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Genetics/Genomics |
GENO-1
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Barb, Jennifer
J. (CIT)
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J.J. Barb, H. Schindel, P.J. Munson
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GO-SCAN, Analysis and Visualization of Gene Ontology Annotations
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GENO-2
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Belfer, Inna
(NIDCR)
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I. Belfer, B. Buzas, H. Hipp, G. Phillips, J. Taubman, I. Lorincz, C. Evans, R.H. Lipsky, M-A. Enoch, M.B. Max and D. Goldman
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Haplotype Structure of Human Adrenergic Receptor Genes
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GENO-3
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Bojanowski, Christine
Marie (NEI)
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C.M. Bojanowski, J. Tuo, E.Y. Chew, K.G. Csaky, C.C. Chan
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Analysis of the Hemicentin-1 Q5345R, hOgg1 S326C, CSB-6530C/G, and E-selectin S149R Single Nucleotide Polymorphisms (SNPs) in Age-related Macular Degeneration
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GENO-4
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Bondy, Carolyn
Ann (NICHD)
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C. Bondy, P. Brown, P. Van, V. Bakalov
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Does the Second X-chromosome Confer Protection from Ischemic Heart Disease (IHD)?
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GENO-5
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Chen, Zehua
(NCI)
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Z. Chen and T.D. Schneider
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Comparative Analysis of T7-like Promoter Bearing Regions in Bacterial Genomes Reveals a Novel Group of Islands
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GENO-6
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Chung, Seyung
(NIDDK)
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S. Chung and D. Masison
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Two Isoforms of Yeast HSP70 Chaperones are Required for Different Prions [PSI+] And [URE3] Propagation in a Distinctive Way
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GENO-7
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Clarence, Anitha
Rachel (NCI)
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A.R.Clarence, M.Upender and T.Ried
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Karyotypic Evolution and Chromosome Stability in Artificially Induced Trisomies
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GENO-8
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Correa-Cerro, Lina
S. (NICHD)
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L.S. Correa-Cerro, C.A. Wassif, L. Kratz, R. Kelly, F.D. Porter
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Simvastatin Therapy Improve the Biochemical Phenotype in a Hypomorphic Smith-Lemli-Opitz Syndrome Mouse Model
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GENO-9
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Cui, Yongzhi
(NIDDK)
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Y. Cui, G. Riedlinger, K. Miyoshi, W. Tang, P. Kovanen, W. Leonard, C. Li, C. Deng, G. Robinson, L. Hennighausen
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Stat5 Revisited: Inactivation of Stat5 in Specific Cells and Defined Time Points
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GENO-10
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Duggal, Priya
(NHGRI)
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P. Duggal, A.P. Klein, K. E. Lee, S. K. Iyengar, R. Klein, J. E. Bailey-Wilson, B.E. Klein
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Identification of Two Novel Loci that Influence Intraocular Pressure in the Beaver Dam Eye Study
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GENO-11
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Dzekunova, Inna
R. (NCI)
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I.R.Dzekunova, B.Peng, D.W.Petersen, E.Kawasaki
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Monkeying Around: Rhesus mRNA Expression Profiles from Human Microarrays
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GENO-12
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Enright, Brian
Patrick (NCI)
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B.P. Enright, S. Maeng, W. Sonoyama, M. Miura, S. Shi, and L. Shen
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Dynamic Remodeling of Hematopoietic Stem Cell Niche in GDNF Haploinsufficient Mice
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GENO-13
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Finch, Thembi
D. (NIAAA)
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T. Finch, K. Xu, E. Westley, A. Roy, W. Maier, D. Goldman
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Linkage Disequilibrium of the GABRA Cluster Genes on Chromosome 4 with Opiate Addiction in an African American and a German Population
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GENO-14
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Goker-Alpan, Ozlem
(NIMH)
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O. Goker-Alpan, K.S. Hruska, B.K. Stubblefield, E. Sidransky
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Does Mutant Glucocerebrosidase Trigger Protein Aggregation?
