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  1. 1.   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. 2.   Mutation Discovered in a Feline Model of Human Congenital Retinal Blinding Disease
  2. Menotti-Raymond, M.; Deckman, K. H.; David, V.; Myrkalo, J.; O'Brien, S. J.; Narfstrom, K.
  3. Investigative Ophthalmology & Visual Science. 2010, Jun; 51(6): 2852-2859.
  1. 3.   Mitochondrial Haplogroups Are Associated With Risk of Neuroretinal Disorder in HIV-Positive Patients
  2. Hendrickson, S. L.; Jabs, D. A.; Van Natta, M.; Lewis, R. A.; Wallace, D. C.; O'Brien, S. J.
  3. Jaids-Journal of Acquired Immune Deficiency Syndromes. 2010, Apr; 53(4): 451-455.
  1. 4.   A suppressive oligodeoxynucleotide inhibits ocular inflammation
  2. Fujimoto, C.; Klinman, D. M.; Shi, G.; Yin, H.; Vistica, B. P.; Lovaas, J. D.; Wawrousek, E. F.; Igarashi, T.; Chan, C. C.; Gery, I.
  3. Clinical and Experimental Immunology. 2009 156(3): 528-534.
  1. 5.   The tetraspanin protein peripherin-2 forms a complex with melanoregulin, a putative membrane fusion regulator
  2. Boesze-Battaglia, K.; Song, H. M.; Sokolov, M.; Lillo, C.; Pankoski-Walker, L.; Gretzula, C.; Gallagher, B.; Rachel, R. A.; Jenkins, N. A.; Copeland, N. G.; Morris, F.; Jacob, J.; Yeagle, P.; Williams, D. S.; Damek-Poprawa, M.
  3. Biochemistry. 2007, Feb; 46(5): 1256-1272.
  1. 6.   Mutation in CEP290 discovered for cat, model of human retinal degeneration
  2. Menotti-Raymond, M.; David, V. A.; Schaffer, A. A.; Stephens, R.; Wells, D.; Kumar-Singh, R.; O'Brien, S. J.; Narfstrom, K.
  3. Journal of Heredity. 2007, May-Jun; 98(3): 211-220.
  1. 7.   Inflammatory processes triggered by TCR engagement or by local cytokine expression: differences in profiles of gene expression and infiltrating cell populations
  2. Takase, H.; Yu, C. R.; Ham, D. I.; Chan, C. C.; Chen, J.; Vistica, B. P.; Wawrousek, E. F.; Durum, S. K.; Egwuagu, C. E.; Gery, I.
  3. Journal of Leukocyte Biology. 2006, Sep; 80(3): 538-545.
  1. 8.   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. 9.   Approaches to identify genes for complex human diseases: Lessons from Mendelian disorders
  2. Dean, M.
  3. Human Mutation. 2003 22(4): 261-274.
  1. 10.   The human ATP binding cassette gene ABCA13, located on chromosome 7p12.3, encodes a 5058 amino acid protein with an extracellular domain encoded in part by a 4.8-kb conserved exon
  2. Prades, C.; Arnould, I.; Annilo, T.; Shulenin, S.; Chen, Z. Q.; Orosco, L.; Triunfol, M.; Devaud, C.; Maintoux-Larois, C.; Lafargue, C.; Lemoine, C.; Denefle, P.; Rosier, M.; Dean, M.
  3. Cytogenetic and Genome Research. 2002 98(2-3): 160-168.
  1. 11.   Genotype-phenotype analysis of ABCR variants in macular degeneration probands and siblings
  2. Bernstein, P. S.; Leppert, M.; Singh, N.; Dean, M.; Lewis, R. A.; Lupski, J. R.; Allikmets, R.; Seddon, J. M.
  3. Investigative Ophthalmology & Visual Science. 2002 43(2): 466-473.
  1. 12.   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. 13.   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. 14.   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. 15.   Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)
  2. Allikmets, R.; Raskind, W. H.; Hutchinson, A.; Schueck, N. D.; Dean, M.; Koeller, D. M.
  3. Human Molecular Genetics. 1999 8(5): 743-749.
  1. 16.   Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies
  2. Allikmets, R.; Seddon, J. M.; Bernstein, P. S.; Hutchinson, A.; Atkinson, A.; Sharma, S.; Gerrard, B.; Li, W.; Metzker, M. L.; Wadelius, C.; Caskey, C. T.; Dean, M.; Petrukhin, K.
  3. Human Genetics. 1999 104(6): 449-453.
  1. 17.   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. 18.   What can we learn about age-related macular degeneration from other retinal diseases?
  2. Zack, D. J.; Dean, M.; Molday, R. S.; Nathans, J.; Redmond, T. M.; Stone, E. M.; Swaroop, A.; Valle, D.; Weber, B. H. F.
  3. Molecular Vision. 1999 5(24-35): NIL_37-NIL_43.
  1. 19.   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. 20.   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.
  1. 21.   Case Report: Ocular toxoplasmosis in a WHIM syndrome immunodeficiency patient
  2. McDermott, David H; Heusinkveld, Lauren E; Zein, Wadih M; Sen, H Nida; Marquesen, Martha M; Parta,Mark; Rosenzweig, Sergio D; Fahle, Gary A; Keller, Michael D; Wiley, Henry E; Murphy, Philip M
  3. F1000Research. 2019 8 2.
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