The Hecyra of Terence.

In submitting this thesis, the writer does not pretend to have made even an approximation of exhaustive study of the Hecyra: this thesis is merely a study of the play from certain viewpoints which also make no claim to completeness. No originality is claimed for the discussion of Terence and of the Hecyra. The rest of the thesis has a fair claim to originality in that it’s the product of the writer’s research, aided of course by various comments and notes. The translation is especially indebted to the Latin paraphrase in the Delphin Classics and to various notes and synonyms in the editions of Terence in the Bibliotheca Classica Latina and in the Delphin Classics. An English translation was consulted in only two or three instances, and then it was not followed as lavishly. The writer can say that he has enjoyed the plot and the language of the play even though some have said that the Hecyra has the least merit of any of Terence’ s plays. In fact the play means more to him than any of the other plays of Terence with which he is acquainted. Of course this would be the natural result of more diligent study. The writer wishes to express his gratitude to Professor Andrew P. Dustin of the University for his aid and encouragement thruout an undergraduate and graduate course in Latin where there have been many vicissitudes. With the above as a forward this thesis is respectfully submitted to the faculty of the College of Arts and Sciences of the University of Louisville

Channel Catfish Diets Include Substantial Vegetation in a Missouri River Reservoir

Channel catfish (Ictalurus punctatus) are native to Lake Sharpe, a Missouri River mainstem reservoir, and are common in angler catches. Channel catfish growth has declined since the formation of the reservoir in 1963. Mean lengths at time of capture for channel catfish ages 9, 10, II, and 12 have decreased by 69, 55, 115, and 21S mm, respectively, since impoundment. The objective of this study was to document monthly food habits of channel catfish throughout the growing season (May-August) in Lake Sharpe to assess potential effects of diet on growth. Although channel catfish consumed both macro invertebrates and fishes as expected, they also consumed large quantities of submergent aquatic vegetation. Consumed vegetation contributed 3S-73% of the diet by weight over 2 channel catfish length groups «2S0 mm and ~2S0 mm total length) during the 4 months sampled. Consumption of substantial amounts of vegetation should be considered a suboptimal diet for channel catfish growth. Consequently, diets of channel catfish in Lake Sharpe could be a factor contributing to the observed slow growth of older catfish in this population

Polynomial functors and combinatorial Dyson-Schwinger equations

We present a general abstract framework for combinatorial Dyson-Schwinger equations, in which combinatorial identities are lifted to explicit bijections of sets, and more generally equivalences of groupoids. Key features of combinatorial Dyson-Schwinger equations are revealed to follow from general categorical constructions and universal properties. Rather than beginning with an equation inside a given Hopf algebra and referring to given Hochschild $1$-cocycles, our starting point is an abstract fixpoint equation in groupoids, shown canonically to generate all the algebraic structure. Precisely, for any finitary polynomial endofunctor $P$ defined over groupoids, the system of combinatorial Dyson-Schwinger equations $X=1+P(X)$ has a universal solution, namely the groupoid of $P$-trees. The isoclasses of $P$-trees generate naturally a Connes-Kreimer-like bialgebra, in which the abstract Dyson-Schwinger equation can be internalised in terms of canonical $B_+$-operators. The solution to this equation is a series (the Green function) which always enjoys a Fa\`a di Bruno formula, and hence generates a sub-bialgebra isomorphic to the Fa\`a di Bruno bialgebra. Varying $P$ yields different bialgebras, and cartesian natural transformations between various $P$ yield bialgebra homomorphisms and sub-bialgebras, corresponding for example to truncation of Dyson-Schwinger equations. Finally, all constructions can be pushed inside the classical Connes-Kreimer Hopf algebra of trees by the operation of taking core of $P$-trees. A byproduct of the theory is an interpretation of combinatorial Green functions as inductive data types in the sense of Martin-L\"of Type Theory (expounded elsewhere).Comment: v4: minor adjustments, 49pp, final version to appear in J. Math. Phy

Engineered Skeletal Muscle Units for Repair of Volumetric Muscle Loss in the Tibialis Anterior Muscle of a Rat

