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  1. 1.   Evidence of association of APOE with age-related macular degeneration - a pooled analysis of 15 studies
  2. McKay, G. J.; Patterson, C. C.; Chakravarthy, U.; Dasari, S.; Klaver, C. C.; Vingerling, J. R.; Ho, L.; de Jong, P.; Fletcher, A. E.; Young, I. S.; Sel, J. H.; Rahu, M.; Soubrane, G.; Tomazzoli, L.; Topouzis, F.; Vioque, J.; Hingorani, A. D.; Sofat, R.; Dean, M.; Sawitzke, J.; Seddon, J. M.; Peter, I.; Webster, A. R.; Moore, A. T.; Yates, J. R. W.; Cipriani, V.; Fritsche, L. G.; Weber, B. H. F.; Keilhauer, C. N.; Lotery, A. J.; Ennis, S.; Klein, M. L.; Francis, P. J.; Stambolian, D.; Orlin, A.; Gorin, M. B.; Weeks, D. E.; Kuo, C. L.; Swaroop, A.; Othman, M.; Kanda, A.; Chen, W.; Abecasis, G. R.; Wright, A. F.; Hayward, C.; Baird, P. N.; Guymer, R. H.; Attia, J.; Thakkinstian, A.; Silvestri, G.
  3. Human Mutation. 2011, Dec; 32(12): 1407-1416.
  1. 2.   Analysis of the ABCA4 Gene by Next-Generation Sequencing
  2. Zernant, J.; Schubert, C.; Im, K. M.; Burke, T.; Brown, C. M.; Fishman, G. A.; Tsang, S. H.; Gouras, P.; Dean, M.; Allikmets, R.
  3. Investigative Ophthalmology & Visual Science. 2011, Oct; 52(11): 8479-8487.
  1. 3.   Variations in Apolipoprotein E Frequency With Age in a Pooled Analysis of a Large Group of Older People
  2. McKay, G. J.; Silvestri, G.; Chakravarthy, U.; Dasari, S.; Fritsche, L. G.; Weber, B. H.; Keilhauer, C. N.; Klein, M. L.; Francis, P. J.; Klaver, C. C.; Vingerling, J. R.; Ho, L.; De Jong, P.; Dean, M.; Sawitzke, J.; Baird, P. N.; Guymer, R. H.; Stambolian, D.; Orlin, A.; Seddon, J. M.; Peter, I.; Wright, A. F.; Hayward, C.; Lotery, A. J.; Ennis, S.; Gorin, M. B.; Weeks, D. E.; Kuo, C. L.; Hingorani, A. D.; Sofat, R.; Cipriani, V.; Swaroop, A.; Othman, M.; Kanda, A.; Chen, W.; Abecasis, G. R.; Yates, J. R.; Webster, A. R.; Moore, A. T.; Seland, J. H.; Rahu, M.; Soubrane, G.; Tomazzoli, L.; Topouzis, F.; Vioque, J.; Young, I. S.; Fletcher, A. E.; Patterson, C. C.
  3. American Journal of Epidemiology. 2011, Jun; 173(12): 1357-1364.
  1. 4.   Genetics of Focal Segmental Glomerulosclerosis and Human Immunodeficiency Virus-Associated Collapsing Glomerulopathy: The Role of MYH9 Genetic Variation
  2. Winkler, C. A.; Nelson, G.; Oleksyk, T. K.; Nava, M. B.; Kopp, J. B.
  3. Seminars in Nephrology. 2010, Mar; 30(2): 111-125.
  1. 5.   Toxicity of Organic Fluorophores Used in Molecular Imaging: Literature Review
