full-screen mode | ScienceGate

In automated Visual GUI Testing (VGT) for Android devices, the available tools often suffer from low robustness to mobile fragmentation, leading to incorrect results when running the same tests on different devices. To soften these issues, we evaluate two feature matching-based approaches for widget detection in VGT scripts, which use, respectively, the complete full-screen snapshot of the application ( Fullscreen ) and the cropped images of its widgets ( Cropped ) as visual locators to match on emulated devices. Our analysis includes validating the portability of different feature-based visual locators over various apps and devices and evaluating their robustness in terms of cross-device portability and correctly executed interactions. We assessed our results through a comparison with two state-of-the-art tools, EyeAutomate and Sikuli. Despite a limited increase in the computational burden, our Fullscreen approach outperformed state-of-the-art tools in terms of correctly identified locators across a wide range of devices and led to a 30% increase in passing tests. Our work shows that VGT tools’ dependability can be improved by bridging the testing and computer vision communities. This connection enables the design of algorithms targeted to domain-specific needs and thus inherently more usable and robust.

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Techniques for Developing Mobile-Friendly Web Sites

Encyclopedia of Organizational Knowledge, Administration, and Technology - Advances in Logistics, Operations, and Management Science ◽

10.4018/978-1-7998-3473-1.ch094 ◽

2021 ◽

pp. 1368-1378

Author(s):

J. Christopher Sandvig

Keyword(s):

Social Media ◽

Mobile Devices ◽

Web Sites ◽

Web Search ◽

Mobile Design ◽

Single Column ◽

Space Saving ◽

Full Screen ◽

Physical Limitations ◽

Display Content

The growing use of mobile devices for e-commerce, news, social media, and web search has created a need for mobile-friendly web sites. Mobile sites are designed to accommodate the physical limitations of mobile devices such as small displays, touch screens, and slow download times. Mobile-friendly sites typically display content in a single column formatted to use the full screen width, utilize vertical scrolling, use smaller images, provide larger touch targets such as buttons and links, and utilize space saving navigation techniques. The objectives of this article are to describe the attributes of mobile friendly web sites, overview current popular mobile design techniques, and discuss their strengths and weaknesses.

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67‐2: 5.5 inch Full Screen Flexible High‐Resolution OLED Display Fabricated by Ink Jet Printing Method

SID Symposium Digest of Technical Papers ◽

10.1002/sdtp.13081 ◽

2019 ◽

Vol 50 (1) ◽

pp. 945-948 ◽

Cited By ~ 4

Author(s):

Dejiang Zhao ◽

Wei Huang ◽

Liwen Dong ◽

Qian Jin ◽

Yu Tian ◽

...

Keyword(s):

High Resolution ◽

Ink Jet Printing ◽

Ink Jet ◽

Full Screen ◽

Jet Printing ◽

Oled Display ◽

Printing Method

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MTT assay to evaluate the cytotoxic potential of a drug

Bangladesh Journal of Pharmacology ◽

10.3329/bjp.v12i2.30892 ◽

2017 ◽

Vol 12 (2) ◽

pp. 8 ◽

Cited By ~ 63

Author(s):

Ashutosh Bahuguna ◽

Imran Khan ◽

Vivek K. Bajpai ◽

Sun Chul Kang

Keyword(s):

Cell Viability ◽

Mtt Assay ◽

Colorimetric Assay ◽

Video Clip ◽

Cell Number ◽

Cytotoxic Potential ◽

Lung Adenocarcinoma Cell Line ◽

Full Screen ◽

Purple Color

Quantification of cell viability and proliferation form the fundamental for numerous in vitro assays in response to external factors. An MTT assay is a colorimetric assay based on assessing the cell metabolic activity. A549 Lung adenocarcinoma cell line was used to see the cytotoxic potential of a new drug for initial screening of apoptosis or necrosis. The biochemical mechanism behind the MTT assay involves NAD(P)H-dependent cellular oxidoreductase enzyme that converts the yellow tetrazolium MTT [3-(4, 5-dimethylthiazolyl-2)-2,5-diphenyltetrazolium bromide] into insoluble (E,Z)-5-(4,5-dimethylthiazol-2-yl)-1,3-diphenylformazan (formazan). The formed formazan can be dissolved with dimethyl sulfoxide (DMSO) to give a purple color with characteristic absorption at 540 nm. Intensity of purple color is directly proportional to the cell number and thus indicating the cell viability.Video Clip of Methodology: 3 min 56 sec <a href="https://www.youtube.com//v/eqFxzDVunt8">Full screen</a> <a href="https://www.youtube.com/watch?v=eqFxzDVunt8">If Failed</a>

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Pharmacological studies on the laxative effects of Fagonia indica on rodents

Bangladesh Journal of Pharmacology ◽

10.3329/bjp.v14i4.41777 ◽

2019 ◽

Vol 14 (4) ◽

pp. 166-173

Author(s):

Muhammad Zeeshan Ali ◽

Malik Hassan Mehmood ◽

Muhammad Saleem ◽

Anwar-ul-Hassan Gilani

Keyword(s):

