74 resultados para Demetrius.


Relevância:

10.00% 10.00%

Publicador:

Resumo:

Mode of access: Internet.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Incluye según índice: Chronici jussu Constantini Porphyrogenneti conscripti, a Leone Armenio usque ad Michaelem Theophili ; Idem Constantinus Porphyrogennetus de Basilii Imp. avi vita & rebus gestis ; Anonymus continuator Theophanis, a Leone Sapiente usque ad Romanum, Constantini Porphyrogenneti ; Orthodoxorum Invectiva adversus Iconomachos ; Joannis Jerosolymitani Narratio de Iconomachis ; Joannes Cameniata, & Demetrius Cydonius, de Excidio Thessalonicae ; Symeonis Magistri ac Logothetae Annales, a Leone Armenio usque ad Nicephorum Phocam ; Georgii Monachi vitae recentiorum Imperatorum, a Leone Armenio usque ad Constantinum Porphyrogennetum.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Back Row: Cam Cameron, Jim Harbaugh, Jim Whitledge, Chris Zurbrugg, Russell Rein, Bob Cernak,

Michael Taylor, Jerry Hanlon, Scott Crawford, Demetrius Brown

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Back Row: Cam Cameron, Jim Harbaugh, Jim Whitledge, Chris Zurbrugg, Russell Rein, Bob Cernak,

Michael Taylor, Jerry Hanlon, Scott Crawford, Demetrius Brown

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Beginning in 1895, includes the Proceedings of the East India Association.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Thesis (doctoral)--Universitat Leipzig.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Thesis (doctoral)--Kgl. Ludwig-Maximilians-Universitat Munchen.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Edited by Emil Kuh.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Includes indexes.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

It remains unclear whether genetic variants in SNCA (the alpha-synuclein gene) alter risk for sporadic Parkinson's disease (PD). The polymorphic mixed sequence repeat (NACP-Rep I) in the promoter region of SNCA has been previously examined as a potential susceptibility factor for PD with conflicting results. We report genotype and allele distributions at this locus from 369 PD cases and 370 control subjects of European Australian ancestry, with alleles designated as -1, 0, +1, +2, and +3 as previously described. Allele frequencies designated (0) were less common in Australian cases compared to controls (OR = 0.80, 95% CI 0.62-1.03). Combined analysis including all previously published ancestral European Rep1 data yielded a highly significant association between the 0 allele and a reduced risk for PD (OR = 0.79, 95% CI 0.70-0.89, p = 0.0001). Further study must now proceed to examine in detail this interesting and biologically plausible genetic association. (C) 2004 Elsevier Ireland Ltd. All rights reserved.

Relevância:

10.00% 10.00%

Publicador:

Resumo:

Epidemiologically related traits may share genetic risk factors, and pleiotropic analysis could identify individual loci associated with these traits. Because of their shared epidemiological associations, we conducted pleiotropic analysis of genome-wide association studies of lung cancer (12 160 lung cancer case patients and 16 838 control subjects) and cardiovascular disease risk factors (blood lipids from 188 577 subjects, type 2 diabetes from 148 821 subjects, body mass index from 123 865 subjects, and smoking phenotypes from 74 053 subjects). We found that 6p22.1 (rs6904596, ZNF184) was associated with both lung cancer (P = 5.50x10(-6)) and blood triglycerides (P = 1.39x10(-5)). We replicated the association in 6097 lung cancer case patients and 204 657 control subjects (P = 2.40 × 10(-4)) and in 71 113 subjects with triglycerides data (P = .01). rs6904596 reached genome-wide significance in lung cancer meta-analysis (odds ratio = 1.15, 95% confidence interval = 1.10 to 1.21 ,: Pcombined = 5.20x10(-9)). The large sample size provided by the lipid GWAS data and the shared genetic risk factors between the two traits contributed to the uncovering of a hitherto unidentified genetic locus for lung cancer.