Globalization, Glocalization, or Global Studies: What\u27s in a Name?

It is only in the concluding section of a painstaking article on the life and time of global studies that Nederveen Pieterse comes to make peace with the competing terminologies and says: \u27The issu..

Globalization and inequality

© The Author(s) 2017. This review essay discusses works of a leading sociologist and a leading economist on the subject of inequality and globalization. The books raise fresh ideas of inequality in the context of globalization by raising questions on the relationship between globalization and inequality throughout history. Although Therborn raises some fundamental questions about inequality, problematizes the concept, and broadens the discussion by adding multiple dimensions to it, Bourguignon’s study deepens our understanding of the problem of inequality by presenting the paradox of its linkage with globalization, which in the last century reduced international inequality while it widened intranational inequality, and the two processes are interrelated. Bourguignon suggests that the growing intranational inequality that threatens economic, political, and social stability can be overcome by concerted efforts of the states. Therborn pins his hope in the rising middle class across the world and their solidarity, which could create a more egalitarian society

Cricket, migration and diasporic communities

Ever since different communities began processes of global migration, sport has been an integral feature in how we conceptualise and experience the notion of being part of a diaspora. Sport provides diasporic communities with a powerful means for creating transnational ties, but also shapes ideas of their ethnic and racial identities. In spite of this, theories of diaspora have been applied sparingly to sporting discourses. Due mainly to its central role in spreading dominant white racial narratives within the British Empire, and the various ways different ethnic groups have ‘played’ with the meanings and associations of the sport in the (post-)colonial period, cricket is an interesting focus for academic research. Despite W.G. Grace’s claim that cricket advances civilisation by promoting a common bond, binding together peoples of vastly different backgrounds, to this day cricket operates strict symbolic boundaries; defining those who do, and equally, do not belong. C.L.R. James’ now famous metaphor of looking ‘beyond the boundary’ captures the belief that, to fully understand the significance of cricket, and the sport’s roles in changing and shaping society, one must consider the wider social and political contexts within which the game is played. The collection of papers in this special issue does just that. Cricket acts as the point of departure in each, but the way in which ideas of power, representation and inequality are ‘played out’ is unique in each

Temporal differences in DNA replication during the S phase using single fiber analysis of normal human fibroblasts and glioblastoma T98G cells

We have recently shown that replication forks pause near origins in normal human fibroblasts (NHF1-hTERT) but not glioblastoma T98G cells. This observation led us to question whether other differences in the replication program may exist between these cell types that may relate to their genetic integrity. To identify differences, we detected immunoflourescently the sequential incorporation of the nucleotide analogs IdU and CldU into replicating DNA at the start of every hour of a synchronized S phase. We then characterized the patterns of labeled replicating DNA tracks and quantified the percentages and lengths of the tracks found at these hourly intervals. From the directionality of labeling in single extended replicating DNA fibers, tracks were categorized as single bidirectional origins, unidirectional elongations, clusters of origins firing in tandem, or merging forks (terminations). Our analysis showed that the start of S phase is enriched in single bidirectional origins in NHF1-hTERT cells, followed by an increase in clustering during mid S phase and an increase in merging forks during late S phase. Early S phase in T98G cells also largely consisted of single bidirectional origin initiations; however, an increase in clustering was delayed until an hour later, and clusters were shorter in mid/late S phase than in NHF1-hTERT cells. The spike in merging forks also did not occur until an hour later in T98G cells. Our observations suggest models to explain the temporal replication of single and clustered origins, and suggest differences in the replication program in a normal and cancer cell line

Ophthalmic Biomarker Detection Using Ensembled Vision Transformers -- Winning Solution to IEEE SPS VIP Cup 2023

This report outlines our approach in the IEEE SPS VIP Cup 2023: Ophthalmic Biomarker Detection competition. Our primary objective in this competition was to identify biomarkers from Optical Coherence Tomography (OCT) images obtained from a diverse range of patients. Using robust augmentations and 5-fold cross-validation, we trained two vision transformer-based models: MaxViT and EVA-02, and ensembled them at inference time. We find MaxViT's use of convolution layers followed by strided attention to be better suited for the detection of local features while EVA-02's use of normal attention mechanism and knowledge distillation is better for detecting global features. Ours was the best-performing solution in the competition, achieving a patient-wise F1 score of 0.814 in the first phase and 0.8527 in the second and final phase of VIP Cup 2023, scoring 3.8% higher than the next-best solution

Order and disorder - An integrative structure of the full-length human growth hormone receptor

Because of its small size (70 kilodalton) and large content of structural disorder (>50%), the human growth hormone receptor (hGHR) falls between the cracks of conventional high-resolution structural biology methods. Here, we study the structure of the full-length hGHR in nanodiscs with small-angle x-ray scattering (SAXS) as the foundation. We develop an approach that combines SAXS, x-ray diffraction, and NMR spectroscopy data obtained on individual domains and integrate these through molecular dynamics simulations to interpret SAXS data on the full-length hGHR in nanodiscs. The hGHR domains reorient freely, resulting in a broad structural ensemble, emphasizing the need to take an ensemble view on signaling of relevance to disease states. The structure provides the first experimental model of any full-length cytokine receptor in a lipid membrane and exemplifies how integrating experimental data from several techniques computationally may access structures of membrane proteins with long, disordered regions, a widespread phenomenon in biology