The Veiled Identity: Hijabistas, Instagram and Branding In The Online Islamic Fashion Industry

What it means to be a Muslim woman is frequently redefined in reaction to the notions of ‘Muslim womanhood’ constructed within neoliberal society. By examining the ways in which Hijabi fashion bloggers use the visual discourse of their Instagram accounts to implement specific notions of taste, authenticity and branding this project aims to address the question of where fashion blogs fit within mainstream fashion frameworks and the ways in which the assumed tensions surrounding veiling and fashion are disrupted

Femme Fatales of Faith : Queer and Deviant Performances of Femme Within Western Protestant Culture

Women and queer folk are changing the religious landscape of Christianity in America, and the scope of visibility for these figures and their apostolic endeavors is widening as more and more Christians are seeking out communities rooted in doctrines of love and connection rather than exclusion and hegemonic piety. Thinking on this phenomenon, this dissertation focuses on the intersectional dilemmas of faith practice and rhetorical discourse with Western Christianity, particularly as it revolves around those female pastors and clergy - considered dangerous by many within the church - who are advocating for a more inclusionary church space. By conducting a rhetorically-motivated investigation centered within feminist and religious dialogues, this project attempts to answer the following questions: How can the femme fatale, as read through a lens of queer performativity, be a hallmark of identity-making for women within religious spaces? How does the rhetorical act of confession, specifically the memoir, work as a performative tool of resistance when used by the femme fatales of faith What do the alternative and \u27out-law\u27 narratives and embodiments of Nadia Bolz-Weber, Paula Stone Williams, and Pamela Lightsey speak to in terms of female church leaders marking themselves as femme fatales of faith

Molecular Organization in Site-Specific Recombination: The Catalytic Domain of Bacteriophage HP1 Integrase at 2.7 Å Resolution

AbstractHP1 integrase promotes site-specific recombination of the HP1 genome into that of Haemophilus influenzae. The isolated C-terminal domain (residues 165–337) of the protein interacts with the recombination site and contains the four catalytic residues conserved in the integrase family. This domain represents a novel fold consisting principally of well-packed α helices, a surface β sheet, and an ordered 17-residue C-terminal tail. The conserved triad of basic residues and the active-site tyrosine are contributed by a single monomer and occupy fixed positions in a defined active-site cleft. Dimers are formed by mutual interactions of the tail of one monomer with an adjacent monomer; this orients active-site clefts antiparallel to each other

The Mississippian Section at Paddys Bluff, Crittenden County, Kentucky

Paddys Bluff (Figs. 1-3) is located on the south side of the Illinois Basin on the Cumberland River, 1.7 miles downstream from Dycusburg in Crittenden County, Ky., in Carter coordinate section 23-I-16 and ecoregion 71f of the Western Highland Rim of Kentucky (Woods and others, 2002). This bluff is on a right-descending bend 18 liver miles above its junction with the Ohio River at Smithland, Livingston County. The bluff (Figs. 4A, B) is locally famous as the location for a scene from the classic 1962 film, How the West Was Won,\u27 a winner of three Academy Awards, starling James Stewart, John Wayne, and others. We observed Paddys Bluff from the starboard Texas deck of the steamboat Della Queen one rainy morning in October 2005; the thick, persistent white bed midway in the bluff especially attracted our attention (Fig. 4). Paddys Bluff is the best natural exposure of Mississippian limestone between Barkley Dam and the Ohio River, a distance of 31 river miles. The bluff, some 1,700 feet long (Fig. 4), rises 160 feet above the Cumberland River and deflects it about 16° into a long westward reach, the river removing all talus at the base of the bluff. The bluff lies in a graben between two inferred faults st liking N40 to 45°E (Amos and Hayes, 1974). Readily seen in the limestones along the river at the base of the bluff is a prominent joint set parallel to these faults. This bluff is mapped on the Dycusburg geologic quadrangle map (Table 1) as the combined Salem and St. Louis Limestones (Amos and Hayes, 1974) and is capped by at least 15 feet of poorly exposed gravel of the Cretaceous Tuscaloosa Formation (Olive, 1980). Across the river less than 2 miles distant are scattered continental deposits of reddish brown Lafayette-type, sandy cobble-gravel (Olive, 1980), below which are outliers of the Cretaceous Tuscaloosa Formation; both cap hilltops of the same underlying Mississippian limestones. Why is Paddys Bluff of interest? There are at least six reasons to study it. First, can the Salem and St. Louis Limestones be individually identified at the bluff? If, in fact, they can be separated, the upper boundary of sequence S4 recognized in the Lake Cumberland area of south-central Kentucky by Khetani and Read (2002, Fig. 12) extends much farther west. Still another challenge is the enigmatic, massive, fine-grained, whitish-weathering carbonate mudstone bed, unit C of our section, high in the bluff. What does it represent? How widespread is it? Why do beds below rt have a strong petroliferous odor and not those above it? Why are some of the coral heads (Fig. 5) at Paddys Bluff overturned and others not? The last challenge is the bluff itself: Why is it there and how long has it been there

