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Results: 1-25 | 26-40 |
Results: 26-40/40
Five plus two equals yellow
Authors: Dixon, MJ Smilek, D Cudahy, C Merikle, PM
Citation: Mj. Dixon et al., Five plus two equals yellow, NATURE, 406(6794), 2000, pp. 365-365
Mapping of dentin-specific acidic phosphoprotein and integrin-binding sialoprotein in sheep defines an inversion breakpoint with respect to human chromosome 4Q
Authors: Lumsden, JM Lord, EA Hirst, KL Dixon, MJ Montgomery, GW
Citation: Jm. Lumsden et al., Mapping of dentin-specific acidic phosphoprotein and integrin-binding sialoprotein in sheep defines an inversion breakpoint with respect to human chromosome 4Q, GENET MOL B, 22(1), 1999, pp. 29-31
Object identification deficits in dementia of the Alzheimer type: Combinedeffects of semantic and visual proximity
Authors: Dixon, MJ Bub, DN Chertkow, H Arguin, M
Citation: Mj. Dixon et al., Object identification deficits in dementia of the Alzheimer type: Combinedeffects of semantic and visual proximity, J INT NEURO, 5(4), 1999, pp. 330-345
Inhibition of FEN-1 processing by DNA secondary structure at trinucleotiderepeats
Authors: Spiro, C Pelletier, R Rolfsmeier, ML Dixon, MJ Lahue, RS Gupta, G Park, MS Chen, X Mariappan, SVS McMurray, CT
Citation: C. Spiro et al., Inhibition of FEN-1 processing by DNA secondary structure at trinucleotiderepeats, MOL CELL, 4(6), 1999, pp. 1079-1085
Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis
Authors: Toomes, C James, J Wood, AJ Wu, CL McCormick, D Lench, N Hewitt, C Moynihan, L Roberts, E Woods, CG Markham, A Wong, M Widmer, R Ghaffar, KA Pemberton, M Hussein, IR Temtamy, SA Davies, R Read, AP Sloan, P Dixon, MJ Thakker, NS
Citation: C. Toomes et al., Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis, NAT GENET, 23(4), 1999, pp. 421-424
Heterogeneity in granular corneal dystrophy: Identification of three causative mutations in the TGFBI (BIGH3) gene - Lessons for corneal amyloidogenesis
Authors: Stewart, HS Ridgway, AE Dixon, MJ Bonshek, R Parveen, R Black, G
Citation: Hs. Stewart et al., Heterogeneity in granular corneal dystrophy: Identification of three causative mutations in the TGFBI (BIGH3) gene - Lessons for corneal amyloidogenesis, HUM MUTAT, 14(2), 1999, pp. 126-132
Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness inmice
Authors: Dixon, MJ Gazzard, J Chaudhry, SS Sampson, N Schulte, BA Steel, KP
Citation: Mj. Dixon et al., Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness inmice, HUM MOL GEN, 8(8), 1999, pp. 1579-1584
Refined genetic and physical localization of the Wagner disease (WGN1) locus and the genes CRTL1 and CSPG2 to a 2- to 2.5-cM region of chromosome 5q14.3
Authors: Perveen, R Hart-Holden, N Dixon, MJ Wiszniewski, W Fryer, AE Brunner, HG Pinkners, AJLH van Beersum, SEC Black, GCM
Citation: R. Perveen et al., Refined genetic and physical localization of the Wagner disease (WGN1) locus and the genes CRTL1 and CSPG2 to a 2- to 2.5-cM region of chromosome 5q14.3, GENOMICS, 57(2), 1999, pp. 219-226
Expressed emotion and relapse in young schizophrenia outpatients
Authors: King, S Dixon, MJ
Citation: S. King et Mj. Dixon, Expressed emotion and relapse in young schizophrenia outpatients, SCHIZO BULL, 25(2), 1999, pp. 377-386
A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late onset form of lattice corneal dystrophy
Authors: Stewart, H Black, GCM Donnai, D Bonshek, RE McCarthy, J Morgan, S Dixon, MJ Ridgway, AAE
Citation: H. Stewart et al., A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late onset form of lattice corneal dystrophy, OPHTHALMOL, 106(5), 1999, pp. 964-970
Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome
Authors: Schutte, BC Basart, AM Watanabe, Y Laffin, JJS Coppage, K Bjork, BC Daack-Hirsch, S Patil, S Dixon, MJ Murray, JC
Citation: Bc. Schutte et al., Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome, AM J MED G, 84(2), 1999, pp. 145-150
The effect of non-stationarity on extreme sea-level estimation
Authors: Dixon, MJ Tawn, JA
Citation: Mj. Dixon et Ja. Tawn, The effect of non-stationarity on extreme sea-level estimation, J ROY STA C, 48, 1999, pp. 135-151
Refinement of the dentinogenesis imperfecta type II locus to an interval of less than 2 centiMorgans at chromosome 4q21 and the creation of a yeast artificial chromosome contig of the critical region
Authors: Aplin, HM Hirst, KL Dixon, MJ
Citation: Hm. Aplin et al., Refinement of the dentinogenesis imperfecta type II locus to an interval of less than 2 centiMorgans at chromosome 4q21 and the creation of a yeast artificial chromosome contig of the critical region, J DENT RES, 78(6), 1999, pp. 1270-1276
Identification and cloning of a novel cellular protein Naf1, Nef-associated factor 1, that increases cell surface CD4 expression
Authors: Fukushi, M Dixon, J Kimura, T Tsurutani, N Dixon, MJ Yamamoto, N
Citation: M. Fukushi et al., Identification and cloning of a novel cellular protein Naf1, Nef-associated factor 1, that increases cell surface CD4 expression, FEBS LETTER, 442(1), 1999, pp. 83-88
Construction of a physical, genetic and transcript map in region q32-qter of human chromosome 5 and relation to a craniosynostosis locus
Authors: Muller, U Monaco, AP Dixon, MJ Boultwood, J
Citation: U. Muller et al., Construction of a physical, genetic and transcript map in region q32-qter of human chromosome 5 and relation to a craniosynostosis locus, BIOM HLTH R, 23, 1998, pp. 72-86
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