Publications by authors named "Grove J"

SARS-CoV-2 variants are mainly defined by mutations in their spike. It is therefore critical to understand how the evolutionary trajectories of spike affect virus phenotypes. So far, it has been challenging to comprehensively compare the many spikes that emerged during the pandemic in a single experimental platform.

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Glioma-associated oncogene (-altered mesenchymal tumors are a newly described entity of neoplasms with very few case reports published in the literature. -altered neoplasms have a moderate degree of variability as they are seen in a broad range of anatomic sites and amongst people of all ages. A common feature that most -altered tumors share is the histologic makeup of monomorphic ovoid cells organized in distinct nests and an arborizing vascular blood supply.

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  • The first act of life involved capturing water within cell membranes, making fluid balance vital for survival.
  • The review explores how neural mechanisms compel animals to seek and consume water and salt, detailing how the brain processes information about blood osmolality and volume to trigger thirst and salt cravings.
  • It also points out gaps in current knowledge about fluid homeostasis, including the identities of sensors that detect fluid imbalances and how drinking is regulated even when there’s no physiological need, like during meals.
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Eating disorders (EDs) commonly co-occur with other psychiatric and neurodevelopmental disorders including attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD); however, the pattern of family history and genetic overlap among them requires clarification. This study investigated the diagnostic, familial, and genetic associations of EDs with ADHD and ASD. The nationwide population-based cohort study included all individuals born in Denmark, 1981-2008, linked to their siblings and cousins.

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Background: Iron deficiency is a common disorder, especially in developing countries. Accurately assessing iron status remains challenging, particularly for patients with chronic diseases such as HIV and chronic kidney disease, prevalent in South Africa.

Objective: This study aimed to determine how ferritin cut-offs affect iron status classification in adult patients treated at a tertiary hospital in South Africa.

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  • Tic disorders (TD) can significantly affect individuals and society, and understanding their genetic causes could lead to better treatments, as family history is a key risk factor.
  • A large-scale GWAS meta-analysis was conducted with nearly 10,000 TD cases and over 981,000 controls, revealing a significant genetic association, though it couldn't be replicated in another study.
  • The findings suggest a complex genetic landscape for TD, highlighting certain genes and brain regions involved, but additional research is needed to firmly establish reliable genetic links.
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Two different hard-radiation phenomena are known to originate from thunderclouds: terrestrial gamma-ray flashes (TGFs) and gamma-ray glows. Both involve an avalanche of electrons accelerated to relativistic energies but are otherwise different. Glows are known to last for one to hundreds of seconds, have moderate intensities and originate from quasi-stationary thundercloud fields.

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Thunderstorms emit fluxes of gamma rays known as gamma-ray glows, sporadically observed by aircraft, balloons and from the ground. Observations report increased gamma-ray emissions by tens of percent up to two orders of magnitude above the background, sometimes abruptly terminated by lightning discharges. Glows are produced by the acceleration of energetic electrons in high-electric-field regions within thunderclouds and contribute to charge dissipation.

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  • Whole-genome sequencing (WGS) of Korean autism families reveals that autistic females have a higher genetic burden than males, indicating a higher liability threshold for females compared to males across different ancestries.
  • The study analyzes data from a large sample of Korean individuals and compares it with European ancestry cohorts, finding that sex differences in genetic burden and autism symptoms vary significantly.
  • Results show that while females carry more damaging genetic variants, male siblings of autistic females display more severe social communication issues, highlighting the complexity of autism's genetic factors and the influence of sex on autistic traits.
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Synovial sarcoma is a malignant soft tissue tumor of uncertain differentiation. It is typically seen in the deep soft tissue of the extremities; however, it has been reported to occur anywhere in the body. Synovial sarcoma by histomorphology has multiple subtypes, including monophasic spindle cell, biphasic and poorly differentiated subtypes.

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Updates of SARS-CoV-2 vaccines are required to generate immunity in the population against constantly evolving SARS-CoV-2 variants of concerns (VOCs). Here we describe three novel in-silico designed spike-based antigens capable of inducing neutralising antibodies across a spectrum of SARS-CoV-2 VOCs. Three sets of antigens utilising pre-Delta (T2_32), and post-Gamma sequence data (T2_35 and T2_36) were designed.

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Viral glycoproteins drive membrane fusion in enveloped viruses and determine host range, tissue tropism and pathogenesis. Despite their importance, there is a fragmentary understanding of glycoproteins within the Flaviviridae, a large virus family that include pathogens such as hepatitis C, dengue and Zika viruses, and numerous other human, animal and emergent viruses. For many flaviviruses the glycoproteins have not yet been identified, for others, such as the hepaciviruses, the molecular mechanisms of membrane fusion remain uncharacterized.

