44 research outputs found

    The MOOC: Rhetoric, Political Economy and the Value of Technological Citizenship

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    This paper offers a critical political-economy of the promise and disappointment of the for- profit Massive Open Online Courses (MOOC) in higher education. Our goal is to encourage awareness, dialogue, and reflexivity about the gap between the rhetoric and reality of the MOOC in higher education and to highlight and interrogate the persuasive and profit power interests served by “the rhetoric of the MOOC.” To this end, the first section outlines our critical approach and defines some key concepts: “the rhetoric of technology,” “the political- economy of edu-tech” and “the public sphere.” The second section highlights the MOOC’s rhetorical promises and real disappointments. The third section contextualizes the “rhetoric of the MOOC” with regard to the persuasive and profit power interests it serves, and then evaluates this rhetoric with regard to the norms and values of the public sphere. We argue this rhetoric is a promotional discourse that is a poor guide to public deliberation and decision making about the role of technology in higher education. In closing, we propose the ideal and practice “technological citizenship” to encourage policy-makers, administrators, professors and students to have more democratic dialogue about educational technology, so that they, not the rhetoric of educational technology and the industry that sells it, can design the future of higher education

    We\u27re Locking The Door : Family Histories in a Sample of Homeless Youth

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    It is well known that the pathways to homelessness for young people are embedded in often ongoing negative childhood experiences. Many of these experiences are rooted in multiple and intersecting problems including, but not limited to: family conflict, abuse, addictions, and mental health issues. The authors draw upon qualitative interviews conducted with 15 homeless male and female youth between the ages of 16 and 24 in a suburban area of Southern Ontario, Canada. We describe these young people\u27s perceptions of family experiences and find support for Elliott Currie\u27s (2004) proposition that a broader ethos of individualism and intolerant parenting underpins many youth experiences in contemporary society

    Gaps Between Theory and Practice: Novice Teachers’ Perspectives

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    This study aimed to explore the novice teachers’ perception of gaps between theory andpractice. Novice teachers’ perceptions were further explored based on teachers’ gender. The surveymethod was used to collect the data. A questionnaire was developed by the researcher consisted of 39items with 5 points Likert rating scale to collect data from randomly selected 600 teachers includingmale and female. The data were analyzed by using the mean, standard deviation, and percentage ofeach five points of the Likert rating scale. The results revealed that most novice teachers were applyingtheir learned theory in their practice regarding lesson planning & delivery, classroom management,and students’ active involvement. They were not only willing to but also were applying learned theoriesin their practice. It also came into the knowledge that there were fewer gaps between novice teachers’theory and practice. It is recommended by the researchers suggested that these pre-service trainingcenters should develop a strong and viable link to make the theory more practical, operational and upto-dat

    Thiamethoxam toxicity: a review in one-health perspective

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    Extensive and frequent use of pesticides has induced numerous abnormalities in target and non-target exposed organisms. Among different various pesticides, neonicotinoids are extensively employed in agro-production sectors. Thiamethoxam (TMX) plays an essential role in keeping the crop safe from insect attack, but on the other hand, it has been reported to induce adverse effects in both humans and animals. Previously, it was thought that neonicotinoids have low toxicity potential in mammals, but widespread use has made it evident that these pesticides have serious toxic effects on both invertebrates and vertebrates. Extensive applications of pesticides also pose serious eco-toxicological threats to aquatic and terrestrial organisms in the ecosystem. This review describes the chemistry, pharmacodynamics, and toxic effects of various TMX on living organisms. Moreover, this review summarizes the excretion/deposition of TMX in different tissues along with potentially adverse effects on production potential, immunity, blood parameters, and male/female reproductive systems. Though the pros of TMX surpass the cons, its reported intrinsic toxicity stresses the need to develop new pesticides that have high potency with little harm to humans and animals. Hence, there is a need for hours to address knowledge gaps related to TMX and design effective rational usage of TMX strategies to keep the ecosystem safe from the potentially harmful effects of TMX

    Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

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    The 2-oxoglutarate dehydrogenase-like (OGDHL) protein is a rate-limiting enzyme in the Krebs cycle that plays a pivotal role in mitochondrial metabolism. OGDHL expression is restricted mainly to the brain in humans. Here, we report nine individuals from eight unrelated families carrying bi-allelic variants in OGDHL with a range of neurological and neurodevelopmental phenotypes including epilepsy, hearing loss, visual impairment, gait ataxia, microcephaly, and hypoplastic corpus callosum. The variants include three homozygous missense variants (p.Pro852Ala, p.Arg244Trp, and p.Arg299Gly), three compound heterozygous single-nucleotide variants (p.Arg673Gln/p.Val488Val, p.Phe734Ser/p.Ala327Val, and p.Trp220Cys/p.Asp491Val), one homozygous frameshift variant (p.Cys553Leufs∗16), and one homozygous stop-gain variant (p.Arg440Ter). To support the pathogenicity of the variants, we developed a novel CRISPR-Cas9-mediated tissue-specific knockout with cDNA rescue system for dOgdh, the Drosophila ortholog of human OGDHL. Pan-neuronal knockout of dOgdh led to developmental lethality as well as defects in Krebs cycle metabolism, which was fully rescued by expression of wild-type dOgdh. Studies using the Drosophila system indicate that p.Arg673Gln, p.Phe734Ser, and p.Arg299Gly are severe loss-of-function alleles, leading to developmental lethality, whereas p.Pro852Ala, p.Ala327Val, p.Trp220Cys, p.Asp491Val, and p.Arg244Trp are hypomorphic alleles, causing behavioral defects. Transcript analysis from fibroblasts obtained from the individual carrying the synonymous variant (c.1464T>C [p.Val488Val]) in family 2 showed that the synonymous variant affects splicing of exon 11 in OGDHL. Human neuronal cells with OGDHL knockout exhibited defects in mitochondrial respiration, indicating the essential role of OGDHL in mitochondrial metabolism in humans. Together, our data establish that the bi-allelic variants in OGDHL are pathogenic, leading to a Mendelian neurodevelopmental disease in humans

    Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies.

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    PURPOSE: We aimed to define a novel autosomal recessive neurodevelopmental disorder, characterize its clinical features, and identify the underlying genetic cause for this condition. METHODS: We performed a detailed clinical characterization of 19 individuals from nine unrelated, consanguineous families with a neurodevelopmental disorder. We used genome/exome sequencing approaches, linkage and cosegregation analyses to identify disease-causing variants, and we performed three-dimensional molecular in silico analysis to predict causality of variants where applicable. RESULTS: In all affected individuals who presented with a neurodevelopmental syndrome with progressive microcephaly, seizures, and intellectual disability we identified biallelic disease-causing variants in Protocadherin-gamma-C4 (PCDHGC4). Five variants were predicted to induce premature protein truncation leading to a loss of PCDHGC4 function. The three detected missense variants were located in extracellular cadherin (EC) domains EC5 and EC6 of PCDHGC4, and in silico analysis of the affected residues showed that two of these substitutions were predicted to influence the Ca2+-binding affinity, which is essential for multimerization of the protein, whereas the third missense variant directly influenced the cis-dimerization interface of PCDHGC4. CONCLUSION: We show that biallelic variants in PCDHGC4 are causing a novel autosomal recessive neurodevelopmental disorder and link PCDHGC4 as a member of the clustered PCDH family to a Mendelian disorder in humans
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