# Editorial: What’s new in endocrinology? volume II

**Authors:** Jeff M. P. Holly, Marc R. Blackman, Sally Radovick, Hubert Vaudry

PMC · DOI: 10.3389/fendo.2025.1561375 · Frontiers in Endocrinology · 2025-02-17

## Full-text entities

- **Genes:** GGH (gamma-glutamyl hydrolase) [NCBI Gene 8836] {aka GATD10, GH}, PRKAA2 (protein kinase AMP-activated catalytic subunit alpha 2) [NCBI Gene 5563] {aka AMPK, AMPK2, AMPKa2, PRKAA}, SIRT1 (sirtuin 1) [NCBI Gene 23411] {aka SIR2, SIR2L1, SIR2alpha}, GH1 (growth hormone 1) [NCBI Gene 2688] {aka GH, GH-N, GHB5, GHN, IGHD1A, IGHD1B}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, MIR1323 (microRNA 1323) [NCBI Gene 100302255] {aka MIRN1323, hsa-mir-1323, mir-1323}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, KISS1 (KiSS-1 metastasis suppressor) [NCBI Gene 3814] {aka HH13, KiSS-1}, GPBAR1 (G protein-coupled bile acid receptor 1) [NCBI Gene 151306] {aka BG37, GPCR19, GPR131, M-BAR, TGR5}, CDKN1B (cyclin dependent kinase inhibitor 1B) [NCBI Gene 1027] {aka CDKN4, KIP1, MEN1B, MEN4, P27KIP1}, GHR (growth hormone receptor) [NCBI Gene 2690] {aka GHBP, GHIP}, LPAR2 (lysophosphatidic acid receptor 2) [NCBI Gene 9170] {aka EDG-4, EDG4, LPA-2, LPA2}, MEN1 (menin 1) [NCBI Gene 4221] {aka MEAI, SCG2}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, TXNIP (thioredoxin interacting protein) [NCBI Gene 10628] {aka ARRDC6, EST01027, HHCPA78, THIF, VDUP1}
- **Diseases:** T1DM (MESH:D003922), CS (MESH:D003480), muscle weakness (MESH:D018908), Laron Syndrome (MESH:D046150), Rickets (MESH:D012279), T2DM (MESH:D003924), obesity (MESH:D009765), IGF-I deficiency (MESH:C563867), fatigue (MESH:D005221), sarcopenia (MESH:D055948), Diabetes (MESH:D003920), MEN (MESH:D009377), endocrine disease (MESH:D004700), skeletal diseases (MESH:D004194), nutritional or hereditary disturbances in calcium and phosphate homeostasis (MESH:D009386), endocrinopathies (MESH:C567425), inflammation (MESH:D007249), hereditary diseases (MESH:D030342), muscle wasting (MESH:D009133), metabolic disease (MESH:D008659), tumours (MESH:D009369), impaired mineralisation of growing bones (MESH:D001847)
- **Chemicals:** lipid (MESH:D008055), fatty acids (MESH:D005227), BAs (MESH:D001647), dox (MESH:D004317), fat (MESH:D005223), amino acid (MESH:D000596), cortisol (MESH:D006854), Melatonin (MESH:D008550)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11874140/full.md

---
Source: https://tomesphere.com/paper/PMC11874140