Jianmei Yang

Jinan, China

Last Updated: 09/26/2026

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Found 17 publications

Regulation of adipocyte metabolism: molecular mechanisms and pharmacological potential.

Regulation of adipocyte metabolism: molecular mechanisms and pharmacological potential.

Journal: Biochemical pharmacology

Published: May 24, 2026

Autocrine and paracrine regulation of pituitary endocrine cells.

Autocrine and paracrine regulation of pituitary endocrine cells.

Journal: Frontiers in endocrinology

Published: February 17, 2026

Clinical and genotypic analysis of 79 children with methylmalonic acidemia: a retrospective single-center study in China.

Clinical and genotypic analysis of 79 children with methylmalonic acidemia: a retrospective single-center study in China.

Journal: Frontiers in endocrinology

Published: February 07, 2026

Novel CACNA1S Mutation c.3491 A>C in Hypokalemic Periodic Paralysis: First Report with Functional Validation.

Novel CACNA1S Mutation c.3491 A>C in Hypokalemic Periodic Paralysis: First Report with Functional Validation.

Journal: Journal of molecular neuroscience : MN

Published: November 19, 2025

A novel compound heterozygous mutation in CYP11B2 (p.A153P and p.Q337*) associated with primary hypoaldosteronism.

A novel compound heterozygous mutation in CYP11B2 (p.A153P and p.Q337*) associated with primary hypoaldosteronism.

Journal: Frontiers in medicine

Published: November 05, 2025

Ghrelin-GHSR-LEAP2 system in the pathophysiology of type 2 diabetes.

Ghrelin-GHSR-LEAP2 system in the pathophysiology of type 2 diabetes.

Journal: iScience

Published: October 10, 2025

Early screening for respiratory and cardiac complications in pediatric mucopolysaccharidosis IVA: Insights from a case.

Early screening for respiratory and cardiac complications in pediatric mucopolysaccharidosis IVA: Insights from a case.

Journal: Intractable & rare diseases research

Published: September 01, 2025

Clinical and genetic analysis of X-linked nephrogenic diabetes insipidus caused by a novel AVPR2 mutation (NM_000054.6:exon3:c.245G>A (p.Cys82Tyr)) in a Chinese boy.

Clinical and genetic analysis of X-linked nephrogenic diabetes insipidus caused by a novel AVPR2 mutation (NM_000054.6:exon3:c.245G>A (p.Cys82Tyr)) in a Chinese boy.

Journal: Intractable & rare diseases research

Published: July 15, 2025

A high-fat diet suppresses growth hormone synthesis and secretion by influencing the Vit D receptor and Pit1.

A high-fat diet suppresses growth hormone synthesis and secretion by influencing the Vit D receptor and Pit1.

Journal: Endocrine

Published: February 07, 2025

Clinical and genetic analysis of ulnar-mammary syndrome caused by a novel TBX3 mutation in a Chinese boy.

Clinical and genetic analysis of ulnar-mammary syndrome caused by a novel TBX3 mutation in a Chinese boy.

Journal: Intractable & rare diseases research

Published: December 29, 2024

ORMDL3‑mediated bronchial epithelial pyroptosis leads to lung inflammation in obese mice with asthma.

ORMDL3‑mediated bronchial epithelial pyroptosis leads to lung inflammation in obese mice with asthma.

Journal: Molecular medicine reports

Published: March 20, 2023

Integrated fecal microbiota and metabolomics analysis of the orlistat intervention effect on polycystic ovary syndrome rats induced by letrozole combined with a high-fat diet.

Integrated fecal microbiota and metabolomics analysis of the orlistat intervention effect on polycystic ovary syndrome rats induced by letrozole combined with a high-fat diet.

Journal: Journal of ovarian research

Published: January 06, 2023

Showing 1-12 of 17

Last Updated: 09/26/2026