Yu-mian L. Gan

P.R. China
Fuzhou, 350001, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 9 publications

Genetic and clinical insights into acute kidney injury in maturity-onset diabetes of the young caused by the ABCC8 c.2500C>T mutation: Potential risk factors associated with SGLT2 inhibitors.

Genetic and clinical insights into acute kidney injury in maturity-onset diabetes of the young caused by the ABCC8 c.2500C>T mutation: Potential risk factors associated with SGLT2 inhibitors.

Journal: Experimental and therapeutic medicine

Published: January 30, 2025

Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome.

Clinical phenotype and genetic function analysis of a rare family with hereditary leiomyomatosis and renal cell carcinoma complicated with Birt-Hogg-Dubé syndrome.

Journal: Journal of medical genetics

Published: April 12, 2023

Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant.

Genetic Analysis and Functional Study of a Pedigree With Bruck Syndrome Caused by PLOD2 Variant.

Journal: Frontiers in pediatrics

Published: February 17, 2022

Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription.

Function of PHEX mutations p.Glu145* and p.Trp749Arg in families with X-linked hypophosphatemic rickets by the negative regulation mechanism on FGF23 promoter transcription.

Journal: Cell death & disease

Published: November 30, 2021

A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.

A novel compound heterozygous variant linked to hematuria in a family with hereditary factor VII deficiency.

Journal: The journal of gene medicine

Published: May 06, 2021

Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.

Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: February 23, 2021

Differences in gut microbiota structure in patients with stages 4-5 chronic kidney disease.

Differences in gut microbiota structure in patients with stages 4-5 chronic kidney disease.

Journal: American journal of translational research

Published: October 28, 2020

Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis.

Genetic diagnosis history and osteoarticular phenotype of a non-transfusion secondary hemochromatosis.

Journal: World journal of clinical cases

Published: April 11, 2020

Evaluation to the effect of B2O3-La2O3-SrO-Na2O-Al2O3 bonding agent on Ti6Al4V-porcelain bonding.

Evaluation to the effect of B2O3-La2O3-SrO-Na2O-Al2O3 bonding agent on Ti6Al4V-porcelain bonding.

Journal: Journal of the mechanical behavior of biomedical materials

Published: April 24, 2016

Showing 1-9 of 9

Last Updated: 09/26/2026