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Results: 1-25 | 26-37
Results: 1-25/37
Complete genomic screen in parkinson disease - Evidence for multiple genes
Authors: Scott, WK Nance, MA Watts, RL Hubble, JP Koller, WC Lyons, K Pahwa, R Stern, MB Colcher, A Hiner, BC Jankovic, J Ondo, WG Allen, FH Goetz, CG Small, GW Masterman, D Mastaglia, F Laing, NG Stajich, JM Slotterbeck, B Booze, MW Ribble, RC Rampersaud, E West, SG Gibson, RA Middleton, LT Roses, AD Haines, JL Scott, BL Vance, JM Pericak-Vance, MA
Citation: Wk. Scott et al., Complete genomic screen in parkinson disease - Evidence for multiple genes, J AM MED A, 286(18), 2001, pp. 2239-2244
Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease
Authors: Martin, ER Scott, WK Nance, MA Watts, RL Hubble, JP Koller, WC Lyons, K Pahwa, R Stern, MB Colcher, A Hiner, BC Jankovic, J Ondo, WG Allen, FH Goetz, CG Small, GW Masterman, D Mastaglia, F Laing, NG Stajich, JM Ribble, RC Booze, MW Rogala, A Hauser, MA Zhang, FY Gibson, RA Middleton, LT Roses, AD Haines, JL Scott, BL Pericak-Vance, MA Vance, JM
Citation: Er. Martin et al., Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease, J AM MED A, 286(18), 2001, pp. 2245-2250
Dissecting a complex disease using modern techniques of molecular biology
Authors: Oliveira, SA Scott, WK Pericak-Vance, MA Vance, JM
Citation: Sa. Oliveira et al., Dissecting a complex disease using modern techniques of molecular biology, LAB MED, 32(10), 2001, pp. 594-598
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia
Authors: Svenson, IK Ashley-Koch, AE Gaskell, PC Riney, TJ Cumming, WJK Kingston, HM Hogan, EL Boustany, RMN Vance, JM Nance, MA Pericak-Vance, MA Marchuk, DA
Citation: Ik. Svenson et al., Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia, AM J HU GEN, 68(5), 2001, pp. 1077-1085
A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis
Authors: Allingham, RR Seo, B Rampersaud, E Bembe, M Challa, P Liu, NP Parrish, T Karolak, L Gilbert, J Pericak-Vance, MA Klintworth, GK Vance, JM
Citation: Rr. Allingham et al., A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis, AM J HU GEN, 68(2), 2001, pp. 491-494
A genomic search for Alzheimer's disease genes
Authors: Haines, JL Bailey, LR Grubber, JM Hedges, D Hall, JL West, S Santoro, L Kemmerer, B Saunders, AM Roses, AD Small, GW Scott, WK Conneally, PM Vance, JM Pericak-Vance, MA
Citation: Jl. Haines et al., A genomic search for Alzheimer's disease genes, ALZHEIMER'S DISEASE, 2001, pp. 33-43
Enantioselective construction of vicinal stereogenic quaternary centers bydialkylation: Practical total syntheses of (+)- and meso-chimonanthine
Authors: Overman, LE Larrow, JF Stearns, BA Vance, JM
Citation: Le. Overman et al., Enantioselective construction of vicinal stereogenic quaternary centers bydialkylation: Practical total syntheses of (+)- and meso-chimonanthine, ANGEW CHEM, 39(1), 2000, pp. 213-215
Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland
Authors: Liu, NP Dew-Knight, S Rayner, M Jonasson, F Akama, TO Fukuda, MN Bao, WJ Gilbert, JR Vance, JM Klintworth, GK
Citation: Np. Liu et al., Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland, MOL VIS, 6(33), 2000, pp. 261-264
Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes
Authors: Liu, NP Dew-Knight, S Jonasson, F Gilbert, JR Klintworth, GK Vance, JM
Citation: Np. Liu et al., Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes, MOL VIS, 6(11), 2000, pp. 95-100
Myotilin is mutated in limb girdle muscular dystrophy 1A
Authors: Hauser, MA Horrigan, SK Salmikangas, P Torian, UM Viles, KD Dancel, R Tim, RW Taivainen, A Bartoloni, L Gilchrist, JM Stajich, JM Gaskell, PC Gilbert, JR Vance, JM Pericak-Vance, MA Carpen, O Westbrook, CA Speer, MC
Citation: Ma. Hauser et al., Myotilin is mutated in limb girdle muscular dystrophy 1A, HUM MOL GEN, 9(14), 2000, pp. 2141-2147
Analysis of association at single nucleotide polymorphisms in the APOE region
Authors: Martin, ER Gilbert, JR Lai, EH Riley, J Rogala, AR Slotterbeck, BD Sipe, CA Grubber, JM Warren, LL Conneally, PM Saunders, AM Schmechel, DE Purvis, I Pericak-Vance, MA Roses, AD Vance, JM
Citation: Er. Martin et al., Analysis of association at single nucleotide polymorphisms in the APOE region, GENOMICS, 63(1), 2000, pp. 7-12
