94 research outputs found

    Simple inhibitors of histone deacetylase activity that combine features of short-chain fatty acid and hydroxamic acid inhibitors

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    Butyric acid and trichostatin A (TSA) are anti-cancer compounds that cause the upregulation of genes involved in differentiation and cell cycle regulation by inhibiting histone deacetylase (HDAC) activity. In this study we have synthesized and evaluated compounds that combine the bioavailability of short-chain fatty acids, like butyric acid, with the bidentate binding ability of TSA. A series of analogs were made to examine the effects of chain length, simple aromatic cap groups, and substituted hydroxamates on the compounds\u27 ability to inhibit rat-liver HDAC using a fluorometric assay. In keeping with previous structure-activity relationships, the most effective inhibitors consisted of longer chains and hydroxamic acid groups. It was found that 5-phenylvaleric hydroxamic acid and 4-benzoylbutyric hydroxamic acid were the most potent inhibitors with IC50\u27s of 5 microM and 133 microM respectively

    SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

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    Variability in SARS-CoV-2 susceptibility and COVID-19 disease severity between individuals is partly due to genetic factors. Here, we identify 4 genomic loci with suggestive associations for SARS-CoV-2 susceptibility and 19 for COVID-19 disease severity. Four of these 23 loci likely have an ethnicity-specific component. Genome-wide association study (GWAS) signals in 11 loci colocalize with expression quantitative trait loci (eQTLs) associated with the expression of 20 genes in 62 tissues/cell types (range: 1:43 tissues/gene), including lung, brain, heart, muscle, and skin as well as the digestive system and immune system. We perform genetic fine mapping to compute 99% credible SNP sets, which identify 10 GWAS loci that have eight or fewer SNPs in the credible set, including three loci with one single likely causal SNP. Our study suggests that the diverse symptoms and disease severity of COVID-19 observed between individuals is associated with variants across the genome, affecting gene expression levels in a wide variety of tissue types

    Finishing the euchromatic sequence of the human genome

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    The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

    Prevalence of chronic HCV infection in EU/EEA countries in 2019 using multiparameter evidence synthesis

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    Publisher Copyright: © 2023 The Author(s)Background: Epidemiological data are crucial to monitoring progress towards the 2030 Hepatitis C Virus (HCV) elimination targets. Our aim was to estimate the prevalence of chronic HCV infection (cHCV) in the European Union (EU)/European Economic Area (EEA) countries in 2019. Methods: Multi-parameter evidence synthesis (MPES) was used to produce national estimates of cHCV defined as: π = πrecρrec + πexρex + πnonρnon; πrec, πex, and πnon represent cHCV prevalence among recent people who inject drugs (PWID), ex-PWID, and non-PWID, respectively, while ρrec, ρex, and ρnon represent the proportions of these groups in the population. Information sources included the European Centre for Disease Prevention and Control (ECDC) national operational contact points (NCPs) and prevalence database, the European Monitoring Centre for Drugs and Drug Addiction databases, and the published literature. Findings: The cHCV prevalence in 29 of 30 EU/EEA countries in 2019 was 0.50% [95% Credible Interval (CrI): 0.46%, 0.55%]. The highest cHCV prevalence was observed in the eastern EU/EEA (0.88%; 95% CrI: 0.81%, 0.94%). At least 35.76% (95% CrI: 33.07%, 38.60%) of the overall cHCV prevalence in EU/EEA countries was associated with injecting drugs. Interpretation: Using MPES and collaborating with ECDC NCPs, we estimated the prevalence of cHCV in the EU/EEA to be low. Some areas experience higher cHCV prevalence while a third of prevalent cHCV infections was attributed to PWID. Further efforts are needed to scale up prevention measures and the diagnosis and treatment of infected individuals, especially in the east of the EU/EEA and among PWID. Funding: ECDC.Peer reviewe

    A first update on mapping the human genetic architecture of COVID-19

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    A theoretical explanation for understanding what motivates women to aspire to the superintendency

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    This study sought to develop a substantive-level theory that would provide an explanation for understanding what motivates women, enrolled in educational administration doctoral programs, to aspire to the superintendency despite the documented obstacles and barriers a female candidate would foreseeably encounter in her pursuit. Utilizing a constructivist grounded theory methodology, The Female Superintendency Aspiration Model emerged. This model was constructed based on three days of semi-structured, in-depth individual interviews with 23 women from across the United States who ranged in age, race, family/marital status, and occupation, who aspire to become superintendents. The Female Superintendency Aspiration Model reveals that women aspiring to the superintendency are motivated to become superintendents as a result of three causal conditions (1) a person of influence, such as a mentor and/or role model, (2) an innate drive to seek out challenging and competitive opportunities, and (3) enrollment in a doctoral program emphasizing superintendency credentials. Each of these factors is further enhanced by multiple outside dynamics, such as women's relationship with her parents, her mother's influence, specific personality characteristics (goal-driven, restless spirit, pressure seekers), and the networking opportunities provided by her university program. Women aspiring to the superintendency demonstrate a strong sense of self-efficacy toward the foreseen literature-documented obstacles and barriers as a result of having a person of influence, networking opportunities, and having goal-driven, realistic personalities. The study's results can be used by university educational leadership programs to (1) facilitate positive mentoring relationships with female students in the program, based on the innate traits presented in the model, and (2) host and facilitate networking opportunities whereby women have the opportunity to meet and build relationships with current and former superintendents, search firms, and school board presidents and members. These positive experiences, actions, and relationships are vital to encouraging more women to pursue the superintendency

    Pregnancy Outcomes of Women With Physical Disabilities: A Matched Cohort Study

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    Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/146996/1/pmr290.pd
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