The Concept of Salvation in Mormonism

The purpose of the thesis is to make clear the Mormon concept of salvation. The development of this concept necessitates a complete discussion of the Mormon philosophy of life. The thesis will show the unchristian character of this philosophy

Temporal endogenous gene expression profiles in response to lipid-mediated transfection

Background — Design of efficient nonviral gene delivery systems is limited as a result of the rudimentary understanding of the specific molecules and processes that facilitate DNA transfer. Methods — Lipoplexes formed with Lipofectamine 2000 (LF2000) and plasmid-encoding green fluorescent protein (GFP) were delivered to the HEK 293T cell line. After treating cells with lipoplexes, HG-U133 Affymetrix microarrays were used to identify endogenous genes differentially expressed between treated and untreated cells (2 h exposure) or between flow-separated transfected cells (GFP+) and treated, untransfected cells (GFP–) at 8, 16 and 24 h after lipoplex treatment. Cell priming studies were conducted using pharmacologic agents to alter endogenous levels of the identified differentially expressed genes to determine effect on transfection levels. Results — Relative to untreated cells 2 h after lipoplex treatment, only downregulated genes were identified ≥ 30-fold: ALMS1, ITGB1, FCGR3A, DOCK10 and ZDDHC13. Subsequently, relative to GFP– cells, the GFP+ cell population showed at least a five-fold upregulation of RAP1A and PACSIN3 (8 h) or HSPA6 and RAP1A (16 and 24 h). Pharmacologic studies altering endogenous levels for ALMS1, FCGR3A, and DOCK10 (involved in filopodia protrusions), ITGB1 (integrin signaling), ZDDHC13 (membrane trafficking) and PACSIN3 (proteolytic shedding of membrane receptors) were able to increase or decrease transgene production. Conclusions — RAP1A, PACSIN3 and HSPA6 may help lipoplex-treated cells overcome a transcriptional shutdown due to treatment with lipoplexes and provide new targets for investigating molecular mechanisms of transfection or for enhancing transfection through cell priming or engineering of the nonviral gene delivery system. Includes supporting materials

Temporal endogenous gene expression profiles in response to polymer-mediated transfection and profile comparison to lipid-mediated transfection

Background Design of efficient nonviral gene delivery systems is limited by the rudimentary understanding of specific molecules that facilitate transfection. Methods Polyplexes using 25-kDa polyethylenimine (PEI) and plasmid encoding green fluorescent protein (GFP) were delivered to HEK 293T cells. After treating cells with polyplexes, microarrays were used to identify endogenous genes differentially expressed between treated and untreated cells (2 h of exposure) or between flow-separated transfected cells (GFP+) and treated, untransfected cells (GFP–) at 8, 16 and 24 h after lipoplex treatment. Cell priming studies were conducted using pharmacologic agents to alter endogenous levels of the identified differentially expressed genes to determine effect on transfection levels. Differentially expressed genes in polyplex-mediated transfection were compared with those differentially expressed in lipoplex transfection to identify DNA carrier-dependent molecular factors. Results Differentially expressed genes were RGS1, ARHGAP24, PDZD2, SNX24, GSN and IGF2BP1 after 2 h; RAP1A and ACTA1 after 8 h; RAP1A, WDR78 and ACTA1 after 16 h; and RAP1A, SCG5, ATF3, IREB2 and ACTA1 after 24 h. Pharmacologic studies altering endogenous levels for ARHGAP24, GSN, IGF2BP1, PDZD2 and RGS1 were able to increase or decrease transgene production. Comparing differentially expressed genes for polyplexes and lipoplexes, no common genes were identified at the 2-h time point, whereas, after the 8-h time point, RAP1A, ATF3 and HSPA6 were similarly expressed. SCG5 and PGAP1 were only upregulated in polyplex-transfected cells. Conclusions The identified genes and pharmacologic agents provide targets for improving transfection systems, although polyplex or lipoplex dependencies must be considered. Includes supplementary materials

Adoptive immunotherapy of cancer with polyclonal, 10(8)-fold hyperexpanded, CD4(+ )and CD8(+ )T cells

T cell-mediated cancer immunotherapy is dose dependent and optimally requires participation of antigen-specific CD4(+ )and CD8(+ )T cells. Here, we isolated tumor-sensitized T cells and activated them in vitro using conditions that led to greater than 10(8)-fold numerical hyperexpansion of either the CD4(+ )or CD8(+ )subset while retaining their capacity for in vivo therapeutic efficacy. Murine tumor-draining lymph node (TDLN) cells were segregated to purify the CD62L(low )subset, or the CD4(+ )subset thereof. Cells were then propagated through multiple cycles of anti-CD3 activation with IL-2 + IL-7 for the CD8(+ )subset, or IL-7 + IL-23 for the CD4(+ )subset. A broad repertoire of TCR Vβ families was maintained throughout hyperexpansion, which was similar to the starting population. Adoptive transfer of hyper-expanded CD8(+ )T cells eliminated established pulmonary metastases, in an immunologically specific fashion without the requirement for adjunct IL-2. Hyper-expanded CD4(+ )T cells cured established tumors in intracranial or subcutaneous sites that were not susceptible to CD8(+ )T cells alone. Because accessibility and antigen presentation within metastases varies according to anatomic site, maintenance of a broad repertoire of both CD4(+ )and CD8(+ )T effector cells will augment the overall systemic efficacy of adoptive immunotherapy

