Jinzhong Yuan

Changsha, China

Last Updated: 09/26/2026

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Found 8 publications

PKD1 Splice and PKD2 Nonsense Variants Identified in Two Chinese Families With Autosomal Dominant Polycystic Kidney Disease.

PKD1 Splice and PKD2 Nonsense Variants Identified in Two Chinese Families With Autosomal Dominant Polycystic Kidney Disease.

Journal: Nephrology (Carlton, Vic.)

Published: October 17, 2024

Identification of COL4A4 variants in Chinese patients with familial hematuria.

Identification of COL4A4 variants in Chinese patients with familial hematuria.

Journal: Frontiers in genetics

Published: October 08, 2022

A COL4A5 Missense Variant in a Han-Chinese Family with X-linked Alport Syndrome.

A COL4A5 Missense Variant in a Han-Chinese Family with X-linked Alport Syndrome.

Journal: Current molecular medicine

Published: April 09, 2019

A novel heterozygous COL4A4 missense mutation in a Chinese family with focal segmental glomerulosclerosis.

A novel heterozygous COL4A4 missense mutation in a Chinese family with focal segmental glomerulosclerosis.

Journal: Journal of cellular and molecular medicine

Published: March 09, 2016

A novel FN1 variant associated with familial hematuria: TBMN?

A novel FN1 variant associated with familial hematuria: TBMN?

Journal: Clinical biochemistry

Published: October 04, 2015

A novel COL4A5 mutation identified in a Chinese Han family using exome sequencing.

A novel COL4A5 mutation identified in a Chinese Han family using exome sequencing.

Journal: BioMed research international

Published: May 14, 2014

Feasibility of continuous extracorporeal normothermic liver perfusion using autologous blood: a study in pigs

Feasibility of continuous extracorporeal normothermic liver perfusion using autologous blood: a study in pigs

Journal: Nan fang yi ke da xue xue bao = Journal of Southern Medical University

Published: March 05, 2014

Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing.

Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing.

Journal: Molecular biology reports

Published: May 01, 2013

Showing 1-8 of 8

Last Updated: 09/26/2026