38 research outputs found
Math Musicians: Exploring the Impact of Content Integrated Pop Music on Students’ Attitudes and Engagement During Math Instruction
Traditional methods of math instruction have been consistently linked to students having negative feelings about math, as well as decreased motivation and engagement during math instruction. This study investigated how arts integration, specifically integrating pop music, impacted students’ attitudes about math and students’ motivation and engagement during math instruction in a fifth-grade classroom. This study was mixed methods, with quantitative data collected through an adapted version of a student dispositions survey to assess students’ attitudes, motivation, and engagement, and qualitative data collected through a short response question about how students feel music impacted their math experiences. Results indicated that the integration of pop music had a significant impact on students’ attitudes about math. Students also noted how pop music integration made math more enjoyable and helped them memorize the information better
Research Methods in Psychology (PSYC 362) Posters: The Interaction Between Stress and Boredom and Their Relationship With Emotional Eating
Students taking Research Methods in Psychology are tasked with generating a novel research question, designing a study to answer that question, and analyzing and interpreting data within the context of their original hypotheses. These posters represent the culmination of this semester-long project
Mindfulness as a Mediator in the Relationship Between Social Media Engagement and Depression
A 491/492 Team Project supervised by Dr. Miriam Liss (Spring 2021)
The Hubble Ultra Deep Field
This paper presents the Hubble Ultra Deep Field (HUDF), a one million second
exposure of an 11 square minute-of-arc region in the southern sky with the
Hubble Space Telescope. The exposure time was divided among four filters, F435W
(B435), F606W (V606), F775W (i775), and F850LP (z850), to give approximately
uniform limiting magnitudes mAB~29 for point sources. The image contains at
least 10,000 objects presented here as a catalog. Few if any galaxies at
redshifts greater than ~4 resemble present day spiral or elliptical galaxies.
Using the Lyman break dropout method, we find 504 B-dropouts, 204 V-dropouts,
and 54 i-dropouts. Using these samples that are at different redshifts but
derived from the same data, we find no evidence for a change in the
characteristic luminosity of galaxies but some evidence for a decrease in their
number densities between redshifts of 4 and 7. The ultraviolet luminosity
density of these samples is dominated by galaxies fainter than the
characteristic luminosity, and the HUDF reveals considerably more luminosity
than shallower surveys. The apparent ultraviolet luminosity density of galaxies
appears to decrease from redshifts of a few to redshifts greater than 6. The
highest redshift samples show that star formation was already vigorous at the
earliest epochs that galaxies have been observed, less than one billion years
after the Big Bang.Comment: 44 pages, 18 figures, to appear in the Astronomical Journal October
200
Identification of a Functional Non-coding Variant in the GABA
GABA type-A (GABA-A) receptors containing the α2 subunit (GABRA2) are expressed in most brain regions and are critical in modulating inhibitory synaptic function. Genetic variation at the GABRA2 locus has been implicated in epilepsy, affective and psychiatric disorders, alcoholism and drug abuse. Gabra2 expression varies as a function of genotype and is modulated by sequence variants in several brain structures and populations, including F2 crosses originating from C57BL/6J (B6J) and the BXD recombinant inbred family derived from B6J and DBA/2J. Here we demonstrate a global reduction of GABRA2 brain protein and mRNA in the B6J strain relative to other inbred strains, and identify and validate the causal mutation in B6J. The mutation is a single base pair deletion located in an intron adjacent to a splice acceptor site that only occurs in the B6J reference genome. The deletion became fixed in B6J between 1976 and 1991 and is now pervasive in many engineered lines, BXD strains generated after 1991, the Collaborative Cross, and the majority of consomic lines. Repair of the deletion using CRISPR-Cas9-mediated gene editing on a B6J genetic background completely restored brain levels of GABRA2 protein and mRNA. Comparison of transcript expression in hippocampus, cortex, and striatum between B6J and repaired genotypes revealed alterations in GABA-A receptor subunit expression, especially in striatum. These results suggest that naturally occurring variation in GABRA2 levels between B6J and other substrains or inbred strains may also explain strain differences in anxiety-like or alcohol and drug response traits related to striatal function. Characterization of the B6J private mutation in the Gabra2 gene is of critical importance to molecular genetic studies in neurobiological research because this strain is widely used to generate genetically engineered mice and murine genetic populations, and is the most widely utilized strain for evaluation of anxiety-like, depression-like, pain, epilepsy, and drug response traits that may be partly modulated by GABRA2 function
