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    Going Beyond Counting First Authors in Author Co-citation Analysis

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    The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed

    Variations on the Author

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    “Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship

    Appropriate Similarity Measures for Author Cocitation Analysis

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    We provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis

    Dispelling the Myths Behind First-author Citation Counts

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    We conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more sophisticated methods

    Author Index

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    alternative splicing and RNA editing of human TPH2 transcripts

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    Serotonin (5-Hydroxytryptamin, 5-HT) ist ein monoaminerger Neurotransmitter, der an zahlreichen Aspekten der Verhaltenskontrolle beteiligt ist. Das serotonerge System nimmt seinen Ursprung in einer handvoll 5-HT synthetisierender Neuronen im Hirnstamm, die zusammen die Raphekerne B1 - B9 bilden. Seit über 40 Jahren ist bekannt, dass die Tryptophan-Hydroxylase (TPH) das geschwindigkeitsbestimmende Enzym in der 5-HT-Biosynthese ist. Erst kürzlich konnte ein zweites TPH-Gen (TPH2) identifiziert werden, das hauptsächlich im Gehirn exprimiert wird, während die Expression des bislang bekannten TPH-Gens (TPH1) vorwiegend in nicht neuronalen Geweben erfolgt. Dysfunktionen des serotonergen Systems im Gehirn konnten mit einer Vielzahl neuropsychiatrischer Erkrankungen, wie Depression, Schizophrenie und Suizidalverhalten in Zusammenhang gebracht werden und umfangreiche Beweise deuten auf TPH2 als Kandidatengen für 5-HT-verwandte psychiatrische Störungen. Zum besseren Verständnis der physiologischen Bedeutung von 5-HT im Gehirn und bei der Ätiologie psychiatrischer Erkrankungen wurde ein induzierbares Mausmodell etabliert. Das Modell basiert auf der spezifischen Expression der E. coli-Nitroreduktase (NTR) in den serotonergen Rapheneuronen und die damit verbundende Metabolisierung des inaktiven Protoxins CB1954 zu einem potenten Zytotoxin, wodurch die Ablation der 5-HT-Neuronen induziert und die zentralnervösen 5-HT-Spiegel konditionell gesenkt werden. Die transgenen NTR1 Mäuse zeigten jedoch trotz spezifischer NTR-Expression keinen Phänotyp nach Behandlung mit CB1954. Die Expression einer gfp markierten NTR in COS7-Zellen zeigte die Aggregation des Fusionsproteins und lies eine beeinträchtigte Translation durch Unterschiede im synonymen Codongebrauch zwischen Donor- und Wirtszelle vermuten. Eine synthetische NTR Version (ntro), deren Codongebrauch an die Präferenzen der Maus angepasst wurde, führte zu höheren Proteinausbeuten in verschiedenen Säugerzelllinien und sensibilisierte diese bereits bei einer zehnfach geringeren CB1954-Konzentration. Die Verbesserung des NTR/CB1954-Systems auf translationeller Ebene sollte sein Potential hinsichtlich der Untersuchung zellulärer Funktionen durch konditionale Zellablation in transgenen Tieren erhöhen und verspricht zusätzlich eine Anwendung in der humanen Krebstherapie durch GDEPT (gene-directed enzyme prodrug therapy). Zahlreiche Studien haben die positive Kopplung von Einzelstrangpolymorphismen (SNPs) im TPH2-Gen mit psychiatrischen Erkrankungen und ihren möglichen Einfluss auf die enzymatische Aktivität der TPH2 gezeigt. In der vorliegenden Arbeit ergab die Sequenzierung von TPH2-cDNAs von post mortem-Gehirnproben des Menschen, dass humane TPH2-Transkripte alternativ gespleißt werden, wobei sich die kinetischen Eigenschaften der kodierten Varianten TPH2A und TPH2B unterscheiden. Zudem werden die prä-mRNAs von TPH2a und TPH2b dynamisch editiert, durch spezifische sich gegenseitig ausschließende Editierungsmuster, die die enzymatische Aktivität der entsprechenden Proteine modulieren. Zusätzlich zur Dichotomie des serotonergen Systems, definiert durch die zwei geschwindigkeitsbestimmenden Enzyme TPH1 und TPH2, in peripheren bzw. neuronalen Geweben, ermöglicht die TPH2a/b-Editierung eine noch komplexere Feinregulation der zentralen 5-HT-Biosynthese. Letztendlich werden molekularbiologische Beweise präsentiert, die vermuten lassen, dass eine Dysregulation von alternativem Spleißen und RNA Editierung an der Ätiologie psychiatrischer Erkrankungen beteiligt ist. Eine wichtige Schlussfolgerung der hier gezeigten Ergebnisse ist die Tatsache, dass weder die aktuell verwendeten RNA- basierten Techniken noch immunhistochemische Proteinnachweismethoden eine Aussage über die TPH2-Aktivität in der psychiatrischen Forschung erlauben, wodurch die bisherigen Daten zu Störungen der TPH2-Expression bei psychiatrischen Erkrankungen sorgfältig nachgeprüft werden sollten.Serotonin (5-hydroxytryptamine, 5-HT) is a monoaminergic neurotransmitter involved in multiple facets of behavioral control. The serotonergic projection system has its roots in a handful of selectively 5-HT-synthesizing neurons within the brainstem, which altogether constitute the raphe nuclei B1 - B9. It is known since more than four decades that tryptophan hydroxylase (TPH) is the rate-limiting enzyme in the 5-HT biosynthesis. Recently, a second TPH gene (TPH2) was identified, which is mainly expressed in the brain, whereas the previously known TPH gene (TPH1) is predominantly expressed in non-neuronal tissues. Dysfunctions of the serotonergic system in the brain have been implicated in a variety of neuropsychatric disorders, like depression, schizophrenia and suicidal behaviour and overwhelming evidence points to TPH2 as a candidate gene for 5- HT-related psychiatric disorders. In order to better understand the physiological role of 5-HT in the brain and the etiology of psychiatric diseases a mouse model was established. The model is based on the specific expression of the E. coli nitroreductase (NTR), which is associated with the bioactivation of the inactive prodrug CB1954 to a powerful cytotoxin in the serotonergic raphe neurons. This leads to the ablation of the 5-HT neurons, thereby conditionally decreasing the 5-HT levels in the CNS. In spite of specific expression of NTR in the 5-HT neurons the transgenic NTR1 mice did not respond to CB1954. The expression of a gfp tagged NTR in COS7 cells showed the aggregation of the corresponding fusion protein, suggesting impaired translation by divergent synonymous codon usage between the donor and host cell. A synthetic NTR version (ntro), in which codon usage was adapted to mouse preferences, showed higher expression levels in different mammalian cell lines rendering them more sensitive to the prodrug CB1954 by one order of magnitude. The improvement of the NTR/CB1954 system at the translational level should increase its potential for the investigation of cellular functions by conditional targeted cell ablation in transgenic animals. Moreover, the ntro developed in this study is a promising candidate for human cancer treatment by GDEPT (gene-directed enzyme prodrug therapy). Numerous studies have proven positive linkage of single nucleotide polymorphisms (SNPs) in the TPH2 gene with psychiatric diseases and their possible influence on TPH2 enzymatic activity. By sequencing TPH2 cDNAs from human post mortem brain samples it could be shown that TPH2 exists in two alternative splice variants with distinct kinetic properties of the encoded TPH2A and TPH2B proteins. Further, the pre-mRNAs of TPH2a and TPH2b are dynamically edited in a mutually exclusive pattern, which modulates the enzymatic activity of the respective proteins. Thus, in addition to the dichotomy of the serotonergic system defined by the two rate limiting enzymes, TPH1 and TPH2, in peripheral and neuronal tissues, respectively, TPH2a/b editing allows an even more complex fine tuning of the central nervous 5-HT biosynthesis. Finally, molecular biological evidence is presented suggesting that a deregulated alternative splicing and RNA editing might be involved in the etiology of psychopathological diseases. An important implication of the results is the fact that neither currently used RNA-based techniques nor immunohistochemical protein detection methods allow estimating the enzymatic activity of TPH2 in psychiatry research. Thus, the here presented data should invite for careful reexamination of present reports on TPH2 expression disturbances in psychiatric disease