Clavicular stress fracture in a cricket fast bowler: A case report

<p>Abstract</p> <p>Introduction</p> <p>Whilst rare, stress fractures of the clavicle have been described in other sports. To our knowledge, this is the first reported case of a stress fracture of the clavicle occurring in a cricket fast bowler.</p> <p>Case presentation</p> <p>A 23-year-old professional cricket fast bowler presented with activity related shoulder pain. Imaging demonstrated a stress fracture of the lateral third of the clavicle. This healed with rest and rehabilitation allowing a full return to professional sport.</p> <p>Conclusion</p> <p>This injury is treated with activity modification and technique adaptation. In a professional sportsman, this needs to be recognised early so that return to play can be as quick as possible.</p

siRNA Screening of a Targeted Library of DNA Repair Factors in HIV Infection Reveals a Role for Base Excision Repair in HIV Integration

Host DNA repair enzymes have long been assumed to play a role in HIV replication, and many different DNA repair factors have been associated with HIV. In order to identify DNA repair pathways required for HIV infection, we conducted a targeted siRNA screen using 232 siRNA pools for genes associated with DNA repair. Mapping the genes targeted by effective siRNA pools to well-defined DNA repair pathways revealed that many of the siRNAs targeting enzymes associated with the short patch base excision repair (BER) pathway reduced HIV infection. For six siRNA pools targeting BER enzymes, the negative effect of mRNA knockdown was rescued by expression of the corresponding cDNA, validating the importance of the gene in HIV replication. Additionally, mouse embryo fibroblasts (MEFs) lacking expression of specific BER enzymes had decreased transduction by HIV-based retroviral vectors. Examining the role BER enzymes play in HIV infection suggests a role for the BER pathway in HIV integration

Productive Hepatitis C Virus Infection of Stem Cell-Derived Hepatocytes Reveals a Critical Transition to Viral Permissiveness during Differentiation

Primary human hepatocytes isolated from patient biopsies represent the most physiologically relevant cell culture model for hepatitis C virus (HCV) infection, but these primary cells are not readily accessible, display individual variability, and are largely refractory to genetic manipulation. Hepatocyte-like cells differentiated from pluripotent stem cells provide an attractive alternative as they not only overcome these shortcomings but can also provide an unlimited source of noncancer cells for both research and cell therapy. Despite its promise, the permissiveness to HCV infection of differentiated human hepatocyte-like cells (DHHs) has not been explored. Here we report a novel infection model based on DHHs derived from human embryonic (hESCs) and induced pluripotent stem cells (iPSCs). DHHs generated in chemically defined media under feeder-free conditions were subjected to infection by both HCV derived in cell culture (HCVcc) and patient-derived virus (HCVser). Pluripotent stem cells and definitive endoderm were not permissive for HCV infection whereas hepatic progenitor cells were persistently infected and secreted infectious particles into culture medium. Permissiveness to infection was correlated with induction of the liver-specific microRNA-122 and modulation of cellular factors that affect HCV replication. RNA interference directed toward essential cellular cofactors in stem cells resulted in HCV-resistant hepatocyte-like cells after differentiation. The ability to infect cultured cells directly with HCV patient serum, to study defined stages of viral permissiveness, and to produce genetically modified cells with desired phenotypes all have broad significance for host-pathogen interactions and cell therapy

Incorporating radiomics into clinical trials: expert consensus on considerations for data-driven compared to biologically-driven quantitative biomarkers

Existing Quantitative Imaging Biomarkers (QIBs) are associated with known biological tissue characteristics and follow a well-understood path of technical, biological and clinical validation before incorporation into clinical trials. In radiomics, novel data-driven processes extract numerous visually imperceptible statistical features from the imaging data with no a priori assumptions on their correlation with biological processes. The selection of relevant features (radiomic signature) and incorporation into clinical trials therefore requires additional considerations to ensure meaningful imaging endpoints. Also, the number of radiomic features tested means that power calculations would result in sample sizes impossible to achieve within clinical trials. This article examines how the process of standardising and validating data-driven imaging biomarkers differs from those based on biological associations. Radiomic signatures are best developed initially on datasets that represent diversity of acquisition protocols as well as diversity of disease and of normal findings, rather than within clinical trials with standardised and optimised protocols as this would risk the selection of radiomic features being linked to the imaging process rather than the pathology. Normalisation through discretisation and feature harmonisation are essential pre-processing steps. Biological correlation may be performed after the technical and clinical validity of a radiomic signature is established, but is not mandatory. Feature selection may be part of discovery within a radiomics-specific trial or represent exploratory endpoints within an established trial; a previously validated radiomic signature may even be used as a primary/secondary endpoint, particularly if associations are demonstrated with specific biological processes and pathways being targeted within clinical trials