Identification of a Functional Non-coding Variant in the GABAA Receptor α2 Subunit of the C57BL/6J Mouse Reference Genome: Major Implications for Neuroscience Research
GABA type-A (GABA-A) receptors containing the α2 subunit (GABRA2) are expressed in most brain regions and are critical in modulating inhibitory synaptic function. Genetic variation at the GABRA2 locus has been implicated in epilepsy, affective and psychiatric disorders, alcoholism and drug abuse. Gabra2 expression varies as a function of genotype and is modulated by sequence variants in several brain structures and populations, including F2 crosses originating from C57BL/6J (B6J) and the BXD recombinant inbred family derived from B6J and DBA/2J. Here we demonstrate a global reduction of GABRA2 brain protein and mRNA in the B6J strain relative to other inbred strains, and identify and validate the causal mutation in B6J. The mutation is a single base pair deletion located in an intron adjacent to a splice acceptor site that only occurs in the B6J reference genome. The deletion became fixed in B6J between 1976 and 1991 and is now pervasive in many engineered lines, BXD strains generated after 1991, the Collaborative Cross, and the majority of consomic lines. Repair of the deletion using CRISPR-Cas9-mediated gene editing on a B6J genetic background completely restored brain levels of GABRA2 protein and mRNA. Comparison of transcript expression in hippocampus, cortex, and striatum between B6J and repaired genotypes revealed alterations in GABA-A receptor subunit expression, especially in striatum. These results suggest that naturally occurring variation in GABRA2 levels between B6J and other substrains or inbred strains may also explain strain differences in anxiety-like or alcohol and drug response traits related to striatal function. Characterization of the B6J private mutation in the Gabra2 gene is of critical importance to molecular genetic studies in neurobiological research because this strain is widely used to generate genetically engineered mice and murine genetic populations, and is the most widely utilized strain for evaluation of anxiety-like, depression-like, pain, epilepsy, and drug response traits that may be partly modulated by GABRA2 function
Phasevarions Mediate Random Switching of Gene Expression in Pathogenic Neisseria
Many host-adapted bacterial pathogens contain DNA methyltransferases (mod genes) that are subject to phase-variable expression (high-frequency reversible ON/OFF switching of gene expression). In Haemophilus influenzae, the random switching of the modA gene controls expression of a phase-variable regulon of genes (a “phasevarion”), via differential methylation of the genome in the modA ON and OFF states. Phase-variable mod genes are also present in Neisseria meningitidis and Neisseria gonorrhoeae, suggesting that phasevarions may occur in these important human pathogens. Phylogenetic studies on phase-variable mod genes associated with type III restriction modification (R-M) systems revealed that these organisms have two distinct mod genes—modA and modB. There are also distinct alleles of modA (abundant: modA11, 12, 13; minor: modA4, 15, 18) and modB (modB1, 2). These alleles differ only in their DNA recognition domain. ModA11 was only found in N. meningitidis and modA13 only in N. gonorrhoeae. The recognition site for the modA13 methyltransferase in N. gonorrhoeae strain FA1090 was identified as 5′-AGAAA-3′. Mutant strains lacking the modA11, 12 or 13 genes were made in N. meningitidis and N. gonorrhoeae and their phenotype analyzed in comparison to a corresponding mod ON wild-type strain. Microarray analysis revealed that in all three modA alleles multiple genes were either upregulated or downregulated, some of which were virulence-associated. For example, in N. meningitidis MC58 (modA11), differentially expressed genes included those encoding the candidate vaccine antigens lactoferrin binding proteins A and B. Functional studies using N. gonorrhoeae FA1090 and the clinical isolate O1G1370 confirmed that modA13 ON and OFF strains have distinct phenotypes in antimicrobial resistance, in a primary human cervical epithelial cell model of infection, and in biofilm formation. This study, in conjunction with our previous work in H. influenzae, indicates that phasevarions may be a common strategy used by host-adapted bacterial pathogens to randomly switch between “differentiated” cell types
The Effects of Sex Offender Registration on Youth with Sexually Problematic Behaviors
The purpose of this proposed qualitative study is to determine the effects of sex offender registration on youth with sexually problematic behaviors and their families, using interviews with parents or guardians of youth on the sex offender registry who have received services from ABC Counseling in Normal, Illinois, to measure the effects. Participants will be invited to a semi-structured interview, which will include twelve questions asking them to rate perceived impact on their child\u27s registration on the sex offender registry on their child using Likert scale type questions and three open-ended questions examining perceived impact of their child\u27s registration on the sex offender registry on their family. Interviews will last approximately fifteen minutes or less and will be analyzed to identify major themes