2,336 research outputs found

    Millettia pseudoracemosa Thothathri & Ravikumar 1997

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    Identities 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&gt

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    sj-xlsx-3-pul-10.1177_20458940211031109 - Supplemental material for Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension

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    Supplemental 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

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    Supplemental 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

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    Supplemental 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

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    Supplemental 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

    A neo-clerodane diterpene from Teucrium tomentosum. Corrigendum

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    The chemical name of the title compound in the paper by Devi, Malathi, Rajan, Aravind, Krishnakumari &amp;amp; Ravikumar [Acta Cryst. (2004), E60, o117&amp;#8211;o119] is corrected and the structural diagram is updated

    A study on the dynamics of the zraP gene expression profile and its application to the construction of zinc adsorption bacteria

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    Zinc 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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