Jie-yuan Y. Jin

Shaoxing, China

Last Updated: 09/26/2026

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Found 61 publications

Ultrasound technologies' new clinical application for chronic liver diseases

Ultrasound technologies' new clinical application for chronic liver diseases

Journal: Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology

Published: June 29, 2026

Identification and growth features of developmental delay with macrocephaly caused by a novel TRIO variant affecting the second SH3 domain.

Identification and growth features of developmental delay with macrocephaly caused by a novel TRIO variant affecting the second SH3 domain.

Journal: BMC medical genomics

Published: April 25, 2026

A novel CACNA1E mutation (c.1256G > A) was identified in a Chinese patient with epilepsy and congenital heart disease.

A novel CACNA1E mutation (c.1256G > A) was identified in a Chinese patient with epilepsy and congenital heart disease.

Journal: Frontiers in medicine

Published: April 25, 2026

Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.

Dent Disease 1 Associated with a Rare Novel Renal Chloride Channel 5 Variant in a Chinese Family.

Journal: DNA and cell biology

Published: April 06, 2026

Case Report: A novel variant in fibrillin-2 identified in a congenital contractural arachnodactyly family with phenotypic heterogeneity.

Case Report: A novel variant in fibrillin-2 identified in a congenital contractural arachnodactyly family with phenotypic heterogeneity.

Journal: Frontiers in medicine

Published: March 12, 2026

Identification of novel tumor protein 63 variant associated with split-hand/foot malformation and tooth agenesis.

Identification of novel tumor protein 63 variant associated with split-hand/foot malformation and tooth agenesis.

Journal: Frontiers in medicine

Published: February 14, 2026

The key regulator of ferroptosis: HIF-1α and its complex roles and treatment strategies in related diseases.

The key regulator of ferroptosis: HIF-1α and its complex roles and treatment strategies in related diseases.

Journal: Life sciences

Published: January 26, 2026

Genetic predisposition to immune dysregulation and extracellular matrix remodeling in cardiac arrhythmia reveals potential mediation by SPP1+ macrophages.

Genetic predisposition to immune dysregulation and extracellular matrix remodeling in cardiac arrhythmia reveals potential mediation by SPP1+ macrophages.

Journal: Frontiers in cell and developmental biology

Published: April 14, 2025

Lipin3 deficiency aggravates cisplatin induced acute kidney injury via activating Sirt1-p21-Caspase 3-GSDME pyroptosis pathway.

Lipin3 deficiency aggravates cisplatin induced acute kidney injury via activating Sirt1-p21-Caspase 3-GSDME pyroptosis pathway.

Journal: International journal of biological sciences

Published: January 08, 2025

Rare SRRM2 mutation in neurodevelopmental disorders involving hyperphagia triggering severe obesity and other complication.

Rare SRRM2 mutation in neurodevelopmental disorders involving hyperphagia triggering severe obesity and other complication.

Journal: Frontiers in medicine

Published: December 23, 2024

RTN3 regulates collagen biosynthesis and profibrotic macrophage differentiation to promote pulmonary fibrosis via interacting with CRTH2.

RTN3 regulates collagen biosynthesis and profibrotic macrophage differentiation to promote pulmonary fibrosis via interacting with CRTH2.

Journal: Molecular medicine (Cambridge, Mass.)

Published: August 27, 2024

Case Report: Allelic and biallelic variants in coagulation factor XI cause factor XI deficiency.

Case Report: Allelic and biallelic variants in coagulation factor XI cause factor XI deficiency.

Journal: Frontiers in cardiovascular medicine

Published: July 09, 2024

Showing 1-12 of 61

Last Updated: 09/26/2026