Volumetric muscle loss (VML) is the traumatic, degenerative, or surgical loss of muscle tissue, which may result in function loss and physical deformity. To date, clinical treatments for VML?the reflected muscle flap or transferred muscle graft?are limited by tissue availability and donor site morbidity. To address the need for more innovative skeletal muscle repair options, our laboratory has developed scaffoldless tissue-engineered skeletal muscle units (SMUs), multiphasic tissue constructs composed of engineered skeletal muscle with engineered bone-tendon ends, myotendinous junctions, and entheses, which in vitro can produce force both spontaneously and in response to electrical stimulation. Though phenotypically immature in vitro, we have shown that following 1 week of implantation in an ectopic site, our muscle constructs develop vascularization and innervation, an epimysium-like outer layer of connective tissue, an increase in myosin protein content, formation of myofibers, and increased force production. These findings suggest that our engineered muscle tissue survives implantation and develops the interfaces necessary to advance the phenotype toward adult muscle. The purpose of this study was to evaluate the potential of our SMUs to restore muscle tissue to sites of acute VML. Our results indicate that our SMUs continue to mature in vivo with longer recovery times and have the potential to repair VML sites by providing additional muscle fibers to damaged muscles. We conclude from this study that our SMUs have the potential to restore lost tissue volume in cases of acute VML.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/140233/1/ten.tea.2014.0060.pd

4,5-Diazafluorene and 9,9’-Dimethyl-4,5-Diazafluorene as Ligands Supporting Redox-Active Mn and Ru Complexes

This work is licensed under a Creative Commons Attribution 4.0 International License.4,5-diazafluorene (daf) and 9,9’-dimethyl-4,5-diazafluorene (Me2daf) are structurally similar to the important ligand 2,2’-bipyridine (bpy), but significantly less is known about the redox and spectroscopic properties of metal complexes containing Me2daf as a ligand than those containing bpy. New complexes Mn(CO)3Br(daf) (2), Mn(CO)3Br(Me2daf) (3), and [Ru(Me2daf)3](PF6)2 (5) have been prepared and fully characterized to understand the influence of the Me2daf framework on their chemical and electrochemical properties. Structural data for 2, 3, and 5 from single-crystal X-ray diffraction analysis reveal a distinctive widening of the daf and Me2daf chelate angles in comparison to the analogous Mn(CO)3(bpy)Br (1) and [Ru(bpy)3]2+ (4) complexes. Electronic absorption data for these complexes confirm the electronic similarity of daf, Me2daf, and bpy, as spectra are dominated in each case by metal-to-ligand charge transfer bands in the visible region. However, the electrochemical properties of 2, 3, and 5 reveal that the redox-active Me2daf framework in 3 and 5 undergoes reduction at a slightly more negative potential than that of bpy in 1 and 4. Taken together, the results indicate that Me2daf could be useful for preparation of a variety of new redox-active compounds, as it retains the useful redox-active nature of bpy but lacks the acidic, benzylic C–H bonds that can induce secondary reactivity in complexes bearing daf.US National Science Foundation (OIA-1833087)NSF REU Program in Chemistry at the University of Kansas (CHE-1560279)NIH T32 GM008545-25NIH S10OD016360NIH S10RR024664CHE-162592

Gas generation from Hanford grout samples

In an extension of our work on the radiolytic processes that occur in the waste tanks at the Hanford site, we studied the gas generation from grout samples that contained nuclear waste simulants. Grout is one option for the long-term storage of low-level nuclear waste solutions but the radiolytic effects on grout have not been thoroughly defined. In particular, the generation of potentially flammable and hazardous gases required quantification. A research team at Argonne examined this issue and found that the total amount of gases generated radiolytically from the WHC samples was an order of magnitude higher than predicted. This implies that novel pathways fro charge migration from the solid grout to the associated water are responsible for gas evolution. The grout samples produced hydrogen, nitrous oxide, and carbon monoxide as well as nitrogen and oxygen. Yields of each of these substances were determined for doses that are equivalent to about 80 years storage of the grout. Carbon monoxide, which was produced in 2% yield, is of particular importance because even small amounts may adversely affect catalytic conversion instrumentation that has been planned for installation in the storage vaults

LOOC UP: Locating and observing optical counterparts to gravitational wave bursts