Actively controlled bearing dampers for aircraft engine applications
Authors: Vance, JM Ying, D Nikolajsen, JL
Citation: Jm. Vance et al., Actively controlled bearing dampers for aircraft engine applications, J ENG GAS T, 122(3), 2000, pp. 466-472
Hybrid brush pocket damper seals for turbomachinery
Authors: Laos, HE Vance, JM Buchanan, SE
Citation: He. Laos et al., Hybrid brush pocket damper seals for turbomachinery, J ENG GAS T, 122(2), 2000, pp. 330-336
Experimental measurements of actively controlled bearing damping with an electrorheological fluid
Authors: Vance, JM Ying, D
Citation: Jm. Vance et D. Ying, Experimental measurements of actively controlled bearing damping with an electrorheological fluid, J ENG GAS T, 122(2), 2000, pp. 337-344
Dynamic force coefficients of a multiple-blade, multiple-pocket gas damperseal: Test results and predictions
Authors: Li, JM Aguilar, R San Andres, L Vance, JM
Citation: Jm. Li et al., Dynamic force coefficients of a multiple-blade, multiple-pocket gas damperseal: Test results and predictions, J TRIBOL, 122(1), 2000, pp. 317-322
Identification of novel genes in late-onset Alzheimer's disease
Authors: Pericak-Vance, MA Grubber, J Bailey, LR Hedges, D West, S Santoro, L Kemmerer, B Hall, JL Saunders, AM Roses, AD Small, GW Scott, WK Conneally, PM Vance, JM Haines, JL
Citation: Ma. Pericak-vance et al., Identification of novel genes in late-onset Alzheimer's disease, EXP GERONT, 35(9-10), 2000, pp. 1343-1352
Applying virtual reality techniques to the interactive stress analysis of a tractor lift arm
Authors: Ryken, MJ Vance, JM
Citation: Mj. Ryken et Jm. Vance, Applying virtual reality techniques to the interactive stress analysis of a tractor lift arm, FINITE EL A, 35(2), 2000, pp. 141-155
Three probands with autistic disorder and isodicentric chromosome 15
Authors: Wolpert, CM Menold, MM Bass, MP Qumsiyeh, MB Donnelly, SL Ravan, SA Vance, JM Gilbert, JR Abramson, RK Wright, HH Cuccaro, ML Pericak-Vance, MA
Citation: Cm. Wolpert et al., Three probands with autistic disorder and isodicentric chromosome 15, AM J MED G, 96(3), 2000, pp. 365-372
Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder
Authors: Martin, ER Menold, MM Wolpert, CM Bass, MP Donnelly, SL Ravan, SA Zimmerman, A Gilbert, JR Vance, JM Maddox, LO Wright, HH Abramson, RK DeLong, GR Cuccaro, ML Pericak-Vance, MA
Citation: Er. Martin et al., Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder, AM J MED G, 96(1), 2000, pp. 43-48
Heterogeneity in Paget disease of the bone
Authors: Nance, MA Nuttall, FQ Econs, MJ Lyles, KW Viles, KD Vance, JM Pericak-Vance, MA Speer, MC
Citation: Ma. Nance et al., Heterogeneity in Paget disease of the bone, AM J MED G, 92(5), 2000, pp. 303-307
The many faces of Charcot-Marie-Tooth disease
Authors: Vance, JM
Citation: Jm. Vance, The many faces of Charcot-Marie-Tooth disease, ARCH NEUROL, 57(5), 2000, pp. 638-640
SNPing away at complex diseases: Analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease
Authors: Martin, ER Lai, EH Gilbert, JR Rogala, AR Afshari, AJ Riley, L Finch, KL Stevens, F Livak, KJ Slotterbeck, BD Slifer, SH Warren, LL Conneally, PM Schmechel, DE Purvis, I Pericak-Vance, MA Roses, AD Vance, JM
Citation: Er. Martin et al., SNPing away at complex diseases: Analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease, AM J HU GEN, 67(2), 2000, pp. 383-394
Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing
Authors: Messiaen, LM Callens, T Roux, KJ Mortier, GR De Paepe, A Abramowicz, M Pericak-Vance, MA Vance, JM Wallace, MR
Citation: Lm. Messiaen et al., Exon 10b of the NF1 gene represents a mutational hotspot and harbors a recurrent missense mutation Y489C associated with aberrant splicing, GENET MED, 1(6), 1999, pp. 248-253
Assessing the effectiveness of traditional and virtual reality interfaces in spherical mechanism design
Authors: Evans, PT Vance, JM Dark, VJ
Citation: Pt. Evans et al., Assessing the effectiveness of traditional and virtual reality interfaces in spherical mechanism design, J MEC DESIG, 121(4), 1999, pp. 507-514
Spherical mechanism synthesis in virtual reality
Authors: Furlong, TJ Vance, JM Larochelle, PM
Citation: Tj. Furlong et al., Spherical mechanism synthesis in virtual reality, J MEC DESIG, 121(4), 1999, pp. 515-520
Risultati: 1-25 | 26-37