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  • - Understanding how viruses like human pegivirus (HPgV) evade host immunity can reveal new aspects of the immune system; HPgV infects about 15% of people but usually doesn't cause disease.
  • - Researchers developed a mouse-adapted version of a pegivirus from rats (maPgV) that established a chronic infection in laboratory mice, lasting over 300 days without causing illness, similar to HPgV behavior in humans.
  • - The study revealed that type-I interferon plays a pro-viral role in chronic infections and identified various ways an immune system can counter PgV, suggesting both shared and unique strategies among persistent viruses; maPgV provides a new model to explore these infections further.
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Postharvest chilling injury (PCI) is a physiological disorder that often impairs tomato fruit ripening; this reduces fruit quality and shelf-life, and even accelerates spoilage at low temperatures. The gene family confers cold tolerance in , and constitutive overexpression of in tomato increases vegetative chilling tolerance, in part by retarding growth, but, whether CBF increases PCI tolerance in fruit is unknown. We hypothesized that overexpression (OE) would be induced in the cold and increase resistance to PCI.

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  • There is increasing awareness that signs of autism can emerge beyond the first three years of life, raising questions about the impact of age at diagnosis on developmental trajectories.
  • Research using data from four birth cohorts reveals two distinct socio-emotional behavior patterns linked to the age when autism is diagnosed.
  • The study also finds that the age at diagnosis has a heritable component and is related to genetic factors, suggesting a complex relationship between autism, the timing of diagnosis, and co-occurring conditions like ADHD and mental health issues.
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  • - The study investigates childhood daytime urinary incontinence (DUI) by identifying genetic variants that increase the risk, shedding light on the condition which is often stigmatized and not well understood.
  • - A genome-wide association study was performed on a large cohort from Denmark and replicated in Iceland, discovering significant genetic variants on chromosomes 6 and 20 linked to genes involved in neuronal development and bladder function.
  • - The research found that DUI has a hereditary component and is genetically correlated with conditions like attention-deficit/hyperactivity disorder and BMI, suggesting new directions for treatment options.
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  • This study examines the links between eating disorders (EDs), attention-deficit/hyperactivity disorder (ADHD), and autism spectrum disorder (ASD) in a large population from Denmark spanning those born between 1981 and 2008.
  • It found significantly higher risks for developing EDs in individuals diagnosed with either ADHD (almost double) or ASD (over two and a half times more likely).
  • Mediation analysis indicated that mood or anxiety disorders might explain a substantial portion of the relationship between ADHD or ASD and EDs, highlighting potential genetic links between anorexia nervosa and these conditions.
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  • Schwannomas are benign tumors that arise from Schwann cells in the peripheral nervous system, featuring both dense (Antoni A) and looser (Antoni B) tissue areas.
  • They mostly occur randomly but can be linked to genetic conditions like neurofibromatosis type 2.
  • A recent case involved a 61-year-old woman whose resected schwannoma showed unusual squamous metaplasia, a finding not previously documented, which could help pathologists identify similar cases in the future.
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  • The prevalence of autism in Denmark is rising, affecting 1.65% of 10-year-olds, with a focus on understanding its molecular causes through neonatal metabolomics of dried blood spots.
  • Researchers analyzed metabolomic profiles from over 1,400 newborns later diagnosed with autism, identifying over 800 metabolite features using advanced mass spectrometry techniques.
  • Key findings include two metabolites, cyclo-leucine-proline and 5-aminovaleric acid betaine (5-AVAB), which are associated with increased autism risk and could serve as early biomarkers, with 5-AVAB also linked to dietary habits and certain genetic variants.
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  • A new method was developed to assess etiologic heterogeneity in mental health disorders, which helps identify how different risk factors affect various subtypes of disorders like autism and ADHD.
  • The study analyzed risks from urban living, maternal smoking during pregnancy, and parental psychiatric history for different diagnostic combinations (autism alone, ADHD alone, and both).
  • Results showed that urban residency primarily increased the risk of autism + ADHD, while maternal smoking was linked only to ADHD, highlighting varying impact of risk factors across disorder subtypes.
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It is commonly held that there is a fundamental relationship between genome size and error rate, manifest as a notional "error threshold" that sets an upper limit on genome sizes. The genome sizes of RNA viruses, which have intrinsically high mutation rates due to a lack of mechanisms for error correction, must therefore be small to avoid accumulating an excessive number of deleterious mutations that will ultimately lead to population extinction. The proposed exceptions to this evolutionary rule are RNA viruses from the order (such as coronaviruses) that encode error-correcting exonucleases, enabling them to reach genome lengths greater than 40 kb.

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  • The study explores positive assortative mating (AM) in autism, focusing on whether AM patterns differ between autism subgroups with and without intellectual disability (ID).
  • It analyzed autism data from two large family-based collections, revealing that both subgroups exhibited similar levels of phenotypic and ancestry-related AM, but no significant AM based on autism polygenic scores.
  • The findings indicate that ancestry-related AM increases genetic linkage disequilibrium, but the study's limitation of focusing on individuals of European ancestry may restrict the applicability of these insights to non-European populations.
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The gold rush at the end of the nineteenth century in south-eastern Australia resulted in the mobilization and re-deposition of vast quantities of tailings that modified the geomorphology of the associated river valleys. Previous studies of contamination risk in these systems have either been performed directly on mine wastes (e.g.

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