991 resultados para White, John, 1685-1755.


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Running title: Plutarch's Lives.

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Reprint of the 1723-51 ed. published by Typ. Societatis Palatinae, Mediolanum.

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A mixed set; imprint varies: v. 1, 2, and 7 as above; v. 3 and 6: sold by John White, Luke Hansard, printer, 1801; v. 4: Printed by H.L. Galabin and sold by R. Faulder, 1800; v. 5: Printed by C. and W. Galabin and sold by W. Richardson, 1801.

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Goldsmith's poems and plays.--Angelo's "Reminiscences".--The latest life of Steele.--The author of "Monsieur Tonson".--Boswell's predecessors and editors.--An English engraver in Paris.--The "Vicar of Wakefield" and its illustrators.--Old Whitehall.--Luttrell's "Letters to Julia".--Changes at Charing Cross.--John Gay.--At Leicester Fields.--Marteilhe's "Memoirs".

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Back Row: Howard Yerges, Bump Elliott, Stu Wilkins, Dick Rifenburg, J.T. White, John Anderson, Alvin Wistert, Dick Kempthorn, Bill Pritula, Bob Chappuis, Bob Mann

3rd Row: Irv Small, Henry Fonde, Tom Peterson, John Ghindia, Dan Hershberger, Irv Wisniewski, Jim Atchison, Lenny Ford, Bob Hollway, Don McClelland, Norm Jackson, Kurt Kampe

2nd Row: Ed McNeil, Pete Elliott, Walt Teninga, George Johnson, Ralph Kohl, H.O. Crisler, Bruce Hilkene, Dan Dworsky, Joe Soboleski, Quentin Sickels, Dick Strauss, Bob Erben

Front Row: Chuck Lentz, Jim Brieske, Pete Dendrinos, Don Kuick, George Kiesel, Bob Ballou, Lloyd Heneveld, Gene Derricotte, Dominic Tomasi, Jack Weisenberger

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Top Row: Ralph Amstutz, Robert McFaddin, William MacDougall, Joseph Rogers, Robert Ingalls, Elmer Madar, George Ceithaml, Fred Dawley

3rd Row: John Harrigan, Charles Haslam, William Kuyper, Rudoph Smeja, Austin Miller, William Pritula, Harlin Fraumann, Jack Petoskey, Vincent Secontine, Robert Stenberg, David Nelson

2nd Row: Walter Freihofer, Harry Anderson, Harold Lockard, Robert Morrison, John Greene, William MacConnachie, Robert Shemky, Reuben Kelto, Angelo Trogan, James Brown, Don Robinson, Donald Boor

Front Row: George Hildebrandt, Tom Kuzma, Philip Sharpe, Ray Sowers, John Karwales, Paul White, John Laine, Julius Franks, Mervin Pregulman, Theodore Denise, Charles Kennedy, Ted Kennedy, Robert Kolesar

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This article examines the neo-liberal reforms that the Kim government implemented in post-crisis Korea. It argues that by embracing the reforms, the state, paradoxicaliy, re-legitimised itself in the national political economy. The process of enacting the reforms completed the power shift from a collusive state-chaebol alliance towards a new alliance based on a more populist social contract - but one that nonetheless generally conformed to the tenets of neo-liberalism. Kim and his closest associates identified the malpractices of the chaebols as the main cause of the crisis, so reforming the chaebols would be the key to economic recovery. Combining populism and neo-liberalism, they drew on support from both domestic and international sources to rein in, rather than nurture, the chaebols.

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Transient receptor potential vanilloid type 4 (TRPV4) is a calcium-permeable nonselective cation channel, originally described in 2000 by research teams led by Schultz (Nat Cell Biol 2: 695-702, 2000) and Liedtke (Cell 103: 525-535, 2000). TRPV4 is now recognized as being a polymodal ionotropic receptor that is activated by a disparate array of stimuli, ranging from hypotonicity to heat and acidic pH. Importantly, this ion channel is constitutively expressed and capable of spontaneous activity in the absence of agonist stimulation, which suggests that it serves important physiological functions, as does its widespread dissemination throughout the body and its capacity to interact with other proteins. Not surprisingly, therefore, it has emerged more recently that TRPV4 fulfills a great number of important physiological roles and that various disease states are attributable to the absence, or abnormal functioning, of this ion channel. Here, we review the known characteristics of this ion channel's structure, localization and function, including its activators, and examine its functional importance in health and disease.

