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Volumn 4, Issue , 2011, Pages

Gene expression in cardiac tissues from infants with idiopathic conotruncal defects

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH RECEPTOR; WNT PROTEIN;

EID: 78650763380     PISSN: None     EISSN: 17558794     Source Type: Journal    
DOI: 10.1186/1755-8794-4-1     Document Type: Article
Times cited : (52)

References (24)
  • 1
    • 0015029234 scopus 로고
    • Congenital heart disease in 56,109 births. Incidence and natural history
    • 5102136
    • Congenital heart disease in 56,109 births. Incidence and natural history. SC Mitchell SB Korones HW Berendes, Circulation 1971 43 3 323 332 5102136
    • (1971) Circulation , vol.43 , Issue.3 , pp. 323-332
    • Mitchell, S.C.1    Korones, S.B.2    Berendes, H.W.3
  • 2
    • 39749191367 scopus 로고    scopus 로고
    • The developmental genetics of congenital heart disease
    • 10.1038/nature06801. 18288184
    • The developmental genetics of congenital heart disease. BG Bruneau, Nature 2008 451 7181 943 948 10.1038/nature06801 18288184
    • (2008) Nature , vol.451 , Issue.7181 , pp. 943-948
    • Bruneau, B.G.1
  • 3
    • 41149125478 scopus 로고    scopus 로고
    • Genetic mechanisms controlling cardiovascular development
    • 10.1196/annals.1420.003. 18375573
    • Genetic mechanisms controlling cardiovascular development. J Bentham S Bhattacharya, Ann N Y Acad Sci 2008 1123 10 19 10.1196/annals.1420.003 18375573
    • (2008) Ann N y Acad Sci , vol.1123 , pp. 10-19
    • Bentham, J.1    Bhattacharya, S.2
  • 4
    • 3242766009 scopus 로고    scopus 로고
    • Outcomes of pregnancy in women with tetralogy of Fallot
    • 10.1016/j.jacc.2003.11.067. 15234429
    • Outcomes of pregnancy in women with tetralogy of Fallot. GR Veldtman HM Connolly M Grogan NM Ammash CA Warnes, J Am Coll Cardiol 2004 44 1 174 180 10.1016/j.jacc.2003.11.067 15234429
    • (2004) J Am Coll Cardiol , vol.44 , Issue.1 , pp. 174-180
    • Veldtman, G.R.1    Connolly, H.M.2    Grogan, M.3    Ammash, N.M.4    Warnes, C.A.5
  • 6
    • 0025124318 scopus 로고
    • Prevalence of significant congenital heart defects in children of parents with Fallot's tetralogy
    • 10.1016/0002-9149(90)90825-L. 2305694
    • Prevalence of significant congenital heart defects in children of parents with Fallot's tetralogy. TM Zellers DJ Driscoll VV Michels, Am J Cardiol 1990 65 7 523 526 10.1016/0002-9149(90)90825-L 2305694
    • (1990) Am J Cardiol , vol.65 , Issue.7 , pp. 523-526
    • Zellers, T.M.1    Driscoll, D.J.2    Michels, V.V.3
  • 7
    • 0043097670 scopus 로고    scopus 로고
    • Congenital heart disease
    • London: Churchill Livingstone Ringmoin DL, Conner JM, Pyeritz RE
    • Congenital heart disease. J Burn J Goodship, Principles and Practice of Medical Genetics London: Churchill Livingstone, Ringmoin DL, Conner JM, Pyeritz RE, 2002
    • (2002) Principles and Practice of Medical Genetics
    • Burn, J.1    Goodship, J.2
  • 8
    • 0242636701 scopus 로고    scopus 로고
    • NKX2.5 mutations in patients with congenital heart disease
    • 10.1016/j.jacc.2003.05.004. 14607454
    • NKX2.5 mutations in patients with congenital heart disease. DB McElhinney E Geiger J Blinder DW Benson E Goldmuntz, J Am Coll Cardiol 2003 42 9 1650 1655 10.1016/j.jacc.2003.05.004 14607454
    • (2003) J Am Coll Cardiol , vol.42 , Issue.9 , pp. 1650-1655
