1,078 research outputs found
Magnetic Response of Magnetospirillum Gryphiswaldense
In this study we modelled and measured the U-turn trajectories of individual
magnetotactic bacteria under the application of rotating magnetic fields,
ranging in ampitude from 1 to 12 mT. The model is based on the balance between
rotational drag and magnetic torque. For accurate verification of this model,
bacteria were observed inside 5 m tall microfluidic channels, so that they
remained in focus during the entire trajectory. From the analysis of hundreds
of trajectories and accurate measurements of bacteria and magnetosome chain
dimensions, we confirmed that the model is correct within measurement error.
The resulting average rate of rotation of Magnetospirillum Gryphiswaldense is
0.74 +- 0.03 rad/mTs.Comment: 17 pages, 12 figure
Macular retinal thickness differs markedly in age-related macular degeneration driven by risk polymorphisms on chromosomes 1 and 10 (vol 10, 21093, 2020)
Protective chromosome 1q32 haplotypes mitigate risk for age-related macular degeneration associated with the CFH-CFHR5 and ARMS2/HTRA1 loci
Background: Single-variant associations with age-related macular degeneration (AMD), one of the most prevalent causes of irreversible vision loss worldwide, have been studied extensively. However, because of a lack of refinement of these associations, there remains considerable ambiguity regarding what constitutes genetic risk and/or protection for this disease, and how genetic combinations affect this risk. In this study, we consider the two most common and strongly AMD-associated loci, the CFH-CFHR5 region on chromosome 1q32 (Chr1 locus)Â and ARMS2/HTRA1 gene on chromosome 10q26 (Chr10 locus). Results: By refining associations within the CFH-CFHR5 locus, we show that all genetic protection against the development of AMD in this region is described by the combination of the amino acid-altering variant CFH I62V (rs800292) and genetic deletion of CFHR3/1. Haplotypes based on CFH I62V, a CFHR3/1 deletion tagging SNP and the risk variant CFH Y402H are associated with either risk, protection or neutrality for AMD and capture more than 99% of control- and case-associated chromosomes. We find that genetic combinations of CFH-CFHR5 haplotypes (diplotypes) strongly influence AMD susceptibility and that individuals with risk/protective diplotypes are substantially protected against the development of disease. Finally, we demonstrate that AMD risk in the ARMS2/HTRA1 locus is also mitigated by combinations of CFH-CFHR5 haplotypes, with Chr10Â risk variants essentially neutralized by protective CFH-CFHR5 haplotypes. Conclusions: Our study highlights the importance of considering protective CFH-CFHR5 haplotypes when assessing genetic susceptibility for AMD. It establishes a framework that describes the full spectrum of AMD susceptibility using an optimal set of single-nucleotide polymorphisms with known functional consequences. It also indicates that protective or preventive complement-directed therapies targeting AMD driven by CFH-CFHR5 risk haplotypes may also be effective when AMD is driven by ARMS2/HTRA1 risk variants
Planar manipulation of magneto-tactic bacteria using unidirectional magnetic fields
We show for the first time that an alternating unidirectional magnetic field generated by a magnetic erase head allows planar manipulation of magneto-tactic bacteria (MTB), and is not restricted to parallel directions only. We used squared-shaped magnetic fields of approximately 4 mT while sweeping from 0.25 to 10 Hz, and found that at frequencies of over 3 Hz the mean orthogonal velocity becomes constant. The erase head offers a significant reduction in size and complexity over conventional manipulators
Progression of Age-Related Macular Degeneration Among Individuals Homozygous for Risk Alleles on Chromosome 1 (CFH-CFHR5) or Chromosome 10 (ARMS2/HTRA1) or Both
Importance: Age-related macular degeneration (AMD) is a common cause of irreversible vision loss among individuals older than 50 years. Although considerable advances have been made in our understanding of AMD genetics, the differential effects of major associated loci on disease manifestation and progression may not be well characterized. Objective: To elucidate the specific associations of the 2 most common genetic risk loci for AMD, the CFH-CFHR5 locus on chromosome 1q32 (Chr1) and the ARMS2/HTRA1 locus on chromosome 10q26 (Chr10)-independent of one another and in combination-with time to conversion to late-stage disease and to visual acuity loss. Design, Setting, and Participants: This case series study included 502 individuals who were homozygous for risk variants at both Chr1 and Chr10 (termed Chr1&10-risk) or at either Chr1 (Chr1-risk) or Chr10 (Chr10-risk) and who had enrolled in Genetic and Molecular Studies of Eye Diseases at the Sharon Eccles Steele Center for Translational Medicine between September 2009 and March 2020. Multimodal imaging data were reviewed for AMD staging, including grading of incomplete and complete retinal pigment epithelium and outer retinal atrophy. Main Outcomes and Measures: Hazard ratios and