1,354,977 research outputs found
James A. Magner
Portrait, head and shoulders. [From Catholic University, Washington, D.C.] (On verso: Rev. James A. Magner. The Catholic University. Washington, D.C. not U of A.
Online Supplement to Der Zusammenhang zwischen dem Geschlecht von Studierenden und Prüfenden sowie der Prüfungsformate auf den Studienerfolg im Lehramtsstudium Sport
Dies ist zur Förderung der Reproduzierbarkeit von Ergebnissen die R Markdown Datei für die Modellierung und die Ergebnisse des Artikels:
Magner, A., Jetzke, M., & Utesch, T. (2023). Der Zusammenhang zwischen dem Geschlecht von Studierenden und Prüfenden sowie der Prüfungsformate auf den Studienerfolg im Lehramtsstudium Sport. Zeitschrift für Studium und Lehre in der Sportwissenschaft, 6(2), 5-20
Online Supplement to Der Zusammenhang zwischen dem Geschlecht von Studierenden und Prüfenden sowie der Prüfungsformate auf den Studienerfolg im Lehramtsstudium Sport
Dies ist zur Förderung der Reproduzierbarkeit von Ergebnissen die R Markdown Datei für die Modellierung und die Ergebnisse des Artikels:
Magner, A., Jetzke, M., & Utesch, T. (2023). Der Zusammenhang zwischen dem Geschlecht von Studierenden und Prüfenden sowie der Prüfungsformate auf den Studienerfolg im Lehramtsstudium Sport. Zeitschrift für Studium und Lehre in der Sportwissenschaft, 6(2), 5-20
Comment on Magner et al. Sulforaphane Treatment in Children with Autism: A Prospective Randomized Double-Blind Study. Nutrients 2023, 15, 718
I read your recent interesting double-blind study by Magner et al. [...
Going Beyond Counting First Authors in Author Co-citation Analysis
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
Specific ion effects on the electrochemical properties of cytochrome c
The range of salts used as supporting electrolytes in electrochemical studies of redox proteins and enzymes varies widely, with the choice of an electrolyte relying on the assumption that the electrolyte used does not affect the electrochemical properties of the proteins and enzymes under investigation. Examination of the electrochemical properties of the redox protein cytochrome c (cyt c) at a 4,4′-bipyridyl modified gold electrode demonstrates that both the redox potential (E o′) and the faradaic current are influenced by the nature of the electrolyte used, in a manner explained primarily by Hofmeister effects. The faradaic peak currents display an atypical trend on switching from kosmotropic to chaotropic anions, with a maximum current observed in the presence of Cl -. For a series of cations, the peak current increased in the sequence: Li + (0.34 μA) Br - (0.35 μA) > ClO 4 - (0.35 μA) > SCN - (0.31 μA) > F - (0.30 μA). E o′ decreased by a total of 24 mV across the series F - > Cl - > Br - > ClO 4 - > SCN - whereas no specific ion effect on E o′ was observed for cations. Factorisation of E o′ into its enthalpic and entropic components showed that while no specific trends were observed, large changes in ΔH o′ and ΔS o′ occurred with individual ions. The effect of anions on the faradaic peak current can be qualitatively explained by considering Collins' empirical rule of 'matching water affinities'. The effect of cations cannot be explained by this rule. However, both anion and cation effects can be understood by taking into account the cooperative action of electrostatic and ion dispersion forces. The results demonstrate that the choice of a supporting electrolyte in electrochemical investigations of redox proteins is important and emphasize that care needs to be taken in the determination and comparison of E o′, ΔH o′ and ΔS o′ in different solutions
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