    • McElhinney, D.B.1    Geiger, E.2    Blinder, J.3    Benson, D.W.4    Goldmuntz, E.5
  • 9
    • 0035830860 scopus 로고    scopus 로고
    • Principles for the buffering of genetic variation
    • 10.1126/science.291.5506.1001. 11232561
    • Principles for the buffering of genetic variation. JLt Hartman B Garvik L Hartwell, Science 2001 291 5506 1001 1004 10.1126/science.291.5506.1001 11232561
    • (2001) Science , vol.291 , Issue.5506 , pp. 1001-1004
    • Jlt, H.1    Garvik, B.2    Hartwell, L.3
  • 10
    • 0037226648 scopus 로고    scopus 로고
    • Quantitative epigenetics
    • 10.1038/ng0103-6. 12509772
    • Quantitative epigenetics. SL Rutherford S Henikoff, Nat Genet 2003 33 1 6 8 10.1038/ng0103-6 12509772
    • (2003) Nat Genet , vol.33 , Issue.1 , pp. 6-8
    • Rutherford, S.L.1    Henikoff, S.2
  • 11
    • 0742287679 scopus 로고    scopus 로고
    • Waddington's widget: Hsp90 and the inheritance of acquired characters
    • 10.1016/j.semcdb.2003.09.024. 14986860
    • Waddington's widget: Hsp90 and the inheritance of acquired characters. DM Ruden MD Garfinkel VE Sollars X Lu, Semin Cell Dev Biol 2003 14 5 301 310 10.1016/j.semcdb.2003.09.024 14986860
    • (2003) Semin Cell Dev Biol , vol.14 , Issue.5 , pp. 301-310
    • Ruden, D.M.1    Garfinkel, M.D.2    Sollars, V.E.3    Lu, X.4
  • 12
    • 0037228526 scopus 로고    scopus 로고
    • Evidence for an epigenetic mechanism by which Hsp90 acts as a capacitor for morphological evolution
    • 10.1038/ng1067. 12483213
    • Evidence for an epigenetic mechanism by which Hsp90 acts as a capacitor for morphological evolution. V Sollars X Lu L Xiao X Wang MD Garfinkel DM Ruden, Nat Genet 2003 33 1 70 74 10.1038/ng1067 12483213
    • (2003) Nat Genet , vol.33 , Issue.1 , pp. 70-74
    • Sollars, V.1    Lu, X.2    Xiao, L.3    Wang, X.4    Garfinkel, M.D.5    Ruden, D.M.6
  • 13
    • 4544235083 scopus 로고    scopus 로고
    • Epigenetic regulation of translation reveals hidden genetic variation to produce complex traits
    • 10.1038/nature02885. 15311209
    • Epigenetic regulation of translation reveals hidden genetic variation to produce complex traits. HL True I Berlin SL Lindquist, Nature 2004 431 7005 184 187 10.1038/nature02885 15311209
    • (2004) Nature , vol.431 , Issue.7005 , pp. 184-187
    • True, H.L.1    Berlin, I.2    Lindquist, S.L.3
  • 16
    • 77949458939 scopus 로고    scopus 로고
    • Identification of novel glial genes by single-cell transcriptional profiling of Bergmann glial cells from mouse cerebellum
    • 10.1371/journal.pone.0009198. 20169146
    • Identification of novel glial genes by single-cell transcriptional profiling of Bergmann glial cells from mouse cerebellum. S Koirala G Corfas, PLoS One 2010 5 2 9198 10.1371/journal.pone.0009198 20169146
    • (2010) PLoS One , vol.5 , Issue.2 , pp. 59198
    • Koirala, S.1    Corfas, G.2
  • 17
    • 33846331967 scopus 로고    scopus 로고
    • Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana
    • 10.1073/pnas.0609063103. 17197417
    • Cross-talk between singlet oxygen- and hydrogen peroxide-dependent signaling of stress responses in Arabidopsis thaliana. C Laloi M Stachowiak E Pers-Kamczyc E Warzych I Murgia K Apel, Proc Natl Acad Sci USA 2007 104 2 672 677 10.1073/pnas.0609063103 17197417
    • (2007) Proc Natl Acad Sci USA , vol.104 , Issue.2 , pp. 672-677
    • Laloi, C.1    Stachowiak, M.2    Pers-Kamczyc, E.3    Warzych, E.4    Murgia, I.5    Apel, K.6
