Poster Session 3
 
Genetics/Genomics
GENO-1 Becker, Kevin Graham (NIA) K.G. Becker, D.G. Leung, A.J. Myers
  Development of a late–onset Alzheimer’s gene expression database.
 
GENO-2 Bhattacharya, Bhaskar (CBER) B. Bhattacharya, Y. Luo, T. Miura, J. Cai, J. Mejido, T.C. Schultz, X. Zheng, S.N. Brimble, M.S. Rao & R.K. Puri
  Characterization of Differentiated Stem Cells on the Basis of Their Gene Expression Profile
 
GENO-3 Birinyi, Paul Vincent (NIDA) P.V. Birinyi, T. Drgon, M.J. Chiocco, G.R. Uhl
  Receptor Protein Tyrosine Phophatase D (PTPRD): Haplotype Structures and Assessments of Associations with Polysubstance Abuse
 
GENO-4 Boyle, Jennifer (NCI) J. Boyle, T. Ueda, V. Gonzalez, K.S. Oh, K. Imoto, H. Inui, D.B. Busch, S.G. Khan, J.J. DiGiovanna, D. Schmidt, K.H. Kraemer
  Xeroderma Pigmentosum Group D Patients Heterozygous for the R683W Mutation with and without Neurological Symptoms
 
GENO-6 Finch, Thembi D. (NIAAA) T. Finch, K. Xu, D. Goldman
  Resequencing of GABRA4 in Nine Populations for SNPs that may Influence Alcohol and Substance Dependence
 
GENO-7 Hahn, Yoonsoo (NCI) Y. Hahn, B. Lee
  Human Lineage-Specific Frameshift and Nonsense Mutations
 
GENO-8 Hung, Graham (NIDDK) G. Hung, D.C. Masison
  Interactions of Hsp104 and Hsp70 in [PSI+] Prion Propagation
 
GENO-9 Imoto, Kyoko (NCI) K. Imoto, H. Slor, S. Orgal, S. G. Khan, K-S Oh, D. Busch, C. Nadem, T. Ueda, N. Gadoth, N.G.J. Jaspers and K.H. Kraemer
  Xeroderma Pigmentosum Group F Patients with Severe Late Onset Neurological Disease
 
GENO-10 Jaluria, Pratik (NIDDK) P. Jaluria,K. Konstantopoulos, M. Betenbaugh, J. Shiloach
  Reverse and Rational Engineering of Mammalian Cells: A Microarray Approach
 
GENO-11 Jemison, Jamileh A (NIDDK) J.A. Jemison, D. Caro, B. Oliver
  Recombinant Mapping of a Menin Effector in Drosophila
 
GENO-12 Khan, Sikandar Gauhar (NCI) S.Khan, A.Lehmann, K.Imoto, K.Oh, C.Baker, S.Clarkson, F.Thorel, A.Nemeth, S.Downes, K.Talbot, C.Nadem and K.Kraemer
  Leaky Splice Donor Site Mutation in the XPG DNA Repair Gene is Associated with Neurological Abnormalities in Two Adult Brothers
 
GENO-13 Khil, Pavel P (NIDDK) P.P. Khil and R.D. Camerini-Otero
  High-Resolution Map of Recombination Hotspots of the Human Genome
 
GENO-14 Liu, Hongfang (NCI) H. Liu, A.Kahn, M. Reimers, B. Zeeberg, J.Weinstein
  Computational Resources for Microarray Data Analysis
 
GENO-15 Narisu, Narisu (NHGRI) N. Narisu and F. Collins
  Identification of Zebrafish Olfactory Receptor Genes
 
GENO-16 Nitto, Takeaki (NIAID) T. Nitto, K.D. Dyer, R.A. Mejia, J. Byström, T.A. Wynn, and H.F. Rosenberg
  Characterization of the Divergent Eosinophil Ribonuclease, mEar 6, and its Expression in Response to Schistosoma Mansoni Infection in vivo
 
GENO-17 Oh, Kyu Seon (NCI) K.S.Oh, D.Schmidt, K.Imoto, J.Boyle, S.G.Khan, J. DiGiovanna, K.H.Kraemer
  A New Xeroderma Pigmentosum Group E kindred with a R273H Mutation in the DDB2 Gene
 
GENO-18 Pang, Alan (NICHD) A.L.Y. Pang, W. Johnson, D.H. Bear, O.M. Rennert, and W.Y. Chan
  Gene Expression Profiling of Murine Spermatogenesis Leads to the Identification of Ard2, a Novel Mouse Ard1 Homolog that is Preferentially Expressed Starting from Meiosis
 
GENO-19 Pangilinan, Faith (NIGMS) F. Pangilinan, M. Miller, A. Weiler, J.L. Mills, P.N. Kirke, A. Parle-McDermott, V.B. O’Leary, A.M. Molloy, J.M. Scott, L.C. Brody
  Evaluation of Thymidylate Synthase Polymorphisms as Genetic Risk Factors for Neural Tube Defects
 
GENO-20 Peters, Linda M. (NIDCD) L. M. Peters, I. A.Belyantseva, J.F. Battey, T. B. Friedman, R. J. Morell
  Analysis of Mouse Inner Ear MPSS Libraries to Select for Rare and Novel Expressed Genes
 
GENO-21 Ross, Robert J (NEI) R.J. Ross, C.M. Bojanowski, C.C. Chan, J. Tuo
  Analysis of a Pigment Epithelium Derived Factor (PEDF) Polymorphism and Age-Related Macular Degeneration
 
GENO-22 Stiles, David A (NIDDK) D. Stiles, J. Lee, P. Tan and M. Cam
  Alternative Splicing and its Possible Effects on Microarray Gene Expression Results
 
GENO-23 Tayebi, Nahid (CBER) N. Tayebi, L. Wood, and J. Lozier
  Genomic Sequences of the Canine Factor VIII gene and Duplicated Sequences Related to a Common Inversion Mutation
 
GENO-24 Tuo, Jingsheng (NEI) J. Tuo, B. Ning, C.M. Bojanowski, Z-N. Lin, D. Shen, E. Chew, F.F. Kadlubar, and C-C Chan
  A Sequence Variation in the 5’-flanking Region of ERCC6 and Predisposition Towards Age-Related Macular Degeneration in Caucasian Patients
 
GENO-25 Wistow, Graeme (NEI) N. Nag, S. Ray, K. Wyatt, D. Bogani, M. Lyon and G. Wistow.
  The Murine No3 Cataract is the Result of Retroviral Insertion in Cryge Resulting in a Non-Cytotoxic Truncation of GammaE-Crystallin
 
GENO-26 Yao, Wenliang (NEI) W. Yao, F. Zulfiqar, S. A. Riazuddin, Q. Zhang, L.A. Kordestani, M. Amer, T. Hussnain, P. Sieving, S. Riazuddin and J. F. Hejtmancik
  A Novel Mutation (Arg413Ter) in the BBS2 Gene in a Consanguineous Pakistani Family
 
GENO-28 Yuen, Peter ST (NIDDK) PST Yuen, SK Jo, MK Holly, X Hu, RA Star
  Comparison of Ischemic and Nephrotoxic Acute Renal Failure by Microarray Analysis, Network Analysis, and Validation