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Results: 1-15 |
Results: 15
Association of a promoter polymorphism of the CD14 gene and atopy
Authors: Koppelman, GH Reijmerink, NE Stine, OC Howard, TD Whittaker, PA Meyers, DA Postma, DS Bleecker, ER
Citation: Gh. Koppelman et al., Association of a promoter polymorphism of the CD14 gene and atopy, AM J R CRIT, 163(4), 2001, pp. 965-969
Hypermethylation of the hMLH1 gene promoter is associated with microsatellite instability in early human gastric neoplasia
Authors: Fleisher, AS Esteller, M Tamura, G Rashid, A Stine, OC Yin, J Zou, TT Abraham, JM Kong, DH Nishizuka, S James, SP Wilson, KT Herman, JG Meltzer, SJ
Citation: As. Fleisher et al., Hypermethylation of the hMLH1 gene promoter is associated with microsatellite instability in early human gastric neoplasia, ONCOGENE, 20(3), 2001, pp. 329-335
Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families
Authors: Mathias, RA Freidhoff, LR Blumenthal, MN Meyers, DA Lester, L King, R Xu, JF Solway, J Barnes, KC Pierce, J Stine, OC Togias, A Oetting, W Marshik, PL Hetmanski, JB Huang, SK Ehrlich, E Dunston, GM Malveaux, F Banks-Schlegel, S Cox, NJ Bleecker, E Ober, C Beaty, TH Rich, SS
Citation: Ra. Mathias et al., Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families, GENET EPID, 20(3), 2001, pp. 340-355
Linkage of prostate cancer susceptibility loci to chromosome 1
Authors: Xu, JF Zheng, SL Chang, BL Smith, JR Carpten, JD Stine, OC Isaacs, SD Wiley, KE Henning, L Ewing, C Bujnovszky, P Bleeker, ER Walsh, PC Trent, JM Meyers, DA Isaacs, WB
Citation: Jf. Xu et al., Linkage of prostate cancer susceptibility loci to chromosome 1, HUM GENET, 108(4), 2001, pp. 335-345
Instabilotyping: Comprehensive identification of frameshift mutations caused by coding region microsatellite instability
Authors: Mori, Y Yin, J Rashid, A Leggett, BA Young, J Simms, L Kuehl, PM Langenberg, P Meltzer, SJ Stine, OC
Citation: Y. Mori et al., Instabilotyping: Comprehensive identification of frameshift mutations caused by coding region microsatellite instability, CANCER RES, 61(16), 2001, pp. 6046-6049
Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease
Authors: Aylward, EH Codori, AM Rosenblatt, A Sherr, M Brandt, J Stine, OC Barta, PE Pearlson, GD Ross, CA
Citation: Eh. Aylward et al., Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease, MOVEMENT D, 15(3), 2000, pp. 552-560
Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees
Authors: Foroud, T Castelluccio, PF Koller, DL Edenberg, HJ Miller, M Bowman, E Rau, NL Smiley, C Rice, JP Goate, A Armstrong, C Bierut, LJ Reich, T Detera-Wadleigh, SD Goldin, LR Badner, JA Guroff, JJ Gershon, ES McMahon, FJ Simpson, S MacKinnon, D McInnis, M Stine, OC DePaulo, JR Blehar, MC Nurnberger, JI
Citation: T. Foroud et al., Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees, AM J MED G, 96(1), 2000, pp. 18-23
Phylogeny of Vibrio cholerae based on recA sequence
Authors: Stine, OC Sozhamannan, S Gou, Q Zheng, SQ Morris, JG Johnson, JA
Citation: Oc. Stine et al., Phylogeny of Vibrio cholerae based on recA sequence, INFEC IMMUN, 68(12), 2000, pp. 7180-7185
Microsatellite instability in inflammatory bowel disease-associated neoplastic lesions is associated with hypermethylation and diminished expression of the DNA mismatch repair gene, hMLHI
Authors: Fleisher, AS Esteller, M Harpaz, N Leytin, A Rashid, A Xu, Y Liang, J Stine, OC Yin, J Zou, TT Ahraham, JM Kong, D Wilson, KT James, SP Herman, JG Meltzer, SJ
Citation: As. Fleisher et al., Microsatellite instability in inflammatory bowel disease-associated neoplastic lesions is associated with hypermethylation and diminished expression of the DNA mismatch repair gene, hMLHI, CANCER RES, 60(17), 2000, pp. 4864-4868
Major genes regulating total serum immunoglobulin E levels in families with asthma
Authors: Xu, JF Postma, DS Howard, TD Koppelman, GH Zheng, SL Stine, OC Bleecker, ER Meyers, DA
Citation: Jf. Xu et al., Major genes regulating total serum immunoglobulin E levels in families with asthma, AM J HU GEN, 67(5), 2000, pp. 1163-1173
Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype
Authors: Friddle, C Koskela, R Ranade, K Hebert, J Cargill, M Clark, CD McInnis, M Simpson, S McMahon, F Stine, OC Meyers, D Xu, JF MacKinnon, D Swift-Scanlan, T Jamison, K Folstein, S Daly, M Kruglyak, L Marr, T DePaulo, JR Botstein, D
Citation: C. Friddle et al., Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype, AM J HU GEN, 66(1), 2000, pp. 205-215
Linkage analysis narrows the critical region for oculodentodigital dysplasia to chromosome 6q22-q23
Authors: Boyadjiev, SA Jabs, EW LaBuda, M Jamal, JE Torbergsen, T Ptacek, LJ Rogers, RC Nyberg-Hansen, R Opjordsmoen, S Zeller, CB Stine, OC Stalker, HJ Zori, RT Shapiro, RE
Citation: Sa. Boyadjiev et al., Linkage analysis narrows the critical region for oculodentodigital dysplasia to chromosome 6q22-q23, GENOMICS, 58(1), 1999, pp. 34-40
Fluorescent allele-specific PCR (FAS-PCR) improves the reliability of single nucleotide polymorphism screening
Authors: Howard, TD Bleecker, ER Stine, OC
Citation: Td. Howard et al., Fluorescent allele-specific PCR (FAS-PCR) improves the reliability of single nucleotide polymorphism screening, BIOTECHNIQU, 26(3), 1999, pp. 380-381
Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of asecond pedigree and effect on protein expression
Authors: Margolis, RL Stine, OC Ward, CM Franz, ML Rosenblatt, A Callahan, C Sherr, M Ross, CA Potter, NT
Citation: Rl. Margolis et al., Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of asecond pedigree and effect on protein expression, J MED GENET, 36(1), 1999, pp. 62-64
Two novel single-base-pair substitutions adjacent to the CAG repeat in theHuntington disease gene (IT15): Implications for diagnostic testing
Authors: Margolis, RL Stine, OC Callahan, C Rosenblatt, A Abbott, MH Sherr, M Ross, CA
Citation: Rl. Margolis et al., Two novel single-base-pair substitutions adjacent to the CAG repeat in theHuntington disease gene (IT15): Implications for diagnostic testing, AM J HU GEN, 64(1), 1999, pp. 323-326
Risultati: 1-15 |