325,060 research outputs found
Millettia pseudoracemosa Thothathri & Ravikumar 1997
No full textIdentities of <i>Millettia pseudoracemosa</i> and <p> <b> <i>Millettia pseudoracemosa</i> Thothathri & Ravikumar (1997: 239) was described on the basis of a single collection (<i>S. Ravikumar 334</i>, Fig. 1: A–B), which was collected on 21 April 1995 from Anamalai Hills, Tamil Nadu, South India. The new species was considered to be similar to <i>M. racemosa</i> (Roxburgh 1832: 329) Bentham (1852: 249) in habit, shape, number and hairiness of leaflets, floral color, and pod shape. The latter species was first described based on specimens also from India, but it has been treated as a monospecific genus <i>Endosamara</i> Geesink (1984: 93) belonging to the tribe Wisterieae because of its true panicles with ebracteole flowers and very peculiar fruits with a lomented endocarp around each seed (Compton <i>et al.</i> 2019). Thothathri & Ravikumar (1997) also pointed out that their new species has a unique character in the genus, i.e. the large sized (2.5–3.0 cm long) and violet flowers.</b> </p>Published as part of <i>Song, Zhu-Qiu, 2023, The identities of Millettia pseudoracemosa and M. pulchra var. munnarensis (Fabaceae: Millettieae) from South India, pp. 55-63 in Phytotaxa 591 (1)</i> on page 56, DOI: 10.11646/phytotaxa.591.1.5, <a href="http://zenodo.org/record/7784270">http://zenodo.org/record/7784270</a>
sj-xlsx-3-pul-10.1177_20458940211031109 - Supplemental material for Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension
No full textSupplemental material, sj-xlsx-3-pul-10.1177_20458940211031109 for Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension by Ravikumar Sitapara, TuKiet T. Lam, Aneta Gandjeva, Rubin M. Tuder and Lawrence S. Zisman in Pulmonary Circulation</p
sj-pdf-4-pul-10.1177_20458940211031109 - Supplemental material for Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension
No full textSupplemental material, sj-pdf-4-pul-10.1177_20458940211031109 for Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension by Ravikumar Sitapara, TuKiet T. Lam, Aneta Gandjeva, Rubin M. Tuder and Lawrence S. Zisman in Pulmonary Circulation</p
sj-xlsx-2-pul-10.1177_20458940211031109 - Supplemental material for Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension
No full textSupplemental material, sj-xlsx-2-pul-10.1177_20458940211031109 for Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension by Ravikumar Sitapara, TuKiet T. Lam, Aneta Gandjeva, Rubin M. Tuder and Lawrence S. Zisman in Pulmonary Circulation</p
sj-pdf-1-pul-10.1177_20458940211031109 - Supplemental material for Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension
No full textSupplemental material, sj-pdf-1-pul-10.1177_20458940211031109 for Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension by Ravikumar Sitapara, TuKiet T. Lam, Aneta Gandjeva, Rubin M. Tuder and Lawrence S. Zisman in Pulmonary Circulation</p
Diffusive author(s), cohesive author: Analysis of S/N (1994)
No full textThis study indicates the ways in which various aspects of the author(s) are brought forth in Dumb type’s performance art, the S/N production. Previous research has suggested a non-hierarchical organization of Dumb type and the absence of a “privileged author” in Dumb type’s collaborative work, S/N. However, the results that I have investigated from member’s interviews on the creative process of S/N along with my analysis of the recorded images of S/N, indicate a different aspect of the author(s). First, S/N was created through, so to speak, the collective ideas of the members of Dumb type. Further, S/N has at least nine quotations from previous performances, installations, and printed writings, besides the work-in-progress technique. Explicating one of the “author functions” as given by Michel Foucault, each text has plural subjects of the author. However, it has been revealed from members’ interviews that Teiji Furuhashi had a decision-making role in selecting the members’ ideas within the performance. Since then, S/N has had plural subjects of creation; however, Furuhashi is one of the subjects of creation along with the “privileged author.” S/N has plural authors (diffusive authors) yet at the same time, it has a “privileged author,” Teiji Furuhashi (cohesive author)
A neo-clerodane diterpene from Teucrium tomentosum. Corrigendum
No full textThe chemical name of the title compound in the paper by Devi, Malathi, Rajan, Aravind, Krishnakumari &amp; Ravikumar [Acta Cryst. (2004), E60, o117&#8211;o119] is corrected and the structural diagram is updated
Going Beyond Counting First Authors in Author Co-citation Analysis
No full textThe 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
A study on the dynamics of the zraP gene expression profile and its application to the construction of zinc adsorption bacteria
No full textZinc ion plays essential roles in biological chemistry. Bacteria acquire Zn(2+) from the environment, and cellular concentration levels are controlled by zinc homeostasis systems. In comparison with other homeostatic systems, the ZraSR two-component system was found to be more efficient in responding to exogenous zinc concentrations. To understand the dynamic response of the bacterium ZraSR two-component system with respect to exogenous zinc concentrations, the genetic circuit of the ZraSR system was integrated with a reporter protein. This study was helpful in the construction of an E. coli system that can display selective metal binding peptides on the surface of the cell in response to exogenous zinc. The engineered bacterial system for monitoring exogenous zinc was successfully employed to detect levels of zinc as low as 0.001 mM, which directly activates the expression of chimeric ompC(t)-zinc binding peptide gene to remove zinc by adsorbing a maximum of 163.6 mu mol of zinc per gram of dry cell weight. These results indicate that the engineered bacterial strain developed in the present study can sense the specific heavy metal and activates a cell surface display system that acts to remove the metal
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