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1,624 results for “steroid”
Summary statistics from "Sex-Specific Causal Relations between Steroid Hormones and Obesity—A Mendelian Randomization Study"
<p>GWAMA summary statistics of four steroid hormone levels and one steroid hormone ratio using fixed-effect model.</p> <p>When using this data, please cite: Pott J, Horn K, Zeidler R, et al.. Sex-Specific Causal Relations between Steroid Hormones and Obesity - A Mendelian Randomization Study. <em>Metabolites</em> <strong>2021</strong>, <em>11</em>, 738. https://doi.org/10.3390/metabo11110738</p> <p>All txt files contain the following columns:</p> <ul> <li>markername</li> <li>chr</li> <li>bp_hg19 (base position according to hg19)</li> <li>ea (effect allele)</li> <li>oa (other allele)</li> <li>eaf (effect allele frequency)</li> <li>info (minimal info score across all used studies)</li> <li>nSamples (sample size per SNP)</li> <li>nStudies (number of studies)</li> <li>beta (effect estimate)</li> <li>se (standard error)</li> <li>p (p-value)</li> <li>I2 (SNP heterogeneity across studies)</li> <li>phenotype (phenotyp setting)</li> </ul>
Summary statistics from "Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease"
<p>GWAMA summary statistics of four steroid hormone levels using fixed-effect model and GWAS summary statistics of four other steroid hormones.</p> <p>When using this data, please cite: Pott J, Bae YJ, Horn K, et al.. Genetic Association Study of Eight Steroid Hormones and Implications for Sexual Dimorphism of Coronary Artery Disease. <em>J Clin Endocrinol Metab</em> <strong>2019</strong> Nov 1;104(11):5008-5023. doi: 10.1210/jc.2019-00757</p> <p>All txt files contain the following columns:</p> <ul> <li>markername</li> <li>chr</li> <li>bp_hg19 (base position according to hg19)</li> <li>effect_allele</li> <li>other_allele</li> <li>effect_allele_freq</li> <li>min_info (minimal info score across all used studies)</li> <li>n (sample size per SNP)</li> <li>beta (effect estimate)</li> <li>se (standard error)</li> <li>p (p-value)</li> <li>CochransQ (only in GWAMA; SNP heterogeneity across studies)</li> <li>pCochransQ (only in GWAMA; p-value of Cochrans Q value)</li> </ul>
Sperm quality parameters and sex steroid concentrations in male and female meagre (Argyrosomus regius) held under constant or cycling temperatures
<p>The dataset contains excel files with sperm quality parameters measured with Computer Assisted Sperm Analysis (CASA), plasma sex steroids (testosterone, 11-ketotestosterone, estradiol and 17a,20β-dihydroxy-4-pregnen-3-one) measured with enzyme-linked immunosorbent assays (ELISAs), oocyte diameters and egg fecundity and % fertilisation data in the meagre <em>Argyrosomus regius</em> held under either attenuated seasonal water temperature (16.4 to 19.6ºC) or relatively constant water temperature (19.4 ± 0.6ºC).</p>
Age, sex, length (mm), weight (g), and plasma sex steroid concentrations (ng/ml) of greater amberjack Seriola dumerili reared in sea cages during the process of sex differentiation
<p>The dataset contains an excel file with the age, sex, total length (mm), wet weight (g) and plasma concentrations (ng/ml) of the following sex steroids, measured with the use of liquid chromatography/tandem mass spectrometry (LC-MS/MS): adrenosterone (Ad), androstenedione (Δ4), 11-ketotestosterone (11ΚΤ), testosterone (Τ), estradiol (Ε2), progesterone (P4) and 17,20β-dihydroxy-4-pregnen-3-one (17,20βP).</p>
Hyperglycemia and steroid use increase the risk of rhino-orbito-cerebral mucormycosis regardless of COVID-19 hospitalization: Case-control study, India
