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Editorial Article

Transcription Factors: Regulators of Gene Expression in Normal and Pathological States

Pages 1-3 | Published online: 08 Jul 2009

References

  • Krajewska W A. Regulation of transcription in eukaryotes by DNA-binding proteins. Int J Biochem 1992; 25: 1885–98
  • Cox P M, Goding C R. Transcription and cancer. Br J Cancer 1991; 63: 651–62
  • Epstein C J. The new dysmorphology: application of insights from basic developmental biology to the understanding of birth defects. Proc Natl Acad Sci USA 1995; 92: 8566–73
  • Roeder R G. The complexities of eukaryotic transcription initiation: regulation of preinitiation complex assembly. Trends Biochem Sci 1991; 16: 402–8
  • Duan R D, Pause A, Burgess W H, et al. Inhibition of transcription elongation by the VHL tumour supressor protein. Science 1995; 269: 1402–6
  • Showe L C, Croce C M. The role of chromosomal translocations in B- and T-cell neoplasms. Annu Rev Immunol 1987; 5: 253–77
  • Heisterkamp N, Stam K, Groffen J, de Klein A, Grosveld G. Structural organization of the bcr gene and its role in the Ph translocation. Nature 1985; 314: 758–61
  • de The H, Chomienne C, Lanotte M, Degos L, Dejean A. The t(15;17) translocation of acute promyelocytic leukemia fuses the retinoic acid receptor I gene to a novel transcribed locus. Nature 1990; 34: 558–61
  • Sabbatini P, Lin J, Levine A J, White E. Essential role for p53-mediated transcription in E1A-induced apoptosis. Genes Dev 1995; 9: 2184–92
  • Chalepakis G, Goulding M, Read A, Strachan T, Gruss P. Molecular basis of splotch and Waardenburg PAX-3 mutations. Proc Natl Acad Sci USA 1994; 91: 3685–9
  • Glaser T, Jepeal L, Edwards J G, Young S R, Favor J, Maas R L. PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia, and central nervous system defects. Nat Genet 1994; 7: 463–71
  • Sanyanusin P, Schimmenti L A, McNoe L A, et al. Mutation of the PAX2 gene in a family with optic nerve colombomas, renal anomalies, and vesicoureteral reflux. War Genef 1995; 9: 358–64
  • Jabs E W, Müller U, Li X, et al. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis. Cell 1993; 75: 443–50
  • Vortkamp A, Gessler M, Grzeschik K-H. GLI3 zinc-finger gene interrupted by tranlocations in Grieg syndromeic families. Nature 1991; 352: 539–40
  • Bruening W, Bardeesy N, Silverman B L, et al. Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development. Nat Genet 1992; 1: 144–8

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