    koamabayili/VECTRON-author-checklist: VECTRON author checklist

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    We have done our best to complete the author checklist relating to the use of animals in the hut study. Note that the objective for the hut study was to evaluate the IRS treatment applications for residual efficacy against Anopheles mosquitoes, including the local An. coluzzii mosquito population. Cows were only used to attract mosquitoes into the huts and no tests were carried out directly on the cows. The author checklist is intended for use with studies where experiments are carried out on animals, which is why we have had such difficulty in completing this for the hut study, as many of the questions do not relate to how the cows were used

    Author Under Sail The Imagination of Jack London, 1893-1902

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    In Author Under Sail, Jay Williams offers the first complete literary biography of Jack London as a professional writer engaged in the labor of writing. It examines the authorial imagination in London's work, the use of imagination in both his fiction and nonfiction, and the ways he defined imagination in the creative process in his business dealings with his publishers, editors, and agents. In this first volume of a two-volume biography, Williams traverses the years 1893 to 1902, from London's "Story of a Typhoon" to The People of the Abyss. The Jack London who emerges in the pages of Author Under Sail is a writer whose partnership with publishers, most notably his productive alliance with George Brett of Macmillan, was one of the most formative in American literary history. London pioneered many author models during the heyday of realism and naturalism, blurring the boundaries of these popular genres by focusing on absorption and theatricality and the representation of the seen and unseen. London created an impassioned, sincere, and extremely personal realism unlike that of other American writers of the time. Author Under Sail is a literary tour de force that reveals the full range of London as writer, creative citizen, and entrepreneur at the same time it sheds light on the maverick side of machine-age literature.Intro -- Title Page -- Copyright Page -- Dedication -- Contents -- Acknowledgments -- Introduction -- 1. Spirit Truth -- 2. From Absorption to Theatricality and Back Again -- 3. "I Will Build a New Present" -- 4. Sons as Authors -- 5. Fathers as Publishers -- 6. The Daughter as Author -- 7. Lovers as Authors -- 8. At Sea with the Family -- 9. Yellow News, Yellow Stories -- 10. The Return Home -- Notes -- Bibliography -- Index -- About Jay WilliamsIn Author Under Sail, Jay Williams offers the first complete literary biography of Jack London as a professional writer engaged in the labor of writing. It examines the authorial imagination in London's work, the use of imagination in both his fiction and nonfiction, and the ways he defined imagination in the creative process in his business dealings with his publishers, editors, and agents. In this first volume of a two-volume biography, Williams traverses the years 1893 to 1902, from London's "Story of a Typhoon" to The People of the Abyss. The Jack London who emerges in the pages of Author Under Sail is a writer whose partnership with publishers, most notably his productive alliance with George Brett of Macmillan, was one of the most formative in American literary history. London pioneered many author models during the heyday of realism and naturalism, blurring the boundaries of these popular genres by focusing on absorption and theatricality and the representation of the seen and unseen. London created an impassioned, sincere, and extremely personal realism unlike that of other American writers of the time. Author Under Sail is a literary tour de force that reveals the full range of London as writer, creative citizen, and entrepreneur at the same time it sheds light on the maverick side of machine-age literature.Description based on publisher supplied metadata and other sources.Electronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, YYYY. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries
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