Thermophysics of metal alkanoates I. Heat capacities and thermodynamic properties of sodium methanoate and ethanoate

The heat capacities of two sodium alkanoates have been studied by adiabatic calorimetry. Earlier measurements from this laboratory on sodium methanoate between 5 and 350 K are supplemented from 300 K to melting. Sodium ethanoate ismeasured from 7 through 350 K; the results differ markedly from those reported by Strelkov in that we find the 21 K transition peak is much larger and the higher temperature values are 15 to 20 per cent higher and in good accord with reported d.s.c. studies at still higher temperatures. We estimate [Delta]traSmo/R of the 21 K peak to be about 1.5 although no isostructural lattice contribution is available. Even with adjuvant X-ray diffraction results by Hsu and Nordman the mechanism of the transition has not been identified. The 298.15 K values of Cp,m/R, Smo/R, {Hmo-Hmo(0)}/R and {Gmo-Hmo(0)}/RT are 12.127, 16.610, 2308.1 K, and -8.868 for form II CH3COONa.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/25417/1/0000866.pd

A novel device to measure power grip forces in squirrel monkeys

Understanding the neural bases for grip force behaviors in both normal and neurologically impaired animals is imperative prior to improving treatments and therapeutic approaches. The present paper describes a novel device for the assessment of power grip forces in squirrel monkeys. The control of grasping and object manipulation represents a vital aspect of daily living by allowing the performance of a wide variety of complex hand movements. However, following neurological injury such as stroke, these grasping behaviors are often severely affected, resulting in persistent impairments in strength, grip force modulation and kinematic hand control. While there is a significant clinical focus on rehabilitative strategies to address these issues, there exists the need for translational animal models. In the study presented here, we describe a simple grip force device designed for use in nonhuman primates, which provides detailed quantitative information regarding distal grip force dynamics. Adult squirrel monkeys were trained to exceed a specific grip force threshold, which was rewarded with a food pellet. One of these subjects then received an infarct of the M1 hand representation area. Results suggest that the device provides detailed and reliable information on grip behaviors in healthy monkeys and can detect deficits in grip dynamics in monkeys with cortical lesions (significantly longer release times). Understanding the physiological and neuroanatomical aspects of grasping function following neurological injury may lead to more effective rehabilitative interventions

Thermophysical properties of the lanthanide sesquisulfides. II. Schottky contributions and magnetic and electronic properties of γ‐phase Pr2S3, Tb2S3, and Dy2S3

Heat‐capacity measurements by adiabatic equilibrium calorimetry are reported for γ‐phase Pr2S3, Tb2S3, and Dy2S3 between 5 and 350 K. Highly purified samples were prepared and their composition verified by chemical analysis. Precision lattice parameters were determined for each compound and are compared with literature values. The total heat capacity has been resolved into lattice, magnetic, and Schottky components by a volumetric approach. The experimental Schottky contributions accord with the calculated curves based on the crystal‐field splitting of the 2S+1LJ ground state of the lanthanide ions occupying sites of S4 symmetry in the Th3P4 lattice. The individual crystal‐field electronic energy levels have been obtained in part from an analysis of the hot‐band data observed in the absorption spectra of Pr2S3, Tb2S3, and Dy2S3, and from a calculated splitting in which the crystal‐field parameters Bkm, were determined from a lattice‐sum calculation. Molar thermodynamic properties are reported for all three compounds. The entropy at 298.15 K {S0−S0 (7 K)}, is 22.78R, 22.93R, and 23.36R, for γ‐phase Pr2S3, Tb2S3, and Dy2S3, respectively.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/70592/2/JCPSA6-95-3-1964-1.pd

Inference on periodicity of circadian time series

Estimation of the period length of time-course data from cyclical biological processes, such as those driven by the circadian pacemaker, is crucial for inferring the properties of the biological clock found in many living organisms. We propose a methodology for period estimation based on spectrum resampling (SR) techniques. Simulation studies show that SR is superior and more robust to non-sinusoidal and noisy cycles than a currently used routine based on Fourier approximations. In addition, a simple fit to the oscillations using linear least squares is available, together with a non-parametric test for detecting changes in period length which allows for period estimates with different variances, as frequently encountered in practice. The proposed methods are motivated by and applied to various data examples from chronobiology

Low-frequency cortical activity is a neuromodulatory target that tracks recovery after stroke.

Recent work has highlighted the importance of transient low-frequency oscillatory (LFO; <4 Hz) activity in the healthy primary motor cortex during skilled upper-limb tasks. These brief bouts of oscillatory activity may establish the timing or sequencing of motor actions. Here, we show that LFOs track motor recovery post-stroke and can be a physiological target for neuromodulation. In rodents, we found that reach-related LFOs, as measured in both the local field potential and the related spiking activity, were diminished after stroke and that spontaneous recovery was closely correlated with their restoration in the perilesional cortex. Sensorimotor LFOs were also diminished in a human subject with chronic disability after stroke in contrast to two non-stroke subjects who demonstrated robust LFOs. Therapeutic delivery of electrical stimulation time-locked to the expected onset of LFOs was found to significantly improve skilled reaching in stroke animals. Together, our results suggest that restoration or modulation of cortical oscillatory dynamics is important for the recovery of upper-limb function and that they may serve as a novel target for clinical neuromodulation