<p><strong>Abstract</strong></p> <p><strong><em>BACKGROUND</em></strong></p> <p>In the context of the ongoing COVID-19 pandemic increased incidence of ROCM was noted in India, among those infected with COVID. We determined risk factors for rhino-orbito-cerebral mucormycosis (ROCM) post Coronavirus disease 2019 (COVID-19) among those never and ever hospitalized for COVID-19 separately through a multi-centric, hospital-based, unmatched case-control study across India.</p> <p><strong><em>METHODS</em></strong></p> <p>We defined cases and controls as those with and without post-COVID ROCM, respectively. We compared their socio-demographics, comorbidities, steroid use, glycaemic status, and practices. We calculated crude and adjusted odds ratio (AOR) with 95% confidence intervals (CI) through logistic regression. The covariates with p-value for crude OR of less 0·20 were considered for the regression model.</p> <p><strong><em>RESULTS</em></strong></p> <p>Among hospitalised, we recruited 267 cases and 256 controls and 116 cases and 231 controls among never hospitalised. Risk factors (AOR; 95% CI) for post-COVID ROCM among the hospitalised were age 45-59 years (2·1; 1·4 to 3·1), having diabetes mellitus (4·9; 3·4 to 7·1), elevated plasma glucose (6·4; 2·4 to 17·2), steroid use (3·2; 2 to 5·2) and frequent nasal washing (4·8; 1·4 to 17). Among those never hospitalised, age ≥ 60 years (6·6; 3·3 to 13·3), having diabetes mellitus (6·7; 3·8 to 11·6), elevated plasma glucose (13·7; 2·2 to 84), steroid use (9·8; 5·8 to 16·6), and cloth facemask use (2·6; 1·5 to 4·5) were associated with increased risk of post-COVID ROCM.</p> <p><strong><em>CONCLUSIONS</em></strong></p> <p>Hyperglycemia irrespective of having diabetes mellitus and steroid use was associated with increased risk of ROCM independent of COVID-19 hospitalisation. Rational steroid usage and glucose monitoring may reduce the risk of post-COVID.</p>
Salivary steroid collection in children under conditions replicating home sampling
<p>This is supplementary materials for the article "Salivary steroid collection in children under conditions replicating home sampling"</p>
Figure 4 in Differential gene expression pattern and plasma sex steroids during testicular development in Genyatremus luteus (Perciforme: Haemulidae) (Bloch, 1790)
Figure 4. Principal component analysis (PCA) used to classify the influence of lhr and er gene expression, plasma steroids (11-KT, 17- OHP and E2), ichthyological parameters and GSI on male G. luteus individuals. Legend: LHR = LH receptor; ER = estrogen receptor; KT = 11-ketotestosterone; E2 = 17β-estradiol; OHP = 17-α-hydroxyprogesterone; TW = total weight; TL = total length; GW = gonad weight; GSI = gonadosomatic index.
Figure 1 in Differential gene expression pattern and plasma sex steroids during testicular development in Genyatremus luteus (Perciforme: Haemulidae) (Bloch, 1790)
Figure 1. Photomicrographs of germ cell and testes development stages of Genyatremus luteus. Stages were determined as (A) Immature, (B) Maturing, (C) Mature. Abbreviations are as follows: SPG, spermatogonia; SPC, spermatocyte; SPZ, spermatozoa. All panels were at 60x magnification.
Figure 2 in Differential gene expression pattern and plasma sex steroids during testicular development in Genyatremus luteus (Perciforme: Haemulidae) (Bloch, 1790)
Figure 2. Steroid concentrations in the blood plasma of male Genyatremus luteus individuals during their reproductive cycle. (A) 11-ketotestosterone. (B) 17 α-hidroxy progesterone. (C) 17β-estradiol. Data are represented as mean ± SEM. abc: indicates statistically significant difference (p<0.05).
Figure 3 in Intragonadal evaluation of sexual steroid hormones during three reproductive events in two species of Peromyscus (Rodentia: Cricetidae)
Figure 3. Fluctuations of each intraovarian [SSH] in the ∆4 pathway throughout three reproductive events in two species of Peromyscus. Mean concentrations of sexual steroid hormones, [SSH], were obtained from estrous cycle, pregnancy and lactation in free-living, adult females of P. melanotis (A) and P. difficilis (B). Symbology as in Fig. 2. Note that scales differ; complete ANOVA information is available in Table S2.