survival times for conversion to any late-stage AMD, atrophic or neovascular, and associated vision loss of 2 or more lines. Results: In total, 317 participants in the Chr1-risk group (median [IQR] age at first visit, 75.6 [69.5-81.7] years; 193 women [60.9%]), 93 participants in the Chr10-risk group (median [IQR] age at first visit, 77.5 [72.2-84.2] years; 62 women [66.7%]), and 92 participants in the Chr1&10-risk group (median [IQR] age at first visit, 71.7 [68.0-76.3] years; 62 women [67.4%]) were included in the analyses. After adjusting for age and AMD grade at first visit, compared with 257 participants in the Chr1-risk group, 56 participants in the Chr1&10-risk group (factor of 3.3 [95% CI, 1.6-6.8]; P < .001) and 58 participants in the Chr10-risk group (factor of 2.6 [95% CI, 1.3-5.2]; P = .007) were more likely to convert to a late-stage phenotype during follow-up. This difference was mostly associated with conversion to macular neovascularization, which occurred earlier in participants with Chr1&10-risk and Chr10-risk. Eyes in the Chr1&10-risk group (median [IQR] survival, 5.7 [2.1-11.1] years) were 2.1 (95% CI, 1.1-3.9; P = .03) times as likely and eyes in the Chr10-risk group (median [IQR] survival, 6.3 [2.7-11.3] years) were 1.8 (95% CI, 1.0-3.1; P = .05) times as likely to experience a visual acuity loss of 2 or more lines compared with eyes of the Chr1-risk group (median [IQR] survival, 9.4 [4.1-* (asterisk indicates event rate did not reach 75%)] years). Conclusions and Relevance: These findings suggest differential associations of the 2 major AMD-related risk loci with structural and functional disease progression and suggest distinct underlying biological mechanisms associated with these 2 loci. These genotype-phenotype associations may warrant consideration when designing and interpreting AMD research studies and clinical trials
Role of transport performance on neuron cell morphology
The compartmental model is a basic tool for studying signal propagation in
neurons, and, if the model parameters are adequately defined, it can also be of
help in the study of electrical or fluid transport. Here we show that the input
resistance, in different networks which simulate the passive properties of
neurons, is the result of an interplay between the relevant conductances,
morphology and size. These results suggest that neurons must grow in such a way
that facilitates the current flow. We propose that power consumption is an
important factor by which neurons attain their final morphological appearance.Comment: 9 pages with 3 figures, submitted to Neuroscience Letter
Quenched QCD at finite density
Simulations of quenched at relatively small but {\it nonzero} chemical
potential on lattices indicate that the nucleon
screening mass decreases linearly as increases predicting a critical
chemical potential of one third the nucleon mass, , by extrapolation.
The meson spectrum does not change as increases over the same range, from
zero to . Past studies of quenched lattice QCD have suggested that
there is phase transition at . We provide alternative
explanations for these results, and find a number of technical reasons why
standard lattice simulation techniques suffer from greatly enhanced
fluctuations and finite size effects for ranging from to
. We find evidence for such problems in our simulations, and suggest
that they can be surmounted by improved measurement techniques.Comment: 23 pages, Revte
Adaptive mesh refinement approach to construction of initial data for black hole collisions
The initial data for black hole collisions is constructed using a
conformal-imaging approach and a new adaptive mesh refinement technique, a
fully threaded tree (FTT). We developed a second-order accurate approach to the
solution of the constraint equations on a non-uniformly refined high resolution
Cartesian mesh including second-order accurate treatment of boundary conditions
at the black hole throats. Results of test computations show convergence of the
solution as the numerical resolution is increased. FTT-based mesh refinement
reduces the required memory and computer time by several orders of magnitude
compared to a uniform grid. This opens up the possibility of using Cartesian
meshes for very high resolution simulations of black hole collisions.Comment: 13 pages, 11 figure
Directional Microwave Emission from Femtosecond-laser Illuminated Linear Arrays of Superconducting Rings
We examine the electromagnetic emission from two photo-illuminated linear arrays composed of inductively charged superconducting ring elements. The arrays are illuminated by an ultrafast infrared laser that triggers microwave broadband emission detected in the 1–26 GHz range. Based on constructive interference from the arrays a narrowing of the forward radiation lobe is observed with increasing element count and frequency demonstrating directed GHz emission. Results suggest that higher frequencies and a larger number of elements are achievable leading to a unique pulsed array emitter concept that can span frequencies from the microwave to the terahertz (THz) regime
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