Jingru Lu

16 Jiangsu Road
Qingdao, 266003, China

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 13 publications

Identification of Four Novel COL4A5 Variants and Detection of Splicing Abnormalities in Three Chinese X-Linked Alport Syndrome Families.

Identification of Four Novel COL4A5 Variants and Detection of Splicing Abnormalities in Three Chinese X-Linked Alport Syndrome Families.

Journal: Frontiers in genetics
Published: January 03, 2022

Body Mass Index and Risk of Diabetic Nephropathy: A Mendelian Randomization Study.

Body Mass Index and Risk of Diabetic Nephropathy: A Mendelian Randomization Study.

Journal: The Journal of clinical endocrinology and metabolism
Published: October 21, 2021

Clinical Acute Kidney Injury and Histologic Acute Tubular-Interstitial Injury and Their Prognosis in Diabetic Nephropathy.

Clinical Acute Kidney Injury and Histologic Acute Tubular-Interstitial Injury and Their Prognosis in Diabetic Nephropathy.

Journal: Nephron
Published: June 09, 2021

A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome with diabetes and the choices of the appropriate hypoglycemic drugs: a case report.

A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome with diabetes and the choices of the appropriate hypoglycemic drugs: a case report.

Journal: BMC medical genomics
Published: December 20, 2020

From Bartter's syndrome to renal tubular acidosis in a patient with Hashimoto's thyroiditis: A case report
.

From Bartter's syndrome to renal tubular acidosis in a patient with Hashimoto's thyroiditis: A case report
.

Journal: Clinical nephrology
Published: July 22, 2020

Influence of guideline adherence and parameter control on the clinical outcomes in patients with diabetic nephropathy.

Influence of guideline adherence and parameter control on the clinical outcomes in patients with diabetic nephropathy.

Journal: BMJ open diabetes research & care
Published: December 29, 2019

Five Novel Mutations in Chinese Children with Primary Distal Renal Tubular Acidosis.

Five Novel Mutations in Chinese Children with Primary Distal Renal Tubular Acidosis.

Journal: Genetic testing and molecular biomarkers
Published: September 27, 2018

Novel compound heterozygous ATP6V1B1 mutations in a Chinese child patient with primary distal renal tubular acidosis: a case report.

Novel compound heterozygous ATP6V1B1 mutations in a Chinese child patient with primary distal renal tubular acidosis: a case report.

Journal: BMC nephrology
Published: November 20, 2017

Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: a case report.

Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: a case report.

Journal: BMC nephrology
Published: October 17, 2017

A novel mutation in exon 9 of Cullin 3 gene contributes to aberrant splicing in pseudohypoaldosteronism type II.

A novel mutation in exon 9 of Cullin 3 gene contributes to aberrant splicing in pseudohypoaldosteronism type II.

Journal: FEBS open bio
Published: September 25, 2017

Genotype/Phenotype Analysis in 67 Chinese Patients with Gitelman's Syndrome.

Genotype/Phenotype Analysis in 67 Chinese Patients with Gitelman's Syndrome.

Journal: American journal of nephrology
Published: May 27, 2016

Two novel AGXT mutations identified in primary hyperoxaluria type-1 and distinct morphological and structural difference in kidney stones.

Two novel AGXT mutations identified in primary hyperoxaluria type-1 and distinct morphological and structural difference in kidney stones.

Journal: Scientific reports
Published: April 25, 2016
Showing 1-12 of 13

Last Updated: 09/26/2026