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The tawny frogmouth is a nocturnal bird species endemic to Australia. While many species of wildlife worldwide experience detrimental outcomes from urbanization, this thesis demonstrates the resilience and adaptability of this unique species to landscape change by human beings.

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Aim: Extreme climatic events and large wildfires are predicted to increase as the world's climate warms. Understanding how they shape species' distributions will be critical for conserving biodiversity. We used a 7-year dataset of mammals collected during and after south-east Australia's Millennium Drought to assess the roles of fire history, climatic extremes and their interactions in shaping mammal distributions. Location: Grampians National Park, south-eastern Australia.

Methods: We surveyed mammals at 36 sites along a ~50-year post-fire chronosequence in each of the 7 years. We modelled ten mammal species in relation to fire history, productivity and recent rainfall. Next, we examined the consistency of species' fire response curves across each of three climatic phases relating to the Millennium Drought. Finally, we identified the optimal distribution of fire ages for small and medium-sized mammal conservation in each of the three climatic phases.

Results:
The majority of species were influenced by fire history, and all native species were negatively associated with recently burned vegetation. Seven of ten species responded positively to the end of the Millennium Drought, but six of these declined quickly thereafter. Species' responses to fire history differed depending on the climatic conditions. However, the optimal distribution of fire-age classes consistently emphasized the importance of older age classes, regardless of climatic phase. This distribution is in stark contrast to the current distribution of fire ages across the study region.

Main conclusions:
Mammals in the study region face an uncertain future. The negative impact of drought, the short-lived nature of post-drought recovery and, now, the possibility of a new drought beginning forewarn of further declines. The stark contrast between the optimal and current fire-age distributions means that reducing the incidence of further fires is critical to enhance the capacity of native mammal communities to weather an increasingly turbulent climate.

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The nanofibrillar structures that underpin self-assembling peptide (SAP) hydrogels offer great potential for the development of finely tuned cellular microenvironments suitable for tissue engineering. However, biofunctionalisation without disruption of the assembly remains a key issue. SAPS present the peptide sequence within their structure, and studies to date have typically focused on including a single biological motif, resulting in chemically and biologically homogenous scaffolds. This limits the utility of these systems, as they cannot effectively mimic the complexity of the multicomponent extracellular matrix (ECM). In this work, we demonstrate the first successful co-assembly of two biologically active SAPs to form a coassembled scaffold of distinct two-component nanofibrils, and demonstrate that this approach is more bioactive than either of the individual systems alone. Here, we use two bioinspired SAPs from two key ECM proteins: Fmoc-FRGDF containing the RGD sequence from fibronectin and Fmoc-DIKVAV containing the IKVAV sequence from laminin. Our results demonstrate that these SAPs are able to co-assemble to form stable hybrid nanofibres containing dual epitopes. Comparison of the co-assembled SAP system to the individual SAP hydrogels and to a mixed system (composed of the two hydrogels mixed together post-assembly) demonstrates its superior stable, transparent, shear-thinning hydrogels at biological pH, ideal characteristics for tissue engineering applications. Importantly, we show that only the coassembled hydrogel is able to induce in vitro multinucleate myotube formation with C2C12 cells. This work illustrates the importance of tissue engineering scaffold functionalisation and the need to develop increasingly advanced multicomponent systems for effective ECM mimicry.

STATEMENT OF SIGNIFICANCE: Successful control of stem cell fate in tissue engineering applications requires the use of sophisticated scaffolds that deliver biological signals to guide growth and differentiation. The complexity of such processes necessitates the presentation of multiple signals in order to effectively mimic the native extracellular matrix (ECM). Here, we establish the use of two biofunctional, minimalist self-assembling peptides (SAPs) to construct the first co-assembled SAP scaffold. Our work characterises this construct, demonstrating that the physical, chemical, and biological properties of the peptides are maintained during the co-assembly process. Importantly, the coassembled system demonstrates superior biological performance relative to the individual SAPs, highlighting the importance of complex ECM mimicry. This work has important implications for future tissue engineering studies.