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  1. 1.   Common Genetic Variants and Risk for HPV Persistence and Progression to Cervical Cancer
  2. Wang, S. S.; Gonzalez, P.; Yu, K.; Porras, C.; Li, Q. Z.; Safaeian, M.; Rodriguez, A. C.; Sherman, M. E.; Bratti, C.; Schiffman, M.; Wacholder, S.; Burk, R. D.; Herrero, R.; Chanock, S. J.; Hildesheim, A.
  3. Plos One. 2010, Jan; 5(1): 7.
  1. 2.   Xeroderma pigmentosum-variant patients from America, Europe, and Asia
  2. Inui, H.; Oh, K. S.; Nadem, C.; Ueda, T.; Khan, S. C.; Metin, A.; Gozukara, E.; Emmert, S.; Slor, H.; Busch, D. B.; Baker, C. C.; DiGiovanna, J. J.; Tamura, D.; Seitz, C. S.; Gratchev, A.; Wu, W. H.; Chung, K. Y.; Chung, H. J.; Azizi, E.; Woodgate, R.
  3. Journal of Investigative Dermatology. 2008 128(8): 2055-2068.
  1. 3.   Epigenetic silencing of the human nucleotide excision repair gene, hHR23B, in interleukin-6-responsive multiple myeloma KAS-6/1 cells
  2. Pengt, B.; Hodge, D. R.; Thomas, S. B.; Cherry, J. M.; Munroe, D. J.; Pompeia, C.; Xiao, W. H.; Farrar, W. L.
  3. Journal of Biological Chemistry. 2005, FEB 11; 280(6): 4182-4187.
  1. 4.   Two essential splice lariat branchpoint sequences in one intron in a xeroderma pigmentosum DNA repair gene: mutations result in reduced XPC mRNA levels that correlate with cancer risk
  2. Khan, S. G.; Metin, A.; Gozukara, E.; Inui, H.; Shahlavi, T.; Muniz-Medina, V.; Baker, C. C.; Ueda, T.; Aiken, J. R.; Schneider, T. D.; Kraemer, K. H.
  3. Human Molecular Genetics. 2004 13(3): 343-352.
  1. 5.   The human XPG gene: gene architecture, alternative splicing and single nucleotide polymorphisms
  2. Emmert, S.; Schneider, T. D.; Khan, S. G.; Kraemer, K. H.
  3. Nucleic Acids Research. 2001 29(7): 1443-1452.
  1. 6.   Characterization of gene expression, genomic structure, and chromosomal localization of Hells (Lsh)
  2. Geiman, T. M.; Durum, S. K.; Muegge, K.
  3. Genomics. 1998 54(3): 477-483.
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