Erzhi Gao
305 East Zhongshan Road
Nanjing, 210016, China
Nanjing, 210016, China
Last Updated: 09/26/2026
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Found 18 publications
Tubular glycogen nuclei in a patient with glycogen storage disease type Ia.
Journal: Kidney international
Published: June 11, 2024
A Prediction Model of Disease Progression in X-Linked Alport syndrome Based on Clinical Characteristics and Genetic Variants.
Journal: Kidney international reports
Published: May 26, 2024
Kidney Organoid Modeling of WT1 Mutations Reveals Key Regulatory Paths Underlying Podocyte Development.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: November 09, 2023
Genetic features and kidney morphological changes in women with X-linked Alport syndrome.
Journal: Journal of medical genetics
Published: February 15, 2023
Pathogenic Gene Spectrum and Clinical Implication in Chinese Patients with Lupus Nephritis.
Journal: Clinical journal of the American Society of Nephrology : CJASN
Published: November 02, 2022
Clinical Implications of a New DDX58 Pathogenic Variant That Causes Lupus Nephritis due to RIG-I Hyperactivation.
Journal: Journal of the American Society of Nephrology : JASN
Published: April 22, 2022
Establishment of the induced pluripotent stem cell line (NCKDi005-A) from a male patient with Alport syndrome carrying a homozygous frameshift mutation in the COL4A4 gene.
Journal: Stem cell research
Published: October 11, 2021
Generation of the induced pluripotent stem cell line (NCKDi004-A) from a 17-year-old patient with Alport syndrome carrying a homozygous mutation in COL4A3 gene.
Journal: Stem cell research
Published: August 26, 2021
Dissecting the genotype-phenotype correlation of COL4A5 gene mutation and its response to renin-angiotensin-aldosterone system blockers in Chinese male patients with Alport syndrome.
Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: August 25, 2021
Next-Generation Sequencing-Based Genetic Diagnostic Strategies of Inherited Kidney Diseases.
Journal: Kidney diseases (Basel, Switzerland)
Published: March 12, 2021
Generation of the induced pluripotent stem cell line (NCKDi002-A) from a 22-year-old patient with Focal Segmental Glomerular Sclerosis carrying a heterozygous mutation in WT1 gene.
Journal: Stem cell research
Published: February 26, 2021
Generation of induced pluripotent stem cell line (NCKDi001-A) from a 19-year-old patient with a novel COL4A5 gene mutation in Alport syndrome.
Journal: Stem cell research
Published: July 14, 2020
Last Updated: 09/26/2026