Ge Lv

Ministry Of Education Key Laboratory Of Child Development And Disorders
Chongqing, China

Last Updated: 09/26/2026

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Found 13 publications

Novel compound heterozygous MRTFA gene variants cause multiple dysfunctions of neutrophils and autoinflammation.

Novel compound heterozygous MRTFA gene variants cause multiple dysfunctions of neutrophils and autoinflammation.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: May 09, 2025

Correction to: Successful Immune Reconstitution in a Patient with a TYK2 Deficiency after Allogeneic Stem Cell Transplantation from Unrelated Donors.

Correction to: Successful Immune Reconstitution in a Patient with a TYK2 Deficiency after Allogeneic Stem Cell Transplantation from Unrelated Donors.

Journal: Journal of clinical immunology

Published: July 03, 2024

Successful Immune Reconstitution in a Patient with a TYK2 Deficiency after Allogeneic Stem Cell Transplantation from Unrelated Donors.

Successful Immune Reconstitution in a Patient with a TYK2 Deficiency after Allogeneic Stem Cell Transplantation from Unrelated Donors.

Journal: Journal of clinical immunology

Published: February 24, 2024

A novel homozygous Y140X mutation of ISG15 causes diverse type I interferonopathies in sibling patients with cutaneous lesions or recurrent parenchymal pneumonia.

A novel homozygous Y140X mutation of ISG15 causes diverse type I interferonopathies in sibling patients with cutaneous lesions or recurrent parenchymal pneumonia.

Journal: Clinical immunology (Orlando, Fla.)

Published: August 01, 2023

Correction to: De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE‑1 Element Insertion Resulting in Chronic Granulomatous Disease.

Correction to: De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE‑1 Element Insertion Resulting in Chronic Granulomatous Disease.

Journal: Journal of clinical immunology

Published: January 20, 2023

De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE-1 Element Insertion Resulting in Chronic Granulomatous Disease.

De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE-1 Element Insertion Resulting in Chronic Granulomatous Disease.

Journal: Journal of clinical immunology

Published: May 27, 2022

A Novel RAC2 Mutation Causing Combined Immunodeficiency.

A Novel RAC2 Mutation Causing Combined Immunodeficiency.

Journal: Journal of clinical immunology

Published: March 01, 2022

Combined Immunodeficiency Caused by a Novel De Novo Gain-of-Function RAC2 Mutation.

Combined Immunodeficiency Caused by a Novel De Novo Gain-of-Function RAC2 Mutation.

Journal: Journal of clinical immunology

Published: January 27, 2022

Novel mutations of TYK2 leading to divergent clinical phenotypes.

Novel mutations of TYK2 leading to divergent clinical phenotypes.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: May 17, 2021

Altered Functions of Neutrophils in Two Chinese Patients With Severe Congenital Neutropenia Type 4 Caused by G6PC3 Mutations.

Altered Functions of Neutrophils in Two Chinese Patients With Severe Congenital Neutropenia Type 4 Caused by G6PC3 Mutations.

Journal: Frontiers in immunology

Published: April 24, 2021

A Missense Mutation rs781536408 (c.2395G>A) of TYK2 Affects Splicing and Causes Skipping of Exon18 in vivo.

A Missense Mutation rs781536408 (c.2395G>A) of TYK2 Affects Splicing and Causes Skipping of Exon18 in vivo.

Journal: Frontiers in genetics

Published: March 12, 2021

CD8+ T-cell senescence and skewed lymphocyte subsets in young Dyskeratosis Congenita patients with PARN and DKC1 mutations.

CD8+ T-cell senescence and skewed lymphocyte subsets in young Dyskeratosis Congenita patients with PARN and DKC1 mutations.

Journal: Journal of clinical laboratory analysis

Published: February 21, 2020

Showing 1-12 of 13

Last Updated: 09/26/2026