16 research outputs found
Legislative Documents
Also, variously referred to as: House bills; House documents; House legislative documents; legislative documents; General Court documents
Additional file 2: of An integrated -omics analysis of the epigenetic landscape of gene expression in human blood cells
eCpG-transcript pairs, plus additional information for MESA. (TXT 44022 kb
Additional file 3: of An integrated -omics analysis of the epigenetic landscape of gene expression in human blood cells
UCSC track for eCpGs from GTP. (BED 2584 kb
Additional file 4: of An integrated -omics analysis of the epigenetic landscape of gene expression in human blood cells
UCSC track for eCpGs from MESA. (BED 8181 kb
<i>Fkbp5</i> DNA methylation decreases with age in mice.
<p>Isolated DNA samples from wild-type mice aged 1 (nβ=β3), 3.5 (nβ=β3), 4 (nβ=β6), 5 (nβ=β7), 6 (nβ=β6), and 12 (nβ=β3) months were subjected to bisulfite pyrosequencing. Multiple CpG sites in intron 5 were analyzed for <i>Fkbp5</i> methylation. Significant demethylation was found at CPG_3 (rβ=ββ0.3890, p<0.05), CPG_4 (rβ=ββ0.4004, p<0.05) and CpG_5 (rβ=ββ0.5044, p<0.01) as measured by linear regression analyses.</p
Blood composition and animal mass of wild-type versus FKBP5<sup>β/β</sup> mice do not differ.
<p>WBC: white blood cells, RBC: red blood cells, Lym: lymphocytes, Mono: monocytes, Gran: granulocytes, HGB: hemoglobin, PLT: platelets. Wild-type, nβ=β11; FKBP5<sup>β/β</sup>, nβ=β12. Values are listed as the mean Β± the standard error of the mean.</p><p>Blood composition and animal mass of wild-type versus FKBP5<sup>β/β</sup> mice do not differ.</p
FKBP51 does not affect longevity.
<p>No significant differences were found in the percent survival of wild-type (wt) and <i>FKBP5<sup>β/β</sup></i> mice, p>0.05. wt, nβ=β34 (18 male and 16 female); <i>FKBP5<sup>β/β</sup></i>, nβ=β32 (18 male and 14 female).</p
<i>FKBP5<sup>β/β</sup></i> mice display enhanced cognitive flexibility in the radial arm water maze.
<p>(A) No differences were found in acquisition learning between genotypes (p>0.05). (B) There was a main effect of genotype (p<0.05) during reversal training, indicating <i>FKBP5<sup>β/β</sup></i> mice made fewer errors across sessions. Data points represent a session of three trials. *p<0.05. wild-type (wt), nβ=β9; <i>FKBP5<sup>β/β</sup></i>, nβ=β10.</p
Deletion of <i>FKBP5</i> does not alter glucose metabolism.
<p><i>FKBP5<sup>β/β</sup></i> mice displayed normal glucose tolerance up to 120 minutes following glucose injection compared to wild-type (wt) mice, p>0.05. wt, nβ=β7; <i>FKBP5<sup>β/β</sup></i>, nβ=β10.</p
Ablation of <i>FKBP5</i> does not alter cytokine levels over time.
<p>Serum levels of interleukin-1Ξ² (A) and interleukin-5 (D) were decreased at 6 months (p<0.05 via t-test) but not across time (p>0.05 by two-way ANOVA). Levels of interleukin-2 (B), interleukin-4 (C), interleukin-10 (E), granulocyte-macrophage colony-stimulating factor (F), interferon gamma (G), or tumor necrosis factor alpha (H) did not differ between genotypes across lifespan, p>0.05. *p<0.05. wild-type (wt), nβ=β6 for each age; <i>FKBP5<sup>β/β</sup></i>, nβ=β7 at 7 and 10 months, nβ=β6 at 21 months.</p