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Institution

University of Georgia

EducationAthens, Georgia, United States
About: University of Georgia is a education organization based out in Athens, Georgia, United States. It is known for research contribution in the topics: Population & Gene. The organization has 41934 authors who have published 93622 publications receiving 3713212 citations. The organization is also known as: UGA & Franklin College.


Papers
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Journal ArticleDOI
TL;DR: In this article, the authors present a predictive QoS model that makes it possible to compute the quality of service (QoS) for workflows automatically based on atomic task QoS attributes.

807 citations

Journal ArticleDOI
TL;DR: The evolution and state of the art of cancer nanotheranostics is described, with an emphasis on clinical impact and translation, and how diagnosis and therapy are interwoven to solve clinical issues and improve treatment outcomes.
Abstract: Advances in nanoparticle synthesis and engineering have produced nanoscale agents affording both therapeutic and diagnostic functions that are often referred to by the portmanteau 'nanotheranostics'. The field is associated with many applications in the clinic, especially in cancer management. These include patient stratification, drug-release monitoring, imaging-guided focal therapy and post-treatment response monitoring. Recent advances in nanotheranostics have expanded this notion and enabled the characterization of individual tumours, the prediction of nanoparticle-tumour interactions, and the creation of tailor-designed nanomedicines for individualized treatment. Some of these applications require breaking the dogma that a nanotheranostic must combine both therapeutic and diagnostic agents within a single, physical entity; instead, it can be a general approach in which diagnosis and therapy are interwoven to solve clinical issues and improve treatment outcomes. In this Review, we describe the evolution and state of the art of cancer nanotheranostics, with an emphasis on clinical impact and translation.

806 citations

Journal ArticleDOI
TL;DR: The profound effects of leptin on regulating body energy balance make it a prime candidate for drug therapies for humans and animals.
Abstract: Leptin, a 16-kDa protein secreted from white adipocytes, has been implicated in the regulation of food intake, energy expenditure, and whole-body energy balance in rodents and humans. The gene encoding leptin was identified by positional cloning and is the mutation leading to the profound obese phenotype of the ob/ob mouse. Exogenous administration of leptin to ob/ob mice leads to a significant improvement in reproductive and endocrine status as well as reduced food intake and weight loss. The expression and secretion of leptin is highly correlated with body fat mass and adipocyte size. Cortisol and insulin are potent stimulators of leptin expression, and expression is attenuated by beta-adrenergic agonists, cAMP, and thiazolidinediones. The role of other hormones and growth factors in the regulation of leptin expression and secretion is emerging. Leptin circulates specifically bound to proteins in serum, which may regulate its half-life and biological activity. Isoforms of the leptin receptor, members of the interleukin-6 cytokine family of receptors, are found in multiple tissues, including the brain. Many of leptin's effects on food intake and energy expenditure are thought to be mediated centrally via neurotransmitters such as neuropeptide Y. Multiple peripheral effects of leptin have also been recently described, including the regulation of insulin secretion by pancreatic beta cells and regulation of insulin action and energy metabolism in adipocytes and skeletal muscle. Leptin is thought to be a metabolic signal that regulates nutritional status effects on reproductive function. Leptin also plays a major role in hematopoeisis and in the anorexia accompanying an acute cytokine challenge. The profound effects of leptin on regulating body energy balance make it a prime candidate for drug therapies for humans and animals.

805 citations

Book ChapterDOI
TL;DR: In this article, the authors present research and theory pertaining to their multicomponent perspective on authentic functioning. And they discuss potential downsides or costs for authentic functioning and describe some future directions for research on authenticity.
Abstract: And if by chance I wake at night and I ask you who I am, oh take me to the slaughterhouse I will wait there with the lamb. —Leonard Cohen Whatever satisfies the soul is truth. —Walt Whitman I prefer to be true to myself, even at the hazard of incurring the ridicule of others, rather than to be false, and to incur my own abhorrence. —Frederick Douglass In this chapter, we present research and theory pertaining to our multicomponent perspective on authentic functioning. We begin with a historical account of various philosophical perspectives on authentic functioning and briefly review several past and contemporary psychological perspectives on authenticity. We then define and discuss our multicomponent conceptualization of authenticity and describe each of its components and their relationships to other constructs in the psychology literature. Next, we present an individual differences measure we have developed to assess dispositional authenticity and each of its components, and we report findings attesting to the adequacy of its psychometric properties. In addition, we present findings from a variety of studies we have conducted to examine how authenticity relates to diverse aspects of healthy psychological and interpersonal functioning. These studies pertain to a wide range of phenomena, including the following: verbal defensiveness, mindfulness, coping styles, self‐concept structure, social‐role functioning, goal pursuits, general well‐being, romantic relationships, parenting styles, and self‐esteem. Following this, we discuss potential downsides or costs for authentic functioning and describe some future directions for research on authenticity.

805 citations

Journal ArticleDOI
TL;DR: The demonstration that RG-II exists in primary walls as a dimer that is covalently cross-linked by a borate diester was a major advance in the understanding of the structure and function of this pectic polysaccharide.
Abstract: ▪ Abstract Rhamnogalacturonan II (RG-II) is a structurally complex pectic polysaccharide that was first identified in 1978 as a quantitatively minor component of suspension-cultured sycamore cell walls. Subsequent studies have shown that RG-II is present in the primary walls of angiosperms, gymnosperms, lycophytes, and pteridophytes and that its glycosyl sequence is conserved in all vascular plants examined to date. This is remarkable because RG-II is composed of at least 12 different glycosyl residues linked together by more than 20 different glycosidic linkages. However, only a few of the genes and proteins required for RG-II biosynthesis have been identified. The demonstration that RG-II exists in primary walls as a dimer that is covalently cross-linked by a borate diester was a major advance in our understanding of the structure and function of this pectic polysaccharide. Dimer formation results in the cross-linking of the two homogalacturonan chains upon which the RG-II molecules are constructed and ...

801 citations


Authors

Showing all 42268 results

NameH-indexPapersCitations
Rob Knight2011061253207
Feng Zhang1721278181865
Zhenan Bao169865106571
Carl W. Cotman165809105323
Yoshio Bando147123480883
Mark Raymond Adams1471187135038
Han Zhang13097058863
Dmitri Golberg129102461788
Godfrey D. Pearlson12874058845
Douglas E. Soltis12761267161
Richard A. Dixon12660371424
Ajit Varki12454258772
Keith A. Johnson12079851034
Gustavo E. Scuseria12065895195
Julian I. Schroeder12031550323
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023125
2022542
20214,670
20204,504
20194,098
20183,994