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GENO-15
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Goonesekere, Nalin
C. (NCI)
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N. C. W. Goonesekere, BK Lee
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Frequency of Gaps Observed in a Structurally Aligned Protein Pair Database Suggests a Simple Gap Penalty Function
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GENO-16
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Habermann, Jens
K. (NCI)
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J. Habermann, U. Paulsen, U. Roblick, M. Upender, L. McShane, E. Korn, S. Krüger, H.-P. Bruch, G. Auer, and T. Ried
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The Pattern of Aneuploidy and Genomic Imbalances Correlates with Specific Gene Expression Changes Along the Adenoma-Carcinoma-Sequence of Colorectal Carcinogenesis
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GENO-17
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Hahn, Yoonsoo
(NCI)
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Y. Hahn, T.K. Bera, K. Gehlhaus, I.R. Kirsch, I.H. Pastan, and B. Lee
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Expressed Sequence Tags Database as Information Source for Discovery of Gene Fusion Resulting from Structural Rearrangement of Chromosomes
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GENO-18
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Haque, Kashif
A. (NCI)
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K.A. Haque, Y. Qi, M.B. Beerman, C.L. Glaser, I. Barrow, J.L. Hartwell, R.A. Welch, M. Garcia-Closas, P. Castle, N. Rothman, S.J. Chanock, A.W. Bergen
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Genotyping Performance of Whole Genome Amplified DNA Derived from Genomic DNA Templates of Variable Quantity and Quality
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GENO-19
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Hildenbrand, Hanna
Lynne (CC)
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H. Hildenbrand, G. Furst, and A.C.M. Smith
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Patterns of Sensory Processing in Children with Smith-Magenis Syndrome, Del (17) (p11.2p11.2)
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GENO-20
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Hodgkinson, Colin
A. (NIAAA)
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C. Hodgkinson, A. Malhotra, S. Persaud, R. Lipsky, and D. Goldman
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Disrupted in Schizophrenia 1 (DISC1) Associates with Schizophrenia, Schizoaffective Disorder and Bipolar Disorder.
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GENO-21
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Ibay, Grace
P. (NHGRI)
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G.P. Ibay, D. Stambolian, L. Reider, D. Dana, M. Schlifka, T. Holmes, R. Owens, E. Ciner, J.E. Bailey –Wilson
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Evidence for a Myopia Susceptibility Locus on Chromosome 22 in an Ashkenazi Jewish Population
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GENO-22
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Khan, Sikandar
Gauhar (NCI)
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S. Khan, K. Oh, S. Emmert, T. Shahlavi, C. Baker, D. Schmidt, J. DiGiovanna1, and K. Kraemer
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An Identical Mutation in the Human XPC DNA Repair Gene in Two Patients With and Without Neurological Abnormalities
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GENO-23
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Khil, Pavel
P. (NIDDK)
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P. Khil, N. Smirnova, P. Romanienko, R. D. Camerini-Otero
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The Mouse X Chromosome is Enriched for Sex-Biased Genes not Subject to Selection by Meiotic Sex Chromosome Inactivation
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GENO-24
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Kimchi-Sarfaty, Chava
(NCI)
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C. Kimchi-Sarfaty, J.M. Oh, J. Gribar, I.W. Kim, A. Sherman, S.V. Ambudkar, and M.M. Gottesman
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Characterization of the Multidrug Drug Resistance 1 (MDR1) Gene Polymorphisms
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GENO-25
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Knutsen, Turid
(NCI)
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T. Knutsen, V. Gobu, R. Knaus, H. Padilla-Nash, T. Groesbeck, T. Ried, K. Sirotkin
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"Cancerchromosomes," A New Entrez Database for Searching NCI and NCBI Cytogenetic Databases
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GENO-26
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LaMarca, Mary
E. (NIMH)
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ME LaMarca, DS Lieber, ME Portnoy, KS Hruska, ED Green, E Sidransky
