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359 results for “food intake”

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ClinicalTrials.gov20/100

The Effects of Mindfulness Training on Eating Behaviors and Food Intake

ClinicalTrials.gov study NCT01616368. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov20/100

The Effects of Ad Libitum Pre-Meal Raisin Snack on Satiety and Food Intake in Children

ClinicalTrials.gov study NCT01712737. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov20/100

The Role of Peptide YY (PYY)Infusions in Inhibiting Food Intake.

ClinicalTrials.gov study NCT00259246. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov20/100

Nutritional Status, Food Intake and Fecal Microbiota of Brazilians Toddlers

ClinicalTrials.gov study NCT02950740. IPD Sharing: NO. Countries: 0. Publications: 0.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov20/100

Study of the Molecular Basis in the Pathophysiology of Food Intake and Growth in Children

ClinicalTrials.gov study NCT00830141. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov20/100

Effect of Soy Protein and Polydextrose on Food Intake in Young Chinese Adult Males

ClinicalTrials.gov study NCT02389114. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov20/100

Food Intake in Older Patients

ClinicalTrials.gov study NCT02490761. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
geo20/100

Fasting-induced miR-7a-5p in AgRP neurons regulates food intake

GEO Series GSE254021. Mus musculus. 7 samples. Type: Non-coding RNA profiling by high throughput sequencing.

openGEO-OpenJan 2025View details →
geo20/100

Targeted Apoptosis of the Angiotensin AT1R (Agtr1a)-Expressing Subtype of Agouti-Related Peptide Neurons in Adult Mice Increases Food Intake and Resting Metabolism, and Alters Blood Pressure Control

GEO Series GSE284096. Mus musculus. 24 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJun 2025View details →
geo16/100

Dnmt1/3a deletion in prefrontal cortical neurons reduces palatable food intake

GEO Series GSE175380. Mus musculus. 8 samples. Type: Methylation profiling by high throughput sequencing.

openGEO-OpenMay 2021View details →
geo16/100

Targeting Clic1 for the Treatment of Obesity: A Novel Therapeutic Strategy to Reduce Food Intake and Body Weight

GEO Series GSE229799. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenJul 2023View details →
geo16/100

Very low protein diets lead to reduced food intake and weight loss, linked to inhibition of hypothalamic mTOR signaling, in mice

GEO Series GSE158215. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenMar 2021View details →
zenodo16/100

Effect of Sourdough Breads Consumption on Postprandial Responses, Satiety and Food Intake at Subsequent Meal (SUPPRESS)

<div><strong>Brief Summary</strong></div> <div> <div>During this project the effect of different types of sourdough breads consumption on satiety, energy intake at subsequent meal and postprandial metabolic responses, will be investigated.</div> </div> <div><strong>Detailed Description</strong></div> <div> <div>A 3-phase randomised cross-over trial will be applied consisting of 3 intervention periods of 2 weeks, with a test day performed at the last day of each intervention period. During each intervention period, participants will consume a fixed amount of test bread, replacing their regular bread, and they will keep food and stool diaries preceding each Test-day. Faecal samples will be collected before each Test-day. On the Test-day, participants will perform a gastric emptying breath test. Furthermore, blood samples and appetite ratings will be collected at regular time points after consumption of the test bread for measurement of glucose, insulin, gut peptides, short-chain fatty acids (SCFA) and blood lipids. Food intake will be assessed by offering the subjects a standard lunch to be consumed ad-libitum.</div> <div>&nbsp;</div> <div> <div><strong>Intervention / Treatment&nbsp;</strong></div> <div> <ul> <li><span>Dietary Supplement</span>:&nbsp;<span>Wholemeal bread</span></li> <li><span>Dietary Supplement</span>:&nbsp;<span>Sourdough bread</span></li> <li><span>Dietary Supplement</span>:&nbsp;<span>Bread with sourdough</span></li> </ul> </div> </div> </div>

restrictedcc-by-4.0Sep 2024View details →
geo16/100

Insights into food intake response in anadromous Coilia nasus through stomach transcriptome analysis

GEO Series GSE138446. Coilia nasus. 12 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenOct 2020View details →
geo12/100

Differences in food intake of tumour-bearing cachectic mice are associated with hypothalamic serotonin signalling

GEO Series GSE57190. Mus musculus. 42 samples. Type: Expression profiling by array.

openGEO-OpenOct 2014View details →
geo12/100

Differences in food intake of tumour-bearing cachectic mice are associated with hypothalamic serotonin signalling [A286_GEO_LLM]

GEO Series GSE57188. Mus musculus. 22 samples. Type: Expression profiling by array.

openGEO-OpenOct 2014View details →
geo12/100

Differences in food intake of tumour-bearing cachectic mice are associated with hypothalamic serotonin signalling [A358_GEO_hypocells]

GEO Series GSE57189. Mus musculus. 20 samples. Type: Expression profiling by array.

openGEO-OpenOct 2014View details →
geo12/100

FoxO1 target Gpr17 activates AgRP neurons to regulate food intake.

GEO Series GSE45858. Mus musculus. 2 samples. Type: Expression profiling by array.

openGEO-OpenApr 2013View details →
zenodo12/100

Dataset related to the article-BDNF Val66Met polymorphism alters food intake and hypothalamic BDNF expression in mice

<p>This record contains raw data related to the article &quot;BDNF Val66Met polymorphism alters food intake and hypothalamic BDNF expression in mice&quot;</p> <p>Abstract</p> <p>Obesity, a rising public health burden, is a multifactorial disease with an increased risk for patients to develop several pathological conditions including type 2 diabetes mellitus, hypertension, and cardiovascular disease. Increasing evidence suggests a relationship between the human brain‐derived neurotrophic factor (BDNF) Val66Met single‐nucleotide polymorphism (SNP) and obesity, although the underlying mechanisms of this connection are still not completely understood. In the present study, we found that homozygous knock‐in BDNFMet/Met&nbsp;mice were overweight and hyperphagic compared to wildtype BDNFVal/Val&nbsp;mice. Increased food intake was associated with&nbsp;reduction of total BDNF and BDNF1, BDNF4 and BDNF6 transcripts in the hypothalamus of BDNFMet/Met&nbsp;mice. In&nbsp;contrast, in the white adipose tissue total BDNF and Glut4 expression levels were augmented, while sirtuin 1 and leptin receptor (Ob‐R) expression levels were reduced in BDNFMet/Met&nbsp;mice. Moreover, plasmatic leptin levels were decreased in BDNFMet/Met&nbsp;mice. However, BDNFVal/Val&nbsp;and BDNFMet/Met&nbsp;mice showed a similar response to the insulin tolerance test and glucose tolerance test. Altogether, these results suggest that BDNF Val66Met SNP strongly contributes to adipose tissue pathophysiology, resulting in reduced circulating leptin levels and hypothalamic expression of BDNF, which, in turn, promote increased food intake and overweight in BDNFMet/Met&nbsp;mice.</p>

restrictedJan 2021View details →

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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.

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OpenNeuro

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Last verified 2026-04-29Open record