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81 results for “Steroid hormones”

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zenodo40/100

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>

opencc-by-4.0Nov 2021View details →
zenodo40/100

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>

opencc-by-4.0Nov 2021View details →
zenodo40/100

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.

opencc-by-4.0Mar 2024View details →
zenodo40/100

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).

opencc-by-4.0Mar 2024View details →
zenodo40/100

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&lt;0.05) between sampling periods. The mean and median overlap in some categories, so both lines may not be visible.

opencc-by-4.0Aug 2021View details →
zenodo40/100

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.

opencc-by-4.0Aug 2021View details →
zenodo40/100

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.

opencc-by-4.0Aug 2021View details →
zenodo40/100

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).

opencc-by-4.0Apr 2022View details →
zenodo40/100

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).

opencc-by-4.0Apr 2022View details →
ClinicalTrials.gov36/100

Does Concomitant Use of Combined Oral Hormonal Steroids Stop Bleeding in Women Using Etonogestrel Implants (Implanon/Nexplanon®)?: A Randomized Controlled Study

ClinicalTrials.gov study NCT01968135. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov36/100

Adrenocorticotropic Hormone (ACTH) for Frequently Relapsing and Steroid Dependent Nephrotic Syndrome

ClinicalTrials.gov study NCT02132195. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
dryad36/100

Steroid hormone profiles in cowbirds and redwings

Open the record for dataset details and reuse information.

publicMay 2025View details →
dryad36/100

Data from: Polybrominated diphenyl ether (DE-71) exposure skews phenotypic sex ratio, and alters steroid hormone levels and steroidogenic enzyme activities in juvenile Silurana tropicalis

Open the record for dataset details and reuse information.

publicJul 2019View details →
dryad32/100

Data from: Feather steroid hormone concentrations in relation to age, sex, and moulting time in a long distance migratory passerine

In birds, concentrations of testosterone (T) and corticosterone (Cort) are closely connected with many morphological, behavioural and other physiological traits, including reproduction, metabolism, immunity, and fitness. The direction of the effect of these hormones on above-mentioned traits, and the potential feedback between hormones are in general unclear; in addition, knowledge on how age and sex can affect T and Cort concentrations is still inconsistent. Our study used a novel method to analyse testosterone and corticosterone in feathers (Tf, Cortf) based on the pre-column chemical derivatization of hormones before LC-MS/MS analysis. Unlike previously used methods (RIA, EIA), our analytical procedure allows simultaneous analysis of both hormones from small amounts of feathers (4-25 mg) and thus overcomes the problem of insufficient detection limits. We applied this method to reveal associations between Tf and Cortf hormone concentrations and feather growth, age, and sex in feathers grown during the post-breeding (flanks) and pre-breeding (tails) periods in barn swallows (Hirundo rustica). There was neither a correlation between pre-breeding and post-breeding Tf, nor between pre-breeding and post-breeding Cortf. Tail Cortf concentrations were negatively associated with tail feather growth rates. Feather hormone concentrations were correlated in the pre-breeding period, negatively in males but positively in females. Both Cortf and Tf were higher in young birds compared to older ones, indicating either an age-related decrease in hormone concentrations within individuals, or the selective disappearance of individuals with high steroid concentrations. Males and females did not differ in Cortf, but Tf concentrations were higher in males than females, particularly during the pre-breeding period. In this study, we provide an effective method for analysing hormones in feathers in an ecological context, especially in situations when the total amount of feathers available for the analysis is limited.

opencc-zeroJul 2019View details →
ClinicalTrials.gov32/100

Neuropsychobiological Correlates of Sex-steroid Hormone Manipulation in Healthy Women: a Risk Model for Depression

ClinicalTrials.gov study NCT02661789. IPD Sharing: YES. Countries: 1. Publications: 2.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov32/100

Incretin Physiology Associated With Steroid Hormone Treatment

ClinicalTrials.gov study NCT00713440. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Study of Adrenocorticotropic Hormone on Children With Frequent Relapse or Steroid-dependent Nephrotic Syndrome: a Prospective, Multicenter, Randomized,Open-label Clinical Trial.

ClinicalTrials.gov study NCT06079788. IPD Sharing: NO. Countries: 1. Publications: 8.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Incremental Clomiphene Citrate Doses in Successive Cycles and FSH, LH and Steroid Hormone Levels

ClinicalTrials.gov study NCT04210765. IPD Sharing: NO. Countries: 1. Publications: 2.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Screening and Stimulation Testing for Residual Secretion of Adrenal Steroid Hormones in Autoimmune Addison's Disease

ClinicalTrials.gov study NCT03793114. IPD Sharing: NO. Countries: 3. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Heritability of Polycystic Ovary Syndrome: Role of Antimullerian Hormone, Steroids and Leptin

ClinicalTrials.gov study NCT03483792. IPD Sharing: Not stated. Countries: 1. Publications: 1.

restrictedIPD-UNDECIDEDFeb 2026View details →

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International Brain Laboratory public data

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OpenNeuro

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Last verified 2026-04-29Open record