ChatGPT in the higher education environment: perspectives from the theory of high order thinking skills.

ChatGPT is a form of technological progress in the 5.0 era. The use of ChatGPT has begun to penetrate all fields of science, including the field of education. Students use ChatGPT to help them complete their assignments in the university environment. Apart from providing many benefits, ChatGPT also has many dangers threatening students. One of the dangers for students who rely too much on ChatGPT is a decrease in higher-order thinking skills.

Career adaptability to prevent unexpected careers and burnout for woman employees in the remote work era.

Since the coronavirus disease 2019 pandemic, female remote workers need career adaptability. The main reason is that women are susceptible to mental health issues like burnout and unexpected career. To balance public and domestic roles, women need access to new skills and professional networks.

The exposure of mom-influencers on social media: a potential threat to public health awareness.

The potential threat to public health awareness posed by mom-influencers on social media must be taken into account. In the meantime, the concept of fostering partnerships between health experts, the government and mom-influencers must be made accessible in order to promote the immediate availability of appropriate, accurate and trustworthy information to the public and adequate health education practices.

Considering ChatGPT to be the first aid for young adults on mental health issues.

Providing mental health support and interventions through artificial intelligence can open up more significant space for young people to get good services. ChatGPT's potential to provide first aid to young adults struggling with mental health issues is noteworthy. Despite its benefits and limitations, today's technology can be a valuable addition to the mental health support available to young adults.

Kinetic Study of Copyrolysis of the Green Microalgae Botryococcus braunii and Victorian Brown Coal by Thermogravimetric Analysis.

The copyrolysis of the green microalgae Botryococcus braunii and Victorian brown coal was studied by thermogravimetric analysis using the Kissinger-Akahira-Sunose (KAS), Flynn-Wall-Ozawa (FWO), and Friedman methods. This research aims to study the synergistic effect of mixing B. braunii and Victorian brown coal in pyrolysis reactions on the kinetic parameter using thermogravimetric analysis. Copyrolysis was carried out at four heating rates, 10, 15, 20, and 25 °C/min. The copyrolysis reaction of B. braunii and Victorian brown coal occurred from 155.79 to 545.27 °C; this temperature range was lower than that for the pyrolysis of only B. braunii under the same conditions. However, mixing the two samples increased the thermal decomposition temperature for each conversion value (α), as well as the average activation energy, due to the presence of compounds that require high temperatures to undergo pyrolysis in the Victorian brown coal. The average activation energies of the copyrolysis reaction of B. braunii and Victorian brown coal determined using the KAS, FWO, and Friedman methods were 195.20 ± 17.40, 195.60 ± 17.70, and 225.93 ± 32.39 kJ/mol, respectively.

Clinical and genetic profile in index patients with spinocerebellar ataxia type 3 in Indonesia: case report.

Spinocerebellar ataxia (SCA) is an autosomal dominant hereditary disease with progressive course, and no causal therapy. Diagnostics are still challenging, due to facility and protocols, and so as in Indonesia. As a national referral center, Dr. Hasan Sadikin Central General Hospital has received a lot of patients from all over Indonesia, particularly from Western Java. Study related to SCA (including clinical and genetic profile) is still limited in Indonesia. We identified index patients from three families with ataxia, hence intend to determine their clinical and genetic pattern. The hereditary pattern is autosomal dominant. Scale for the assessment and rating of ataxia (SARA) shows mild and moderate ataxia. Inventory of non-ataxia signs (INAS) scores of the patients were 3, 5 and 6. Montreal cognitive assessment-Indonesian version (MOCA-INA) shows only one patient has mild cognitive impairment, despite young age. Barthel index shows 1 subject has moderate dependency. Mutation in Ataxin3 polyQ repeats shows pathologically long CAG repeats, 72,10; 72,10; and 72,23 respectively in mutant and wild type allele. We diagnosed the index patients with spinocerebellar ataxia type 3. This study is the first case series study in Indonesia. The hereditary pattern is clearly shown as an autosomal dominant ataxia. The clinical and genetic profile was varied, and the symptom is progressive and deteriorates overtime, including wide based gait, speech problem, motor and sensor complaint, and cognitive decline complaint. Despite the same polyQ stretch length, the onset and clinical characteristics of patients are diverse.

Dataset of short-term prediction of CO2 concentration based on a wireless sensor network.

This CO2 data is gathered from WSN (Wireless Sensor Network) sensors that is placed in some areas. To make this observation framework run effectively, examining the relationships between factors is required. We can utilize multiple wireless sensor devices. There are three parts of the system, including the sensor device, the sink node device, and the server. We use those devices to acquire data over a three-month period. In terms of the server infrastructure, we utilized an application server, a user interface server, and a database server to store our data. This study built a WSN framework for CO2 observations. We investigate, analyze, and predict the level of CO2, and the results have been collected. The Random Forest algorithm achieved a 0.82 R2 Score.

A cytogenetic study in a large population of intellectually disabled Indonesians.

Genetic factors play a significant role in the etiology of intellectual disability (ID). The goal of this study was to identify microscopically visible chromosomal abnormalities in an Indonesian ID population and to determine their frequency, pattern, and clinical features. A total of 527 intellectually disabled individuals from special schools and institutions in 4 different areas on Java Island, Indonesia, were screened for cytogenetic abnormalities. Additional analyses were carried out for verification or further characterization by using fluorescence in situ hybridization, multiplex ligation-dependent probe amplification, or analysis of the FMR1 promoter CGG(n) repeat. Of the 527 individuals with ID, chromosomal abnormalities were found in 87 (16.5%). Trisomy 21 was the major chromosomal abnormality, identified in 74 patients (14%). Other chromosome abnormalities included 8 X-chromosomal and 5 autosomal aberrations. Details on chromosome aberrations and confirmation analyses are discussed. This study shows that chromosomal abnormalities are an important cause of ID in Indonesia. Cytogenetic analysis is important for an adequate diagnosis in patients and subsequent genetic counseling for their families, especially in developing countries with limited facilities, such as Indonesia.