Ubiquitin fusion degradation 1-like gene dysregulation in bicuspid aortic valve

Journal of Thoracic and Cardiovascular Surgery

Volumn 130, Issue 6, 2005, Pages 1531-1536

  Mohamed, Salah Ali ^a   Hanke, Thorsten ^a   Schlueter, Claudia ^b   Bullerdiek, Joern ^b   Sievers, Hans Hinrich ^a  

^a UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^b UNIVERSITY OF BREMEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT;

AORTA VALVE; ARTICLE; CHROMOSOME 22; CHROMOSOME DELETION; CONTROLLED STUDY; DOWN REGULATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE CONTROL; GENE DELETION; GENE EXPRESSION; GENETIC DISORDER; HUMAN; HUMAN TISSUE; HYPOTHESIS; INTRAOPERATIVE PERIOD; MALE; MITRAL VALVE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; STATISTICAL SIGNIFICANCE; TRICUSPID VALVE; UBIQUITIN FUSION DEGRADATION 1 LIKE GENE; WESTERN BLOTTING;

AORTIC VALVE; FEMALE; GENE EXPRESSION REGULATION; HUMANS; MALE; MIDDLE AGED; PROTEINS; UBIQUITINS;

EID: 27944503483     PISSN: 00225223     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jtcvs.2005.08.017     Document Type: Article

References (30)

1. W.C. Roberts The congenitally bicuspid aortic valve Am J Cardiol 26 1970 72 82
2. M.W. Wessels, R.M. Berger, I.M. Frohn-Mulder, J.W. Roos-Hesselink, J.J. Hoogeboom, G.S. Mancini Autosomal dominant inheritance of left ventricular outflow tract obstruction Am J Med Genet A 134 2005 171 179
3. V.A. McKusick Association of congenital bicuspid aortic valve and Erdheim's cystic medial necrosis Lancet 1 1972 1026 1027
4. Nataatmadja M, West M, West J, Summers K, Walker P, Nagata M, et al. Abnormal extracellular matrix protein transport associated with increased apoptosis of vascular smooth muscle cells in Marfan syndrome and bicuspid aortic valve thoracic aortic aneurysm Circulation. 2003;108 Suppl 1:II329-34.
5. D. Bonderman, E. Gharehbaghi-Schnell, G. Wollenek, G. Maurer, H. Baumgartner, I.M. Lang Mechanisms underlying aortic dilatation in congenital aortic valve malformation Circulation 99 1999 2138 2143
6. M.J. Zigmond, F.E. Bloom, S.C. Landis, J.L. Roberts, L.R. Squire Neurogenesis and migration M.J. Zigmond F.E. Bloom S.C. Landis J.L. Roberts L.R. Squire Fundamental neuroscience 1998 Academic Press San Diego p. 451-80
7. N.M. Le Douarin, M.A. Teillet Experimental analysis of the migration and differentiation of neurectodernam mesenchymal derivatives, using a biological cell making technique Dev Biol 41 1974 162 184
8. M.L. Kirby, K.L. Waldo Role of neural crest in congenital heart disease Circulation 82 1990 332 340
9. D. Srivastava, P. Cserjesi, E.N. Olson A subclass of bHLH proteins required for cardiac morphogenesis Science 270 1995 1995 1999
10. T. Thomas, H. Yamagishi, P.A. Overbeek, E.N. Olson, D. Srivastava The bHLH factors, dHAND and eHAND, specify pulmonary and systemic cardiac ventricles independent of left-right sidedness Dev Biol 196 1998 228 236
11. H. Yamagishi, V. Garg, R. Matsuoka, T. Thomas, D. Srivastava A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects Science 283 1999 1158 1161
12. U.K. Laemmli Cleavage of structural proteins during the assembly of the head of bacteriophage T4 Nature 227 1970 680 685
13. J.R. Hove, R.W. Koster, A.S. Forouhar, G. Acevedo-Bolton, S.E. Fraser, M. Gharib Intracardiac fluid forces are an essential epigenetic factor for embryonic cardiogenesis Nature 421 2003 172 177
14. K. Momma, C. Kondo, M. Ando, R. Matsuoka, A. Takao Tetralogy of Fallot associated with chromosome 22q11 deletion Am J Cardiol 76 1995 618 621
15. A.K. Ryan, J.A. Goodship, D.I. Wilson, N. Philip, A. Levy, H. Seidel Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study J Med Genet 34 1997 798 804
16. Yamagishi C, Hierck BP, Gittenberger-De Groot AC, Yamagishi H, Srivastava D. Functional attenuation of UFD1L, a 22q11.2 deletion syndrome candidate gene, leads to cardiac outflow septation defects in chicken embryos. Pediatr Res. 2003;53:546-53.
17. V. Sans-Coma, B. Fernandez, A.C. Duran, G. Thiene, J.M. Arque, R. Munoz-Chapuli Fusion of valve cushions as a key factor in the formation of congenital bicuspid aortic valves in Syrian hamsters Anat Rec 244 1996 490 498
18. D.I. Wilson, J.A. Goodship, J. Burn, I.E. Cross, P.J. Scambler Deletions within chromosome 22q11 in familial congenital heart disease Lancet 340 1992 573 575
19. X. Jiang, D.H. Rowitch, P. Soriano, A.P. McMahon, H.M. Sucov Fate of the mammalian cardiac neural crest Development 127 2000 1607 1616
20. P.J. Mitchell, P.M. Timmons, J.M. Hebert, P.W. Rigby, R. Tjian Transcription factor AP-2 is expressed in neural crest cell lineages during mouse embryogenesis Genes Dev 5 1991 105 119
21. H. Schorle, P. Meier, M. Buchert, R. Jaenisch, P.J. Mitchell Transcription factor AP-2 essential for cranial closure and craniofacial development Nature 381 1996 235 238
22. D. Wang, T.H. Shin, J.E. Kudlow Transcription factor AP-2 controls transcription of the human transforming growth factor-alpha gene J Biol Chem 272 1997 14244 14250
23. L.A. McPherson, V.R. Baichwal, R.J. Weigel Identification of ERF-1 as a member of the AP2 transcription factor family Proc Natl Acad Sci U S A 94 1997 4342 4347
24. S.M. Frisch, J.H. Morisaki Positive and negative transcriptional elements of the human type IV collagenase gene Mol Cell Biol 10 1990 6524 6532
25. C. Duan, D.R. Clemmons Transcription factor AP-2 regulates human insulin-like growth factor binding protein-5 gene expression J Biol Chem 270 1995 24844 24851
26. Hierck BP, Molin DG, Boot MJ, Poelmann RE, Gittenberger-De Groot AC. A chicken model for DGCR6 as a modifier gene in the DiGeorge critical region. Pediatr Res. 2004;56:440-8.
27. A.M. Ranger, M.J. Grusby, M.R. Hodge, E.M. Gravallese, F.C. de la Brousse, T. Hoey The transcription factor NF-Atc is essential for cardiac valve formation Nature 12 1998 186 190
28. J.L. de la Pompa, L.A. Timmerman, H. Takimoto, H. Yoshida, A.J. Elia, E. Samper Role of the NF-Atc transcription factor in morphogenesis of cardiac valves and septum Nature 12 1998 182 186
29. M.W. Schilham, M.A. Oosterwegel, P. Moerer, J. Ya, P.A. de Boer, M. van de Wetering Defects in cardiac outflow tract formation and pro-B-lymphocyte expansion in mice lacking Sox-4 Nature 380 1996 711 714
30. M.H. Yacoub, L.H. Cohn Novel approaches to cardiac valve repair from structure to function: part I Circulation 109 2004 942 950