    Snijders, R.4    Nicolaides, K.H.5
  • 27
    • 0037329890 scopus 로고    scopus 로고
    • VEGF: a modifier of the del22q11 (DiGeorge) syndrome?
    • Stalmans I, Lambrechts D, De Smet F, et al. 2003. VEGF: a modifier of the del22q11 (DiGeorge) syndrome?. Nat Med 9(2): 173-182.
    • (2003) Nat Med , vol.9 , Issue.2 , pp. 173-182
    • Stalmans, I.1    Lambrechts, D.2    De Smet, F.3
  • 28
    • 0031006692 scopus 로고    scopus 로고
    • Cardiac morphology at late fetal stages in the mouse with trisomy 16: consequences for different formation of the atrioventricular junction when compared to humans with trisomy 21
    • Webb S, Brown NA, Anderson RH. 1997. Cardiac morphology at late fetal stages in the mouse with trisomy 16: consequences for different formation of the atrioventricular junction when compared to humans with trisomy 21. Cardiovasc Res 34(3): 515-524.
    • (1997) Cardiovasc Res , vol.34 , Issue.3 , pp. 515-524
    • Webb, S.1    Brown, N.A.2    Anderson, R.H.3
  • 29
    • 0033578853 scopus 로고    scopus 로고
    • Prox1 function is required for the development of the murine lymphatic system
    • Wigle JT, Oliver G. 1999. Prox1 function is required for the development of the murine lymphatic system. Cell 98(6): 769-778.
    • (1999) Cell , vol.98 , Issue.6 , pp. 769-778
    • Wigle, J.T.1    Oliver, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.