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| Genomics |
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P-1
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Becker, Kevin
Graham (NIA)
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K.G. Becker
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Comparative genomics of Autism, Tourette’s Syndrome, and Autoimmune/Inflammatory disorders.
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P-2
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Betts, Elizabeth
Shavonne (NIDA)
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M.T. McCoy, J. L. Cadet
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Induction of fos and jun by apoptotic doses of methamphetamine: Evidence from cDNA array and RT-PCR.
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P-3
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Boissy, Robert
James (NIEHS)
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R. J. Boissy, A. E. Dellinger, D. A. Bell
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A Relational Database Application for "Structured Query Fragment" (SQF) Analysis Of Genomic DNA Sequence Data Using Process-Patterns.
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P-4
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Cheadle, Chris
(NIA)
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C.Cheadle, M.Buchholz, X.Shan, J.Nagel, D.Taub, K.Becker, P.Ghosh
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Delineation of Differential Gene Expression in Alternative Pathways of Human T Cell Activation Using cDNA MicroArrays
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P-5
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Desai, Kartiki
V (NCI)
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K.V.Desai, W.Wang, L.Gangi, J.Green, J.Powell, R. Kuchelapati, E.Liu, J.E.Green
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Molecular Signatures in Transgenic Mouse Models of Mammary Cancer By cDNA Microarray Technology : a comparison to human breast cancer
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P-6
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Finnegan, Ronald
W. (NIAAA)
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Ronald W. Finnegan, MS, David Goldman, M.D., NIH, NIAAA, DICBR, Laboratory of Neurogenetics, Rockville, MD 20852
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Large Scale SNP Genotyping and NT SQL Server Services
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P-7
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Grouse, Lynette
H. (NCI)
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L.H. Grouse, S. F. Greenhut, and R. L. Strausberg
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The Cancer Genome Anatomy Project (CGAP): Current Progress and New Directions
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P-8
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Hansen, Carl
T. (OD)
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C. Hansen
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The NIH Animal Genetic Resource
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P-9
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Johnston, Jennifer
J. (NHGRI)
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J. Johnston, R. Kelley, T. Crawford, D. HolmesMorton, R.Agarwala, T. Koch, A. Schäffer, C. Francomano, and L. Biesecker
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A novel nemaline myopathy in the Amish caused by a mutation in troponin T1
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P-10
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Khan, Sikandar
G. (NCI)
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S.G. Khan, T. Ueda, S.Emmert, T. Shahlavi , D. Busch* and K. H. Kraemer
Basic Research Laboratory, DBS, NCI and *Armed Forces Institute of Pathology, Washington, D.C.
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A G to A Change at the Splice Donor Site of Intron 2 in the Xeroderma Pigmentosum Group C (XPC) Gene Alters the Efficiency of Pre-mRNA Splicing
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P-11
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Khil, Pavel
(NIDDK)
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P. Khil, R.D. Camerini-Otero
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Profiling gene expression of E. coli in response to DNA damage
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P-12
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Khoshnevisan, Mohammad
H (NIDCR)
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M.H. Khoshnevisan1, T. Wu1, C. Sun1, M. Mazeheri2, R. Long2, A. Miller-Chisholm1, S.R. Diehl1. 1) Craniofacial Epidemiology and Genetics Branch, NIDCR, NIH, Bethesda, MD; 2) Lancaster Cleft Palate Clinic, Lancaster, PA.
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Single nucleotide polymorphisms (SNPs) in alcohol dehydrogenases and risk of oral clefts in humans: different effects of maternal and child genotypes.
