Publications by authors named "Jessica Bertol"

Article Synopsis
  • Disease risk prediction can be enhanced by analyzing genomic sequences and transcriptional profiles, though identifying harmful non-coding DNA variations remains challenging for common diseases.
  • This study explores the interactions between P53 and cMYC proteins in regulation of target genes, revealing co-occupancy patterns in DNA regions that are conserved through evolution.
  • Results indicate that doxorubicin treatment leads to changes in protein levels and gene expression, suggesting a method to connect non-coding variations to gene regulation and disease risk screening.
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Article Synopsis
  • * The study focused on the co-occupancy and competitive interactions between the transcription factors P53 and cMYC in regulating gene expression, identifying that approximately 344-366 genomic regions were co-occupied by both factors in human and mouse embryonic stem cells.
  • * Treatment with doxorubicin altered protein levels of P53 and cMYC in certain cell types and resulted in significant changes in the expression of nearby genes, indicating that variations in non-coding DNA influence the binding affinity of these transcription factors, which in turn affects gene regulation
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There is growing interest in exploring Digitalis cardenolides as potential antiviral agents. Hence, we herein investigated the influence of structural features and lipophilicity on the antiherpes activity of 65 natural and semisynthetic cardenolides assayed in vitro against HSV-1. The presence of an α,β-unsaturated lactone ring at C-17, a β-hydroxy group at C-14 and C-3β-OR substituents were considered essential requirements for this biological activity.

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Cell fate determination is a necessary and tightly regulated process for producing different cell types and structures during development. Cranial neural crest cells (CNCCs) are unique to vertebrate embryos and emerge from the neural plate borders into multiple cell lineages that differentiate into bone, cartilage, neurons and glial cells. We have previously reported that Irf6 genetically interacts with Twist1 during CNCC-derived tissue formation.

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The role of human adenovirus (HAdV) infection in different acute diseases, such as febrile exudative tonsillitis, conjunctivitis, and pharyngoconjunctival fever is well established. However, the relationships, if any, of HAdV persistence and reactivation in the development of the chronic adenotonsillar disease is not fully understood. The present paper reports a 3-year cross-sectional hospital-based study aimed at detecting and quantifying HAdV DNA and mRNA of the HAdV hexon gene in adenoid and palatine tonsil tissues and nasopharyngeal secretions (NPS) from patients with adenotonsillar hypertrophy or recurrent adenotonsillitis.

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Background: Interferon regulatory factor 6 (IRF6) plays a critical role in embryonic tissue development, including differentiation of epithelial cells. Besides orofacial clefting due to haploinsufficiency of IRF6, recent human genetic studies indicated that mutations in IRF6 are linked to small mandible and digit abnormalities. The function of IRF6 has been well studied in oral epithelium; however, its role in craniofacial skeletal formation remains unknown.

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Article Synopsis
  • Mandibular disorders are a prevalent birth defect in humans, often leading to secondary issues like airway obstruction and feeding difficulties that can impact quality of life.
  • The study aims to uncover hormonal and genetic factors linked to nonsyndromic mandibular disorders, identifying significant interactions in the FGF and BMP signaling pathways.
  • Findings suggest that certain genes related to skeletal formation may play a crucial role as genetic risk factors for common mandibular disorders, indicating a need for further research into their implications.
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To assess the impact of genetic variation in regulatory loci on human health, we constructed a high-resolution map of allelic imbalances in DNA methylation, histone marks, and gene transcription in 71 epigenomes from 36 distinct cell and tissue types from 13 donors. Deep whole-genome bisulfite sequencing of 49 methylomes revealed sequence-dependent CpG methylation imbalances at thousands of heterozygous regulatory loci. Such loci are enriched for stochastic switching, which is defined as random transitions between fully methylated and unmethylated states of DNA.

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A major issue in developmental biology is to determine how embryonic tissues respond to molecular signals in a timely manner and given the position-restricted instructions during morphogenesis, of which Meckel's cartilage is a classical example. The explant model is a practical and convenient system that allows investigation of bone and cartilage responses to specific stimuli under a controlled manner that closely mimics the conditions. In this protocol, the explant model was applied to test whether Meckel's cartilage and surrounding tissues are responsive to the Endothelin1 (Edn1) signaling molecule and whether it would rescue the phenotype of genetic mutations.

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  • Rapid detection methods for infectious viruses are essential, particularly for studying rotavirus-induced diarrhea, as current cultivation techniques are challenging.
  • Molecular beacons (MBs) have been shown to effectively detect human rotavirus group A (HuRVA) in cell culture, providing a specific method to identify viral infectivity.
  • The proposed MB assay demonstrated increased fluorescence in infected cells, allowing for quick and efficient detection of HuRVA without lengthy viral culture processes, potentially aiding in vaccine development.
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Culture supernatant of sepsis-associated Escherichia coli (SEPEC) isolated from patients with sepsis caused loss of intercellular junctions and elongation of human umbilical vein endothelial cells (HUVEC). The cytotoxic factor was purified from culture supernatant of SEPEC 15 (serogroup O153) by liquid chromatography process. PAGE (polyacrylamide gel electrophoresis) showed that the purified SEPEC cytotoxic factor had a molecular mass of ∼150kDa and consisted of at least two subunits.

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Group A human rotaviruses (HuRVA) are causative agents of acute gastroenteritis. Six viral structural proteins (VPs) and six nonstructural proteins (NSPs) are produced in RV-infected cells. NSP4 is a diarrhoea-inducing viral enterotoxin and NSP4 gene analysis revealed at least 15 (E1-E15) genotypes.

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Cardiac glycosides, known ligands of the sodium pump, are widely used in the treatment of heart failure, such as digoxin and digitoxin. Besides this important activity, other biological activities, such as the antiviral activity, have been described for this group. HSV are responsible for many infections of oral, ocular and genital regions.

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