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Multispecies Comparative Sequence Analysis of the Glucocerebrosidase Gene Locus
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GENO-27
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Lee, Yun-Sil
(NIDCR)
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Y. Lee, H. Kim, and R.A. Dionne
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Expression Patterns and Genetic Polymorphisms of Cyclooxygenase (COX) Genes in a Clinical Model of Tissue Injury
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GENO-28
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Lustig, Ana
(NIA)
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A. Lustig, K. Becker, W. Wood, D. Teichberg, A. Weeraratna, D. Bertak, S. Poosala, J. Firman, A. Zonderman, D. Longo, and D. Taub
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Age and Diet- Associated Changes in Gene Expression Patterns in the Murine Thymus
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GENO-29
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Mattapallil, Mary
J. (NEI)
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M.J. Mattapallil, A.M. Viley, C.C. Chan, P.B. Silver, L.A. Donoso, J.A. Hanson, C.S. David and R.R. Caspi
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HLA DR and DQ Interact to Control Susceptibility to Experimental Autoimmune Uveitis (EAU)
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GENO-30
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Packer, Bernice
R. (NCI)
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B. Packer, M. Yeager, B. Staats, R. Welch, A. Crenshaw, M. Kiley, A. Eckert, M. Beerman, A. Bergen, and S. Chanock
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SNP500 Cancer Database: Sequence Validation and Assay Optimization of Candidate Gene SNPs for Molecular Epidemiology Studies in Cancer
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GENO-31
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Pang, Lap-Yin
(NICHD)
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A.L.Y. Pang, M.M. Martin, D.H. Bellan, A.L.A. Martin, O.M. Rennert and W.Y. Chan
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Alterations of Gene Expression Pattern in Testicular Biopsy from A Patient with DAX-1 Mutation
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GENO-32
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Pangilinan, Faith
(NIGMS)
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F. Pangilinan, D. Swanson, A. Weiler, V. O'Leary, A. Parle-McDermott, M. Conley, C. Cox, T. Frey, A. Molloy, P. Kirke, J. Mills, J. Scott, L. Brody
|
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Transcobalamin II Polymorphisms Influence Plasma Levels of Vitamin B12 But are Not Major Risk Factors for Neural Tube Defects
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GENO-33
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Penzak, Scott
R. (CC)
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S.R. Penzak, R.M. Alfaro, E. Formentini, J. Falloon
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Influence of MDR1 Genotypes on Saquinavir Pharmacokinetics in Healthy Human Subjects
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GENO-34
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Pezza, Roberto
Jose (NIDDK)
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R.J. Pezza, G. Pethukova, E. Boja, H.M. Fales and R.D. Camerini-Otero
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Biochemical and Biophysical Characterization of The Mouse Meiotic Proteins Hop2 and Mnd1
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GENO-35
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Pierce, Michael
M. (NIDDK)
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M.M. Pierce, U. Baxa, A. Bax & R.B. Wickner
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The Ure2p Prion Domain is Unstructured in the Soluble Form
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GENO-36
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Rajkumar, Jonathan
N. (NCI)
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J. Rajkumar, A. Kahn, B. Zeeberg, W. Feng, G. Wang, M. Wang, A. Fojo, M. Sunshine, S. Narasimhan, D. Kane, W. Reinhold, S. Lababidi, K. Bussey, and J. Weinstein
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Enhancing the Perception of Information in Scalable Vector Graphics (SVG) for Analysis of Gene Expression Microarray Data
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GENO-37
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Reimers, Mark
(NCI)
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M Reimers
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Quality Control of Spatial Artifacts in Raw Microarray Data
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GENO-38
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Scalco, Fernanda
(NICHD)
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F.B. Scalco, L.S. Correa-Cerro, C.A. Wassif, D. Moretti-Ferreira, F.D. Porter