Figure 1 in Intragonadal evaluation of sexual steroid hormones during three reproductive events in two species of Peromyscus (Rodentia: Cricetidae)
Figure 1. Intraovarian contents of selected ∆ 4 pathway's SSH in two Peromyscus species. Sexual steroid hormones (SSH: progesterone, P4; androstenedione, A; testosterone, T; estradiol, E2) were obtained from free-living, adult females of P. melanotis (A) and P. difficilis (B), during a complete estrous cycle (CEC: proestrus to diestrus), and after ovulation (vertical arrows) followed by fecundation in a successful estrous cycle (SEC: proestrus, estrus + early gestation 1 and late gestation 2 + overall lactation); note that proestrus and estrus data from CEC are duplicated in SEC). The oogenetic and anabolic/ catabolic phases of the ovarian cycle are also depicted (see Table 1).
Fig. 3 in Trends in ovarian development, plasma vitellogenin, and steroid hormones in female Malaclemys terrapin (Schoepff, 1793) from coastal Louisiana
Fig. 3. Concentrations of vitellogenin (A), testosterone (B), and estradiol (C) throughout sampling periods of female Diamondback Terrapins captured in Louisiana. Dashed lines within each box indicate the mean of the data, bold lines within each box indicate the median of the data, the upper and lower edges of the boxes represent the 75% and 25% quartiles, and bars represent the minimum and maximum values. Solid black circles represent outliers, and different letters indicate significant differences (P<0.05) between sampling periods. The mean and median overlap in some categories, so both lines may not be visible.
Fig. 2 in Trends in ovarian development, plasma vitellogenin, and steroid hormones in female Malaclemys terrapin (Schoepff, 1793) from coastal Louisiana
Fig. 2. Ovarian follicle diameter throughout sampling periods of female Diamondback Terrapins captured in Louisiana. Dashed lines within each box indicate the mean of the data, bold lines within each box indicate the median of the data, and the upper and lower edges of the boxes represent the 75% and 25% quartiles. T bars represent the minimum and maximum values. Solid black circles represent outliers. Note n = 4 for late nesting period, but only two samples were used in the analysis as the others lacked any detectable follicles. The mean and median overlap in some categories, so both lines may not be visible.
Fig. 1 in Trends in ovarian development, plasma vitellogenin, and steroid hormones in female Malaclemys terrapin (Schoepff, 1793) from coastal Louisiana
Fig. 1. Examples of various follicular size classes from different sampling periods of Diamondback Terrapins. (A) Class II and IV follicles from late May. (B) Class I follicles from August samples. (C–D). Class II and III follicles from October samples.
Fig. 2. Geometric mean ratio and 95 in Associations between Toxoplasma gondii infection and steroid hormone levels in spotted hyenas
Fig. 2. Geometric mean ratio and 95% CI estimates from separate sex stratified models of the relationship between T. gondii infection and plasma cortisol. The red dashed line represents the null, and estimates are based on percentile bootstrapping (2000 simulations).
Fig. 1. Geometric mean ratio and 95 in Associations between Toxoplasma gondii infection and steroid hormone levels in spotted hyenas
Fig. 1. Geometric mean ratio and 95% CI estimates from separate sex and age stratified models of the relationship between T. gondii infection and plasma testosterone. The red dashed line represents the null, and estimates are based on percentile bootstrapping (2000 simulations).
Efficacy, Tolerability and Safety of Early Introduction of Everolimus, Reduced Calcineurin Inhibitors and Early Steroid Elimination Compared to Standard CNI, Mycophenolate Mofetil and Steroid Regimen
ClinicalTrials.gov study NCT01544491. IPD Sharing: UNDECIDED. Countries: 13. Publications: 2.
Special Drug Use Surveillance of Vonoprazan for "Prevention of Recurrence of Gastric/Duodenal Ulcer in Patients Receiving Non-steroidal Anti-inflammatory Drugs: Long-term Use"
ClinicalTrials.gov study NCT03214198. IPD Sharing: YES. Countries: 1. Publications: 1.
Virtual Reality as a Substitute for Procedural Sedation During Epidural Steroid Injections
ClinicalTrials.gov study NCT04887285. IPD Sharing: YES. Countries: 1. Publications: 2.
Effect of Perimenstrual Ovarian Steroid Supplementation on Perimenstrual Suicidality
ClinicalTrials.gov study NCT03720847. IPD Sharing: YES. Countries: 1. Publications: 3.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.