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P-13
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Lee, Ju-Seog
(NCI)
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J-S. Lee and S. S. Thorgeirsson
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Dictinct subtypes of Hepatocellular Carcinoma identified by genome-wide gene expression profiling
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P-14
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Li, Tao
(NICHD)
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T. Li, K. Okano and H. Kambara
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Template DNA Size-reduction Sequencing Strategy with a Set of 16 Selective Primers
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P-15
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Li, Wenping
(NCI)
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W.Li, J.Cimorelli, M.Endres, C.Perry, L.Shen
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Predicting Hirschsprung disease susceptibility in GDNF +/- mice using real-time RT-PCR
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P-16
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Luo, Yongquan
(NIA)
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Y. Luo, J. M. Long, E. L. Spangler, D. L. Longo, D. K. Ingram, and N-P. Weng
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Identification of Learning- and Aging-associated Genes in Rat Hippocampus by cDNA Microarray
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P-17
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Myakishev, Maxim
V. (NCI)
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M.V. Myakishev (1),
Y. Khripin (2),
S. Hu (1),
K. Lueders (1),
D. Hamer (1).
(1) - NIH, NCI, Bethesda, MD
(2) - Intergen, Gaithersburg, MD.
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A new method for SNP genotyping based on allele-specific PCR with universal FRET primers.
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P-18
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Nagaraja, Ramaiah
(NIA)
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R. Nagaraja, P. Waeltz, E. Jones, S.M. Amyot, Y. Qian, D. Dudekula, M. Brathwaite, M.S.H. Ko and D. Schlessinger.
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Genomic sequence analysis in the mouse t-complex region.
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P-19
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Permana, Paska
A (NIDDK)
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X. Yang, R.E. Pratley, P.A. Permana
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Use of oligonucleotide microarrays to identify novel candidate genes for insulin resistance in non-diabetic Pima Indians
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P-20
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Piotrowski, Tatjana
(NICHD)
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T.Piotrowski; C.Nuesslein-Volhard; I.B.Dawid
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Genetic Screen for Defects in the Lateral Line Sensory System in the Zebrafish
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P-21
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Riazuddin, Saima
(NIDCD)
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S. Riazuddin,C.M. Castelein, T.B. Friedman, A.K. Lalwani, A.J. Griffith, S. Naz, T.N. Smith, N.A. Liburd,M.A. Mastroianni, S. Riazuddin, E.R. Wilcox
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A dominant modifier DFNM1 protects seven individuals from DFNB26 hearing impairment
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P-22
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Scherpbier, J. Titia
(NCI)
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Titia Scherpbier, Jenny Kelley, Michael Gandolph and Kenneth Buetow
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Genetic Polymorphisms in Breast Cancer
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P-23
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Shatkay, Hagit
(NLM)
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H. Shatkay, S. W. Edwards, W. J. Wilbur, M. Boguski
|
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Genes, Themes and Microarrays:Automated Genome-Wide Extraction of Gene Function from PubMed
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P-24
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Silk, Wesam
(NEI)
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A Pilot Study Examining Gene Expression Patterns in Circulating Monocytes and Dermal Fibroblasts in Patients with Age-related Macular Degeneration
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P-25
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Suh, Edward
B (CIT)
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Edward B. Suh
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Genetic Linkage Analysis Software on High-Performance Computer Systems
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P-26
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Velasco, Alfredo
A. (NCI)
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A. Velasco , S. Hewitt ,C. Martinez , H. Rosenberg , M. Hossein Saboorian , W.M. Linehan ,J.D. McConnell and F.S. Leach .
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Altered Expression of the Mismatch Repair Gene, hMSH2, in Normal and Neoplastic Prostate Tissue.
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P-27
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Wilcox, Edward
R (NIDCD)
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E.R. Wilcox, S. Naz, S, Riazuddin, T.N. Smith, I. Belyantseva, Q. Burton, T. Ben-Yosef, A.J. Griffith, R.J. Morell, D.K. Wu, B. Kachar, S. Riazuddin, T.B. Friedman
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Mapping DFNB29 and Cloning this Novel Nonsyndromic Deafness Gene on Chromosome 21q22
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P-28
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Yuan, Fang
(NCI)
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F. Yuan and C.C.Baker
|
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Profiling Gene Expression in Cervical Cancer by Microdissection-based cDNA Libraries and High throughput Microarrays
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