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IVS8-1G>C and T93M are the Most Frequent 7-Dehydrocholesterol Reductase Mutations Identified in a Cohort of Smoith-Lemli-Opitz Syndrome Patients from Brazil
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GENO-39
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Shankavaram, Uma
(NCI)
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U.Shankavaram, W.C. Reinhold, M. Reimers, U. Scherf, D. Doginow, and J.W.Weinstein
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Molecular, Biological, and Therapeutic Profiling of the NCI-60 Cells
|
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GENO-40
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Sidransky, Ellen
(NIMH)
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E. Sidransky, J. Nguyen, J. Walker, O. Goker-Alpan, H.I. Hurtig, J.Q. Trojanowski, B. Giasson
|
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Glucocerebrosidase Mutations in Autopsy Samples from Subjects with Parkinsonian Syndromes
|
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GENO-41
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Sokolov, Mykyta
(CC)
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M.V. Sokolov, I.G. Panyutin, N.A. Smirnova, R.D. Camerini-Otero, R.D. Neumann
|
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Probing Signaling Pathways Induced by I-125-Mediated DNA Double Strand Breaks: Lessons from the Genome-Wide Transcriptome Analysis in Human Cells
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GENO-42
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Staats, Brian
J. (NCI)
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B. Staats, L. Qi, M. Beerman, H. Sicotte, B. R. Packer, S. J. Chanock, M. Yeager
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Visualization of Valid Polymorphisms within the Human Genome
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GENO-43
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Stiles, David
A. (NIDDK)
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D.A. Stiles, P.K. Tan, P.A. Henning, M.C. Cam
|
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Alternative Splicing and its Possible Affects on Microarray Gene Expression Results
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GENO-44
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Tibriwal, Aruna
Rani (NCI)
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A. Tibriwal, E. Mathe, M. Reimers, J. Weinstein
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Quality Control of Affymetrix Chips By Use Of False-Color Images
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GENO-45
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Tuo, Jingsheng
(NEI)
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J.Tuo, B. Smith, C.M. Bojanowski, A.D. Meleth, I. Gery, K. Csaky, E. Chew and C. Chan
|
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The Involvement of Sequence Variation and Expression of CX3CR1 in the Pathogenesis of Age-related Macular Degeneration
|
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GENO-46
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Wanke, Kay
L. (NCI)
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K.L. Wanke, E.M. Augustson, N.E. Caporaso, A.W. Bergen, D.N. Paltoo, T.A. Lehman, R. Modali, N. Chatterjee, J.M. Hayes, S.I. Malik, P.R. Taylor, D. Albanes
|
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The Genetic Determinants of Smoking Cessation: An Analysis from the Alpha-Tocopherol Beta-Carotene Cancer Prevention (ATBC) Study
|
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GENO-47
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Wasson, Katherine
(NCI)
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K. Wasson, K.J. Helzlsouer, E.D. Cook
|
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Ethical Issues in Direct-to-Consumer Online Genetic Testing
|
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GENO-48
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Weiss, George
H. (CIT)
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J. Nolan, P. J. Munson, G.H. Weiss
|
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Statistical Detection of Abnormal Gene Clustering
|
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GENO-49
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Wheeler, David
L. (NLM)
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A. Gabrielian, V. Pham, M. Romiti, E. Sayers, D. Wheeler
|
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Implementation of Pipelines for Genomic Analysis using the Entrez Programming Utilities
|
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GENO-50
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Yu, Qing
(NHLBI)
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Q. Yu, Y. Shen, B. Chatterjee, B.H.Siegfried, L.Leatherbury, J.Rosenthal, J.F.Lucas, A. Wessels, C.F.Spurney, Y.J.Wu, M.L.Kirby, K. Svenson, and C.W. Lo
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ENU Induced Mutations Causing Congenital Cardiovascular Anomalies
|
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