Hypogonadism - OmicsDI

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biostudies-arrayexpress (251)
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Hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism (1)

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Instrument Platform

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Metabolite Name

Pyridoxamine (2)
Glycerophosphocholine (2)
3-hydroxybuteric acid (1)
Xanthosine-5-phosphate (1)
Thiamine-phosphate (1)
Succinyl-CoA-methylmalonyl-CoA (1)
SBP (1)
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OBP (1)
O8P-O1P (1)
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Methylnicotinamide (1)
Metabolite name (1)
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M289T243_pos (1)
M333T310_pos (1)
M569T333_pos (1)
M153T188_pos (1)
M783T190_pos (1)
M265T174_pos (1)
M233T281_pos (1)
M209T140_1_pos (1)
M318T163_1_pos (1)
M271T261_2_pos (1)

First Public Date

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2014 (7)
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2023 (5)
2020 (4)
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2024 (3)
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2019 (2)
2018 (2)
2015 (2)
2017 (1)
2016 (1)
2012 (1)

Study status

Recruiting (2)

Study type

Transcription profiling by array (136)
ChIP-seq (36)
RNA-seq of coding RNA (36)
Comparative genomic hybridization by array (8)
ATAC-seq (6)
Other (4)
RNA-seq of non coding RNA (4)
Methylation profiling by array (3)
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Animal - High-throughput sequencing (2)
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Human - High-throughput sequencing (1)
Cell line - High-throughput sequencing (1)
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Genotyping by array (1)
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RIP-seq (1)
MicroRNA profiling by array (1)
CUT&RUN (1)
RNA-seq of coding RNA from single cells (1)
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Release Date

2022 (132)
2021 (130)
2023 (114)
2020 (74)
2014 (73)
2025 (67)
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2024 (63)
2013 (59)
2015 (56)
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2011 (48)
2012 (45)
2010 (40)
2008 (24)
2009 (17)
2007 (12)
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2004 (2)
2003 (2)
2001 (1)
1993 (1)

Lab affiliation

Center for Stem Cell Biology and Tissue Engineering, Key Laboratory for Stem Cells and Tissue Engineering, Ministry of Education, Sun Yat-sen University, Guangzhou, Guangdong, China. (2)
Proteomics Center, Erasmus MC (2)
Department Of Pharmacy (1)
Genetics Unit, Department of Biomedical Sciences, Faculty of Medicine, Casanova 143, 08036 Barcelona, Spain (1)
Professor at the Section for Clinical Chemistry, Department of Translational Medicine, Lund University. Sweden (1)
Translational Proteomics Laboratory, Institut de recherches cliniques de Montréal (IRCM), Québec, Montréal, Canada. Departement of Biochemistry and Molecular Medicine, Université de Montréal, Québec, Montréal, Canada. (Laboratory Director) (1)
Translational Proteomics, IRCM, Canada (1)

Location

United States (1)
Australia (1)
United Kingdom (1)

Keyword

Neglected Diseases (1)
Orphan Diseases (1)
Rare Disease Research (1)
Registries (1)
Batten Disease (1)
Mucolipidosis IV (1)
Undiagnosed (1)
Uncommon Disease (1)
Hypersomnia (1)
Marinesco-Sjogren Syndrome (1)
4p-/Wolf-Hirschhorn Syndrome (1)
Wiedermann-Steiner Syndrome (1)
Hemophagocytic Lymphohistiocytosis (HLH) (1)
Behcet’s Disease (1)
Jansen metaphyseal chondrodysplasia (1)
Chronic recurrent multifocal osteomyelitis (CRMO) (1)
Hereditary Sensory and Autonomic Neuropathy (1)
Nephropathic infantile cystinosis (1)
Ocular cystinosis (1)
Spinal Bulbar Muscular Atrophy (SBMA) (1)
Mucolipidosis (1)
Mitochondrial aminoacyl-tRNA synthetases (Mt-aaRS Disorders) (1)
Shine Syndrome (1)
Intestinal Bromhidrosis Syndrome (1)
Autosomal recessive extra oral halitosis (1)
CACNA1H mutation (1)
Dimethylglycine dehydrogenase deficiency (1)
Testosterone (1)

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Seminal lipid depletion and gut microbiome–metabolome alterations in men with gonadotropin-treated idiopathic hypogonadotropic hypogonadism: an integrated multi-omics study

This study investigated seminal plasma lipid alterations and gut microbiome–metabolome changes in men with gonadotropin-treated idiopathic hypogonadotropic hypogonadism. Seminal plasma metabolomics, fecal metagenomic sequencing, and fecal metabolomics were performed in patients and healthy controls....

2026-07-20 | MTBLS15080 | MetaboLights

Effect of Xq28 deletion on hypergonadotropic hypogonadism

PRJNA662636 | ENA

Effect of Xq28 deletion on hypergonadotropic hypogonadism

PRJNA662637 | ENA

KLB mutations in congenital hypogonadotropic hypogonadism

To test if patients with congenital hypogonadotropic hypogonadism harbor mutations in FGF21 and KLB (encoding the co-receptor of FGF21)

EGAS00001002568 | EGA

The role of testosterone in spermatogenesis: lessons from proteome profiling of human spermatozoa in testosterone deficiency

Testosterone is essential to maintain qualitative spermatogenesis. Nonetheless, no studies have been yet performed in humans to analyze the testosterone-mediated expression of the sperm proteins and their importance in reproduction. Thus, this study aimed to identify sperm protein alterations in mal...

ORGANISM(S): Homo sapiens (Human)

2022-05-09 | PXD032270 | Pride