Gravitational wave (GW) bursts (short duration signals) are expected to be associated with highly energetic astrophysical processes. With such high energies present, it is likely these astrophysical events will have signatures in the EM spectrum as well as in gravitational radiation. We have initiated a program, "Locating and Observing Optical Counterparts to Unmodeled Pulses in Gravitational Waves" (LOOC UP) to promptly search for counterparts to GW burst candidates. The proposed method analyzes near real-time data from the LIGO-Virgo network, and then uses a telescope network to seek optical-transient counterparts to candidate GW signals. We carried out a pilot study using S5/VSR1 data from the LIGO-Virgo network to develop methods and software tools for such a search. We will present the method, with an emphasis on the potential for such a search to be carried out during the next science run of LIGO and Virgo, expected to begin in 2009.Comment: 11 pages, 2 figures; v2) added acknowledgments, additional references, and minor text changes v3) added 1 figure, additional references, and minor text changes. v4) Updated references and acknowledgments. To be published in the GWDAW 12 Conf. Proc. by Classical and Quantum Gravit

Leveraging in vitro and pharmacokinetic models to support bench to bedside investigation of XTMAB-16 as a novel pulmonary sarcoidosis treatment

Background: Sarcoidosis is a chronic, multisystem inflammatory disorder characterized by non-caseating epithelioid granulomas; infiltration of mononuclear cells; and destruction of microarchitecture in the skin, eye, heart, and central nervous system, and the lung in >90% of cases. XTMAB-16 is a chimeric anti-tumor necrosis factor alpha (TNFα) antibody, distinct from other anti-TNF antibodies based on its molecular structure. The efficacy of XTMAB-16 has not been clinically demonstrated, and it is still undergoing clinical development as a potential treatment for sarcoidosis. The current study demonstrates the activity of XTMAB-16 in a well-established in vitro sarcoidosis granuloma model, although XTMAB-16 is not yet approved by the United States Food and Drug Administration (FDA) for treatment of sarcoidosis, or any other disease.Objective: To provide data to guide safe and efficacious dose selection for the ongoing clinical development of XTMAB-16 as a potential treatment for sarcoidosis.Methods: First, XTMAB-16 activity was evaluated in an established in vitro model of granuloma formation using peripheral blood mononuclear cells from patients with active pulmonary sarcoidosis to determine a potentially efficacious dose range. Second, data obtained from the first-in-human study of XTMAB-16 (NCT04971395) were used to develop a population pharmacokinetic (PPK) model to characterize the pharmacokinetics (PK) of XTMAB-16. Model simulations were performed to evaluate the sources of PK variability and to predict interstitial lung exposure based on concentrations in the in vitro granuloma model.Results: XTMAB-16 dose levels of 2 and 4 mg/kg, once every 2 weeks (Q2W) or once every 4 weeks (Q4W) for up to 12 weeks, were supported by data from the non-clinical, in vitro secondary pharmacology; the Phase 1 clinical study; and the PPK model developed to guide dose level and frequency assumptions. XTMAB-16 inhibited granuloma formation and suppressed interleukin-1β (IL-1β) secretion in the in vitro granuloma model with a half maximal inhibitory concentration (IC50) of 5.2 and 3.5 μg/mL, respectively. Interstitial lung concentrations on average, following 2 or 4 mg/kg administered Q2W or Q4W, are anticipated to exceed the in vitro IC50 concentrations.Conclusion: The data presented in this report provide a rationale for dose selection and support the continued clinical development of XTMAB-16 for patients with pulmonary sarcoidosis

Myelinating Schwann cells ensheath multiple axons in the absence of E3 ligase component Fbxw7

In the central nervous system (CNS), oligodendrocytes myelinate multiple axons; in the peripheral nervous system (PNS), Schwann cells (SCs) myelinate a single axon. Why are the myelinating potentials of these glia so fundamentally different? Here, we find that loss of Fbxw7, an E3 ubiquitin ligase component, enhances the myelinating potential of SCs. Fbxw7 mutant SCs make thicker myelin sheaths and sometimes appear to myelinate multiple axons in a fashion reminiscent of oligodendrocytes. Several Fbxw7 mutant phenotypes are due to dysregulation of mTOR; however, the remarkable ability of mutant SCs to ensheathe multiple axons is independent of mTOR signaling. This indicates distinct roles for Fbxw7 in SC biology including modes of axon interactions previously thought to fundamentally distinguish myelinating SCs from oligodendrocytes. Our data reveal unexpected plasticity in the myelinating potential of SCs, which may have important implications for our understanding of both PNS and CNS myelination and myelin repair