  • 18
    • 33847417017 scopus 로고    scopus 로고
    • Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome
    • 17036336
    • Whole genome microarray analysis of gene expression in an imprinting center deletion mouse model of Prader-Willi syndrome. DC Bittel N Kibiryeva SG McNulty DJ Driscoll MG Butler RA White, Am J Med Genet A 2007 143 5 422 429 17036336
    • (2007) Am J Med Genet A , vol.143 , Issue.5 , pp. 422-429
    • Bittel, D.C.1    Kibiryeva, N.2    McNulty, S.G.3    Driscoll, D.J.4    Butler, M.G.5    White, R.A.6
  • 20
    • 34547662012 scopus 로고    scopus 로고
    • Whole genome microarray analysis of gene expression in subjects with fragile X syndrome
    • DOI 10.1097/GIM.0b013e3180ca9a9a, PII 0012581720070700000008
    • Whole genome microarray analysis of gene expression in subjects with fragile X syndrome. DC Bittel N Kibiryeva MG Butler, Genet Med 2007 9 7 464 472 10.1097/GIM.0b013e3180ca9a9a 17666893 (Pubitemid 47222139)
    • (2007) Genetics in Medicine , vol.9 , Issue.7 , pp. 464-472
    • Bittel, D.C.1    Kibiryeva, N.2    Butler, M.G.3
  • 21
    • 10644257888 scopus 로고    scopus 로고
    • Microarray analysis of gene/transcript expression in Angelman syndrome: Deletion versus UPD
    • 10.1016/j.ygeno.2004.10.010. 15607424
    • Microarray analysis of gene/transcript expression in Angelman syndrome: deletion versus UPD. DC Bittel N Kibiryeva Z Talebizadeh DJ Driscoll MG Butler, Genomics 2005 85 1 85 91 10.1016/j.ygeno.2004.10.010 15607424
    • (2005) Genomics , vol.85 , Issue.1 , pp. 85-91
    • Bittel, D.C.1    Kibiryeva, N.2    Talebizadeh, Z.3    Driscoll, D.J.4    Butler, M.G.5
  • 22
    • 0036801060 scopus 로고    scopus 로고
    • Distinct requirements for extra-embryonic and embryonic bone morphogenetic protein 4 in the formation of the node and primitive streak and coordination of left-right asymmetry in the mouse
    • 12361961
    • Distinct requirements for extra-embryonic and embryonic bone morphogenetic protein 4 in the formation of the node and primitive streak and coordination of left-right asymmetry in the mouse. T Fujiwara DB Dehart KK Sulik BL Hogan, Development 2002 129 20 4685 4696 12361961
    • (2002) Development , vol.129 , Issue.20 , pp. 4685-4696
    • Fujiwara, T.1    Dehart, D.B.2    Sulik, K.K.3    Hogan, B.L.4
  • 23
    • 0034119237 scopus 로고    scopus 로고
    • The hypoplastic heart in congenital diaphragmatic hernia: Reduced expression of basic fibroblast growth factor and platelet-derived growth factor
    • 10.1007/s003830050737. 10898222
    • The hypoplastic heart in congenital diaphragmatic hernia: reduced expression of basic fibroblast growth factor and platelet-derived growth factor. N Guarino H Shima P Puri, Pediatr Surg Int 2000 16 4 243 246 10.1007/s003830050737 10898222
    • (2000) Pediatr Surg Int , vol.16 , Issue.4 , pp. 243-246
    • Guarino, N.1    Shima, H.2    Puri, P.3
  • 24
    • 0032764442 scopus 로고    scopus 로고
    • Advances in the molecular genetics of congenital structural heart disease
    • 10464664
    • Advances in the molecular genetics of congenital structural heart disease. CS Mah CJ Vaughan CT Basson, Genet Test 1999 3 2 157 172 10464664
    • (1999) Genet Test , vol.3 , Issue.2 , pp. 157-172
    • Mah, C.S.1    Vaughan, C.J.2    Basson, C.T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.