dadiScripts

Set of Python scripts used to run all dadi analyse

Monarcha_nexus_files

Set of nexus input files for running in SNAPP phylogenetic analysi

RADsysBio_Scripts

Set of all Perl and R scripts used in analysis pipelin

Demographic/Socioeconomic Characteristics of Focus Group Participants vs MB Total Population.

1<p>Information not completed by participants at their own discretion. Marital Status, Education and Household Income were unfortunately not collected during first pilot testing of the instrument in the rural First Nations community prior to Wave 2 of H1N1. This represents 16 participants each for these three Missing values.</p>2<p>We over-sampled the 18–34 age category during our pilot testing phase (8 focus groups in total) as this was believed to be the age category at highest risk of more severe outcomes from pandemic H1N1.</p>3<p>Statistics Canada, 2011 Census of Population. At the time of writing, only age and sex data from the 2011 Census were available from Statistics Canada.</p>4<p>Statistics Canada, 2006 Census of Population. Includes all data on marital status, education, household income.</p>5<p>Statistics Canada, 2006 Census of Population. For MB Totals in education for Grades 11 to 12, number given is the High School Certificate or equivalent. For category of Some or completed university or college, number represents aggregate of those with College, CEGEP or other non-university certificate or diploma, university certificate or diploma below bachelor level, and university certificate, diploma or degree.</p

Study Locations for the Manitoba H1N1 Project.

<p>Study Locations for the Manitoba H1N1 Project.</p

Additional file 1 of Involvement of the tumour necrosis factor receptor system in glioblastoma cell death induced by palbociclib-heptamethine cyanine dye conjugate

Additional file 1: Supplementary Figure 1. Cyclin-dependent kinase inhibitor-MHI-148 conjugates, 1 are not synergistic with TMZ. Patient-derived glioblastoma cells were treated with up to 100 μM of palbociclib, and 1 with and without 100 μM of TMZ for 96 h. Concentration-dependent effects of each compound on the toxicity of glioblastoma cells was measured by the percentage of Hoechst-positive cells after 96 h (EC50). A non-linear curve was fitted using Graphpad Prism using the concentration of each compound versus the percentage of hoechst-positive cells (A). Combination index (CI) was calculated from the CI equation algorithms using CompuSyn software. CI=1, 1 indicates additive effect, synergism, and antagonism, respectively (B). The pEC50 of each compound with and without TMZ (100 μM) on each glioblastoma cell line is summarised in B and D. The CI for palbociclib (A) and 1 (C), with TMZ across a range of effect sizes is presented per case. Data represents mean ±SEM for at least six independent glioblastoma cases, ns = p > 0.05. Supplementary Figure 2. Trafficking and expression of TNFR1 in response to 1 in patient-derived glioblastoma cells in the presence of vesicle trafficking inhibitor, BFA and protein translation inhibitor, CHX. Residual starting surface expression TNFR1 (Method A) (A). To investigate the net surface expression of TNFR1 (Method B) (B). C summarises method A and B detection of TNFR1. Total TNFR1 expression in response to 1 in the presence of absence of BFA or CHX (D) Summary data of the pEC50 (E) and Emax (F) of 1 on the total TNFR1 expression in the presence or absence of BFA or CHX. Basal total TNFR1 expression in G. Data represents mean ± SEM from three independent glioblastoma cases. ns = p > 0.05, * p < 0.05, ** p< 0.01, *** p < 0.001, One-way ANOVA relative to 1 plus vehicle inhibitor