  2. Alford, R.; Simpson, H. M.; Duberman, J.; Hill, G. C.; Ogawa, M.; Regino, C.; Kobayashi, H.; Choyke, P. L.
  3. Molecular Imaging. 2009, Nov-Dec; 8(6): 341-354.
  1. 6.   Multilocus analysis of age-related macular degeneration
  2. Bergeron-Sawitzke, J.; Gold, B.; Olsh, A.; Schlotterbeck, S.; Lemon, K.; Visvanathan, K.; Allikmets, R.; Dean, M.
  3. European Journal of Human Genetics. 2009 17(9): 1190-1199.
  1. 7.   Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: Characterization, ethnic distribution and evolutionary implications
  2. Hageman, G. S.; Hancox, L. S.; Taiber, A. J.; Gehrs, K. M.; Anderson, D. H.; Johnson, L. V.; Radeke, M. J.; Kavanagh, D.; Richards, A.; Atkinson, J.; Meri, S.; Bergeron, J.; Zernant, J.; Merriam, J.; Gold, B.; Allikmets, R.; Dean, Michael; Grp, A. M. D. C. S.
  3. Annals of Medicine. 2006 38(8): 592-604.
  1. 8.   A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration
  2. Hageman, G. S.; Anderson, D. H.; Johnson, L. V.; Hancox, L. S.; Taiber, A. J.; Hardisty, L. I.; Hageman, J. L.; Stockman, H. A.; Borchardt, J. D.; Gehrs, K. M.; Smith, R. J. H.; Silvestri, G.; Russell, S. R.; Klaver, C. C. W.; Barbazetto, I.; Chang, S.; Yannuzzi, L. A.; Barile, G. R.; Merriam, J. C.; Smith, R. T.; Olsh, A. K.; Bergeron, J.; Zernant, J.; Merriam, J. E.; Gold, B.; Dean, M.; Allikmets, R.
  3. Proceedings of the National Academy of Sciences of the United States of America. 2005, MAY 17; 102(20): 7227-7232.
  1. 9.   Evolution of the ATP-binding cassette (ABC) transporter superfamily in vertebrates
  2. Dean, M.; Annilo, T.
  3. Annual review of genomics and human genetics. 2005 6: 123-142.
  1. 10.   Mutational scanning of the ABCR gene with double-gradient denaturing-gradient gel electrophoresis (DG-DGGE) in Italian Stargardt disease patients
  2. Fumagalli, A.; Ferrari, M.; Soriani, N.; Gessi, A.; Foglieni, B.; Martina, E.; Manitto, M. P.; Brancato, R.; Dean, M.; Allikmets, R.; Cremonesi, L.
  3. Human Genetics. 2001 109(3): 326-338.
  1. 11.   Complete characterization of the human ABC gene family
  2. Dean, M.; Allikmets, R.
  3. Journal of Bioenergetics and Biomembranes. 2001 33(6): 475-479.
  1. 12.   New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease
  2. Simonelli, F.; Testa, F.; de Crecchio, G.; Rinaldi, E.; Hutchinson, A.; Atkinson, A.; Dean, M.; D'Urso, M.; Allikmets, R.
  3. Investigative Ophthalmology & Visual Science. 2000 41(3): 892-897.
  1. 13.   The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial
  2. Shroyer, N. F.; Lewis, R. A.; Allikmets, R.; Singh, N.; Dean, M.; Leppert, M.; Lupski, J. R.
  3. Vision Research. 1999 39(15): 2537-2544.
  1. 14.   Genotype/phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease
  2. Lewis, R. A.; Shroyer, N. F.; Singh, N.; Allikmets, R.; Hutchinson, A.; Li, Y. X.; Lupski, J. R.; Leppert, M.; Dean, M.
  3. American Journal of Human Genetics. 1999 64(2): 422-434.
  1. 15.   A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease
  2. Zhang, K.; Garibaldi, D. C.; Kniazeva, M.; Albini, T.; Chiang, M. F.; Kerrigan, M.; Sunness, J. S.; Han, M.; Allikmets, R.
  3. American Journal of Ophthalmology. 1999 128(6): 720-724.
  1. 16.   Mammalian Homolog of Drosophila Retinal Degeneration B Rescues the Mutant Fly Phenotype
  2. Chang, J. H. T.; Milligan, S.; Li, Y. Y.; Chew, C. E.; Wiggs, J.; Copeland, N. G.; Jenkins, N. A.; Campochiaro, P. A.; Hyde, D. R.; Zack, D. J.
  3. Journal of Neuroscience. 1997 17(15): 5881-5890.
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