Ursolic Acid ◽

Video Clip ◽

In Vitro Assays ◽

Aqueous Fraction ◽

Laxative Effects ◽

Pharmacological Studies ◽

Full Screen ◽

Species Specific

This study explores the pharmacological basis for the folk use of Fagonia indica in constipation using in vivo and in vitro assays. The crude extract of F. indica contained tannins, saponins, anthraquinones, alkaloids, flavonoids, glycosides and phenols. The administration of F. indica extract (100 and 300 mg/kg) to mice caused a partially atropine-sensitive 35 and 42.6% laxation, respectively, similar to ursolic acid which showed 22 and 36% laxation at 10 and 30 mg/kg, respectively. In loperamide-induced constipation mice, F. indica (27.3 and 34.6%) and ursolic acid (15 and 28%) also displayed laxative effects at the aforementioned doses. In mice and rats ileum, F. indica, its fractions (ethyl acetate, aqueous) and ursolic acid produced atropine-sensitive stimulatory effects, while in rats ileum, F. indica and aqueous fraction showed partially atropine-sensitive effects. F. indica and ursolic acid possess laxative and species-specific gut stimulant effects predominantly involving the activation of muscarinic receptor, thus eliciting its folk use in constipation. Video Clip of Methodology: 7 min 7 sec: Full Screen Alternate

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Ameliorative potential of Anacyclus pyrethrum extract in generalized seizures in rat: Possible cholinergic mediated mechanism

Bangladesh Journal of Pharmacology ◽

10.3329/bjp.v14i4.40537 ◽

2019 ◽

Vol 14 (4) ◽

pp. 188-195

Author(s):

Kenza Bezza ◽

Zineb El Gabbas ◽

Jawad Laadraoui ◽

Mehdi Ait Laaradia ◽

Sara Oufquir ◽

...

Keyword(s):

Anticonvulsant Activity ◽

Video Clip ◽

Ethanol Extract ◽

Control Group ◽

Anticonvulsant Effect ◽

Onset Seizure ◽

Generalized Seizures ◽

Full Screen ◽

Time Latency ◽

Latency Duration

The present study evaluates the anticonvulsant activity of the roots of Anacyclus pyrethrum using pilocarpine-induced experimental model of epilepsy in rat, and to determine its possible anticonvulsant mechanism. Ethanol extract (200 and 400 mg/kg) or alkylamides (25 and 50 mg/kg) was administered orally 45 min before the injection of pilocarpine-induced (400 mg/kg) seizures. The possible anticonvulsant mechanism was investigated by testing the effect of atropine (2 mL/kg) and scopolamine (1 mg/kg). The scoring of seizure severity, seizures time latency, duration of total seizures and percentage of mortality protection were recorded. Ethanol extract and alkylamides prolonged the time of onset seizure and decreased the duration of seizures compared to control group (p<0.001). The seizure protection was 100%. The co-administered of ethanol extract of A. pyrethrum and alkylamides with atropine completely abolished the pilocarpine-induced seizures. Video Clip of Methodology: Anticonvulsant effect: 6 min 7 sec: Full Screen Alternate

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A new class of potential antidiabetic acetohydrazides: Synthesis, in vivo antidiabetic activity and molecular docking studies

Bangladesh Journal of Pharmacology ◽

10.3329/bjp.v12i3.31428 ◽

2017 ◽

Vol 12 (3) ◽

pp. 319 ◽

Cited By ~ 1

Author(s):

Mubeen Arif ◽

Furukh Jabeen ◽

Aamer Saeed ◽

Irfan Zia Qureshi ◽

Nadia Mushtaq

Keyword(s):

Molecular Docking ◽

Video Clip ◽

Docking Studies ◽

Antidiabetic Activity ◽

Molecular Docking Studies ◽

H Nmr ◽

New Class ◽

Full Screen ◽

Pharmacologically Active

Two new pharmacologically active series of tetrazolopyridine-acetohydrazide conjugates [9 (a-n), 10 (a-n)] were synthesized by reacting a variety of suitably substituted benzaldehydes and isomeric 2-(5-(pyridin-3/4-yl)-2H-tetrazol-2-yl)acetohydrazides (7, 8). The synthesized compounds were analyzed through FTIR, 1H NMR, 13C NMR and elemental techniques. These acetohydrazides were screened for their in vivo antidiabetic activity and molecular docking studies. An excellent agreement was obtained as the best docked poses show-ed important binding features mostly based on interactions due to an oxygen atom and aromatic moieties of the series. The compounds 9a, 9c and 10l were found to be the most active in lowering blood glucose, having the potential of being good antidiabetic agents.Video Clip of Methodology:Synthesis of 3/4-(2H-tetrazole-5-yl)pyridine: 1 min 57 sec <a href="https://www.youtube.com/v/CHp8HxlEa2M">Full Screen</a> <a href="https://www.youtube.com/watch?v=CHp8HxlEa2M">Alternate</a>

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